Enhancing the longevity of microparticle-based glucose sensors towards 1 month continuous operation
Open accessAbstract
Luminescent microspheres encapsulating glucose oxidase have recently been reported as potential implantable sensors, but the operational lifetime of these systems has been limited by enzyme degradation. We report here that the longevity of these enzymatic microparticle-based sensors has been extended by the coimmobilization of glucose oxidase (GOx) and catalase (CAT) into the sensor matrix. A mathematical model was used to compare the response and longevity of the sensors with and without catalase. To experimentally test the longevity, sensors were continuously operated under normoglycemic dermal substrate concentrations and physiological conditions (5.5 mM glucose and 140 microM O(2), 37 degrees C and pH 7.4). The sensors incorporating CAT were experimentally shown to be approximately 5 times more stable than those without CAT; nevertheless, the response of sensors with CAT still changed by approximately 20%, when operated continuously for 7 days. The experimentally determined trends obtained for the variation in sensor response due to enzyme deactivation were in close agreement with modeling predictions, which also revealed a significant apparent loss in enzyme activity upon immobilization. It was further predicted via modeling that by incorporating 0.1 mM each of active GOx and CAT, the sensors will exhibit less than 2% variation in response over 1 month of continuous operation.
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The average glucose level of tears for fasting diabetic patients typically exceeds 0.9 mM, and for fasting people without diabetes it is below 0.6 mM.
“Because the average glucose level of tears for fasting diabetic patients typically exceeds 0.9 mM and the concentration for fasting people without diabetes is below 0.6 mM (39)”
From Soft, smart contact lenses with integrations of wireless circuits, glucose sensors, and displays (2018) · cites this paper as [39]
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Soft, smart contact lenses with integrations of wireless circuits, glucose sensors, and displays
Park, J., Kim, J., Kim, S.-Y., Cheong, W. H., Jang, J., Park, Y.-G., Na, K., Kim, Y.-T., Heo, J. H., Lee, C. Y., et al. (2018) · Science Advances · doi:10.1126/sciadv.aap9841 · Cited by 671 · see citing works
- Authors
- Singh, S., & McShane, M.
- Affiliations
- Texas A&M University (US)
- ORCID
- Singh, Saurabh
- Venue
- Biosensors and Bioelectronics
- Publisher
- Elsevier BV
- Published
- 2010-01
- Volume
- 25
- Issue
- 5
- Pages
- 1075-1081
- ISSN
- 0956-5663 (ISSN-L)
- PMC
- PMC2818267
- OpenAlex
- W1964611095
- Cited by
- 35
- References
- 22
- Citations by year
- 2025: 1 · 2024: 2 · 2023: 2 · 2021: 2 · 2019: 1 · 2018: 1 · 2017: 1 · 2016: 1 · 2015: 1 · 2014: 3 · 2013: 4 · 2012: 5
- FWCI
- 4.23
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Biosensors and Bioelectronics (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Biomedical Imaging and Bioengineering (R01EB000739)
- Topics
- Physical Sciences › Engineering › Electrical and Electronic Engineering › Electrochemical sensors and biosensors
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Enzyme Catalysis and Immobilization
- Physical Sciences › Chemical Engineering › Bioengineering › Analytical Chemistry and Sensors
- Keywords
- glucose sensor, glucose oxidase, catalase, enzyme co-immobilization, enzyme degradation, implantable sensors, continuous glucose monitoring, oxygen scavenging
- MeSH terms
- Catalase, Computer Simulation, Equipment Design, Glucose, Glucose Oxidase, Luminescent Measurements, Microspheres, Models, Chemical, Sensitivity and Specificity, Reproducibility of Results, Biosensing Techniques, Computer-Aided Design, Equipment Failure Analysis
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