Plasmonic nanobubble-enhanced endosomal escape processes for selective and guided intracellular delivery of chemotherapy to drug-resistant cancer cells.

Plasmonic nanobubble-enhanced endosomal escape processes for selective and guided intracellular delivery of chemotherapy to drug-resistant cancer cells.
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DOI:
10.1016/j.biomaterials.2011.11.015
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发表时间:
2012-02
期刊:
影响因子:
14
通讯作者:
Lapotko, Dmitri O.
Lapotko, Dmitri O.
中科院分区:
工程技术1区
文献类型:
--
作者:
Lukianova-Hleb, Ekaterina Y.;Belyanin, Andrey;Kashinath, Shruti;Wu, Xiangwei;Lapotko, Dmitri O.

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肿瘤化疗具有多药耐药、高非特异性毒性和肿瘤异质性等特点。我们报告了一种等离子体纳米气泡增强内体逃逸(PNBEE)的方法,用于通过癌细胞的单独靶向的金纳米颗粒和封装的药物(Doxil)的自组装来选择性地、快速地和引导性地向细胞内递送药物。与癌细胞中光学产生的Doxil等离子体纳米泡共定位,将药物释放到细胞质中,从而将针对这些耐药细胞的治疗功效提高了31倍,将药物剂量减少了20倍,治疗时间减少了3倍,与标准治疗相比,非特异性毒性增加了10倍。因此,PNBEE机制提供了在异质环境中选择性、安全和有效的细胞内药物递送,为药物治疗开辟了新的机会。
Cancer chemotherapies suffer from multi drug resistance, high non-specific toxicity and heterogeneity of tumors. We report a method of plasmonic nanobubble-enhanced endosomal escape (PNBEE) for the selective, fast and guided intracellular delivery of drugs through a self-assembly by cancer cells of separately targeted gold nanoparticles and encapsulated drug (Doxil). The co-localized with Doxil plasmonic nanobubbles optically generated in cancer cells released the drug into the cytoplasm thus increasing the therapeutic efficacy against these drug-resistant cells by 31-fold, reducing drug dose by 20-fold, the treatment time by 3-fold and the non-specific toxicity by 10-fold compared to standard treatment. Thus the PNBEE mechanism provided selective, safe and efficient intracellular drug delivery in heterogeneous environment opening new opportunities for drug therapies.
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