Reversal of multidrug resistance using poly(L-lactide)-vitamin E TPGS micelles in breast cancer cell

P. Y. Li, P. Lai, C. Lin
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引用次数: 5

Abstract

Drug resistance is a frequent clinical problem that seriously reduces the efficacy of many chemotherapy agents. In this study, the effect of micellar encapsulation using poly(L-lactide)-vitamin E TPGS (PLA-TPGS) copolymer on intracellular distribution of doxorubicin was studied in vitro. As our results, doxorubicin can be encapsulated successfully into PLA-TPGS formed micelle with a uniform particle size (≪ 200nm) that could exhibit the passive targeting ability to cancer tissue. Moreover, the nuclear accumulation of doxorubicin can be improved significantly in micelle form that can utilize as a potential carrier to overcome doxorubicin-resistance in breast MCF-7 cancer cells.
利用聚l -丙交酯-维生素E TPGS胶束逆转乳腺癌细胞的多药耐药
耐药是一个常见的临床问题,严重降低了许多化疗药物的疗效。本实验研究了聚l -丙交酯-维生素E TPGS (PLA-TPGS)共聚物胶束包封对阿霉素胞内分布的影响。我们的研究结果表明,阿霉素可以被成功地封装在PLA-TPGS形成的胶团中,该胶团具有均匀的粒径(≪200nm),能够表现出对癌症组织的被动靶向能力。此外,多柔比星的核积累可以以胶束形式显著改善,可以作为克服乳腺癌MCF-7癌细胞中多柔比星耐药的潜在载体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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