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Single-step assembly of polymer-lipid hybrid nanoparticles for mitomycin C delivery

机译:用于丝裂霉素C递送的聚合物-脂质杂化纳米颗粒的一步组装

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摘要

Mitomycin C is one of the most effective chemotherapeutic agents for a wide spectrum of cancers, but its clinical use is still hindered by the mitomycin C (MMC) delivery systems. In this study, the MMC-loaded polymer-lipid hybrid nanoparticles (NPs) were prepared by a single-step assembly (ACS Nano 2012, 6:4955 to 4965) of MMC-soybean phosphatidyhlcholine (SPC) complex (Mol. Pharmaceutics 2013, 10:90 to 101) and biodegradable polylactic acid (PLA) polymers for intravenous MMC delivery. The advantage of the MMC-SPC complex on the polymer-lipid hybrid NPs was that MMC-SPC was used as a structural element to offer the integrity of the hybrid NPs, served as a drug preparation to increase the effectiveness and safety and control the release of MMC, and acted as an emulsifier to facilitate and stabilize the formation. Compared to the PLA NPs/MMC, the PLA NPs/MMC-SPC showed a significant accumulation of MMC in the nuclei as the action site of MMC. The PLA NPs/MMC-SPC also exhibited a significantly higher anticancer effect compared to the PLA NPs/MMC or free MMC injection in vitro and in vivo. These results suggested that the MMC-loaded polymer-lipid hybrid NPs might be useful and efficient drug delivery systems for widening the therapeutic window of MMC and bringing the clinical use of MMC one step closer to reality.
机译:丝裂霉素C是用于多种癌症的最有效的化学治疗剂之一,但丝裂霉素C(MMC)递送系统仍然阻碍了它的临床应用。在这项研究中,通过MMC-大豆磷脂酰胆碱(SPC)复合物的单步组装(ACS Nano 2012,6:4955至4965)制备了载有MMC的聚合物-脂质杂化纳米颗粒(NPs)(Mol。Pharmaceutics 2013, 10:90至101)和可生物降解的聚乳酸(PLA)聚合物,用于静脉内MMC递送。 MMC-SPC复合物在聚合物-脂质杂化NP上的优势在于,MMC-SPC被用作提供杂化NP完整性的结构元素,用作药物制剂以提高有效性和安全性并控制释放MMC,并充当乳化剂以促进和稳定地层。与PLA NPs / MMC相比,PLA NPs / MMC-SPC在核中作为MMC的作用部位表现出大量的MMC积累。与PLA NPs / MMC或在体外和体内进行免费MMC注射相比,PLA NPs / MMC-SPC还表现出明显更高的抗癌作用。这些结果表明,载有MMC的聚合物-脂质杂化NP可能是有用和有效的药物递送系统,可拓宽MMC的治疗范围,并使MMC的临床应用更加接近现实。

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