肽
水溶液
聚乙二醇化
化学
降级(电信)
生物利用度
治疗指标
组合化学
生化工程
药品
计算机科学
药理学
生物化学
医学
有机化学
聚乙二醇
工程类
电信
作者
Primawan Putra Nugrahadi,Wouter L.J. Hinrichs,Henderik W. Frijlink,Christian Schöneich,Christina Avanti
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2023-03-14
卷期号:15 (3): 935-935
被引量:55
标识
DOI:10.3390/pharmaceutics15030935
摘要
Over the past few decades, there has been a tremendous increase in the utilization of therapeutic peptides. Therapeutic peptides are usually administered via the parenteral route, requiring an aqueous formulation. Unfortunately, peptides are often unstable in aqueous solutions, affecting stability and bioactivity. Although a stable and dry formulation for reconstitution might be designed, from a pharmaco-economic and practical convenience point of view, a peptide formulation in an aqueous liquid form is preferred. Designing formulation strategies that optimize peptide stability may improve bioavailability and increase therapeutic efficacy. This literature review provides an overview of various degradation pathways and formulation strategies to stabilize therapeutic peptides in aqueous solutions. First, we introduce the major peptide stability issues in liquid formulations and the degradation mechanisms. Then, we present a variety of known strategies to inhibit or slow down peptide degradation. Overall, the most practical approaches to peptide stabilization are pH optimization and selecting the appropriate type of buffer. Other practical strategies to reduce peptide degradation rates in solution are the application of co-solvency, air exclusion, viscosity enhancement, PEGylation, and using polyol excipients.
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