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通过化学偶联和临床应用来设计肽类药物治疗剂。

Engineering peptide drug therapeutics through chemical conjugation and implication in clinics.

机构信息

State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, Gansu, China.

Key Laboratory of Preclinical Study for New Drugs of Gansu Province, Institute of Pathology, School of Basic Medical Sciences, Lanzhou University, Lanzhou, Gansu, China.

出版信息

Med Res Rev. 2024 Nov;44(6):2420-2471. doi: 10.1002/med.22046. Epub 2024 May 5.

Abstract

The development of peptide drugs has made tremendous progress in the past few decades because of the advancements in modification chemistry and analytical technologies. The novel-designed peptide drugs have been modified through various biochemical methods with improved diagnostic, therapeutic, and drug-delivery strategies. Researchers found it a helping hand to overcome the inherent limitations of peptides and bring continued advancements in their applications. Furthermore, the emergence of peptide-drug conjugates (PDCs)-utilizes target-oriented peptide moieties as a vehicle for cytotoxic payloads via conjugation with cleavable chemical agents, resulting in the key foundation of the new era of targeted peptide drugs. This review summarizes the various classifications of peptide drugs, suitable chemical modification strategies to improve the ADME (adsorption, distribution, metabolism, and excretion) features of peptide drugs, and recent (2015-early 2024) progress/achievements in peptide-based drug delivery systems as well as their fruitful implication in preclinical and clinical studies. Furthermore, we also summarized the brief description of other types of PDCs, including peptide-MOF conjugates and peptide-UCNP conjugates. The principal aim is to provide scattered and diversified knowledge in one place and to help researchers understand the pinching knots in the science of PDC development and progress toward a bright future of novel peptide drugs.

摘要

在过去的几十年中,由于修饰化学和分析技术的进步,肽类药物的发展取得了巨大的进展。新型设计的肽类药物已经通过各种生化方法进行了修饰,改进了诊断、治疗和药物输送策略。研究人员发现,这些方法有助于克服肽类药物的固有局限性,并持续推动其应用的发展。此外,肽药物偶联物(PDC)的出现——利用靶向肽作为载体,通过与可切割的化学试剂结合,将细胞毒性有效载荷递送至靶标,为靶向肽药物的新时代奠定了基础。本综述总结了各种肽类药物的分类、合适的化学修饰策略,以改善肽类药物的 ADME(吸收、分布、代谢和排泄)特性,以及最近(2015 年初至 2024 年初)基于肽的药物输送系统的进展/成就及其在临床前和临床研究中的富有成效的应用。此外,我们还总结了其他类型的 PDC 的简要描述,包括肽-金属有机框架(MOF)偶联物和肽-上转换纳米粒子(UCNP)偶联物。主要目的是提供分散和多样化的知识,帮助研究人员了解 PDC 发展中的症结,并为新型肽类药物的美好未来指明方向。

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