Block copolymer micelles for delivery of cancer therapy: Transport at the whole body, tissue and cellular levels

被引:385
作者
Mikhail, Andrew S. [1 ]
Allen, Christine [1 ]
机构
[1] Univ Toronto, Inst Biomat & Biomed Engn, Leslie Dan Fac Pharm, Toronto, ON M5S 3M2, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
Block copolymer; Micelle; Tumor; Transport; Drug delivery; MULTIFUNCTIONAL POLYMERIC MICELLES; VIVO ANTITUMOR-ACTIVITY; TARGETED DRUG-DELIVERY; HUMAN TUMOR XENOGRAFT; POORLY SOLUBLE DRUGS; IN-VIVO; SOLID TUMORS; ANTICANCER DRUGS; GROWTH-FACTOR; PHASE-I;
D O I
10.1016/j.jconrel.2009.04.010
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The use of block copolymer micelles (BCMs) for the targeted delivery of chemotherapeutics has proven to be a promising approach for improving the therapeutic efficacy of pharmaceutical cancer therapy. Acceleration of the translation of BCM-based drug formulations from the fundamental stages of pre-clinical development to clinical use requires a greater understanding of the transport mechanisms that influence the fate of these nano-carrier systems at the whole body, tissue, and cellular levels. New information emerging regarding the intratumoral distribution, and tumor penetration of BCMs and other nanosystems in vivo, by non-invasive image-based assessment, has the potential to revolutionize our understanding and current approach to drug delivery in this field. This review aims to highlight these and other important advancements as well as to bring attention to the many critical questions that remain to be addressed regarding the fate of BCM-based drug formulations in vivo. (c) 2009 Elsevier R.V. All rights reserved.
引用
收藏
页码:214 / 223
页数:10
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