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The Next Generation of Platinum Drugs: Targeted Pt(II) Agents, Nanoparticle Delivery, and Pt(IV) Prodrugs

机译:下一代铂类药物:靶向pt(II)剂,纳米粒子递送和pt(IV)前药

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摘要

The platinum drugs, cisplatin, carboplatin, and oxaliplatin, prevail in the treatment of cancer, but new platinum agents have been very slow to enter the clinic. Recently, however, there has been a surge of activity, based on a great deal of mechanistic information, aimed at developing nonclassical platinum complexes that operate via mechanisms of action distinct from those of the approved drugs. The use of nanodelivery devices has also grown, and many different strategies have been explored to incorporate platinum warheads into nanomedicine constructs. In this Review, we discuss these efforts to create the next generation of platinum anticancer drugs. The introduction provides the reader with a brief overview of the use, development, and mechanism of action of the approved platinum drugs to provide the context in which more recent research has flourished. We then describe approaches that explore nonclassical platinum(II) complexes with trans geometry or with a monofunctional coordination mode, polynuclear platinum(II) compounds, platinum(IV) prodrugs, dual-threat agents, and photoactivatable platinum(IV) complexes. Nanoparticles designed to deliver platinum(IV) complexes will also be discussed, including carbon nanotubes, carbon nanoparticles, gold nanoparticles, quantum dots, upconversion nanoparticles, and polymeric micelles. Additional nanoformulations, including supramolecular self-assembled structures, proteins, peptides, metal–organic frameworks, and coordination polymers, will then be described. Finally, the significant clinical progress made by nanoparticle formulations of platinum(II) agents will be reviewed. We anticipate that such a synthesis of disparate research efforts will not only help to generate new drug development ideas and strategies, but also will reflect our optimism that the next generation of approved platinum cancer drugs is about to arrive.
机译:铂药物(顺铂,卡铂和奥沙利铂)在癌症的治疗中占主导地位,但是新的铂药物进入临床的过程非常缓慢。然而,最近,基于大量的机械信息,激增了许多活动,旨在开发非经典的铂络合物,这些络合物通过不同于批准药物的作用机理起作用。纳米递送装置的使用也在增长,并且已经探索了许多不同的策略来将铂弹头整合到纳米药物构造中。在本综述中,我们讨论了创建下一代铂类抗癌药物的这些努力。引言为读者提供了已获批准的铂类药物的使用,开发和作用机理的简要概述,以提供最新研究蓬勃发展的背景。然后,我们描述探索具有反式几何或单功能配位模式的非经典铂(II)配合物,多核铂(II)化合物,铂(IV)前药,双重威胁剂和可光活化的铂(IV)配合物的方法。还将讨论设计用于传递铂(IV)配合物的纳米粒子,包括碳纳米管,碳纳米粒子,金纳米粒子,量子点,上转换纳米粒子和聚合物胶束。然后将介绍其他纳米制剂,包括超分子自组装结构,蛋白质,肽,金属有机骨架和配位聚合物。最后,将对铂(II)剂的纳米颗粒制剂取得的重大临床进展进行回顾。我们预计,这样分散的研究工作将综合在一起,不仅有助于产生新的药物开发思路和策略,而且将反映出我们对下一代已获批准的铂金抗癌药物即将到来的乐观态度。

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