赛马鲁肽
肠促胰岛素
医学
兴奋剂
2型糖尿病
糖尿病
胰岛素
药理学
车辆段
受体
内分泌学
利拉鲁肽
内科学
历史
考古
作者
Andrea I. d’Aquino,Changxin Dong,Leslee T. Nguyen,Jerry Yan,Carolyn K. Jons,Olivia M. Saouaf,Ye Eun Song,Noah Eckman,Sara Kapasi,Christian Milton Williams,Vanessa M. Doulames,Samya Sen,Manoj K. Manna,Alakesh Alakesh,Katie Lu,Ian P. Hall,Eric A. Appel
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2025-07-05
被引量:2
标识
DOI:10.1101/2025.07.02.662867
摘要
Several incretin hormone therapies have been clinically approved and have revolutionized the treatment of diabetes and obesity. Promising therapeutics include semaglutide (Ozempic and Wegovy), an agonist for glucagon-like peptide-1 (GLP-1) receptor, and tirzepatide (Mounjaro), a dual agonist for GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) receptors. These molecules help to regulate blood glucose levels, enhance insulin secretion and sensitivity, and reduce appetite. Currently, these treatments require weekly injections, which can be challenging for patients to adhere to. We recently reported the development of an injectable hydrogel depot technology enabling months-long release of semaglutide (Sema). Here, we further develop this technology for improved prolonged release of both Sema and tirzepatide (TZP). In a rat model of diabetes, we show a single administration of hydrogel-based formulations of either Sema or TZP maintained relevant drug levels for over 6 weeks. In these studies, single administrations of long-acting hydrogel-based therapies of Sema or TZP were similarly effective at regulating blood glucose and weight compared to daily injections of either Sema or TZP in standard aqueous vehicles. This hydrogel depot technology is easy to manufacture, injectable, and exhibits excellent biocompatibility, enabling months-long-acting treatments with the potential to improve management of diabetes and weight.
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