化学
血糖性
生物结合
胰高血糖素样肽-1
免疫原性
肽
共轭体系
肠促胰岛素
分泌物
效力
生物化学
药理学
胰岛素
糖尿病
内科学
内分泌学
聚合物
抗原
2型糖尿病
体外
有机化学
免疫学
生物
医学
作者
Caroline Tsao,Peng Zhang,Zhefan Yuan,Dianyu Dong,Kan Wu,Liqian Niu,Patrick McMullen,Sijin Luozhong,Hsiang‐Chieh Hung,Rene Yu-Hong Cheng,Shaoyi Jiang
标识
DOI:10.1021/acs.bioconjchem.0c00286
摘要
Glucagon-like peptide-1 (GLP-1) is of particular interest for treating type 2 diabetes mellitus (T2DM), as it induces insulin secretion in a glucose-dependent fashion and has the potential to facilitate weight control. However, native GLP-1 is a short incretin peptide that is susceptible to fast proteolytic inactivation and rapid clearance from the circulation. Various GLP-1 analogs and bioconjugation of GLP-1 analogs have been developed to counter these issues, but these modifications are frequently accompanied by the sacrifice of potency and the induction of immunogenicity. Here, we demonstrated that with the conjugation of a zwitterionic polymer, poly(carboxybetaine) (pCB), the pharmacokinetic properties of native GLP-1 were greatly enhanced without serious negative effects on its potency and secondary structure. The pCB conjugated GLP-1 further provided glycemic control for up to 6 days in a mouse study. These results illustrate that the conjugation of pCB could realize the potential of using native GLP-1 for prolonged glycemic control in treating T2DM.
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