基于聚合物的胰高血糖素样肽-1 给药技术用于治疗糖尿病。

ISRN endocrinology Pub Date : 2012-01-01 Epub Date: 2012-05-30 DOI:10.5402/2012/340632
Pyung-Hwan Kim, Sung Wan Kim
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引用次数: 0

摘要

增量素激素、胰高血糖素样肽-1(GLP-1)及其受体激动剂(exendin-4)因具有葡萄糖稳态、促胰岛素作用以及减轻体重和促进食物摄入的功效而广为人知。然而,由于 GLP-1 会被二肽基肽酶-IV(DPP-IV)酶快速降解,且 exendin-4 会被肾脏排出体外,因此其临床应用一直受到限制。虽然 exendin-4 的半衰期比 GLP-1 长,但仍需要频繁注射才能维持治疗糖尿病的疗效。近几十年来,人们开发了各种聚合物输送系统,用于输送 GLP-1 和 exendin-4 基因或肽,使其长期发挥作用并在异位组织中额外产生。在此,我们将讨论如何对表达盒和肽进行修饰,以实现本地肽的长期生产和分泌。此外,还介绍了用于递送经修饰的 GLP-1 或 exendin-4 的非病毒或病毒系统的特点。此外,还讨论了与原生肽相比,最近通过与各种智能聚合物化学共轭来改善 GLP-1 或 exendin-4 肽的生物半衰期的努力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Polymer-based delivery of glucagon-like Peptide-1 for the treatment of diabetes.

Polymer-based delivery of glucagon-like Peptide-1 for the treatment of diabetes.

Polymer-based delivery of glucagon-like Peptide-1 for the treatment of diabetes.

The incretin hormones, glucagon-like peptide-1 (GLP-1) and its receptor agonist (exendin-4), are well known for glucose homeostasis, insulinotropic effect, and effects on weight loss and food intake. However, due to the rapid degradation of GLP-1 by dipeptidylpeptidase-IV (DPP-IV) enzyme and renal elimination of exendin-4, their clinical applications have been restricted. Although exendin-4 has longer half-life than GLP-1, it still requires frequent injections to maintain efficacy for the treatment of diabetes. In recent decades, various polymeric delivery systems have been developed for the delivery of GLP-1 and exendin-4 genes or peptides for their long-term action and the extra production in ectopic tissues. Herein, we discuss the modification of the expression cassettes and peptides for long-term production and secretion of the native peptides. In addition, the characteristics of nonviral or viral system used for a delivery of a modified GLP-1 or exendin-4 are described. Furthermore, recent efforts to improve the biological half-life of GLP-1 or exendin-4 peptide via chemical conjugation with various smart polymers via chemical conjugation compared with native peptide are discussed.

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