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Clinical Evidence for Use of a Noninvasive Biosensor for Tear Glucose as an Alternative to Painful Finger-Prick for Diabetes Management Utilizing a Biopolymer Coating

[Image: see text] Diabetes is a metabolic condition that is exponentially increasing worldwide. Current monitoring methods for diabetes are invasive, painful, and expensive. Herein, we present the first multipatient clinical trial that demonstrates clearly that tear fluid may be a valuable marker fo...

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Autores principales: Kownacka, Alicja E., Vegelyte, Dovile, Joosse, Maurits, Anton, Nicoleta, Toebes, B. Jelle, Lauko, Jan, Buzzacchera, Irene, Lipinska, Katarzyna, Wilson, Daniela A., Geelhoed-Duijvestijn, Nel, Wilson, Christopher J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6234487/
https://www.ncbi.nlm.nih.gov/pubmed/30350599
http://dx.doi.org/10.1021/acs.biomac.8b01429
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author Kownacka, Alicja E.
Vegelyte, Dovile
Joosse, Maurits
Anton, Nicoleta
Toebes, B. Jelle
Lauko, Jan
Buzzacchera, Irene
Lipinska, Katarzyna
Wilson, Daniela A.
Geelhoed-Duijvestijn, Nel
Wilson, Christopher J.
author_facet Kownacka, Alicja E.
Vegelyte, Dovile
Joosse, Maurits
Anton, Nicoleta
Toebes, B. Jelle
Lauko, Jan
Buzzacchera, Irene
Lipinska, Katarzyna
Wilson, Daniela A.
Geelhoed-Duijvestijn, Nel
Wilson, Christopher J.
author_sort Kownacka, Alicja E.
collection PubMed
description [Image: see text] Diabetes is a metabolic condition that is exponentially increasing worldwide. Current monitoring methods for diabetes are invasive, painful, and expensive. Herein, we present the first multipatient clinical trial that demonstrates clearly that tear fluid may be a valuable marker for systemic glucose measurements. The NovioSense Glucose Sensor, worn under the lower eye lid (inferior conjunctival fornix), is reported to continuously measure glucose levels in the basal tear fluid with good correlation to blood glucose values, showing clear clinical feasibility in both animals and humans. Furthermore, the polysaccharide coated device previously reported by our laboratory when worn, does not induce pain or irritation. In a phase II clinical trial, six patients with type 1 Diabetes Mellitus were enrolled and the capability of the device to measure glucose in the tear fluid was evaluated. The NovioSense Glucose Sensor gives a stable signal and the results correlate well to blood glucose values obtained from finger-prick measurements determined by consensus error grid analysis.
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spelling pubmed-62344872018-11-15 Clinical Evidence for Use of a Noninvasive Biosensor for Tear Glucose as an Alternative to Painful Finger-Prick for Diabetes Management Utilizing a Biopolymer Coating Kownacka, Alicja E. Vegelyte, Dovile Joosse, Maurits Anton, Nicoleta Toebes, B. Jelle Lauko, Jan Buzzacchera, Irene Lipinska, Katarzyna Wilson, Daniela A. Geelhoed-Duijvestijn, Nel Wilson, Christopher J. Biomacromolecules [Image: see text] Diabetes is a metabolic condition that is exponentially increasing worldwide. Current monitoring methods for diabetes are invasive, painful, and expensive. Herein, we present the first multipatient clinical trial that demonstrates clearly that tear fluid may be a valuable marker for systemic glucose measurements. The NovioSense Glucose Sensor, worn under the lower eye lid (inferior conjunctival fornix), is reported to continuously measure glucose levels in the basal tear fluid with good correlation to blood glucose values, showing clear clinical feasibility in both animals and humans. Furthermore, the polysaccharide coated device previously reported by our laboratory when worn, does not induce pain or irritation. In a phase II clinical trial, six patients with type 1 Diabetes Mellitus were enrolled and the capability of the device to measure glucose in the tear fluid was evaluated. The NovioSense Glucose Sensor gives a stable signal and the results correlate well to blood glucose values obtained from finger-prick measurements determined by consensus error grid analysis. American Chemical Society 2018-10-12 2018-11-12 /pmc/articles/PMC6234487/ /pubmed/30350599 http://dx.doi.org/10.1021/acs.biomac.8b01429 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Kownacka, Alicja E.
Vegelyte, Dovile
Joosse, Maurits
Anton, Nicoleta
Toebes, B. Jelle
Lauko, Jan
Buzzacchera, Irene
Lipinska, Katarzyna
Wilson, Daniela A.
Geelhoed-Duijvestijn, Nel
Wilson, Christopher J.
Clinical Evidence for Use of a Noninvasive Biosensor for Tear Glucose as an Alternative to Painful Finger-Prick for Diabetes Management Utilizing a Biopolymer Coating
title Clinical Evidence for Use of a Noninvasive Biosensor for Tear Glucose as an Alternative to Painful Finger-Prick for Diabetes Management Utilizing a Biopolymer Coating
title_full Clinical Evidence for Use of a Noninvasive Biosensor for Tear Glucose as an Alternative to Painful Finger-Prick for Diabetes Management Utilizing a Biopolymer Coating
title_fullStr Clinical Evidence for Use of a Noninvasive Biosensor for Tear Glucose as an Alternative to Painful Finger-Prick for Diabetes Management Utilizing a Biopolymer Coating
title_full_unstemmed Clinical Evidence for Use of a Noninvasive Biosensor for Tear Glucose as an Alternative to Painful Finger-Prick for Diabetes Management Utilizing a Biopolymer Coating
title_short Clinical Evidence for Use of a Noninvasive Biosensor for Tear Glucose as an Alternative to Painful Finger-Prick for Diabetes Management Utilizing a Biopolymer Coating
title_sort clinical evidence for use of a noninvasive biosensor for tear glucose as an alternative to painful finger-prick for diabetes management utilizing a biopolymer coating
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6234487/
https://www.ncbi.nlm.nih.gov/pubmed/30350599
http://dx.doi.org/10.1021/acs.biomac.8b01429
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