Use of a biomimetic hydrogel depot technology for sustained delivery of GLP-1 receptor agonists reduces burden of diabetes management

被引:13
作者
d'Aquino, Andrea I. [1 ]
Maikawa, Caitlin L. [2 ]
Nguyen, Leslee T. [3 ]
Lu, Katie [4 ]
Hall, Ian A. [2 ]
Jons, Carolyn K. [1 ]
Kasse, Catherine M. [1 ]
Yan, Jerry [2 ]
Prossnitz, Alexander N. [1 ]
Chang, Enmian [1 ]
Baker, Sam W. [5 ]
Hovgaard, Lars [6 ]
Steensgaard, Dorte B. [6 ]
Andersen, Hanne B. [6 ]
Simonsen, Lotte [7 ]
Appel, Eric A. [1 ,2 ,8 ,9 ,10 ]
机构
[1] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94025 USA
[2] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Biochem, Palo Alto, CA 94305 USA
[4] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Comparat Med, Palo Alto, CA 94305 USA
[6] Global Res Technol, Dept Biophys & Formulat, Novo Nord Pk, DK-2760 Malov, Denmark
[7] Global Drug Discovery, Dept Obes Res, Novo Nord Pk, DK-2760 Malov, Denmark
[8] Stanford Univ, ChEM H Inst, Stanford, CA 94305 USA
[9] Stanford Univ, Dept Pediat Endocrinol, Stanford, CA 94305 USA
[10] Stanford Univ, Woods Inst Environm, Stanford, CA 94305 USA
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
LIRAGLUTIDE; ADHERENCE; INSULIN; STREPTOZOTOCIN; SEMAGLUTIDE; ABSORPTION; STRATEGIES; INCRETINS; RELEASE; PEPTIDE;
D O I
10.1016/j.xcrm.2023.101292
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glucagon-like peptide-1 (GLP-1) is an incretin hormone and neurotransmitter secreted from intestinal L cells in response to nutrients to stimulate insulin and block glucagon secretion in a glucose-dependent manner. Long-acting GLP-1 receptor agonists (GLP-1 RAs) have become central to treating type 2 diabetes (T2D); however, these therapies are burdensome, as they must be taken daily or weekly. Technological innovations that enable less frequent administrations would reduce patient burden and increase patient compliance. Herein, we leverage an injectable hydrogel depot technology to develop a GLP-1 RA drug product capable of months-long GLP-1 RA delivery. Using a rat model of T2D, we confirm that one injection of hydrogel-based therapy sustains exposure of GLP-1 RA over 42 days, corresponding to a once-every-4-months therapy in humans. Hydrogel therapy maintains management of blood glucose and weight comparable to daily injections of a leading GLP-1 RA drug. This long-acting GLP-1 RA treatment is a promising therapy for more effective T2D management.
引用
收藏
页数:19
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