前药
奥沙利铂
顺铂
卡铂
合理设计
药品
组合化学
化学
药理学
癌症
化疗
纳米技术
医学
材料科学
内科学
结直肠癌
作者
Lingkai Tang,Yafei Luo,Wenqin Luo,Guangzhou Sun,Yu Jiang,Zhigang Zhang,Xinru Yue,Siyao Li,Liang Li,Wei Liu,Jianping Hu
出处
期刊:Current Protein & Peptide Science
[Bentham Science Publishers]
日期:2024-06-26
卷期号:25 (10): 797-813
标识
DOI:10.2174/0113892037297416240525155628
摘要
: Platinum (II) drugs, including cisplatin, carboplatin, and oxaliplatin, have achieved significant clinical success in cancer treatment. However, their clinical application has been greatly hindered by various adverse factors, such as non-specific activation and drug resistance. Compared with Pt(II) drugs, the axial ligands within Pt(IV) compounds can improve the pharmacokinetic properties, selectivity, and biological activity, implementing alternative cytotoxic mechanisms beyond DNA cross-linking and partially overcoming drug resistance. The controlled conversion of Pt(IV) prodrugs into Pt(II) agents at the tumor site has been extensively explored internationally. In this review, Pt(IV) prodrug modification strategies are first summarized, and the development of the predominant external and internal photosensitizers is listed. Finally, three representative photoreduction mechanisms and strategies for developing corresponding Pt(IV) prodrugs are discussed. This work provides constructive instruction for the subsequent molecular design of Pt(IV) prodrugs.
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