
doi: 10.1038/ncomms2282
pmid: 23250412
Cellular microparticles are vesicular plasma membrane fragments with a diameter of 100-1,000 nanometres that are shed by cells in response to various physiological and artificial stimuli. Here we demonstrate that tumour cell-derived microparticles can be used as vectors to deliver chemotherapeutic drugs. We show that tumour cells incubated with chemotherapeutic drugs package these drugs into microparticles, which can be collected and used to effectively kill tumour cells in murine tumour models without typical side effects. We describe several mechanisms involved in this process, including uptake of drug-containing microparticles by tumour cells, synthesis of additional drug-packaging microparticles by these cells that contribute to the cytotoxic effect and the inhibition of drug efflux from tumour cells. This study highlights a novel drug delivery strategy with potential clinical application.
Ovarian Neoplasms, Drug Carriers, Mice, Inbred BALB C, Cell Membrane, Liver Neoplasms, Antineoplastic Agents, Mice, SCID, Neoplasms, Experimental, Mice, Methotrexate, Cell-Derived Microparticles, Cell Line, Tumor, Neoplasms, Animals, Female, Cisplatin
Ovarian Neoplasms, Drug Carriers, Mice, Inbred BALB C, Cell Membrane, Liver Neoplasms, Antineoplastic Agents, Mice, SCID, Neoplasms, Experimental, Mice, Methotrexate, Cell-Derived Microparticles, Cell Line, Tumor, Neoplasms, Animals, Female, Cisplatin
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