Glucagon-like peptide-1 receptor agonists for treatment of diabetes and obesity: advantage of oral delivery.

Frontiers in drug delivery Pub Date : 2024-11-06 eCollection Date: 2024-01-01 DOI:10.3389/fddev.2024.1456654
R R C New, M Bogus, G N Travers, U Hahn, A Vaiceliunaite, M Burnet, J H Wang, H Wen
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Abstract

GLP-1 receptor agonists ((GLP-1 RAs) are currently receiving a lot of attention because of their impact in diabetes, weight loss and other areas. While GLP-1 RAs in injectable form are highly efficacious, further work is required to develop oral versions which can deliver these peptides efficiently without requiring use of excessively high doses. This paper describes the ability of an oral peptide delivery formulation, Axcess™, to enhance uptake of GLP-1 receptor agonists via the intestine, resulting in changes in insulin and glucose blood levels indicative of biopotencies of 9% for exendin-4 and 14.8% for semaglutide in preclinical models. The route of delivery suggests that the peptides will be able to interact with the GLP-1 receptors on the vagal afferents of the intestine, as is the case for native GLP-1 in healthy individuals. GLP-1 receptor agonists administered via this route will be a valuable addition to the therapeutic modalities available for treatment of diabetes and obesity.

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治疗糖尿病和肥胖症的胰高血糖素样肽-1受体激动剂:口服给药的优势。
GLP-1受体激动剂(GLP-1 receptor agonists,简称GLP-1 RAs)因其在糖尿病、减肥等领域的作用而受到广泛关注。虽然注射形式的GLP-1 RAs是非常有效的,但需要进一步的工作来开发口服版本,以便在不需要使用过高剂量的情况下有效地递送这些肽。本文描述了口服肽递送制剂axess™的能力,通过肠道增强GLP-1受体激动剂的吸收,导致胰岛素和血糖水平的变化,表明临床前模型中exendin-4和semaglutide的生物效价分别为9%和14.8%。传递途径表明,肽将能够与肠迷走神经传入的GLP-1受体相互作用,就像健康个体的天然GLP-1一样。通过这种途径给药的GLP-1受体激动剂将是治疗糖尿病和肥胖症的一种有价值的治疗方式。
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