首页> 外文会议>Controlled Release Society 31st annual meeting transactions: abstracts >Micelles as Carriers for Poorly Soluble Drugs: Preparation and Anticancer Activity In Vitroof Paclitaxel in Mixed Micelles of PEG-PE and Positively Charged Lipids
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Micelles as Carriers for Poorly Soluble Drugs: Preparation and Anticancer Activity In Vitroof Paclitaxel in Mixed Micelles of PEG-PE and Positively Charged Lipids

机译:胶束作为难溶药物的载体:紫杉醇在PEG-PE和带正电荷的脂质混合胶束中的制备及其体外抗癌活性

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摘要

Mixed micelles (MM) consisting of poly (ethylenernglycol)-phosphatidylethanolamine conjugates (PEGPE)rnand cationic Lipofectin? lipids (LL) and loadedrnwith paclitaxel (MM-PT) were prepared. The averagernsize of such micelles was ca. 98 nm, zeta-potentialrnca. -6 mV, and paclitaxel content ca. 4 wt %. In vitrorncytotoxicity of MM-P was significantly greater thanrnthat of free paclitaxel (PT) or paclitaxel in LL-freernPEG-PE micelles (M-PT). MM seem to be able tornescape from endosomes and deliver the drug into therncytoplasm of cancer cells.
机译:混合胶束(MM),由聚(乙二醇)-磷脂酰乙醇胺共轭物(PEGPE)rn和阳离子脂转染蛋白组成?制备脂质(LL)和紫杉醇(MM-PT)。这种胶束的平均尺寸为约。 98 nm,ζ电势。 -6 mV,紫杉醇含量约为4重量%。 MM-P在LL-freernPEG-PE胶束(M-PT)中的体外细胞毒性显着大于游离紫杉醇(PT)或紫杉醇。 MM似乎能够从内体中解脱出来并将药物递送到癌细胞的细胞质中。

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