The DOI matches its Crossref record; 244 of the 246 references it cites were found in a registry or an index; 1 of the 236 sources its claims cite were checked for support.
Biocompatible Materials for Continuous Glucose Monitoring Devices
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ADVERTISEMENT RETURN TO ISSUEPREVReviewNEXTBiocompatible Materials for Continuous Glucose Monitoring DevicesScott P. Nichols†, Ahyeon Koh†, Wesley L. Storm†, Jae Ho Shin‡, and Mark H. Schoenfisch*†View Author Information† Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States‡ Department of Chemistry, Kwangwoon University, Seoul, Korea*Address: Chemistry Department of Chemistry, University of North Carolina at Chapel Hill, CB#3290, Chapel Hill, North Carolina, 27599, USA. Tel: +1 (919) 843-8714. Fax: +1 (919) 962-2388. E-mail: [email protected]Cite this: Chem. Rev. 2013, 113, 4, 2528–2549Publication Date (Web):February 7, 2013Publication History Received19 September 2012Published online7 February 2013Published inissue 10 April 2013https://pubs.acs.org/doi/10.1021/cr300387jhttps://doi.org/10.1021/cr300387jreview-articleACS PublicationsCopyright © 2013 American Chemical SocietyRequest reuse permissionsArticle Views8353Altmetric-Citations268LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Anatomy,Carbohydrates,Inflammation,Peptides and proteins,Sensors Get e-Alerts
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Claims the paper makes
190 Not checked yet · 37 Own interpretation · 26 No basis given · 1 Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Accurate glucose measurements were carried out for >1 year by taking into account the difference in oxygen reduction at an electrode producing a glucose-modulated current and a reference electrode producing an oxygen-dependent current.31”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.2. Short-term and long-term electrochemical implantable glucose sensors (fully implantable versus percutaneous)
What the sources say
- Supportedcites [31] Gough D. A., 2010, Sci. Transl. Med. source
The Results (Sensing Principle) describe glucose oxidase and catalase, a glucose-modulated oxygen electrode, a reference oxygen electrode, and subtraction of their currents to obtain the glucose signal. The Results (Implantation and Accuracy; page numbers unavailable) report operation for 520 days in one pig and glucose measurements assessed for accuracy in the diabetic animals. The finding is in pigs, not humans. (LLM, conf=0.92)
plaindirect- Asserted: passes — The authors put it forward as true.
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- Supported
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In the paper
“Optical detection of glucose via near infrared (NIR) spectroscopy enables 90–95% of the light to pass through the human stratum corneum and epidermis into subcutaneous space with minimal tissue adsorption independent of skin pigmentation.19,40–41”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.3. Glucose detection based on optical approaches or combination technologies
What the sources say
plain- Asserted: passes — The authors put it forward as true.
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In the paper
“Continuous glucose monitoring (CGM) provides real-time information on trends (i.e., whether the glucose levels are increasing or decreasing), magnitude, duration, and frequency of glucose fluctuations during the day.5–6”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 1. Introduction
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
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The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Frequent calibration (e.g., 2 times per day) is required even after the stabilization period due to changes in sensor response.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.2. Short-term and long-term electrochemical implantable glucose sensors (fully implantable versus percutaneous)
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“The subcutaneous nature of the sensors likely minimized any micromotion effects associated with the foreign body response.32”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.2. Short-term and long-term electrochemical implantable glucose sensors (fully implantable versus percutaneous)
What the sources say
- Not checked yetcites [32] Helton K. L., 2011, J. Diabetes Sci. Technol. source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“Due to their ability to be miniaturized and give high selectivity and sensitivity governed by the specific biocatalytic reactions of an immobilized enzyme, electrochemical biosensors are among the most widely studied devices.4”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.1. Electrochemical continuous glucose monitoring biosensors
What the sources say
- Not checked yetcites [4] Wang J., 2008, Chem. Rev. source
plaindirect- Asserted: passes — The authors put it forward as true.
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None of the sources cited for this claim have been checked yet.
In the paper
“As described earlier, the use of mediators to shuttle electrons between the enzyme and the electrode can also minimize the impact of interfering species by lowering the working potential required to oxidize hydrogen peroxide.56,58,62”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.1. Interferences
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
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A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“A one-point calibration is thus considered more appropriate.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.4. In vivo calibration
plain- Asserted: passes — The authors put it forward as true.
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In the paper
“However, deactivation by endogenously produced hydrogen peroxide from oxidase reactions also contributes to the loss of activity.71”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.3. Stability and degradation of sensor components
What the sources say
- Not checked yetcites [71] Tse P. H. S., 1987, Biotechnol. Bioeng. source
plaindirect- Asserted: passes — The authors put it forward as true.
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A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Sensor performance issues due to changing oxygen levels are exacerbated due to the foreign body response that results in local consumption of oxygen and glucose by inflammatory cells at the vicinity of the sensor.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.2. Oxygen dependence
plaindirect- Asserted: passes — The authors put it forward as true.
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- It may state two separate claims as one. 93
- Probably not a substantial claim. 15
- The quote only partly states this claim. 1
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“However, the continuous applied current causes skin erythema and irritation.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.1. Electrochemical continuous glucose monitoring biosensors
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Photobleaching of the fluorophore and scattering in tissue are significant drawbacks.19,35–36”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.3. Glucose detection based on optical approaches or combination technologies
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Enzyme-immobilized amperometric biosensors have been implanted fully subcutaneously as CGM devices for extended periods (months to years) or percutaneously for <1 month.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.2. Short-term and long-term electrochemical implantable glucose sensors (fully implantable versus percutaneous)
plain- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Unfortunately, most mediators are toxic and competition between the mediator and oxygen still exists.19,22”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.1. Electrochemical continuous glucose monitoring biosensors
What the sources say
- Not checked yetcites [19] Vaddiraju S., 2010, J. Diabetes Sci. Technol. source
- Not checked yetcites [22]
plain- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
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In the paper
“Microdialysis avoids direct implantation of a sensor but the glucose measurement (i.e., recovery) remains erratic in vivo due to the foreign body response.19,24–25”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.1. Electrochemical continuous glucose monitoring biosensors
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
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None of the sources cited for this claim have been checked yet.
In the paper
“Additionally, sweating, often associated with hypoglycemia, affects the rate of extraction of glucose and therefore causes erroneous results when readings must be most accurate.29–30”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.1. Electrochemical continuous glucose monitoring biosensors
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Although enzyme-based electrochemical glucose biosensors are characterized with high selectivity and sensitivity due their enzymatic nature, the dynamic range of such sensors is limited by co-substrate (i.e., oxygen) availability.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.1. Electrochemical continuous glucose monitoring biosensors
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
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In the paper
“Almost all invasive sensing devices are characterized by infection risks, discomfort, and analytical response issues related to the foreign body response (FBR).29–30”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.3. Glucose detection based on optical approaches or combination technologies
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“Moreover, miniaturization of the instrumentation is not currently possible thus precluding personalized devices for continuous monitoring.19”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.3. Glucose detection based on optical approaches or combination technologies
What the sources say
- Not checked yetcites [19] Vaddiraju S., 2010, J. Diabetes Sci. Technol. source
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Iontophoretic electrochemical sensors are not invasive and experience less fouling because of the skin’s ability to filter large biomolecules.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.1. Electrochemical continuous glucose monitoring biosensors
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
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It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Though such sensors typically are characterized as having a shorter stabilization period (e.g., 2–4 h) compared to subcutaneous glucose sensors, the device penetrates through an opening in the dermis with concomitant infection risk.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.2. Short-term and long-term electrochemical implantable glucose sensors (fully implantable versus percutaneous)
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“While Raman spectroscopy gives narrow and distinct peaks (in contrast to NIR absorbance), long spectral acquisition and stabilization times are required.30”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.3. Glucose detection based on optical approaches or combination technologies
What the sources say
- Not checked yetcites [30] Vashist S. K., 2012, Anal. Chim. Acta source
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“While optical detection provides sensitive detection without damaging the host, skin pigmentation and epidermal thickness can negatively impact the analytical response among hosts.35–36”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.3. Glucose detection based on optical approaches or combination technologies
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“Additionally, the working electrode potential required to monitor hydrogen peroxide (i.e., ~+0.6 V vs. Ag/AgCl) will also oxidize electroactive endogenous species (e.g., ascorbic acid and acetaminophen) and create high current densities.19”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.1. Electrochemical continuous glucose monitoring biosensors
What the sources say
- Not checked yetcites [19] Vaddiraju S., 2010, J. Diabetes Sci. Technol. source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Electrode fouling (often called electrode passivation) is another cause of sensor instability, and occurs when diffusible small molecules come into contact with the surface of the electrode after penetration of the sensor membrane.74”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.3. Stability and degradation of sensor components
What the sources say
- Not checked yetcites [74] Wisniewski N., 2000, Colloid. Surface. B source
plaindirect- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“For example, Gilligan et al. found that long-term implanted glucose sensors in humans provided accurate sensor readings while immobile, but posture changes (i.e., standing and/or moving) led to erratic outputs.85”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.5. Physiological fluctuations and sensor performance
What the sources say
- Not checked yetcites [85] Gilligan B. C., 2004, Diabetes Technol. Ther. source
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“However, these sensors are not intended as warning or prognostic devices but rather as tools to inform users and physicians of trends in glucose fluctuations.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.4. Commercially available glucose sensors
plain- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Current numerical and clinical accuracy criteria for CGM includes linear regressions and correlation coefficients; mean (or median) absolute and relative absolute difference (MAD and MARD); Clarke Error Grid Analysis (Clarke EGA); and, International Standard Organization (ISO) criteria.76”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.4. In vivo calibration
What the sources say
- Not checked yetcites [76] Clarke W. L., 2007, J. Diabetes Sci. Technol. source
plain- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper’s conclusions may not depend on it.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Unfortunately, the changes in blood dielectric properties are not specific to glucose, resulting in poor accuracy.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.3. Glucose detection based on optical approaches or combination technologies
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Subcutaneous oxygen tension for humans ranges from 40 mm Hg (~5 kPa) to 130 mm Hg (~17kPa) with partial pressures affected by anesthetics and hypoxia at the implantation site.70”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.2. Oxygen dependence
What the sources say
- Not checked yetcites [70] Koschwanez H. E., 2007, Biomaterials source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Pressures as low as 2 kPa have been shown to diminish blood flow near the skin while only 7 kPa completely occluded blood circulation in diabetic patients whereas non-diabetics withstood pressures up to 22 kPa before total blood occlusion.88”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.5. Physiological fluctuations and sensor performance
What the sources say
- Not checked yetcites [88] Petrofsky J. S., 2011, J. Diabetes Sci. Technol. source
boosteddirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“Because CGM systems also provide information on glucose fluctuations, the continuous glucose-error grid (CG-EGA) has been introduced comprising of (1) a point-error grid analysis (P-EGA) that evaluates the sensor accuracy in terms of accurate blood glucose measurements; and, (2) a rate-error grid analysis (R-EGA) that assesses the prediction capability of the sensor.77”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.4. In vivo calibration
What the sources say
- Not checked yetcites [77] Kovatchev B. P., 2004, Diabetes Care source
plain- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Oxygen concentration in interstitial fluid is approximately ten times lower than the concentration of glucose in interstitial fluid resulting in an “oxygen deficit” state that is addressed by an outer diffusion-controlled membrane.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.2. Oxygen dependence
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Since the analytical performance of CGM sensors changes drastically upon implantation, methods for defining and assessing sensor accuracy are critical for clinical use.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.4. In vivo calibration
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
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It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Even with an accurate calibration, repeated calibration is required as the sensor sensitivity changes over time due to physiological fluctuations and the foreign body response to the sensor.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.4. In vivo calibration
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“Since 1999, CGM systems have been approved by the FDA but only percutaneously implanted electrochemical glucose sensors are currently for sale in the United States.53”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.4. Commercially available glucose sensors
What the sources say
- Not checked yetcites [53] Henning T., 2010
plain- Asserted: passes — The authors put it forward as true.
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- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“The electrochemical detection of hydrogen peroxide requires oxygen, a cofactor in the GOx enzymatic reaction.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 3. Issues in bioanalytical performance > 3.2. Oxygen dependence
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Recent advances have demonstrated that surface enhanced Raman spectroscopy (SERS) dramatically decreases acquisition times with concomitant improvements in both sensitivity and limit of detection.45–46”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.3. Glucose detection based on optical approaches or combination technologies
What the sources say
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Due to finite FDA-regulated sensor lifetimes (5–7 d), the biosensor must be replaced on a regular basis with significant financial burden on the individual patient.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 2. Continuous glucose monitoring technologies > 2.4. Commercially available glucose sensors
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“empirical data suggests that lag times range from 10–15 min in vivo, indicating the integral function of angiogenesis in early granulation tissue.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: unclear — It is unclear why the paper says it holds.
It may state two separate claims as one.
In the paper
“Nevertheless, this reversibility indicated that the process was passive and likely caused by biofouling on the sensor.100”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [100] Thomé-Duret V., 1996, Diabetes Metab.
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Sensor lag times for native tissue was estimated at ~20 min, but tripled when modeled with decreased diffusion due to a capsule.107”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [107] Sharkawy A. A., 1997, J. Biomed. Mater. Res. source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Indeed, macrophages serve three primary functions in the body: host defense, wound healing, and immune regulation.95”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [95] Mosser D. M., 2008, Nat. Rev. Immunol. source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“While glucose sensor performance recovered soon after injection (~15 min), the sensor response to glucose decreased after 1–2 days”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [106] Klueh U., 2010, Biomaterials source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“This process can result in a local pH’s dropping as low as 3.6 and disrupting biosensor performance as the activity of GOx is pH dependent.94”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [94] Zhao Q. H., 1993, J. Biomed. Mater. Res. source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The glucose sensitivity in vivo peaked at day 7, but then decreased for the duration of the study.108”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [108] Dungel P., 2008, J. Biomed. Mater. Res. Part A source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Sensor performance in mast cell-deficient mice was markedly better with reliable sensor function throughout the 28-day period.106”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [106] Klueh U., 2010, Biomaterials source
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“microdialysis probes consume significantly more glucose than electrochemical glucose sensors and therefore may underestimate the effects of biofouling in vivo.105”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [105] Lowry J. P., 1998, J. Neurochem. source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“response to glucose improved after rinsing, albeit not to pre-implantation levels.100”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [100] Thomé-Duret V., 1996, Diabetes Metab.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The collagen encapsulation will persist for the lifetime of the device, negatively impacting sensor performance with respect to sensitivity and response (e.g., lag times).”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The Tecoflex SG-85A membrane provided the biocompatibility often observed with polyurethane while also ensuring ideal sensor performance by limiting glucose diffusion.34”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.3. Polymer coatings
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“the physical properties of the implant (e.g., size) impact the FBR, and the large size of the stainless steel cage will influence the overall immune response to the materials.115”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.1. Models for assessing biocompatibility
What the sources say
- Not checked yetcites [115] Ward W. K., 2002, Biomaterials source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“At 20 months, thinner capsules were observed at the implant’s corners while the face of the implant closest to the skin had a thicker capsule than the opposite side.130”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.2. Effects of sensor geometry and physical stress
What the sources say
- Not checked yetcites [130] Li D. J., 1999, J. Biomed. Mater. Res. source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
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It may state two separate claims as one.
In the paper
“Histological analysis revealed delayed neovascularization and less matrix production in the diabetic rabbits”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.1. Models for assessing biocompatibility
What the sources say
- Not checked yetcites [128] Gerritsen H., 2000, J. Biomed. Mater. Res. source
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“While examination of the subcutaneous implant noted no blood vessels or collagen within the interior of the porous material, the percutaneous experiments revealed significant levels of collagen and vascularization, indicating a differential FBR dependent on the nature (i.e., purely subcutaneous vs. percutaneous) of the implant.121”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.2. Effects of sensor geometry and physical stress
What the sources say
- Not checked yetcites [121] Koschwanez H. E., 2008, J. Biomed. Mater. Res. Part A source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Histology samplings from human subcutaneous tissue showed a high concentration of adipose cells while rat tissue was characterized with larger amounts of collagen.126”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.1. Models for assessing biocompatibility
What the sources say
- Not checked yetcites [126] Wisniewski N., 2002, Am. J. Physiol.-Endocrinol. Metab source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“the increases to mass transfer were not attributed to any specific part of the FBR and could originate from collagen capsule thickness, blood vessel density, or other unanticipated factors.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [110] Jablecki M., 2000, Anal. Chem. source
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The optical tissue window enables tissue monitoring and correlation to the sensor performance.116–118”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.1. Models for assessing biocompatibility
What the sources say
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Moussy et al. implanted Nafion-coated CGM probes into canines that proved functional for up 10 days, but ultimately the membranes were deemed unstable with significant cracking and eventual failure.122”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.3. Polymer coatings
What the sources say
- Not checked yetcites [122] Moussy F., 1994, Int. J. Artif. Organs source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Taken together, these results necessitate careful consideration and caution when extrapolating results from animal models to humans.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.1. Models for assessing biocompatibility
What the sources say
- Not checked yetcites [126] Wisniewski N., 2002, Am. J. Physiol.-Endocrinol. Metab source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
In the paper
“While textured surfaces elicited a more favorable FBR, much of the response that did occur was attributed to differential sheer stress caused by the interaction between the textured surface of the device and the surrounding fatty tissue.132”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.2. Effects of sensor geometry and physical stress
What the sources say
- Not checked yetcites [132] Picha G. J., 1996, J. Biomed. Mater. Res. source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Anesthesia is not required to observe the tissue in real-time, an important consideration for glucose sensor performance correlation as anesthesia can alter microvasculature circulation.116”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.1. Models for assessing biocompatibility
What the sources say
- Not checked yetcites [116] Makale M. T., 2005, Am. J. Physiol.-Heart C source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Therefore, temporary signal reductions may actually be the result of local tissue damage caused by forces exerted on the sensor and may be solved by using more flexible materials.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.2. Effects of sensor geometry and physical stress
What the sources say
- Not checked yetcites [133] Klueh U., 2011, J. Diabetes Sci. Technol. source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“the results do identify the histological parameters of key interest when assessing the biocompatibility of materials for glucose sensors.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [111] Novak M. T., 2010, Anal. Bioanal. Chem. source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
In the paper
“The model was ultimately used to conclude that collagen capsule thickness, a common histological parameter, was the primary source of sensor lag time with little impact on sensor response attenuation.111”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [111] Novak M. T., 2010, Anal. Bioanal. Chem. source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“when the same materials were implanted percutaneously, histological differences were less apparent, with porous coatings giving a twofold increase in vascularization and a twofold increase, rather than decrease, in collagen content compared to bare sensors at 2 weeks.121”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.2. Effects of sensor geometry and physical stress
What the sources say
- Not checked yetcites [121] Koschwanez H. E., 2008, J. Biomed. Mater. Res. Part A source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Simulations of glucose concentration oscillations by Jablecki and Gough concluded that increases in mass transfer would increase lag and could potentially decrease the magnitude and differences when fluctuating between high and low glucose sensor signals.110”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 4. Consequences of the foreign body response on in vivo glucose sensor performance
What the sources say
- Not checked yetcites [110] Jablecki M., 2000, Anal. Chem. source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“PU allows for sufficient oxygen transport while limiting glucose diffusion to the sensor.136”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.3. Polymer coatings
What the sources say
- Not checked yetcites [136] Zhang Y., 1993, Anal. Chim. Acta source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The collagen encapsulation surrounding the PU-S-PEO substrates was ~45% thinner than those around the PU substrates though no differences in capillary density were observed.115”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.3. Polymer coatings
What the sources say
- Not checked yetcites [115] Ward W. K., 2002, Biomaterials source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“When coated onto non-functioning sensors and implanted subcutaneously, the PLLA foams exhibited the expected decrease in collagen capsule thickness and increased capillary density compared to bare non-functional sensors.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.4. Porosity
What the sources say
- Not checked yetcites [121] Koschwanez H. E., 2008, J. Biomed. Mater. Res. Part A source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“In vitro examination of silicone-modified PU was also found to significantly inhibit adhesion and FBGC formation, possibly explaining the in vivo benefits observed.140”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.3. Polymer coatings
What the sources say
- Not checked yetcites [140] Jones J. A., 2004, J. Biomater. Sci., Polym. Ed. source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Following subcutaneous implantation into humans, one of five biosensors functioned for ~6 months with ≥90% of all measured glucose concentrations falling within the A and B regions of the resulting Clarke Error Grid (i.e., clinically accurate and acceptable, respectively).”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.4. Porosity
What the sources say
- Not checked yetcites [85] Gilligan B. C., 2004, Diabetes Technol. Ther. source
plainSingle case- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The authors reported that this membrane allowed for the fabrication of functional glucose sensors in rats for up to 56 days with good sensitivity.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.3. Polymer coatings
What the sources say
- Not checked yetcites [141] Yu B., 2006, Biosens. Bioelectron. source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one. The quote only partly states this claim.
In the paper
“poly(2-hydroxyethylmethacrylate-co-methacrylic acid) implants with 30–40 μm pores were reported to increase vascularization and reduce capsule thickness when placed into the myocardium of rats over a 4-week period.160”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.4. Porosity
What the sources say
- Not checked yetcites [160] Madden L. R., 2010, Proc. Natl. Acad. Sci. U.S.A. source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Even with these benefits, the accuracy was not examined and it is unclear what impact the hydrogel coating would provide in this respect.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.3. Polymer coatings
What the sources say
- Not checked yetcites [147] Yu B. Z., 2008, Biosens. Bioelectron. source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“the tissue around the porous materials exhibited increased vascularization and decreased collagen capsule thickness.107”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.4. Porosity
What the sources say
- Not checked yetcites [107] Sharkawy A. A., 1997, J. Biomed. Mater. Res. source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The observed vascular density adjacent to the porous PVA samples was increased relative to controls, with the 60 μm pores exhibiting the greatest vascular density”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.4. Porosity
What the sources say
- Not checked yetcites [153] Sharkawy A. A., 1998, J. Biomed. Mater. Res. source
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“sensors lacking the ePTFE membrane (i.e., having only an underlying layer of unspecified composition) were functional for approximately 94 d with a best-case recalibration interval of 18 d.156”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.4. Porosity
What the sources say
- Not checked yetcites [156] Updike S. J., 2000, Diabetes Care source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Hydrogel-coated biosensors were still functional after 21 days whereas only 13.5% of the controls were still functional.147”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.3. Polymer coatings
What the sources say
- Not checked yetcites [147] Yu B. Z., 2008, Biosens. Bioelectron. source
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“However, only one of the nine sensors functioned this long. Indeed, seven of the nine sensors lost functionality in 17 d or less.141”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.3. Polymer coatings
What the sources say
- Not checked yetcites [141] Yu B., 2006, Biosens. Bioelectron. source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These results suggest that chemical modifications may improve tissue biocompatibility, but ultimately they have not led to major improvements on sensor performance in vivo.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.3. Polymer coatings
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“porous materials demonstrated a statistically significant increase in total macrophage biomarkers, yet a significant reduction (P < 0.05) in macrophage biomarkers associated with the pro-inflammatory macrophage phenotype.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.4. Porosity
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Control sensor membranes (epoxy-polyurethane) at 28 days were characterized with a fibrous capsule of ~500 Vm while the capsules around hydrogel-based sensors were roughly 30–60 Vm.15”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.3. Polymer coatings
What the sources say
- Not checked yetcites [15] Wang C., 2008, Biomacromolecules source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Updike and coworkers implanted biosensors with an affixed expanded PTFE (ePTFE) membrane having 1–10 μm pores in non-diabetic canines and found they were operable for greater than 160 d with a best-case recalibration interval of 20 d.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.4. Porosity
What the sources say
- Not checked yetcites [156] Updike S. J., 2000, Diabetes Care source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Conversely, tissue surrounding materials with either larger or smaller pores were avascular with thicker, denser collagen capsules.157”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.4. Porosity
What the sources say
- Not checked yetcites [157] Marshall A. J., 2004, ACS Polym. Prepr.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“While Pellethane (i.e., polyurethane) control substrates exhibited significant inflammatory cell adherence and collagen encapsulation, PEG-modified hydrogels were characterized by less cells indicating improved biocompatibility.144”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.3. Polymer coatings
What the sources say
- Not checked yetcites [144] Quinn C. A. P., 1997, Biomaterials source
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Norton et al. carefully examined the tissue response to VEGF-, DX-, and VEGF/DX-releasing hydrogels in a rat subcutaneous model,191 observing the expected increase in vascularization due to VEGF but no decrease in local inflammation from DX release.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [191] Norton L. W., 2007, J. Biomed. Mater. Res. Part A source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Overall, these studies suggest that decreased inflammation likely enhances long-term glucose biosensor functionality, though the challenges of achieving long-term DX release while avoiding systemic effects remains.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“initial experiments examining the simultaneous delivery of VEGF and DX from PLGA particles showed enhanced tissue integration, decreased inflammation, and increased vascularization in a rat model.189”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [189] Patil S. D., 2007, J. Controlled Release source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“DX-releasing glucose biosensors retained >50% of their original sensitivity 2 weeks after implantation, the sensitivity of control membranes dropped to 15–42% of their original levels.187”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [187] Ju Y. M., 2010, J. Biomed. Mater. Res. Part A source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Histology surrounding PLGA particle-containing hydrogels with combined DX and VEGF release revealed a 50% reduction in inflammation after the first week, similar to that of DX release alone, though inflammation at weeks 2–4 was still greater than DX alone.189”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [189] Patil S. D., 2007, J. Controlled Release source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Although more empirical evidence is needed, this strategy may prove helpful in reducing chronic inflammation from motion-damaged tissue.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.5. Material modulus
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“As chronic inflammation set in at ~3 weeks, the DX-releasing composites still exhibited reduced inflammation and fibrosis compared to control hydrogels, demonstrating the ability of local DX release to arrest fibrous encapsulation.188”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [188] Patil S. D., 2004, Diabetes Technol. Ther. source
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Vascular endothelial growth factor, or VEGF, is a cytokine released by macrophages and keratinocytes during wound reconstruction to promote angiogenesis.195–197”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Local delivery of DX from glucose biosensors was hypothesized to circumvent undesirable systemic side effects of DX.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
plainconditional- Asserted: fails — The authors may not put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The authors may not put it forward as true.
In the paper
“The functional lifetime of the sensors near the pump was 63 days whereas control (saline) sensors stopped working accurately at 34 days.203”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [203] Ward W. K., 2004, Diabetes Technol. Ther.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The acute inflammatory response was diminished at 3 and 8 d, but inflammation was significantly increased at 30 d compared to the shorter time points (i.e., 3 and 8 d), indicating that DX release simply delayed the immune response.186”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [186] Bhardwaj U., 2007, J. Diabetes Sci. Technol. source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“high concentrations of DX over 28 d (i.e., 0.17 mg/kg) led to a systemic reduction in cortisol levels while low concentrations (i.e., <0.10 mg/kg) did not cause such effects.181”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [181] Ward W. K., 2010, J. Biomed. Mater. Res. Part A source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Nitric oxide is an endogenously produced free radical synthesized from L-arginine by one of three isoforms of nitric oxide synthase (NOS): neuronal NOS (nNOS), endothelial NOS (eNOS), and inducible NOS (iNOS).211”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [211] Walford G., 2003, J. Thromb. Haemost. source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The difference in the outcome of these studies may be the result of differences in polymer composition, DX release kinetics, and or total DX payload, clearly indicating the importance of many biomaterial parameters on tissue biocompatibility.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Within 24 h biosensors in control mice suffered large reductions in sensitivity while mice receiving the daily DX injection at the sensor site experienced sustained sensitivity and functionality through 2 weeks, regardless of DX concentration.192”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [192] Klueh U., 2007, J. Diabetes Sci. Technol. source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“the polyimide material demonstrated a 94% reduction in applied strain to the surrounding tissue, while strain with the theoretical 6 MPa material was reduced by two orders of magnitude.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.5. Material modulus
What the sources say
- Not checked yetcites [169] Subbaroyan J., 2005, J. Neural Eng. source
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“These particles are simple to synthesize, enable slow DX release, and biodegrade over 2–3 months.183”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [183] Burgess D., 1994
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“The combined use of these factors was thus hypothesized to decrease inflammation and enhance vascularization.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
plainconditional- Asserted: fails — The authors may not put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The authors may not put it forward as true. It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Dexamethasone (DX) is a glucocorticoid that reduces inflammation.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“research to date is still in early stages with respect to NO storage and release, and combining the chemistry of NO release with enzymatic glucose sensing.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“New strategies for directing rather than avoiding the FBR by the active release of drugs and/or the body’s own signaling mediators of wound healing have created a unique path to alter the natural host response.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 6. Conclusions
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: fails — The paper may give no reason why it holds.
Probably not a substantial claim. The paper may give no reason why it holds.
In the paper
“Carreau et al. reported reduced leukocyte adhesion at elevated NO concentrations, suggesting NO could reduce localization of inflammatory cells at the device-tissue interface.216”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [216] Carreau A., 2011, Exp. Cell Res. source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The anti-inflammation correlated with the NO-release duration indicating that the observed benefits may only persist as long as the interface is releasing NO, in contrast to observations by Hetrick et al. where long-term reduction in inflammation were observed after cessation of NO release.103,238”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Collagen encapsulation was reduced at 3 and 6 weeks, and the greatest effect was observed for the largest payloads and longest release.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [240] Nichols S. P., 2012, Biomaterials source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Multiple reports indicate that NO serves as an angiogenic signaling model, up-regulating VEGF production and increasing blood vessel growth.213–214”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“In addition to reduced collagen encapsulation (~20–25% vs. controls) observed at 3 and 6 weeks, the NO mitigated inflammation (determined by reduced inflammatory cells near the implant) and appeared to enhance vascular density at 1 and 3 weeks.238”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
What the sources say
- Not checked yetcites [238] Hetrick E. M., 2007, Biomaterials source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper relies on this without support.
Traditional finger-prick glucose monitoring yields only instantaneous readings and cannot provide advance warning of hyperglycemic or hypoglycemic events.
“such monitoring only provides instantaneous blood glucose concentrations that are unable to warn of hyperglycemic or hypoglycemic events in advance.”
The paper relies on this without support.
Finger-prick sample collection is inconvenient and leads to poor patient compliance.
“Additionally, the sample collection (i.e., finger prick) method is inconvenient resulting in poor patient compliance.”
The authors state this as an assumption.
CGM systems estimate blood glucose by assuming interstitial fluid glucose is similar enough to blood glucose.
“CGM systems inherently estimate the blood glucose concentration by assuming the concentration of glucose in interstitial fluids will be similar enough.”
The paper relies on this without support.
The foreign body response is a major hurdle for continuous glucose monitoring performance.
“address the major hurdles related to the FBR.”
The paper relies on this without support.
The outer sensor membrane protects the enzyme.
