聚乙二醇脂质体阿霉素:目前和未来的应用综述

Conrad R Lewanski, Simon Stewart
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引用次数: 11

摘要

蒽环类药物,如阿霉素,在人类肿瘤中具有广谱的活性,但在一定程度上,由于它们非选择性地递送到正常组织宿主,从而产生毒性,因此受到限制。脂质体的发展提供了一种具有重大潜力的药物输送系统,可以靶向肿瘤,同时保留正常组织。一项重大突破是用聚乙二醇(聚乙二醇化)包裹脂质体,从而大大改变了药物的药代动力学。在这篇综述中,作者讨论了目前出现的聚乙二醇脂质体阿霉素的有希望的数据,并描述了可能的未来应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pegylated liposomal adriamycin: a review of current and future applications

Anthracyclines such as adriamycin have a broad spectrum of activity in human tumours, but are limited, to an extent, by their non-selective delivery to a host of normal tissues and hence, subsequent toxicity. The development of liposomes has offered a drug delivery system with significant potential to target tumours whilst sparing normal tissues. A significant breakthrough has been achieved by coating the liposome with polyethylene glycol (pegylation), and thus altering the pharmacokinetics of the drug considerably. In this review, the authors discuss the promising data now emerging with pegylated liposomal adriamycin, and also describe possible future applications.

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