| Literature DB >> 33710398 |
Mark A Jarosinski1, Balamurugan Dhayalan1, Nischay Rege2, Deepak Chatterjee1, Michael A Weiss3,4,5.
Abstract
Insulin replacement therapy for diabetes mellitus seeks to minimise excursions in blood glucose concentration above or below the therapeutic range (hyper- or hypoglycaemia). To mitigate acute and chronic risks of such excursions, glucose-responsive insulin-delivery technologies have long been sought for clinical application in type 1 and long-standing type 2 diabetes mellitus. Such 'smart' systems or insulin analogues seek to provide hormonal activity proportional to blood glucose levels without external monitoring. This review highlights three broad strategies to co-optimise mean glycaemic control and time in range: (1) coupling of continuous glucose monitoring (CGM) to delivery devices (algorithm-based 'closed-loop' systems); (2) glucose-responsive polymer encapsulation of insulin; and (3) mechanism-based hormone modifications. Innovations span control algorithms for CGM-based insulin-delivery systems, glucose-responsive polymer matrices, bio-inspired design based on insulin's conformational switch mechanism upon insulin receptor engagement, and glucose-responsive modifications of new insulin analogues. In each case, innovations in insulin chemistry and formulation may enhance clinical outcomes. Prospects are discussed for intrinsic glucose-responsive insulin analogues containing a reversible switch (regulating bioavailability or conformation) that can be activated by glucose at high concentrations.Entities:
Keywords: Artificial pancreas; Glucose sensor; Glucose-responsive insulin; Glucose-responsive polymers; Hormone-receptor recognition; Review
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Year: 2021 PMID: 33710398 PMCID: PMC8158166 DOI: 10.1007/s00125-021-05422-6
Source DB: PubMed Journal: Diabetologia ISSN: 0012-186X Impact factor: 10.122