Volume 6, Issue 2 , Pages 210-213, April 2010
Doxorubicin-loaded solid lipid nanoparticles to overcome multidrug resistance in cancer therapy
Abstract
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.
Key words: Solid lipid nanoparticles, Multidrug resistance, Doxorubicin, P-glycoprotein, Doxorubicin-resistant breast cancer
To access this article, please choose from the options below
This work was supported by a National Research Foundation of Korea (NRF) grant funded by the Ministry of Education, Science and Technology (MEST) through the Research Center for Resistant Cells (R13-2003-009).
PII: S1549-9634(10)00006-7
doi:10.1016/j.nano.2009.12.006
© 2010 Elsevier Inc. All rights reserved.
Volume 6, Issue 2 , Pages 210-213, April 2010
