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Insulin delivery using dynamic covalent boronic acid/ester-controlled release

Insulin delivery using dynamic covalent boronic acid/ester-controlled release
Insulin delivery using dynamic covalent boronic acid/ester-controlled release
The number of people affected by diabetes mellitus increases globally year on year. Elevated blood glucose levels may result from a lack of insulin to manage these levels and can, over a prolonged period, lead to serious repercussions. Diabetes mellitus patients must monitor and control their blood-glucose levels with invasive testing and often alongside administration of intravenous doses of insulin, which can often lead to suboptimal compliance. To mitigate these issues, “closed-loop” insulin delivery systems are deemed to be among superior options for rapid relief from the demanding and troublesome necessity of self-directed care. The reversible dynamic covalent chemistry of boronic acid derivatives and their competitive affinity to 1,2- and 1,3-diols (such as those present in saccharides) allows for the design and preparation of responsive self-regulated insulin delivery materials which respond to elevated and changing glucose levels. A range of meritorious and noteworthy contributions in the domain of boron-mediated insulin delivery materials is surveyed, and providing a multidisciplinary context in the realisation of the ambitious goal of ultimately addressing the desire to furnish glucose-responsive insulin delivery materials through innovative synthesis and rigorous testing is targetted.
boronic acid, controlled release, diabetes mellitus, glucose, insulin
2366-3987
Banach, Łukasz
d733d7ea-25bf-44b6-881d-1e6adb8ffe82
Williams, George T.
26810522-92ef-4b61-a766-582bf15be280
Fossey, John S.
e080d7fe-9246-4d09-b598-e516f27168fd
Banach, Łukasz
d733d7ea-25bf-44b6-881d-1e6adb8ffe82
Williams, George T.
26810522-92ef-4b61-a766-582bf15be280
Fossey, John S.
e080d7fe-9246-4d09-b598-e516f27168fd

Banach, Łukasz, Williams, George T. and Fossey, John S. (2021) Insulin delivery using dynamic covalent boronic acid/ester-controlled release. Advanced Therapeutics, 4 (11), [2100118]. (doi:10.1002/adtp.202100118).

Record type: Article

Abstract

The number of people affected by diabetes mellitus increases globally year on year. Elevated blood glucose levels may result from a lack of insulin to manage these levels and can, over a prolonged period, lead to serious repercussions. Diabetes mellitus patients must monitor and control their blood-glucose levels with invasive testing and often alongside administration of intravenous doses of insulin, which can often lead to suboptimal compliance. To mitigate these issues, “closed-loop” insulin delivery systems are deemed to be among superior options for rapid relief from the demanding and troublesome necessity of self-directed care. The reversible dynamic covalent chemistry of boronic acid derivatives and their competitive affinity to 1,2- and 1,3-diols (such as those present in saccharides) allows for the design and preparation of responsive self-regulated insulin delivery materials which respond to elevated and changing glucose levels. A range of meritorious and noteworthy contributions in the domain of boron-mediated insulin delivery materials is surveyed, and providing a multidisciplinary context in the realisation of the ambitious goal of ultimately addressing the desire to furnish glucose-responsive insulin delivery materials through innovative synthesis and rigorous testing is targetted.

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Advanced Therapeutics - 2021 - Banach - Insulin Delivery - Version of Record
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More information

e-pub ahead of print date: 15 August 2021
Published date: 18 November 2021
Keywords: boronic acid, controlled release, diabetes mellitus, glucose, insulin

Identifiers

Local EPrints ID: 474081
URI: http://eprints.soton.ac.uk/id/eprint/474081
ISSN: 2366-3987
PURE UUID: 650ffb1d-f854-467e-8577-e8ee8e577211
ORCID for George T. Williams: ORCID iD orcid.org/0000-0001-6162-8895

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Date deposited: 10 Feb 2023 18:03
Last modified: 17 Mar 2024 04:17

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Contributors

Author: Łukasz Banach
Author: George T. Williams ORCID iD
Author: John S. Fossey

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