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Novel nanocrystal formulation of megestrol acetate has improved bioavailability compared with the conventional micronized formulation in the fasting state

机译:与空腹状态下的常规微粉化制剂相比醋酸孕甾酮的新型纳米晶体制剂具有更高的生物利用度

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摘要

BackgroundMegestrol acetate is an effective treatment for improving appetite and increasing body weight in patients with cancer-associated anorexia. However, Megace® oral suspension (OS), a micronized formulation of megestrol acetate, has low bioavailability in the fasting state. To overcome this limitation, a nanocrystal formulation has been developed. This study was performed to evaluate the pharmacokinetics and tolerability of the nanocrystal formulation and to compare them with those of Megace® OS in the fed and fasting states.
机译:背景醋酸孕甾酮是一种改善癌症相关厌食症患者食欲并增加体重的有效疗法。然而,Megace ®口服混悬液(OS)是醋酸孕甾酮的微粉化制剂,在禁食状态下生物利用度较低。为了克服该限制,已经开发了纳米晶体制剂。进行这项研究以评估纳米晶体制剂的药代动力学和耐受性,并将其与在进食和禁食状态下的Megace ® OS进行比较。

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