首页> 美国卫生研究院文献>other >Mixed Micelles made of Poly(ethylene glycol)-Phosphatidylethanolamine Conjugate and D-α-tocopheryl Polyethylene Glycol 1000 Succinate as Pharmaceutical Nanocarriers for Camptothecin
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Mixed Micelles made of Poly(ethylene glycol)-Phosphatidylethanolamine Conjugate and D-α-tocopheryl Polyethylene Glycol 1000 Succinate as Pharmaceutical Nanocarriers for Camptothecin

机译:聚(乙二醇)-磷脂酰乙醇胺缀合物和D-α-生育酚基聚乙二醇1000琥珀酸酯制成的混合胶束作为喜树碱的药物纳米载体

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摘要

Micelles from the mixture of poly(ethylene glycol)-phosphatidyl ethanolamine conjugate (PEG-PE) and D-α-tocopheryl polyetheyene glycol 1000 succinate (TPGS) were prepared loaded with the poorly soluble anticancer drug camptothecin (CPT). The solubilization of CPT by the mixed micelles was more efficient than with earlier described micelles made of PEG-PE alone. CPT-loaded mixed micelles were stable upon storage and dilution and firmly retained the incorporated drug. The cytotoxicity of the CPT-loaded mixed micelles against various cancer cells in vitro was remarkably higher than that of the free drug. PEG-PE/TPGS mixed micelles may serve as pharmaceutical nanocarriers with improved solubilization capacity for poorly soluble drugs.
机译:从聚(乙二醇)-磷脂酰乙醇胺缀合物(PEG-PE)和D-α-生育酚基聚乙二醇1000琥珀酸酯(TPGS)的混合物中制备胶束,并在其中加入难溶的抗癌药物喜树碱(CPT)。混合胶束对CPT的溶解作用比以前描述的单独由PEG-PE制成的胶束更有效。载有CPT的混合胶束在储存和稀释后稳定,并牢固地保留了掺入的药物。载有CPT的混合胶束对各种癌细胞的体外细胞毒性明显高于游离药物。 PEG-PE / TPGS混合胶束可作为药物纳米载体,对难溶性药物具有更高的增溶能力。

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