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Designing a liposomal formulation for idarubicin: Prolonging drug circulation lifetime and increased antitumour activity

机译:设计脂质酸脂质体的脂质体制剂:延长药物循环寿命和增加的抗肿瘤活性

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Prolonged idarubicin (IDA) plasma circulation lifetime was demonstrated in liposomes prepared with low (2 mole%) PEG concentrations and isoosmotic internal citrate concentrations (150 mM). Therapeutic activity of liposomal IDA was evaluated in a murine leukemia model, and treatment resulted in a significant increase in lifespan (ILS) when compared to equivalent doses of free drug.
机译:在用低(2摩尔%)PEG浓度和Isoosmotic柠檬酸盐浓度(150mM)制备的脂质体中,在脂质体中展示了延长的近似偶像素血液循环寿命。在鼠白血病模型中评价脂质体IDA的治疗活性,与当量的游离药物相比,治疗导致寿命(ILS)的显着增加。

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