“the outer sensor membrane that serves to protect the enzyme, tune response, and ultimately is responsible for the magnitude of the FBR”
The paper relies on this without support.
The outer sensor membrane tunes the sensor response.
“the outer sensor membrane that serves to protect the enzyme, tune response, and ultimately is responsible for the magnitude of the FBR”
The paper relies on this without support.
The outer sensor membrane determines the magnitude of the foreign body response.
“the outer sensor membrane that serves to protect the enzyme, tune response, and ultimately is responsible for the magnitude of the FBR”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The latter, generally requires 2-3 weeks stabilization period after surgery and are larger than the subcutaneous counterparts 88.”
From Glucose biosensors in clinical practice: principles, limits and perspectives of currently used devices (2022) · cites this paper as [88]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“This protocol allows transferring state information in small blocks of data at regular intervals, where the processor operates in a low power mode.107”
From Wearables in Medicine (2018) · cites this paper as [107]
Experimental — accuracy not yet measuredIn the citing paper
“At the macro level (>100 μm in size), it is generally held that thicker materials produce a proportionally higher magnitude of foreign body responses and fibrosis3, 21.”
From Size- and shape-dependent foreign body immune response to materials implanted in rodents and non-human primates (2015) · cites this paper as [3]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Rated minor: it would not touch a result — a value no result rests on, a p-value that stays on the same side of the significance level, or a conflict that is clerical, resolved elsewhere in the paper, or outside its own findings.
In the paper
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
“Furthermore, studies evaluating the benefits of VEGF-, DX-, or VEGF/DX-release on the analytical performance of glucose biosensors have not been evaluated.”
§ Biocompatible Materials for Continuous Glucose Monitoring Devices > 5. Mitigating the foreign body response to improve analytical performance of in vivo glucose sensors > 5.6. Active release materials
“DX-releasing glucose biosensors retained >50% of their original sensitivity 2 weeks after implantation, the sensitivity of control membranes dropped to 15–42% of their original levels.187”
Citations
Cites
Exploring the full spectrum of macrophage activation
Mosser, D. M., & Edwards, J. P. (2008) · Nature Reviews Immunology · doi:10.1038/nri2448 · Cited by 9,144
Hydrogels for Tissue Engineering
Lee, K. Y., & Mooney, D. J. (2001) · Chemical Reviews · doi:10.1021/cr000108x · Cited by 5,295
Foreign body reaction to biomaterials
Anderson, J. M., Rodriguez, A., & Chang, D. T. (2008) · Seminars in Immunology · doi:10.1016/j.smim.2007.11.004 · Cited by 5,138
Electrospinning: A Fascinating Method for the Preparation of Ultrathin Fibers
Greiner, A., & Wendorff, J. H. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200604646 · Cited by 4,260
ELECTRODE SYSTEMS FOR CONTINUOUS MONITORING IN CARDIOVASCULAR SURGERY
Clark, L. C., & Lyons, C. (1962) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1962.tb13623.x · Cited by 3,945
Vascular Endothelial Growth Factor: Basic Science and Clinical Progress
Ferrara, N. (2004) · Endocrine Reviews · doi:10.1210/er.2003-0027 · Cited by 3,788
Regulation of Wound Healing by Growth Factors and Cytokines
WERNER, S., & GROSE, R. (2003) · Physiological Reviews · doi:10.1152/physrev.2003.83.3.835 · Cited by 3,629
Electrochemical Glucose Biosensors
Wang, J. (2008) · Chemical Reviews · doi:10.1021/cr068123a · Cited by 3,498
Antiinflammatory Action of Glucocorticoids — New Mechanisms for Old Drugs
Rhen, T., & Cidlowski, J. A. (2005) · New England Journal of Medicine · doi:10.1056/nejmra050541 · Cited by 3,149
On the mechanisms of biocompatibility
Williams, D. F. (2008) · Biomaterials · doi:10.1016/j.biomaterials.2008.04.023 · Cited by 2,772
Coutinho, A. E., & Chapman, K. E. (2011) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2010.04.005 · Cited by 1,815
Encyclopedia of pharmaceutical technology
(2003) · Choice Reviews Online · doi:10.5860/choice.40-6157 · Cited by 1,744
Myotubes differentiate optimally on substrates with tissue-like stiffness
Engler, A. J., Griffin, M. A., Sen, S., Bönnemann, C. G., Sweeney, H. L., & Discher, D. E. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200405004 · Cited by 1,743
Electrochemical Glucose Sensors and Their Applications in Diabetes Management
Heller, A., & Feldman, B. (2008) · Chemical Reviews · doi:10.1021/cr068069y · Cited by 1,707
Mediation of biomaterial-cell interactions by adsorbed proteins: a review
Wilson, C. J., Clegg, R. E., Leavesley, D. I., & Pearcy, M. J. (2005) · Tissue Engineering · doi:10.1089/ten.2005.11.1 · Cited by 1,696
Biological Responses to Materials
Anderson, J. M. (2001) · Annual Review of Materials Research · doi:10.1146/annurev.matsci.31.1.81 · Cited by 1,465
Electrospun nanofibers: solving global issues
Ramakrishna, S., Fujihara, K., Teo, W. E., Yong, T., Ma, Z., & Ramaseshan, R. (2006) · Materials Today · doi:10.1016/s1369-7021(06)71389-x · Cited by 1,420
Updike, S. J., & Hicks, G. P. (1967) · Nature · doi:10.1038/214986a0 · Cited by 1,379
Nitric oxide donors: chemical activities and biological applications
Wang, P. G., Xian, M., Tang, X., Wu, X., Wen, Z., Cai, T., & Janczuk, A. J. (2002) · Chemical Reviews · doi:10.1021/cr000040l · Cited by 1,337
Nitric Oxide Synthases: Properties and Catalytic Mechanism
Griffith, O. W., & Stuehr, D. J. (1995) · Annual Review of Physiology · doi:10.1146/annurev.ph.57.030195.003423 · Cited by 1,311
Reducing implant-related infections: active release strategies
Hetrick, E. M., & Schoenfisch, M. H. (2006) · Chemical Society Reviews · doi:10.1039/b515219b · Cited by 1,201
Self-citationElectrochemical non-enzymatic glucose sensors
Park, S., Boo, H., & Chung, T. D. (2005) · Analytica Chimica Acta · doi:10.1016/j.aca.2005.05.080 · Cited by 1,164
Preparation of bioactive Ti and its alloys via simple chemical surface treatment
Kim, H. M., Miyaji, F., Kokubo, T., & Nakamura, T. (1996) · Journal of Biomedical Materials Research · doi:10.1002/(sici)1097-4636(199611)32:3 · Cited by 1,009
Nitric oxide release: Part II. Therapeutic applications
Carpenter, A. W., & Schoenfisch, M. H. (2012) · Chemical Society Reviews · doi:10.1039/c2cs15273h · Cited by 964
Self-citationHome blood glucose biosensors: a commercial perspective
Newman, J. D., & Turner, A. P. F. (2005) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2004.11.012 · Cited by 931
Brown, L. F., Yeo, K. T., Berse, B., Yeo, T. K., Senger, D. R., Dvorak, H. F., & van de Water, L. (1992) · The Journal of experimental medicine · doi:10.1084/jem.176.5.1375 · Cited by 878
Glucose Biosensors: 40 Years of Advances and Challenges
Wang, J. (2001) · Electroanalysis · doi:10.1002/1521-4109(200108)13:12 · Cited by 765
Regulation of Vascular Endothelial Growth Factor Expression in Cultured Keratinocytes.
Frank, S., Hübner, G., Breier, G., Longaker, M. T., Greenhalgh, D. G., & Werner, S. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.21.12607 · Cited by 764
Proangiogenic scaffolds as functional templates for cardiac tissue engineering
Madden, L. R., Mortisen, D. J., Sussman, E. M., Dupras, S. K., Fugate, J. A., Cuy, J. L., Hauch, K. D., Laflamme, M. A., Murry, C. E., & Ratner, B. D. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006442107 · Cited by 662
Biosensors for real-time in vivo measurements
Wilson, G. S., & Gifford, R. (2005) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2004.12.003 · Cited by 660
Toward a Glucose Biosensor Based on Surface-Enhanced Raman Scattering
Shafer-Peltier, K. E., Haynes, C. L., Glucksberg, M. R., & Van Duyne, R. P. (2003) · Journal of the American Chemical Society · doi:10.1021/ja028255v · Cited by 653
The molecular biology of chronic wounds and delayed healing in diabetes
Blakytny, R., & Jude, E. (2006) · Diabetic Medicine · doi:10.1111/j.1464-5491.2006.01773.x · Cited by 632
Vascular permeability, vascular hyperpermeability and angiogenesis
Nagy, J. A., Benjamin, L. E., Zeng, H., Dvořàk, A. M., & Dvorak, H. F. (2008) · Angiogenesis · doi:10.1007/s10456-008-9099-z · Cited by 629
Fluorescence-based glucose sensors
Pickup, J. C., Hussain, F., Evans, N. D., Rolinski, O. J., & Birch, D. J. S. (2005) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2004.10.002 · Cited by 616
An enzyme electrode for the amperometric determination of glucose
Guilbault, G. G., & Lubrano, G. J. (1973) · Analytica Chimica Acta · doi:10.1016/s0003-2670(01)82476-4 · Cited by 586
Glucose sensors: a review of current and emerging technology
Oliver, N. S., Toumazou, C., Cass, A. E. G., & Johnston, D. G. (2009) · Diabetic Medicine · doi:10.1111/j.1464-5491.2008.02642.x · Cited by 584
Non-invasive glucose monitoring technology in diabetes management: A review
Vashist, S. K. (2012) · Analytica Chimica Acta · doi:10.1016/j.aca.2012.03.043 · Cited by 575
Degani, Y., & Heller, A. (1987) · The Journal of Physical Chemistry · doi:10.1021/j100290a001 · Cited by 574
Methods for reducing biosensor membrane biofouling
Wisniewski, N., & Reichert, M. (2000) · Colloids and Surfaces B: Biointerfaces · doi:10.1016/s0927-7765(99)00148-4 · Cited by 543
Neovascularization of synthetic membranes directed by membrane microarchitecture
Brauker, J. H., Carr‐Brendel, V. E., Martinson, L. A., Crudele, J., Johnston, W. D., & Johnson, R. C. (1995) · Journal of Biomedical Materials Research · doi:10.1002/jbm.820291208 · Cited by 517
The Chemistry of S-Nitrosothiols
Williams, D. L. H. (1999) · Accounts of Chemical Research · doi:10.1021/ar9800439 · Cited by 499
Nitric oxide release: Part I. Macromolecular scaffolds
Riccio, D. A., & Schoenfisch, M. H. (2012) · Chemical Society Reviews · doi:10.1039/c2cs15272j · Cited by 475
Self-citationA review of the immobilization of enzymes in electropolymerized films
Barlett, P. N., & Cooper, J. M. (1993) · Journal of Electroanalytical Chemistry · doi:10.1016/0022-0728(93)80001-x · Cited by 472
Hrabie, J. A., & Keefer, L. K. (2002) · Chemical Reviews · doi:10.1021/cr000028t · Cited by 466
Enzyme-Based Biosensors for in Vivo Measurements
Wilson, G. S., & Hu, Y. (2000) · Chemical Reviews · doi:10.1021/cr990003y · Cited by 434
Handbook of non-invasive methods and the skin
Guy, R. H. (1996) · Journal of Controlled Release · doi:10.1016/0168-3659(96)01365-x · Cited by 414
Cellular and Molecular Dynamics in the Foreign Body Reaction
Luttikhuizen, D. T., Harmsen, M. C., & Luyn, M. J. A. V. (2006) · Tissue Engineering · doi:10.1089/ten.2006.12.1955 · Cited by 396
A Tale of Two Compartments: Interstitial Versus Blood Glucose Monitoring
Cengiz, E., & Tamborlane, W. V. (2009) · Diabetes Technology & Therapeutics · doi:10.1089/dia.2009.0002 · Cited by 390
Tierney, M. J., Tamada, J. A., Potts, R. O., Jovanovic, L., & Garg, S. (2001) · Biosensors and Bioelectronics · doi:10.1016/s0956-5663(01)00189-0 · Cited by 390
Nitric oxide and wound repair: role of cytokines?
