Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, USA.
Department of Medicine, Yale University School of Medicine, New Haven, CT, USA.
Diabetologia. 2021 May;64(5):1016-1029. doi: 10.1007/s00125-021-05422-6. Epub 2021 Mar 12.
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.
糖尿病的胰岛素替代疗法旨在将血糖浓度的波动最小化至治疗范围(高血糖或低血糖)之上或之下。为了减轻这些波动带来的急性和慢性风险,人们长期以来一直在寻求用于 1 型和长期 2 型糖尿病的临床应用的葡萄糖响应型胰岛素输送技术。这些“智能”系统或胰岛素类似物旨在提供与血糖水平成比例的激素活性,而无需外部监测。本综述强调了三种广泛的策略来共同优化平均血糖控制和血糖达标时间:(1)将连续血糖监测(CGM)与输送设备相结合(基于算法的“闭环”系统);(2)胰岛素的葡萄糖响应性聚合物包封;和(3)基于机制的激素修饰。创新涵盖了基于 CGM 的胰岛素输送系统的控制算法、葡萄糖响应性聚合物基质、基于胰岛素受体结合时胰岛素构象开关机制的仿生设计,以及新胰岛素类似物的葡萄糖响应性修饰。在每种情况下,胰岛素化学和配方的创新都可能改善临床结果。讨论了含有可逆开关(调节生物利用度或构象)的内在葡萄糖响应性胰岛素类似物的前景,该开关可以在高浓度下被葡萄糖激活。