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双配体功能化纳米金刚石通过靶向癌细胞线粒体的药物传递来规避耐药性。

Cancer-Cell-Specific Mitochondria-Targeted Drug Delivery by Dual-Ligand-Functionalized Nanodiamonds Circumvent Drug Resistance.

机构信息

Department of Biology and Chemistry, City University of Hong Kong , Kowloon Tong, Hong Kong SAR.

Key Laboratory of Biochip Technology, Biotech and Health Care, Shenzhen Research Institute of City University of Hong Kong , Shenzhen 518057, China.

出版信息

ACS Appl Mater Interfaces. 2017 Apr 5;9(13):11780-11789. doi: 10.1021/acsami.6b15954. Epub 2017 Mar 21.

Abstract

We demonstrate a nanotechnology approach for the development of cancer-cell-specific subcellular organelle-targeted drug nanocarriers based on photostable nanodiamonds (ND) functionalized with folic acid and mitochondrial localizing sequence (MLS) peptides. We showed that these multifunctional NDs not only distinguish between cancer cells and normal cells, and transport the loaded drugs across the plasma membrane of cancer cells, but also selectively deliver them to mitochondria and induce significant cytotoxicity and cell death compared with free Dox localized in lysosomes. Importantly, the cellular uptake of Dox was dramatically increased in a resistant model of MCF-7 cells, which contributed to the significant circumvention of P-glycoprotein-mediated drug resistance. Our work provides a novel method of designing nanodiamond-based carriers for targeted delivery and for circumventing drug resistance in doxorubicin-resistant human breast adenocarcinoma cancer cells.

摘要

我们展示了一种基于光敏纳米金刚石(ND)的纳米技术方法,该方法可用于开发针对癌细胞亚细胞细胞器的靶向药物纳米载体,纳米金刚石经过叶酸和线粒体定位序列(MLS)肽的功能化修饰。我们表明,这些多功能 ND 不仅可以区分癌细胞和正常细胞,而且可以将负载的药物穿过癌细胞的质膜运输,并且与定位于溶酶体的游离 Dox 相比,它们还可以选择性地将其递送至线粒体并诱导明显的细胞毒性和细胞死亡。重要的是,在 MCF-7 细胞的耐药模型中,Dox 的细胞摄取量大大增加,这有助于显著克服 P-糖蛋白介导的耐药性。我们的工作为设计基于纳米金刚石的载体进行靶向递药以及克服多柔比星耐药的人乳腺癌腺癌细胞中的耐药性提供了一种新方法。

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