Schwentker, A., Vodovotz, Y., Weller, R., & Billiar, T. R. (2002) · Nitric Oxide · doi:10.1016/s1089-8603(02)00002-2 · Cited by 386
Yonzon, C. R., Haynes, C. L., Zhang, X., Walsh, & Van Duyne, R. P. (2004) · Analytical Chemistry · doi:10.1021/ac035134k · Cited by 376
Photonic Crystal Glucose-Sensing Material for Noninvasive Monitoring of Glucose in Tear Fluid
Alexeev, V. L., Das, S., Finegold, D. N., & Asher, S. A. (2004) · Clinical Chemistry · doi:10.1373/clinchem.2004.039701 · Cited by 370
Subbaroyan, J., Martin, D. C., & Kipke, D. R. (2005) · Journal of Neural Engineering · doi:10.1088/1741-2560/2/4/006 · Cited by 368
Nitric Oxide: A Unique Endogenous Signaling Molecule in Vascular Biology (Nobel Lecture)
Ignarro, L. J. (1999) · Angewandte Chemie International Edition · doi:10.1002/(sici)1521-3773(19990712)38:13/14 · Cited by 367
Jones, J. A., Chang, D. T., Meyerson, H., Colton, E., Kwon, I. K., Matsuda, T., & Anderson, J. M. (2007) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.31221 · Cited by 352
A numerical‐experimental method to characterize the non‐linear mechanical behaviour of human skin
Hendriks, F. M., Brokken, D., Van Eemeren, J. T. W. M., Oomens, C. W. J., Baaijens, F. P. T., & Horsten, J. B. A. M. (2003) · Skin Research and Technology · doi:10.1034/j.1600-0846.2003.00019.x · Cited by 347
Shoji, E., & Freund, M. S. (2001) · Journal of the American Chemical Society · doi:10.1021/ja005906j · Cited by 344
Jhon, M. S., & Andrade, J. D. (1973) · Journal of Biomedical Materials Research · doi:10.1002/jbm.820070604 · Cited by 326
WEARABLE ARTIFICIAL ENDOCRINE PANCREAS WITH NEEDLE-TYPE GLUCOSE SENSOR
Shichiri, M., Yamasaki, Y., Kawamori, R., Hakui, N., & Abe, H. (1982) · The Lancet · doi:10.1016/s0140-6736(82)92788-x · Cited by 323
Zhao, Q., Topham, N., Anderson, J. M., Hiltner, A., Lodoen, G., & Payet, C. R. (1991) · Journal of Biomedical Materials Research · doi:10.1002/jbm.820250205 · Cited by 318
Evaluating the Accuracy of Continuous Glucose-Monitoring Sensors
Kovatchev, B. P., Gonder-Frederick, L. A., Cox, D. J., & Clarke, W. L. (2004) · Diabetes Care · doi:10.2337/diacare.27.8.1922 · Cited by 312
Long-term in vivo glucose monitoring using fluorescent hydrogel fibers
Heo, Y. J., Shibata, H., Okitsu, T., Kawanishi, T., & Takeuchi, S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1104954108 · Cited by 311
Design and in vitro studies of a needle-type glucose sensor for subcutaneous monitoring
Bindra, D. S., Zhang, Y., Wilson, G. S., Sternberg, R., Thevenot, D. R., Moatti, D., & Reach, G. (1991) · Analytical Chemistry · doi:10.1021/ac00017a008 · Cited by 309
Nitric Oxide in Vascular Biology
Walford, G., & Loscalzo, J. (2003) · Journal of Thrombosis and Haemostasis · doi:10.1046/j.1538-7836.2003.00345.x · Cited by 302
Noninvasive Blood Glucose Monitoring With Optical Coherence Tomography
Larin, K. V., Eledrisi, M. S., Motamedi, M., & Esenaliev, R. O. (2002) · Diabetes Care · doi:10.2337/diacare.25.12.2263 · Cited by 300
Injectable hydrogel microbeads for fluorescence-based in vivo continuous glucose monitoring
Shibata, H., Heo, Y. J., Okitsu, T., Matsunaga, Y. T., Kawanishi, T., & Takeuchi, S. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006911107 · Cited by 293
Technologies for Continuous Glucose Monitoring: Current Problems and Future Promises
Vaddiraju, S., Burgess, D. J., Tomazos, I., Jain, F. C., & Papadimitrakopoulos, F. (2010) · Journal of Diabetes Science and Technology · doi:10.1177/193229681000400632 · Cited by 285
Minireview: Latest Perspectives on Antiinflammatory Actions of Glucocorticoids
De Bosscher, K., & Haegeman, G. (2009) · Molecular Endocrinology · doi:10.1210/me.2008-0283 · Cited by 284
Gibney, M. A., Arce, C. H., Byron, K. J., & Hirsch, L. J. (2010) · Current Medical Research and Opinion · doi:10.1185/03007995.2010.481203 · Cited by 283
Tura, A., Maran, A., & Pacini, G. (2007) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2006.10.027 · Cited by 283
Barone, P. W., Parker, R. S., & Strano, M. S. (2005) · Analytical Chemistry · doi:10.1021/ac0511997 · Cited by 279
Potentiometric Saccharide Detection Based on the p K a Changes of Poly(aniline boronic acid)
Shoji, E., & Freund, M. S. (2002) · Journal of the American Chemical Society · doi:10.1021/ja0267371 · Cited by 277
Anti-inflammatory functions of glucocorticoid-induced genes
Clark, A. R. (2007) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2007.04.013 · Cited by 276
van Tienen, T. G., Heijkants, R. G. J. C., Buma, P., de Groot, J. H., Pennings, A. J., & Veth, R. P. H. (2002) · Biomaterials · doi:10.1016/s0142-9612(01)00280-0 · Cited by 270
Current development in non-invasive glucose monitoring
Ferrante do Amaral, C. E., & Wolf, B. (2008) · Medical Engineering & Physics · doi:10.1016/j.medengphy.2007.06.003 · Cited by 269
Hickey, T., Kreutzer, D., Burgess, D. J., & Moussy, F. (2002) · Biomaterials · doi:10.1016/s0142-9612(01)00291-5 · Cited by 268
Raman spectroscopy for noninvasive glucose measurements
Enejder, A. M. K., Scecina, T. G., Oh, J., Hunter, M., Shih, W., Šašić, S., Horowitz, G. L., & Feld, M. S. (2005) · Journal of Biomedical Optics · doi:10.1117/1.1920212 · Cited by 268
Cooke, J. P. (2003) · Atherosclerosis Supplements · doi:10.1016/s1567-5688(03)00034-5 · Cited by 266
Synthesis of Nitric Oxide-Releasing Silica Nanoparticles
Shin, J. H., O’Neal, S., & Schoenfisch, M. H. (2007) · Journal of the American Chemical Society · doi:10.1021/ja0674338 · Cited by 253
Self-citationProinflammatory functions of vascular endothelial growth factor in alloimmunity
Reinders, M. E. J., Sho, M., Izawa, A., Wang, P., Mukhopadhyay, D., Koss, K. E., Geehan, C. S., Luster, A. D., Sayegh, M. H., & Briscoe, D. M. (2003) · Journal of Clinical Investigation · doi:10.1172/jci17712 · Cited by 251
Glucose monitoring by reverse iontophoresis
Potts, R. O., Tamada, J. A., & Tierney, M. J. (2002) · Diabetes/Metabolism Research and Reviews · doi:10.1002/dmrr.210 · Cited by 246
Edelman, J. L., Lutz, D., & Castro, M. R. (2005) · Experimental Eye Research · doi:10.1016/j.exer.2004.09.013 · Cited by 246
Cao, H., Mchugh, K., Chew, S. Y., & Anderson, J. M. (2010) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.32609 · Cited by 243
Engineering the tissue which encapsulates subcutaneous implants. I. Diffusion properties
Sharkawy, A. A., Klitzman, B. M., Truskey, G. A., & Reichert, W. M. (1997) · Journal of Biomedical Materials Research · doi:10.1002/(sici)1097-4636(19971205)37:3 · Cited by 239
Comparison of the Numerical and Clinical Accuracy of Four Continuous Glucose Monitors
Kovatchev, B. P., Anderson, S. M., Heinemann, L., & Clarke, W. L. (2008) · Diabetes Care · doi:10.2337/dc07-2401 · Cited by 236
