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Co-delivery of doxorubicin and imatinib by pH sensitive cleavable PEGylated nanoliposomes with folate-mediated targeting to overcome multidrug resistance. | LitMetric

AI Article Synopsis

  • Multidrug resistance is a significant challenge in treating breast cancer, and the study focuses on overcoming this issue using a novel drug delivery system.
  • Researchers created folate receptor-targeted, pH-sensitive liposomes that co-load doxorubicin (DOX) and imatinib (IM) for effective drug release in acidic tumor environments.
  • The combination of DOX and IM in these liposomes not only improves drug stability and efficacy but also helps to reverse drug resistance, enhancing anti-tumor effects in both lab and live settings.

Article Abstract

Multidrug resistance to chemotherapeutic drugs is a major obstacle to breast cancer treatment. In this study, doxorubicin (DOX) and imatinib (IM) were co-loaded into folate receptor targeted (FR-targeted) pH-sensitive liposomes (denoted as FPL-DOX/IM) to fulfill intracellular acid-sensitive release and reverse drug resistance. FPL-DOX/IM could maintain stability in blood circulation with approximate diameters of 100 nm and rapidly release encapsulated drugs in tumor acidic microenvironment. Moreover, the IM in combination therapy could overcome chemoresistance associated with DOX effectively by inhibiting ABC transporter function and improving chemotherapy sensitivity. The designed liposomes co-loaded with DOX and IM significantly enhanced anti-tumor effects both in vitro and in vivo. These findings suggest that FPL-DOX/IM provides a novel strategy to improve chemotherapeutic efficacy against MDR tumors.

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Source
http://dx.doi.org/10.1016/j.ijpharm.2018.03.024DOI Listing

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