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载多柔比星的固体脂质纳米粒克服癌症治疗中的多药耐药性。

Doxorubicin-loaded solid lipid nanoparticles to overcome multidrug resistance in cancer therapy.

机构信息

BK21 Project Team, College of Pharmacy, Chosun University, Gwangju, South Korea.

出版信息

Nanomedicine. 2010 Apr;6(2):210-3. doi: 10.1016/j.nano.2009.12.006. Epub 2010 Jan 6.


DOI:10.1016/j.nano.2009.12.006
PMID:20060074
Abstract

UNLABELLED: In the present study we developed doxorubicin-loaded solid lipid nanoparticles (SLN-Dox) using biocompatible compounds, assessed the in vitro hemolytic effect, and examined their in vivo effects on drug retention and apoptosis intensity in P-glycoprotein-overexpressing MCF-7/ADR cells, a representative Dox-resistant breast cancer cell line. Our SLNs did not show hemolytic activity in human erythrocytes. In comparison with Dox, SLN-Dox efficiently enhanced apoptotic cell death through the higher accumulation of Dox in MCF-7/ADR cells. Therefore, SLN-Dox have potential to serve as a useful therapeutic approach to overcome the chemoresistance of adriamycin-resistant breast cancer. FROM THE CLINICAL EDITOR: Doxorubicin loaded solid lipid nanoparticles (SLN-Dox) were studied in a cell line representative of doxorubicin resistant breast cancer. The nanoparticles did not show hemolytic activity; furthermore, they efficiently enhanced apoptotic cell death through higher accumulation of doxorubicin in cancer cells. This approach may be viable in overcoming the chemoresistance of adriamycin resistant breast cancer.

摘要

未注明:在本研究中,我们使用生物相容性化合物制备了多柔比星负载的固体脂质纳米粒(SLN-Dox),评估了其体外溶血效应,并研究了它们在 P 糖蛋白过表达的 MCF-7/ADR 细胞(一种代表性的多柔比星耐药乳腺癌细胞系)中对药物保留和细胞凋亡强度的体内作用。我们的 SLN 在人红细胞中没有显示出溶血活性。与多柔比星相比,SLN-Dox 通过多柔比星在 MCF-7/ADR 细胞中的更高积累,有效地增强了细胞凋亡死亡。因此,SLN-Dox 有可能成为克服阿霉素耐药乳腺癌化疗耐药性的一种有用的治疗方法。

临床编辑:多柔比星负载的固体脂质纳米粒(SLN-Dox)在代表多柔比星耐药乳腺癌的细胞系中进行了研究。这些纳米粒没有显示出溶血活性; 此外,它们通过在癌细胞中更高地积累多柔比星,有效地增强了细胞凋亡死亡。这种方法在克服阿霉素耐药乳腺癌的化疗耐药性方面可能是可行的。

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