Concurrent delivery of dexamethasone and VEGF for localized inflammation control and angiogenesis
Patil, S. D., Papadmitrakopoulos, F., & Burgess, D. J. (2007) · Journal of Controlled Release · doi:10.1016/j.jconrel.2006.10.013 · Cited by 230
Accuracy of the 5-Day FreeStyle Navigator Continuous Glucose Monitoring System
Weinstein, R. L., Schwartz, S. L., Brazg, R., Bugler, J., Peyser, T. A., & McGarraugh, G. V. (2007) · Diabetes Care · doi:10.2337/dc06-1602 · Cited by 228
Initial in vivo experience with steady‐state subzone‐based MR elastography of the human breast
Van Houten, E. E. W., Doyley, M. M., Kennedy, F. E., Weaver, J. B., & Paulsen, K. D. (2003) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.10232 · Cited by 224
Implanted Electrochemical Glucose Sensors for the Management of Diabetes
Heller, A. (1999) · Annual Review of Biomedical Engineering · doi:10.1146/annurev.bioeng.1.1.153 · Cited by 215
Davies, K. M., Wink, D. A., Saavedra, J. E., & Keefer, L. K. (2001) · Journal of the American Chemical Society · doi:10.1021/ja002899q · Cited by 209
Nitric oxide-releasing sol–gels as antibacterial coatings for orthopedic implants
Nablo, B. J., Rothrock, A. R., & Schoenfisch, M. H. (2004) · Biomaterials · doi:10.1016/j.biomaterials.2004.03.031 · Cited by 207
Self-citationEnzyme-induced biodegradation of polycarbonate-polyurethanes: Dependence on hard-segment chemistry
Tang, Y. W., Labow, R. S., & Santerre, J. P. (2001) · Journal of Biomedical Materials Research · doi:10.1002/1097-4636(20011215)57:4 · Cited by 198
Delays in Minimally Invasive Continuous Glucose Monitoring Devices: A Review of Current Technology
Keenan, D. B., Mastrototaro, J. J., Voskanyan, G., & Steil, G. M. (2009) · Journal of Diabetes Science and Technology · doi:10.1177/193229680900300528 · Cited by 198
Polymer‐Based Nitric Oxide Therapies: Recent Insights for Biomedical Applications
Jen, M. C., Serrano, M. C., van Lith, R., & Ameer, G. A. (2012) · Advanced Functional Materials · doi:10.1002/adfm.201101707 · Cited by 194
The chick chorioallantoic membrane as a novel in vivo model for the testing of biomaterials
Valdes, T. I., Kreutzer, D. L., & Moussy, F. G. (2002) · Journal of Biomedical Materials Research · doi:10.1002/jbm.10152 · Cited by 192
Measurement of glucose in diabetic subjects using noninvasive transdermal extraction
Tamada, J. A., Bohannon, N. J. V., & Potts, R. O. (1995) · Nature Medicine · doi:10.1038/nm1195-1198 · Cited by 182
Koschwanez, H. E., & Reichert, W. M. (2007) · Biomaterials · doi:10.1016/j.biomaterials.2007.03.034 · Cited by 181
In vivo biocompatibility studies. I. The cage implant system and a biodegradable hydrogel
Marchant, R., Hiltner, A., Hamlin, C., Rabinovitch, A., Slobodkin, R., & Anderson, J. M. (1983) · Journal of Biomedical Materials Research · doi:10.1002/jbm.820170209 · Cited by 181
A fibrinogen-based precision microporous scaffold for tissue engineering
Linnes, M. P., Ratner, B. D., & Giachelli, C. M. (2007) · Biomaterials · doi:10.1016/j.biomaterials.2007.08.020 · Cited by 180
Jamieson, A. M., Yu, S., Annicelli, C. H., & Medzhitov, R. (2010) · Cell Host & Microbe · doi:10.1016/j.chom.2010.01.010 · Cited by 180
Function of an Implanted Tissue Glucose Sensor for More than 1 Year in Animals
Gough, D. A., Kumosa, L. S., Routh, T. L., Lin, J. T., & Lucisano, J. Y. (2010) · Science Translational Medicine · doi:10.1126/scitranslmed.3001148 · Cited by 179
In-Vivo Electrochemistry: What Can We Learn about Living Systems?
Wilson, G. S., & Johnson, M. A. (2008) · Chemical Reviews · doi:10.1021/cr068082i · Cited by 178
Ward, W. K., Slobodzian, E. P., Tiekotter, K. L., & Wood, M. D. (2002) · Biomaterials · doi:10.1016/s0142-9612(02)00160-6 · Cited by 176
Wu, W.-S., Wang, F.-S., Yang, K. D., Huang, C.-C., & Kuo, Y.-R. (2006) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700274 · Cited by 174
Quinn, C. P., Pathak, C. P., Heller, A., & Hubbell, J. A. (1995) · Biomaterials · doi:10.1016/0142-9612(95)98856-9 · Cited by 172
A paradigm shift: biomaterials that heal
Ratner, B. D. (2007) · Polymer International · doi:10.1002/pi.2319 · Cited by 162
Viscoelastic response of human skin to low magnitude physiologically relevant shear
Holt, B., Tripathi, A., & Morgan, J. (2008) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2008.06.008 · Cited by 161
Moussy, F. G., Harrison, D. J., O'Brien, D. W., & Rajotte, R. V. (1993) · Analytical Chemistry · doi:10.1021/ac00063a023 · Cited by 158
Reduced foreign body response at nitric oxide-releasing subcutaneous implants
Hetrick, E. M., Prichard, H. L., Klitzman, B., & Schoenfisch, M. H. (2007) · Biomaterials · doi:10.1016/j.biomaterials.2007.06.036 · Cited by 158
Self-citationCaduff, A., Dewarrat, F., Talary, M., Stalder, G., Heinemann, L., & Feldman, Y. (2006) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2006.01.031 · Cited by 155
Biomaterial–microvasculature interactions
Sieminski, A. L., & Gooch, K. J. (2000) · Biomaterials · doi:10.1016/s0142-9612(00)00149-6 · Cited by 155
Fluorescence Glucose Detection: Advances Toward the Ideal In Vivo Biosensor
Moschou, E. A., Sharma, B. V., Deo, S. K., & Daunert, S. (2004) · Journal of Fluorescence · doi:10.1023/b:jofl.0000039341.64999.83 · Cited by 154
Rebrin, K., Sheppard, N. F., & Steil, G. M. (2010) · Journal of Diabetes Science and Technology · doi:10.1177/193229681000400507 · Cited by 152
The Microcirculation and Inflammation: Site of Action for Glucocorticoids
Perretti, M., & Ahluwalia, A. (2000) · Microcirculation · doi:10.1111/j.1549-8719.2000.tb00117.x · Cited by 150
Redepenning, J. G., Schlessinger, T., Burnham, S., Lippiello, L., & Miyano, J. (1996) · Journal of Biomedical Materials Research · doi:10.1002/(sici)1097-4636(199603)30:3 · Cited by 145
Sachedina, N., & Pickup, J. C. (2003) · Diabetic Medicine · doi:10.1046/j.1464-5491.2003.01037.x · Cited by 142
Yu, B., Long, N., Moussy, Y., & Moussy, F. (2006) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2005.11.002 · Cited by 141
Zhao, Q. H., McNally, A. K., Rubin, K. R., Renier, M., Wu, Y., Rose‐Caprara, V., Anderson, J. M., Hiltner, A., Urbanski, P., & Stokes, K. (1993) · Journal of Biomedical Materials Research · doi:10.1002/jbm.820270311 · Cited by 140
Zhao, Q., Egashira, K., Inoue, S., Usui, M., Kitamoto, S., Ni, W., Ishibashi, M., Hiasa, K.-I., Ichiki, T., Shibuya, M., et al. (2002) · Circulation · doi:10.1161/hc0902.104718 · Cited by 136
Patil, S. D., Papadimitrakopoulos, F., & Burgess, D. J. (2004) · Diabetes Technology & Therapeutics · doi:10.1089/dia.2004.6.887 · Cited by 135
A subcutaneous glucose sensor with improved longevity, dynamic range, and stability of calibration.
