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Evaluation of synthetic/reconstituted high-density lipoproteins as delivery vehicles for paclitaxel.

机译:评估合成/重构的高密度脂蛋白作为紫杉醇的递送载体。

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摘要

Reconstituted (synthetic) high-density lipoprotein particles carrying paclitaxel (rHDL/PTX) were prepared with substantially higher PTX content than reported earlier. The rHDL/PTX complexes seemed to be primarily spherical nanoparticles when examined via electron microscopy, with a constant composition, molecular weight and exceptional stability even after ultracentrifugation and storage for up to 6 months. The rHDL/PTX nanoparticles had superior cytotoxicity against several cancer cell lines (MCF7, DU145, OV1063 and OVCAR-3), the half maximal inhibitory concentration (IC50) having been found to be 5-20 times lower than that of the free drug. Studies with mice showed that the rHDL/PTX nanoparticles were substantially better tolerated than the corresponding dosages of either Taxol or Abraxane.
机译:携带紫杉醇(rHDL / PTX)的重组(合成)高密度脂蛋白颗粒的制备所产生的PTX含量比先前报道的要高得多。当通过电子显微镜检查时,rHDL / PTX复合物似乎主要是球形纳米颗粒,具有恒定的组成,分子量和出色的稳定性,即使在超速离心和储存长达6个月之后也是如此。 rHDL / PTX纳米颗粒对几种癌细胞系(MCF7,DU145,OV1063和OVCAR-3)具有优异的细胞毒性,发现最大抑制浓度(IC50)的一半是游离药物的5-20倍。小鼠研究表明,rHDL / PTX纳米颗粒的耐受性比紫杉醇或Abraxane的相应剂量要好得多。

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