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Antibody-targeting of Drug-loaded Micelles to Acute Myeloid Leukemia Cells

机译:载药胶束针对急性髓样白血病细胞的抗体靶向。

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Antibody targeting greatly enhanced the ability of PSMA-b-PS micelles to bind CD123 positive cells in vitro. Homing of PTL-loaded micelles has not significantly enhanced PTL cytotoxicity compared to untargeted micelles in vitro, but may drastically improve PTL efficacy in vivo due to increased bioavailability and LSC-specific delivery. Future studies will focus on PTL delivery mechanisms of targeted and non-targeted micelles, and the ability to reduce off-target drug accumulation in mixed primary cell culture systems.
机译:靶向抗体极大地增强了PSMA-b-PS胶束在体外结合CD123阳性细胞的能力。与体外未靶向的胶束相比,归巢于PTL的胶束的归巢并没有显着增强PTL的细胞毒性,但是由于增加的生物利用度和LSC特异性递送,可以显着提高体内的PTL效力。未来的研究将集中于靶向和非靶向胶束的PTL传递机制,以及减少混合原代细胞培养系统中脱靶药物积累的能力。

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