Updike, S. J., Shults, M. C., Gilligan, B. J., & Rhodes, R. K. (2000) · Diabetes Care · doi:10.2337/diacare.23.2.208 · Cited by 135
Progress Toward an In Vivo Surface-Enhanced Raman Spectroscopy Glucose Sensor
Lyandres, O., Yuen, J. M., Shah, N. C., Duyne, R. P. V., Walsh, J. T., & Glucksberg, M. R. (2008) · Diabetes Technology & Therapeutics · doi:10.1089/dia.2007.0288 · Cited by 135
Sol−Gel Derived Nitric-Oxide Releasing Materials that Reduce Bacterial Adhesion
Nablo, B. J., Chen, T.-Y., & Schoenfisch, M. H. (2001) · Journal of the American Chemical Society · doi:10.1021/ja0165077 · Cited by 134
Self-citationImpact of nicotine on bone healing
Hollinger, J. O., Schmitt, J., Hwang, K., Soleymani, P., & Buck, D. C. (1999) · Journal of Biomedical Materials Research · doi:10.1002/(sici)1097-4636(19990615)45:4 · Cited by 131
Regulation of Vascular Endothelial Growth Factor Synthesis by Nitric Oxide: Facts and Controversies
Dulak, J., & Józkowicz, A. (2003) · Antioxidants & Redox Signaling · doi:10.1089/152308603321223612 · Cited by 130
Norton, L. W., Koschwanez, H. E., Wisniewski, N. A., Klitzman, B., & Reichert, W. M. (2007) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.31088 · Cited by 128
Reverse Iontophoresis: Development of a Noninvasive Approach for Glucose Monitoring
Rao, G., Glikfeld, P., & Guy, R. H. (1993) · Pharmaceutical Research · doi:10.1023/a:1018926215306 · Cited by 126
Biocompatible, glucose-permeable hydrogel for in situ coating of implantable biosensors
Quinn, C. A. P., Connor, R. E., & Heller, A. (1997) · Biomaterials · doi:10.1016/s0142-9612(97)00125-7 · Cited by 126
Helton, K. L., Ratner, B. D., & Wisniewski, N. A. (2011) · Journal of Diabetes Science and Technology · doi:10.1177/193229681100500317 · Cited by 125
On the parameters affecting the characteristics of the “wired” glucose oxidase anode
Mano, N., Mao, F., & Heller, A. (2004) · Journal of Electroanalytical Chemistry · doi:10.1016/j.jelechem.2004.08.014 · Cited by 120
Chen, X., Matsumoto, N., Hu, Y., & Wilson, G. S. (2002) · Analytical Chemistry · doi:10.1021/ac015628m · Cited by 120
Protein interactions with subcutaneously implanted biosensors
Gifford, R., Kehoe, J. J., Barnes, S. L., Kornilayev, B. A., Alterman, M. A., & Wilson, G. S. (2006) · Biomaterials · doi:10.1016/j.biomaterials.2005.11.033 · Cited by 117
ChemInform Abstract: Nitric Oxide Release. Part 2. Therapeutic Applications
Carpenter, A. W., & Schoenfisch, M. H. (2012) · ChemInform · doi:10.1002/chin.201231269 · Cited by 115
Self-citation*The Diabetes Research in Children Network (DirecNet) Study Group (2004) · Diabetes Care · doi:10.2337/diacare.27.3.722 · Cited by 114
Machein, Kullmer, Rönicke, Machein, Krieg, Damert, Breier, Risau, & Plate (1999) · Neuropathology and Applied Neurobiology · doi:10.1046/j.1365-2990.1999.00166.x · Cited by 113
Karp, R. D., Johnson, K. H., Buoen, L. C., Ghobrial, H. K. G., Brand, I., & Brand, K. G. (1973) · JNCI: Journal of the National Cancer Institute · doi:10.1093/jnci/51.4.1275 · Cited by 112
In vivo cytokine-associated responses to biomaterials
Schutte, R. J., Xie, L., Klitzman, B., & Reichert, W. M. (2009) · Biomaterials · doi:10.1016/j.biomaterials.2008.09.026 · Cited by 111
Sharkawy, A. A., Klitzman, B. M., Truskey, G. A., & Reichert, W. M. (1998) · Journal of Biomedical Materials Research · doi:10.1002/(sici)1097-4636(19980615)40:4 · Cited by 110
Nitric oxide-releasing S-nitrosothiol-modified xerogels
Riccio, D. A., Dobmeier, K. P., Hetrick, E. M., Privett, B. J., Paul, H. S., & Schoenfisch, M. H. (2009) · Biomaterials · doi:10.1016/j.biomaterials.2009.05.006 · Cited by 107
Self-citationS‐nitrosoglutathione‐containing hydrogel accelerates rat cutaneous wound repair
Amadeu, T. P., Seabra, A. B., Oliveira, M. D., & Monte‐Alto‐Costa, A. (2007) · Journal of the European Academy of Dermatology and Venereology · doi:10.1111/j.1468-3083.2006.02032.x · Cited by 106
Lowry, J. P., O'Neill, R. D., Boutelle, M. G., & Fillenz, M. (1998) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1998.70010391.x · Cited by 105
Preparation of Nitric Oxide (NO)-Releasing Sol−Gels for Biomaterial Applications
Marxer, S. M., Rothrock, A. R., Nablo, B. J., Robbins, M. E., & Schoenfisch, M. H. (2003) · Chemistry of Materials · doi:10.1021/cm034347n · Cited by 105
Self-citationModulus-dependent macrophage adhesion and behavior
Irwin, E. F., Saha, K., Rosenbluth, M., Gamble, L. J., Castner, D. G., & Healy, K. E. (2008) · Journal of Biomaterials Science, Polymer Edition · doi:10.1163/156856208786052407 · Cited by 105
Use of hydrogel coating to improve the performance of implanted glucose sensors
Yu, B., Wang, C., Ju, Y. M., West, L., Harmon, J., Moussy, Y., & Moussy, F. (2008) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2007.11.010 · Cited by 105
A glucose-sensing contact lens: from bench top to patient
Badugu, R., Lakowicz, J. R., & Geddes, C. D. (2005) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2004.12.007 · Cited by 105
Inorganic/Organic Hybrid Silica Nanoparticles as a Nitric Oxide Delivery Scaffold
Shin, J. H., & Schoenfisch, M. H. (2007) · Chemistry of Materials · doi:10.1021/cm702526q · Cited by 104
Self-citationNorton, L. W., Tegnell, E., Toporek, S. S., & Reichert, W. M. (2004) · Biomaterials · doi:10.1016/j.biomaterials.2004.07.069 · Cited by 104
Hetrick, E. M., & Schoenfisch, M. H. (2007) · Biomaterials · doi:10.1016/j.biomaterials.2007.01.006 · Cited by 104
Self-citationHelton, K. L., Ratner, B. D., & Wisniewski, N. A. (2011) · Journal of Diabetes Science and Technology · doi:10.1177/193229681100500318 · Cited by 102
Monocyte, macrophage and foreign body giant cell interactions with molecularly engineered surfaces
Anderson, J. M., Defife, K., Mcnally, A., collier, T., & jenney, C. (1999) · Journal of Materials Science: Materials in Medicine · doi:10.1023/a:1008976531592 · Cited by 100
Sex‐ and site‐dependent variations in the thickness and mechanical properties of human skin in vivo
Diridollou, S., Black, D., Lagarde, J. M., Gall, Y., Berson, M., Vabre, V., Patat, F., & Vaillant, L. (2000) · International Journal of Cosmetic Science · doi:10.1111/j.1468-2494.2000.00037.x · Cited by 99
Bhardwaj, U., Sura, R., Papadimitrakopoulos, F., & Burgess, D. J. (2007) · Journal of Diabetes Science and Technology · doi:10.1177/193229680700100103 · Cited by 99
Pishko, M. V., Katakis, I., Lindquist, S., Ye, L., Gregg, B. A., & Heller, A. (1990) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199000821 · Cited by 99
Nonenzymatic continuous glucose monitoring in human whole blood using electrified nanoporous Pt
Park, S., Park, S., Jeong, R.-A., Boo, H., Park, J., Kim, H. C., & Chung, T. D. (2011) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2011.10.033 · Cited by 97
Nitric Oxide Donor Improves Healing if Applied on Inflammatory and Proliferative Phase
Amadeu, T. P., Seabra, A. B., de Oliveira, M. G., & Monte‐Alto‐Costa, A. (2007) · Journal of Surgical Research · doi:10.1016/j.jss.2007.10.015 · Cited by 96
Mediation of in vivo glucose sensor inflammatory response via nitric oxide release
Gifford, R., Batchelor, M. M., Lee, Y., Gokulrangan, G., Meyerhoff, M. E., & Wilson, G. S. (2005) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.30359 · Cited by 96
Shichiri, M., Asakawa, N., Yamasaki, Y., Kawamori, R., & Abe, H. (1986) · Diabetes Care · doi:10.2337/diacare.9.3.298 · Cited by 96
A Novel Noninvasive Blood Glucose Monitor
Malchoff, C. D., Shoukri, K., Landau, J. I., & Buchert, J. M. (2002) · Diabetes Care · doi:10.2337/diacare.25.12.2268 · Cited by 96
Amperometric Glucose Sensors: Sources of Error and Potential Benefit of Redundancy
Castle, J. R., & Ward, W. K. (2010) · Journal of Diabetes Science and Technology · doi:10.1177/193229681000400127 · Cited by 95
Time‐dependent inactivation of immobilized glucose oxidase and catalase
Tse, P. H. S., & Gough, D. A. (1987) · Biotechnology and Bioengineering · doi:10.1002/bit.260290607 · Cited by 95
Stöber Synthesis of Nitric Oxide-Releasing S-Nitrosothiol-Modified Silica Particles
Riccio, D. A., Nugent, J. L., & Schoenfisch, M. H. (2011) · Chemistry of Materials · doi:10.1021/cm102510q · Cited by 94
Self-citationZhang, Y., & Wilson, G. S. (1993) · Analytica Chimica Acta · doi:10.1016/0003-2670(93)85009-9 · Cited by 92
Turner, R. F. B., Harrison, D. J., & Rojotte, R. V. (1991) · Biomaterials · doi:10.1016/0142-9612(91)90003-s · Cited by 91
Pendra goes Dutch: lessons for the CE mark in Europe
Wentholt, I. M. E., Hoekstra, J. B. L., Zwart, A., & DeVries, J. H. (2005) · Diabetologia · doi:10.1007/s00125-005-1754-y · Cited by 90
Influence of inflammatory cells and serum on the performance of implantable glucose sensors
Gerritsen, M., Jansen, J. A., Kros, A., Vriezema, D. M., Sommerdijk, N. A. J. M., Nolte, R. J. M., Lutterman, J. A., van Hövell, S. W. F. M., & van der Gaag, A. (2000) · Journal of Biomedical Materials Research · doi:10.1002/1097-4636(200101)54:1 · Cited by 89
Carreau, A., Kieda, C., & Grillon, C. (2011) · Experimental Cell Research · doi:10.1016/j.yexcr.2010.08.011 · Cited by 88
Klueh, U., Dorsky, D. I., & Kreutzer, D. L. (2005) · Biomaterials · doi:10.1016/j.biomaterials.2004.04.017 · Cited by 87
Weiss, R., Yegorchikov, Y., Shusterman, A., & Raz, I. (2007) · Diabetes Technology & Therapeutics · doi:10.1089/dia.2006.0059 · Cited by 86
Kao, W. J., Zhao, Q. H., Hiltner, A., & Anderson, J. M. (1994) · Journal of Biomedical Materials Research · doi:10.1002/jbm.820280110 · Cited by 85
A new amperometric glucose microsensor: in vitro and short-term in vivo evaluation
Ward, W. K., Jansen, L. B., Anderson, E., Reach, G., Klein, J.-C., & Wilson, G. S. (2002) · Biosensors and Bioelectronics · doi:10.1016/s0956-5663(01)00268-8 · Cited by 81
In vivo glucose monitoring: Towards ‘Sense and Act’ feedback-loop individualized medical systems
Wang, J. (2007) · Talanta · doi:10.1016/j.talanta.2007.10.023 · Cited by 81
Kim, T.-K., & Burgess, D. J. (2002) · Journal of Pharmacy and Pharmacology · doi:10.1211/002235702760089009 · Cited by 79
Quantifying the Composition of Human Skin for Glucose Sensor Development
Groenendaal, W., von Basum, G., Schmidt, K. A., Hilbers, P. A. J., & van Riel, N. A. W. (2010) · Journal of Diabetes Science and Technology · doi:10.1177/193229681000400502 · Cited by 79
Antibacterial properties of nitric oxide–releasing sol‐gels
Nablo, B. J., & Schoenfisch, M. H. (2003) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.20030 · Cited by 78
Self-citationCold- and hot-pack contrast therapy: subcutaneous and intramuscular temperature change.
