Reversal of multidrug resistance in vitro by co-delivery of MDR1 targeting siRNA and doxorubicin using a novel cationic poly(lactide-co-glycolide) nanoformulation

作者: Ranjita Misra , Manasi Das , Bhabani Sankar Sahoo , Sanjeeb K. Sahoo

DOI: 10.1016/J.IJPHARM.2014.08.056

关键词: Multiple drug resistanceDoxorubicinChemistryPoly lactide co glycolideCationic polymerizationPharmacologyDrug resistanceIn vitroNanocarriersDrug

摘要: Over expression of drug efflux transporters such as P-glycoprotein (P-gp) cumulatively leading to multidrug resistance (MDR) embodies a major hindrance for successful cancer therapy. A paradigm nanomedicinal approach involving an anticancer and modulators within one multifunctional nanocarrier-based delivery system represent ideal modality the treatment MDR. In this regards, we have developed cationic polymeric nanoparticulate loaded with MDR1-siRNA doxorubicin. Results indicated augmented synergistic effect combinational nanoformulation in overcoming MDR MCF-7/ADR cells. Therefore, above regime could be promising co-delivery effective therapy resistant breast cancer.

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