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Isolated cell-bound membrane vesicles (CBMVs) as a novel class of drug nanocarriers

Yang Zhang, Yang Liu, Wendiao Zhang, Qisheng Tang, Yun Zhou, Yuanfang Li, Tong Rong, Huaying Wang, Yong Chen

2020Journal of Nanobiotechnology31 citationsDOIOpen Access PDF

Abstract

BACKGROUND: Cell-bound membrane vesicles (CBMVs) are a type of membrane vesicles different from the well-known extracellular vesicles (EVs). In recent years, the applications of EVs as drug delivery systems have been studied widely. A question may arise whether isolated CBMVs also have the possibility of being recruited as a drug delivery system or nanocarrier? METHODS: To test the possibility, CBMVs were isolated/purified from the surfaces of cultured endothelial cells, loaded with a putative antitumor drug doxorubicin (Dox), and characterized. Subsequently, cellular experiments and animal experiments using mouse models were performed to determine the in vitro and in vivo antitumor effects of Dox-loaded CBMVs (Dox-CBMVs or Dox@CBMVs), respectively. RESULTS: Both Dox-free and Dox-loaded CBMVs were globular-shaped and nanometer-sized with an average diameter of ~ 300-400 nm. Dox-CBMVs could be internalized by cells and could kill multiple types of cancer cells. The in vivo antitumor ability of Dox-CBMVs also was confirmed. Moreover, Quantifications of blood cells (white blood cells and platelets) and specific enzymes (aspartate aminotransferase and creatine kinase isoenzymes) showed that Dox-CBMVs had lower side effects compared with free Dox. CONCLUSIONS: The data show that the CBMV-entrapped Doxorubicin has the antitumor efficacy with lower side effects. This study provides evidence supporting the possibility of isolated cell-bound membrane vesicles as a novel drug nanocarrier.

Topics & Concepts

NanocarriersDoxorubicinIn vivoVesicleDrug deliveryChemistryIn vitroTargeted drug deliveryPharmacologyBiochemistryBiologyMembraneChemotherapyOrganic chemistryBiotechnologyGeneticsExtracellular vesicles in diseaseNanoplatforms for cancer theranosticsNanoparticle-Based Drug Delivery
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