Myrer, J. W., Measom, G. J., Durrant, E., & Fellingham, G. W. (1997) · Europe PMC (PubMed Central) · Cited by 76
Calibration of a subcutaneous amperometric glucose sensor implanted for 7 days in diabetic patients
Choleau, C., Klein, J. C., Reach, G., Aussedat, B., Demaria-Pesce, V., Wilson, G. S., Gifford, R., & Ward, W. K. (2002) · Biosensors and Bioelectronics · doi:10.1016/s0956-5663(01)00304-9 · Cited by 76
In vitro and in vivo mineralization of Nafion membrane used for implantable glucose sensors
Mercado, R. C., & Moussy, F. (1998) · Biosensors and Bioelectronics · doi:10.1016/s0956-5663(97)00112-7 · Cited by 73
Continuous Glucose Sensors: Continuing Questions about Clinical Accuracy
Clarke, W. L., & Kovatchev, B. (2007) · Journal of Diabetes Science and Technology · doi:10.1177/193229680700100510 · Cited by 71
Feasibility of Continuous Long-Term Glucose Monitoring from a Subcutaneous Glucose Sensor in Humans
Gilligan, B. C., Shults, M., Rhodes, R. K., Jacobs, P. G., Brauker, J. H., Pintar, T. J., & Updike, S. J. (2004) · Diabetes Technology & Therapeutics · doi:10.1089/152091504774198089 · Cited by 71
Macrophage behavior on surface-modified polyurethanes
Jones, J. A., Dadsetan, M., Collier, T. O., Ebert, M., Stokes, K. S., Ward, R. S., Hiltner, P. A., & Anderson, J. M. (2004) · Journal of Biomaterials Science, Polymer Edition · doi:10.1163/156856204323046843 · Cited by 70
Ju, Y. M., Yu, B., Koob, T. J., Moussy, Y., & Moussy, F. G. (2007) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.31756 · Cited by 70
Koschwanez, H. E., Yap, F. Y., Klitzman, B., & Reichert, W. M. (2008) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.31824 · Cited by 69
A Miniaturized Nafion-Based Glucose Sensor: in vitro and in vivo evaluation in dogs
Moussy, F., Harrison, D. J., & Rajotte, R. V. (1994) · The International Journal of Artificial Organs · doi:10.1177/039139889401700206 · Cited by 67
The effect of nitric oxide surface flux on the foreign body response to subcutaneous implants
Nichols, S. P., Koh, A., Brown, N. L., Rose, M. B., Sun, B., Slomberg, D. L., Riccio, D. A., Klitzman, B., & Schoenfisch, M. H. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.05.053 · Cited by 67
Self-citationIn vivo glucose sensing for diabetes management: progress towards non-invasive monitoring
Pickup, J., McCartney, L., Rolinski, O., & Birch, D. (1999) · BMJ · doi:10.1136/bmj.319.7220.1289 · Cited by 66
Barman, I., Kong, C.-R., Singh, G., Dasari, R. R., & Feld, M. S. (2010) · Analytical Chemistry · doi:10.1021/ac100810e · Cited by 65
Synthesis and Performance of Novel Hydrogels Coatings for Implantable Glucose Sensors
Wang, C., Yu, B., Knudsen, B., Harmon, J., Moussy, F., & Moussy, Y. (2008) · Biomacromolecules · doi:10.1021/bm701102y · Cited by 63
Metabolic Biofouling of Glucose Sensors in Vivo : Role of Tissue Microhemorrhages
Klueh, U., Liu, Z., Feldman, B., Henning, T. P., Cho, B., Ouyang, T., & Kreutzer, D. (2011) · Journal of Diabetes Science and Technology · doi:10.1177/193229681100500313 · Cited by 63
Linke, B., Kerner, W., Kiwit, M., Pishko, M. V., & Heller, A. (1994) · Biosensors and Bioelectronics · doi:10.1016/0956-5663(94)80107-x · Cited by 61
Calibration of a subcutaneous amperometric glucose sensor
Choleau, C., Klein, J. C., Reach, G., Aussedat, B., Demaria-Pesce, V. H., Wilson, G. S., Gifford, R., & Ward, W. K. (2002) · Biosensors and Bioelectronics · doi:10.1016/s0956-5663(01)00306-2 · Cited by 60
Gourzi, M., Rouane, A., Guelaz, R., Alavi, M., McHugh, M. B., Nadi, M., & Roth, P. (2004) · Journal of Medical Engineering & Technology · doi:10.1080/03091900410001720247 · Cited by 60
Ward, W. K., Quinn, M. J., Wood, M. D., Tiekotter, K. L., Pidikiti, S., & Gallagher, J. A. (2003) · Biosensors and Bioelectronics · doi:10.1016/s0956-5663(03)00180-5 · Cited by 55
Pfützner, A., Caduff, A., Larbig, M., Schrepfer, T., & Forst, T. M. (2004) · Diabetes Technology & Therapeutics · doi:10.1089/1520915041705839 · Cited by 55
Novak, M. T., Yuan, F., & Reichert, W. M. (2010) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-010-4097-6 · Cited by 55
Photoinitiated Nitric Oxide-Releasing Tertiary S-Nitrosothiol-Modified Xerogels
Riccio, D. A., Coneski, P. N., Nichols, S. P., Broadnax, A. D., & Schoenfisch, M. H. (2012) · ACS Applied Materials & Interfaces · doi:10.1021/am201443r · Cited by 53
Self-citationErtefai, S., & Gough, D. A. (1989) · Journal of Biomedical Engineering · doi:10.1016/0141-5425(89)90097-6 · Cited by 52
Ju, Y. M., Yu, B., West, L., Moussy, Y., & Moussy, F. (2010) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.32400 · Cited by 52
Implant Healing in Experimental Animal Models of Diabetes
Le, N. N., Rose, M. B., Levinson, H., & Klitzman, B. (2011) · Journal of Diabetes Science and Technology · doi:10.1177/193229681100500315 · Cited by 52
Wagner, J. G., Schmidtke, D. W., Quinn, C. P., Fleming, T. F., Bernacky, B. J., & Heller, A. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.11.6379 · Cited by 51
Wisniewski, N., Rajamand, N., Adamsson, U., Lins, P. E., Reichert, W. M., Klitzman, B., & Ungerstedt, U. (2002) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00259.2001 · Cited by 50
Research works printed but not linked: 14
- 2012, World Health Statistics 2012
- Wang J., 2008, Chem. Rev., 108, 814, 10.1021/cr068123a · DOI · Paper page
- Arnold M. A., 2010, In Vivo Glucose Sensing
- Vashist S. K., 2012, Anal. Chim. Acta, 750, 16, 10.1016/j.aca.2012.03.043 · DOI · Paper page
- 2012, Continuous Glucose Monitoring (CGM) Systems - Global Pipeline Analysis, Competitive Landscape and Market Forecasts to 2017
- Henning T., 2010, In Vivo Glucose Sensing
- Myrer J. W., 1997, J. Athletic Training, 32, 238
- Wilson G. S., 2009, In Vivo Glucose Sensing
- Thomé-Duret V., 1996, Diabetes Metab., 22, 174
- Helton K. L., 2011, J. Diabetes Sci. Technol., 5, 647, 10.1177/193229681100500318 · DOI · Paper page
- Sharkawy A. A., 1998, J. Biomed. Mater. Res., 40, 598, 10.1002/(sici)1097-4636(19980615)40:4 · DOI
- Marshall A. J., 2004, ACS Polym. Prepr., 45, 100
- Ratner B. D., 2009, ACS Polym. Prepr., 50, 286
- Ward W. K., 2004, Diabetes Technol. Ther., 19, 155
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Veiseh, O., Doloff, J. C., Ma, M., Vegas, A. J., Tam, H. H., Bader, A. R., Li, J., Langan, E., Wyckoff, J., Loo, W. S., et al. (2015) · Nature Materials · doi:10.1038/nmat4290 · Cited by 897
Electrochemical glucose sensors in diabetes management: an updated review (2010–2020)
Teymourian, H., Barfidokht, A., & Wang, J. (2020) · Chemical Society Reviews · doi:10.1039/d0cs00304b · Cited by 915
Design of biodegradable, implantable devices towards clinical translation
Li, C., Guo, C., Fitzpatrick, V., Ibrahim, A. G. A., Zwierstra, M. J., Hanna, P. C., Lechtig, A., Nazarian, A., Lin, S. J., & Kaplan, D. L. (2019) · Nature Reviews Materials · doi:10.1038/s41578-019-0150-z · Cited by 828
Yetisen, A. K., Martinez‐Hurtado, J. L., Ünal, B., Khademhosseini, A., & Butt, H. (2018) · Advanced Materials · doi:10.1002/adma.201706910 · Cited by 569
Metadata
- Authors
- Nichols, S. P., Koh, A., Storm, W. L., Shin, J. H., & Schoenfisch, M. H.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- Kwangwoon University (KR)
- Corresponding author
- Schoenfisch, Mark H.
- Venue
- Chemical Reviews
- Publisher
- American Chemical Society (ACS)
- Published
- 2013-02-07
- Volume
- 113
- Issue
- 4
- Pages
- 2528-2549
- ISSN
- 0009-2665 (ISSN-L)
- 1520-6890
- PMC
- PMC3624030
- OpenAlex
- W1993893772
- Semantic Scholar
- 15d86c3915bf4d8443f91beee6a62f80dcdc9ac4
- Cited by
- 347
- References
- 246
- Citations by year
- 2026: 20 · 2025: 25 · 2024: 26 · 2023: 26 · 2022: 28 · 2021: 31 · 2020: 23 · 2019: 23 · 2018: 31 · 2017: 20 · 2016: 37 · 2015: 21 · 2014: 20 · 2013: 14
- FWCI
- 2.55
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Chemical Reviews (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Biomedical Imaging and Bioengineering (EB 000708, R01EB000708)
- Topics
- Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Physical Sciences › Chemistry › Analytical Chemistry › Electrochemical sensors and biosensors
- Keywords
- biomaterials, continuous glucose monitoring, biomedical implants, diabetes mellitus, biocompatibility, glucose sensor, tissue response to implants, inflammation, diabetes complications, diabetes management, diabetes prevention
- MeSH terms
- Animals, Biocompatible Materials, Blood Glucose, Diabetes Mellitus, Disease Models, Animal, Humans, Polymers, Blood Glucose Self-Monitoring, Biosensing Techniques, Porosity, Elastic Modulus, Electrochemical Techniques
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