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铂(IV)类抗癌前药——假说与事实

Platinum(iv) anticancer prodrugs - hypotheses and facts.

作者信息

Gibson Dan

机构信息

Institute of Drug Research, School of Pharmacy, The Hebrew University, Jerusalem, Israel.

出版信息

Dalton Trans. 2016 Aug 16;45(33):12983-91. doi: 10.1039/c6dt01414c.

Abstract

In this manuscript we focus on Pt(iv) anticancer prodrugs. We explore the main working hypotheses for the design of effective Pt(iv) prodrugs and note the exceptions to the common assumptions that are prevalent in the field. Special attention was devoted to the emerging class of "dual action" Pt(iv) prodrugs, where bioactive ligands are conjugated to the axial positions of platinum in order to obtain orthogonal or complementary effects that will increase the efficacy of killing the cancer cells. We discuss the rationale behind the design of the "dual action" prodrugs and the results of the pharmacological studies obtained. Simultaneous release of two bioactive moieties inside the cancer cells often triggers several processes that together determine the fate of the cell. Pt(iv) complexes provide many opportunities for applying new concepts in targeting, synergistic cell killing and exploiting novel nanodelivery systems.

摘要

在本手稿中,我们聚焦于铂(IV)抗癌前药。我们探究了设计有效铂(IV)前药的主要工作假设,并指出了该领域普遍存在的常见假设的例外情况。特别关注了新兴的“双功能”铂(IV)前药类别,其中生物活性配体与铂的轴向位置共轭,以获得正交或互补效应,从而提高杀死癌细胞的功效。我们讨论了“双功能”前药设计背后的原理以及所获得的药理学研究结果。癌细胞内两个生物活性部分的同时释放通常会触发多个共同决定细胞命运的过程。铂(IV)配合物为在靶向、协同细胞杀伤和开发新型纳米递送系统中应用新概念提供了许多机会。

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