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用于癌症治疗的纳米颗粒作为药物载体的设计

Design of Nanoparticles as Drug Carriers for Cancer Therapy.

作者信息

Zhang Jin, Lan Christopher Q, Post Michael, Simard Benoit, Deslandes Yves, Hsieh Tsung Han

机构信息

Department of Chemical Engineering, University of Ottawa, Ottawa, Ontario, K1N 6N5

Department of Chemical Engineering, University of Ottawa, Ottawa, Ontario, K1N 6N5.

出版信息

Cancer Genomics Proteomics. 2006 May-Aug;3(3-4):147-157. Epub 2006 Jan 1.

Abstract

This review explores the recent chemotherapeutic work on drug delivery using nanoparticles as carriers for the targeted treatment of cancer. Compared to direct drug delivery, delivery through a carrier can increase the efficacy of a drug, but decrease the side-effects by utilizing the enhanced permeability and retention (EPR) effect and tumor-specific targeting. The search for efficient and safe transport vehicles (carriers) to achieve better drug availability at the target site has been a challenging yet exciting area of research. Current interest focuses on the colloidal nanoparticles (diameter <500 nm), including the biodegradable polymer- and liposome-systems, bioconjugating with antitumor drugs. These biocompatible nanoparticles, with an enlarged surface area-volume ratio can overcome non-cellular and cellular-based mechanisms of resistance and increase the selectivity of drugs towards cancer cells, while reducing their toxicity towards normal tissues. This review focuses on the evolution of nanoparticles as carriers for anticancer drug delivery, with emphasis on the biocompatible magnetic nanohybrids.

摘要

本综述探讨了近期利用纳米颗粒作为载体进行药物递送以实现癌症靶向治疗的化疗研究工作。与直接给药相比,通过载体给药可提高药物疗效,并利用增强的渗透与滞留(EPR)效应及肿瘤特异性靶向作用降低副作用。寻找高效且安全的运输工具(载体)以在靶位点实现更好的药物可用性一直是一个具有挑战性但又令人兴奋的研究领域。当前的研究兴趣集中在胶体纳米颗粒(直径<500 nm),包括可生物降解的聚合物和脂质体系统,它们与抗肿瘤药物进行生物共轭。这些具有增大的表面积与体积比的生物相容性纳米颗粒能够克服基于非细胞和细胞的耐药机制,并提高药物对癌细胞的选择性,同时降低其对正常组织的毒性。本综述重点关注纳米颗粒作为抗癌药物递送载体的发展,尤其着重于生物相容性磁性纳米杂化物。

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