State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science , Fudan University , Shanghai 200438 , China.
Department of Orthopaedic Surgery , Shanghai Jiaotong University Affiliated Sixth People's Hospital , Shanghai 200233 , China.
ACS Appl Mater Interfaces. 2019 Aug 21;11(33):29604-29618. doi: 10.1021/acsami.9b10346. Epub 2019 Aug 9.
Diabetes and its complications have become a global challenge of public health. Herein, we aimed to develop a long-acting delivery system of lixisenatide (Lixi), a glucose-dependent antidiabetic peptide, based on an injectable hydrogel for the synchronous treatment of type 2 diabetes mellitus (T2DM) and associated complications. Two triblock copolymers, poly(ε-caprolactone--glycolic acid)-poly(ethylene glycol)-poly(ε-caprolactone--glycolic acid) and poly(d,l-lactic acid--glycolic acid)-poly(ethylene glycol)-poly(d,l-lactic acid--glycolic acid) possessing temperature-induced sol-gel transitions, were synthesized by us. Compared to the two single-component hydrogels, their 1/1 mixture hydrogel not only maintained the temperature-induced gelation but also exhibited a steadier degradation profile in vivo. Both in vitro and in vivo release studies demonstrated that the mixture hydrogel provided the sustained release of Lixi for up to 9 days, which was attributed to balanced electrostatic interactions between the positive charges in the peptide and the negative charges in the polymer carrier. The hypoglycemic efficacy of Lixi delivered from the mixture hydrogel after a single subcutaneous injection into diabetic db/db mice was comparable to that of twice-daily administrations of Lixi solution for up to 9 days. Furthermore, three successive administrations of the abovementioned gel system within a month significantly increased the plasma insulin level, lowered glycosylated hemoglobin, and improved the pancreatic function of the animals. These results were superior or equivalent to those of twice-daily injections of Lixi solution for 30 days, but the number of injections was markedly reduced from 60 to 3. Finally, an improvement in hyperlipidemia, augmentation of nerve fiber density, and enhancement of motor nerve conduction velocity in the gel formulation-treated db/db mice indicated that the sustained delivery of Lixi arrested and even ameliorated diabetic complications. These findings suggested that the Lixi-loaded mixture hydrogel has great potential for the treatment of T2DM with significant improvements in the health and quality of life of patients.
糖尿病及其并发症已成为全球公共卫生的挑战。在此,我们旨在开发一种基于可注射水凝胶的长效递药系统,用于递送利西那肽(Lixi),这是一种葡萄糖依赖性抗糖尿病肽,用于同步治疗 2 型糖尿病(T2DM)及其相关并发症。我们合成了两种具有温度诱导溶胶-凝胶转变的嵌段共聚物,聚(ε-己内酯-乙交酯)-聚乙二醇-聚(ε-己内酯-乙交酯)和聚(D,L-乳酸-乙交酯)-聚乙二醇-聚(D,L-乳酸-乙交酯)。与两种单一组分水凝胶相比,其 1/1 混合物水凝胶不仅保持了温度诱导的凝胶化,而且在体内还表现出更稳定的降解曲线。体外和体内释放研究表明,混合物水凝胶能够持续释放 Lixi 长达 9 天,这归因于肽中的正电荷与聚合物载体中的负电荷之间的平衡静电相互作用。将混合物水凝胶单次皮下注射到糖尿病 db/db 小鼠后,Lixi 的降血糖效果可与 Lixi 溶液每天两次给药长达 9 天的效果相媲美。此外,在一个月内连续三次给予上述凝胶系统可显著增加动物的血浆胰岛素水平,降低糖化血红蛋白,并改善动物的胰腺功能。这些结果优于或等同于 Lixi 溶液每天两次注射 30 天的结果,但注射次数从 60 次显著减少到 3 次。最后,在接受凝胶制剂治疗的 db/db 小鼠中,高血脂的改善、神经纤维密度的增加以及运动神经传导速度的提高表明,Lixi 的持续递送可阻止甚至改善糖尿病并发症。这些结果表明,载有 Lixi 的混合物水凝胶具有很大的潜力,可用于治疗 T2DM,显著改善患者的健康和生活质量。