用于癌症治疗的可刺激激活金属前体药物的最新进展

Jinzhe Liang, Fangmian Wei, Hui Chao
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摘要

过去几十年来,铂类药物的临床批准促使了新型金属络合物的开发,但同时也出现了一些严重问题,特别是水溶性差、耐药性和对患者的毒性,这些问题极大地阻碍了临床试验和疗效的提高。为了解决这些问题,人们提出了肿瘤金属药物的概念。一些可刺激活化的金属原药为设计和制备具有最大疗效和可忽略不利副作用的特定位点原药提供了新的思路。本综述概述了过去 20 年来刺激可激活金属原药的最新进展,其中涉及内源性和外源性刺激。文中讨论了智能刺激可激活金属前药的典型例子,包括其分子结构、激活机制和有前景的生物医学应用。最后,还讨论了金属原药面临的挑战和未来展望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Recent progress in stimuli-activable metallo-prodrugs for cancer therapy
The clinical approval of platinum-based drugs has prompted the development of novel metallo-complexes during the last several decades, while severe problems, especially for poor water solubility, drug resistance and toxicity in patients, greatly hindered the clinical trials and curative efficacy. To address these issues, the concept of metallo-prodrugs has been proposed for oncology. Some stimuli-activable metallo-prodrugs provide new insights for designing and preparing site-specific prodrugs with maximized therapeutic efficacy and negligible unfavorable by-effects. In this review, recent progress in stimuli-activable metallo-prodrugs in the past 20 years has been overviewed, where endogenous and exogenous stimuli have been involved. Typical examples of smart stimuli-activable metallo-prodrugs are discussed regarding to their molecular structure, activation mechanism, and promising biomedical applications. In the end, challenges and future perspectives in metallo-prodrugs have been discussed.
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