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Preparation and characterization of Pluronic/TPGS mixed micelles for solubilization of camptothecin

机译:Pluronic / TPGS混合胶束的制备与表征Camptothecin的溶解

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To increase the solubility and bioavailability of poorly soluble anticancer drug camptothecin (CPT), CPT-loaded mixed micelles were prepared. METHODS. Mixed micelles made of Pluronic P105 (P105) and D--tocopheryl polyethylene glycol 1000 succinate (TPGS) were prepared by film formation method and poorly soluble anticancer drug CPT was incorporated into the mixed micelles. The amount of CPT in the micellar phase was determined by the reversed phase-HPLC. The cytotoxicity of the CPT-loaded mixed micelles against MCF-7 cancer cell in vitro was assessed by the MTS colorimetric assay for the dehydrogenase activity of viable cell. RESULTS. The solubility of CPT by the mixed micelles was more than that of the free drug. The cytotoxicity of the CPT-loaded mixed micelles against MCF-7 cancer cell in vitro was remarkably higher than that of the free drug. CONCLUSIONS. Mixed micelles made of Pluronic P105 and TPGS may represent potential delivery system for sparingly soluble anticancer drugs.
机译:为了提高可溶性抗癌药物喜树碱(CPT)的溶解度和生物利用度,制备了加载负载的混合胶束。方法。通过薄膜形成方法制备由Pluronic P105(P105)和D - 生育基聚乙二醇1000琥珀酸盐(TPG)制成的混合胶束并将可溶性抗癌药物CPT掺入混合胶束中。胶束相中的CPT量由反相HPLC测定。通过MTS比色测定评估了对体外CPT加载的混合胶束对MCF-7癌细胞的细胞毒性进行了可活细胞的脱氢酶活性。结果。 CPT通过混合胶束的溶解度大于游离药物的溶解度。 CPT加载的混合胶束对MCF-7癌细胞体外的细胞毒性显着高于游离药物。结论。由Pluronic P105和TPG制造的混合胶束可以代表潜在的递送系统,用于避免溶于抗癌药物。

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