胰岛素
葡萄糖转运蛋白
内科学
内分泌学
低血糖
糖尿病
脂质体
2型糖尿病
化学
小泡
药理学
医学
生物化学
膜
作者
Qian Chen,Zhisheng Xiao,Chao Wang,Guojun Chen,Yuqi Zhang,Xudong Zhang,Xiao Han,Jinqiang Wang,Ye Xiao,Mark R. Prausnitz,Song Li,Zhen Gu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-11-02
卷期号:16 (11): 18223-18231
被引量:44
标识
DOI:10.1021/acsnano.2c05687
摘要
Glucose-responsive insulin delivery systems that mimic insulin secretion activity in the pancreas show great potential to improve clinical therapeutic outcomes for people with type 1 and advanced type 2 diabetes. Here, we report a glucose-responsive insulin delivery microneedle (MN) array patch that is loaded with red blood cell (RBC) vesicles or liposome nanoparticles containing glucose transporters (GLUTs) bound with glucosamine-modified insulin (Glu-Insulin). In hyperglycemic conditions, high concentrations of glucose in interstitial fluid can replace Glu-Insulin via a competitive interaction with GLUT, leading to a quick release of Glu-Insulin and subsequent regulation of blood glucose (BG) levels in vivo. To prolong the effective glucose-responsive insulin release from MNs, additional free Glu-Insulin, which serves as "stored insulin", is loaded after RBC vesicles or liposome nanoparticles bound with Glu-Insulin. In the streptozotocin (STZ)-induced type 1 diabetic mouse model, this smart GLUT-based insulin patch can effectively control BG levels without causing hypoglycemia.
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