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Overcoming cancer multidrug resistance by codelivery of doxorubicin and verapamil with hydrogel nanoparticles.
Qin, Ming; Lee, Yong-Eun Koo; Ray, Aniruddha; Kopelman, Raoul.
Afiliación
  • Qin M; Department of Chemistry, University of Michigan, Ann Arbor, MI, 48109, USA.
Macromol Biosci ; 14(8): 1106-15, 2014 Aug.
Article en En | MEDLINE | ID: mdl-24771682
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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sistemas de Liberación de Medicamentos / Resistencia a Múltiples Medicamentos / Resistencia a Antineoplásicos / Hidrogel de Polietilenoglicol-Dimetacrilato / Nanopartículas / Neoplasias / Antineoplásicos Límite: Humans Idioma: En Revista: Macromol Biosci Asunto de la revista: BIOQUIMICA Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sistemas de Liberación de Medicamentos / Resistencia a Múltiples Medicamentos / Resistencia a Antineoplásicos / Hidrogel de Polietilenoglicol-Dimetacrilato / Nanopartículas / Neoplasias / Antineoplásicos Límite: Humans Idioma: En Revista: Macromol Biosci Asunto de la revista: BIOQUIMICA Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos