胶体药物载体的治疗应用

Gillian M. Barratt
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引用次数: 290

摘要

胶体药物载体,如脂质体和纳米颗粒,可以通过改变其分布来改善现有药物和新药的治疗指数,从而提高其疗效和/或降低其毒性。这是因为药物的分布遵循载体的分布,而不是依赖于药物本身的物理化学性质。如果这些给药系统在靶点和给药途径方面经过精心设计,它们可能会为新一类活性分子(如肽和蛋白质、基因和寡核苷酸)带来的一些给药问题提供一种解决方案。它们也可能为更传统的药物提供替代模式,比如高度疏水的小分子。本文综述了胶体颗粒载体系统(直径25 nm至1 μm)在此类应用中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic applications of colloidal drug carriers

Colloidal drug carriers such as liposomes and nanoparticles can be used to improve the therapeutic index of both established and new drugs by modifying their distribution, and thus increasing their efficacy and/or reducing their toxicity. This is because the drug distribution then follows that of the carrier, rather than depending on the physicochemical properties of the drug itself. If these delivery systems are carefully designed with respect to the target and the route of administration, they may provide one solution to some of the delivery problems posed by new classes of active molecules, such as peptides and proteins, genes and oligonucleotides. They may also offer alternative modes for more conventional drugs, such as highly hydrophobic small molecules. This review discusses the use of colloidal, particulate carrier systems (25 nm to 1 μm in diameter) in such applications.

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