| Literature DB >> 24771682 |
Ming Qin1, Yong-Eun Koo Lee, Aniruddha Ray, Raoul Kopelman.
Abstract
The efficacy of chemotherapy is often inhibited by multidrug resistance (MDR). A highly engineerable hydrogel nanoparticle (NP) serves as a carrier for the optimal codelivery to tumor cells of the chemodrug, doxorubicin (Dox) and the chemosensitizer, verapamil (Vera), aiming at alleviating tumor MDR. The hydrogel NPs are prepared via the copolymerization of acrylamide and 2-carboxyethyl acrylate. Dox and Vera are post-loaded into the respective NPs, with drug loading around 7.7 wt% and 8.0 wt%, respectively. The codelivery of Dox-NPs and Vera-NPs increases the intracellular accumulation of Dox, and significantly enhances the cell killing ability of Dox with respect to NCI/ADR-RES cells in vitro. These findings suggest that such codelivery nanoplatforms provide a promising route for overcoming tumor MDR.Entities:
Keywords: cancer therapy; doxorubicin; hydrogel nanoparticles; multidrug resistance; verapamil
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Year: 2014 PMID: 24771682 DOI: 10.1002/mabi.201400035
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979