胰岛素
葡萄糖氧化酶
血糖性
材料科学
胰岛素释放
右旋糖酐
内科学
内分泌学
糖尿病
医学
化学
纳米技术
生物化学
1型糖尿病
生物传感器
作者
Lisa R. Volpatti,Amanda Facklam,Abel B. Cortinas,Yen‐Chun Lu,Morgan A. Matranga,Corina MacIsaac,Michael C. Hill,Róbert Langer,Daniel G. Anderson
出处
期刊:Biomaterials
[Elsevier BV]
日期:2020-11-04
卷期号:267: 120458-120458
被引量:60
标识
DOI:10.1016/j.biomaterials.2020.120458
摘要
An insulin delivery system that self-regulates blood glucose levels has the potential to limit hypoglycemic events and improve glycemic control. Glucose-responsive insulin delivery systems have been developed by coupling glucose oxidase with a stimuli-responsive biomaterial. However, the challenge of achieving desirable release kinetics (i.e., insulin release within minutes after glucose elevation and duration of release on the order of weeks) still remains. Here, we develop a glucose-responsive delivery system using encapsulated glucose-responsive, acetalated-dextran nanoparticles in porous alginate microgels. The nanoparticles respond rapidly to changes in glucose concentrations while the microgels provide them with protection and stability, allowing for extended glucose-responsive insulin release. This system reduces blood sugar in a diabetic mouse model at a rate similar to naked insulin and responds to a glucose challenge 3 days after administration similarly to a healthy animal. With 2 doses of microgels containing 60 IU/kg insulin each, we are able to achieve extended glycemic control in diabetic mice for 22 days.
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