Fluorescence-based glucose sensors
Abstract
There is an urgent need to develop technology for continuous in vivo glucose monitoring in subjects with diabetes mellitus. Problems with existing devices based on electrochemistry have encouraged alternative approaches to glucose sensing in recent years, and those based on fluorescence intensity and lifetime have special advantages, including sensitivity and the potential for non-invasive measurement when near-infrared light is used. Several receptors have been employed to detect glucose in fluorescence sensors, and these include the lectin concanavalin A (Con A), enzymes such as glucose oxidase, glucose dehydrogenase and hexokinase/glucokinase, bacterial glucose-binding protein, and boronic acid derivatives (which bind the diols of sugars). Techniques include measuring changes in fluorescence resonance energy transfer (FRET) between a fluorescent donor and an acceptor either within a protein which undergoes glucose-induced changes in conformation or because of competitive displacement; measurement of glucose-induced changes in intrinsic fluorescence of enzymes (e.g. due to tryptophan residues in hexokinase) or extrinsic fluorophores (e.g. using environmentally sensitive fluorophores to signal protein conformation). Non-invasive glucose monitoring can be accomplished by measurement of cell autofluorescence due to NAD(P)H, and fluorescent markers of mitochondrial metabolism can signal changes in extracellular glucose concentration. Here we review the principles of operation, context and current status of the various approaches to fluorescence-based glucose sensing.
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Optical glucose detection is sensitive and does not damage the host, but skin pigmentation and epidermal thickness can worsen analytical response.
“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”
From Biocompatible Materials for Continuous Glucose Monitoring Devices (2013) · cites this paper as [36]
Photobleaching of fluorophores and tissue scattering are significant drawbacks of optical glucose detection.
“Photobleaching of the fluorophore and scattering in tissue are significant drawbacks.19,35–36”
From Biocompatible Materials for Continuous Glucose Monitoring Devices (2013) · cites this paper as [36]
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References 75 · Cited by 616
- Authors
- Pickup, J. C., Hussain, F., Evans, N. D., Rolinski, O. J., & Birch, D. J. S.
- Affiliations
- Guy's Hospital (GB)
- University of Strathclyde (GB)
- Corresponding author
- Pickup, John C.
- Venue
- Biosensors and Bioelectronics
- Publisher
- Elsevier BV
- Published
- 2005-06
- Volume
- 20
- Issue
- 12
- Pages
- 2555-2565
- ISSN
- 0956-5663 (ISSN-L)
- OpenAlex
- W1993772396
- Cited by
- 616
- References
- 75
- Citations by year
- 2026: 14 · 2025: 21 · 2024: 30 · 2023: 26 · 2022: 25 · 2021: 23 · 2020: 31 · 2019: 34 · 2018: 31 · 2017: 34 · 2016: 38 · 2015: 39 · 2014: 36 · 2013: 40 · 2012: 49
- FWCI
- 1.06
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biosensors and Bioelectronics (publishedVersion)
- PubMed (publishedVersion)
- ePrints Soton (University of Southampton) (submittedVersion)
- Funders
- Wellcome Trust
- Engineering and Physical Sciences Research Council
- Topics
- Physical Sciences › Chemistry › Spectroscopy › Molecular Sensors and Ion Detection
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biophysics › Advanced Fluorescence Microscopy Techniques
- Physical Sciences › Chemical Engineering › Bioengineering › Analytical Chemistry and Sensors
- Keywords
- glucose sensor, continuous glucose monitoring, diabetes mellitus, non-invasive glucose monitoring, near-infrared fluorescence, fluorescence resonance energy transfer, concanavalin A, glucose oxidase, glucose dehydrogenase, hexokinase, glucokinase, boronic acid derivatives, tryptophan fluorescence, NAD(P)H autofluorescence, protein conformational change
- MeSH terms
- Blood Glucose, Diabetes Mellitus, Glucose, Humans, Spectrometry, Fluorescence, Blood Glucose Self-Monitoring, Biosensing Techniques
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