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靶向递送铂类抗癌配合物。

Targeted delivery of platinum-based anticancer complexes.

机构信息

Department of Chemistry, University of Warwick, Coventry CV4 7AL, UK.

出版信息

Curr Opin Chem Biol. 2013 Apr;17(2):175-88. doi: 10.1016/j.cbpa.2013.01.004. Epub 2013 Feb 7.

Abstract

The most widely used anticancer drugs are platinum-based. Their efficacy might be improved by carriers which can transport large numbers of Pt centres, shield the drug from premature activation, and/or deliver Pt specifically to cancer cells using vectors which recognise specific targets. We describe recent progress using functionalized carbon nanotubes (CNTs) and nanorods, hollow Prussian blue (HPB), magnetic iron oxide and gold nanoparticles, liposomes, nanogels and polymers, as well as active targeting by conjugation to biodegradable proteins and peptides (e.g. EGF, heparin, herceptin, somatostatin and TAT). Spatially targeted activation of Pt(IV) prodrugs using light is also a promising approach. Interestingly, use of these new delivery and targeting systems for platinum drugs can lead to species with unusual reactivity which can kill cancer cells by new mechanisms.

摘要

最广泛使用的抗癌药物是基于铂的。通过载体可以提高它们的疗效,这些载体可以运输大量的 Pt 中心,防止药物过早激活,并且/或者使用能够识别特定靶标的载体将 Pt 特异性递送到癌细胞中。我们描述了最近使用功能化碳纳米管(CNT)和纳米棒、空心普鲁士蓝(HPB)、磁性氧化铁和金纳米粒子、脂质体、纳米凝胶和聚合物的进展,以及通过与可生物降解的蛋白质和肽(例如 EGF、肝素、曲妥珠单抗、生长抑素和 TAT)缀合进行主动靶向。用光对 Pt(IV)前药进行空间靶向激活也是一种很有前途的方法。有趣的是,这些新的递药和靶向系统用于铂类药物可以产生具有异常反应性的物质,这些物质可以通过新的机制杀死癌细胞。

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