Long-Acting Hydrogel-Based Depot Formulations of Tirzepatide and Semaglutide for the Management of Type 2 Diabetes and Weight

IF 3.2 4区 医学 Q2 PHARMACOLOGY & PHARMACY
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 M. Williams, Vannessa Doulames, Samya Sen, Manoj K. Manna, Alakesh Alakesh, Katie Lu, Ian Hall, Eric A. Appel
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Abstract

Several incretin hormone therapies have been clinically approved and have revolutionized the treatment of diabetes and obesity. Promising therapeutics include semaglutide (Ozempic and Wegovy), a glucagon-like peptide-1 (GLP-1) receptor agonist, and tirzepatide (Mounjaro), a dual agonist for GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) receptors. These molecules help 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 previously reported the development of an injectable hydrogel depot technology enabling months-long release of semaglutide (Sema). Here, we further developed this technology for improved prolonged release of both Sema and tirzepatide (TZP). In a type 2 diabetes rat model, we show that 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 injectable hydrogel depot is easy to manufactureand exhibits excellent biocompatibility, enabling months-long treatments with the potential to improve the management of diabetes and weight.

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替西帕肽和西马鲁肽的长效水凝胶储备制剂用于治疗2型糖尿病和体重
几种促肠促胰岛素激素疗法已被临床批准,并彻底改变了糖尿病和肥胖的治疗。有希望的治疗方法包括semaglutide (Ozempic和Wegovy),一种胰高血糖素样肽-1 (GLP-1)受体激动剂,以及tirzepatide (Mounjaro),一种GLP-1和葡萄糖依赖性胰岛素性多肽(GIP)受体的双重激动剂。这些分子有助于调节血糖水平,增强胰岛素分泌和敏感性,降低食欲。目前,这些治疗需要每周注射一次,这对患者来说是一个挑战。我们之前报道了一种可注射水凝胶储存技术的开发,该技术可以使Sema释放数月之久。在这里,我们进一步开发了该技术,以改善Sema和替西帕肽(TZP)的延长释放。在2型糖尿病大鼠模型中,我们发现单次给药Sema或TZP的水凝胶制剂可以维持相关的药物水平超过6周。在这些研究中,与每日在标准水溶液中注射Sema或TZP相比,单次给药Sema或TZP的长效水凝胶疗法在调节血糖和体重方面同样有效。这种可注射的水凝胶储库易于制造,具有良好的生物相容性,可以进行长达数月的治疗,有可能改善糖尿病和体重的管理。
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来源期刊
Advanced Therapeutics
Advanced Therapeutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.10
自引率
2.20%
发文量
130
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