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多肽的合成及其在抗肿瘤药物输送中的生物医学应用。

Syntheses of Polypeptides and Their Biomedical Application for Anti-Tumor Drug Delivery.

机构信息

Institute for Physical Chemistry, CeNIDE, University of Duisburg-Essen, 45141 Essen, Germany.

People's Hospital of Zhengzhou University, Zhengzhou University, Zhengzhou 450003, China.

出版信息

Int J Mol Sci. 2022 May 2;23(9):5042. doi: 10.3390/ijms23095042.

Abstract

Polypeptides have attracted considerable attention in recent decades due to their inherent biodegradability and biocompatibility. This mini-review focuses on various ways to synthesize polypeptides, as well as on their biomedical applications as anti-tumor drug carriers over the past five years. Various approaches to preparing polypeptides are summarized, including solid phase peptide synthesis, recombinant DNA techniques, and the polymerization of activated amino acid monomers. More details on the polymerization of specifically activated amino acid monomers, such as amino acid N-carboxyanhydrides (NCAs), amino acid N-thiocarboxyanhydrides (NTAs), and N-phenoxycarbonyl amino acids (NPCs), are introduced. Some stimuli-responsive polypeptide-based drug delivery systems that can undergo different transitions, including stability, surface, and size transition, to realize a better anti-tumor effect, are elaborated upon. Finally, the challenges and opportunities in this field are briefly discussed.

摘要

近几十年来,由于其固有可生物降解性和生物相容性,多肽引起了相当大的关注。本综述主要关注各种合成多肽的方法,以及过去五年中作为抗肿瘤药物载体的生物医学应用。总结了各种制备多肽的方法,包括固相肽合成、重组 DNA 技术和活性氨基酸单体的聚合。更详细地介绍了特定活化氨基酸单体的聚合,如氨基酸 N-羧酸酐(NCAs)、氨基酸 N-硫代羧酸酐(NTAs)和 N-苯甲酰基氨基酸(NPCs)。阐述了一些对刺激响应的基于多肽的药物输送系统,这些系统可以经历不同的转变,包括稳定性、表面和大小转变,以实现更好的抗肿瘤效果。最后,简要讨论了该领域的挑战和机遇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b8c/9104059/aa38c7f6c99f/ijms-23-05042-g001.jpg

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