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首页> 外文期刊>Drug Design, Development and Therapy >Novel nanocrystal formulation of megestrol acetate has improved bioavailability compared with the conventional micronized formulation in the fasting state
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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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Background: Megestrol 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.Methods: A randomized, open-label, two-treatment, two-period, two-sequence, crossover study was performed in three parts in 93 healthy subjects. A single 625 mg/5 mL oral dose of a nanocrystal formulation was administered in the fasting and fed states (part I). In parts II and III, a single 625 mg/5 mL oral dose of the nanocrystal formulation or Megace? OS 800 mg/20 mL was given in the fed and fasting states, respectively. Blood samples were collected for up to 120 hours post dose for pharmacokinetic analysis. Tolerability was evaluated throughout the entire study period.Results: The nanocrystal formulation of megestrol acetate was rapidly absorbed in both the fed and fasting states. In the fed state, systemic exposure was comparable between the nanocrystal formulation of megestrol acetate and Megace? OS. In the fasting state, however, the peak plasma concentration and area under the plasma concentration-time curve to the last measurable concentration of megestrol acetate was 6.7-fold and 1.9-fold higher, respectively, for the nanocrystal formulation than for Megace? OS. No serious adverse events were reported.Conclusion: Systemic exposure to megestrol acetate is less affected by lack of concomitant food intake when it is administered using the nanocrystal formulation. The nanocrystal formulation of megestrol acetate could be more effective in treating patients with cachexia or anorexia.
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。可是,梅嘉丝?口服悬浮液(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Megace?的药代动力学和耐受性进行比较。方法:对93名健康受试者的三个部分进行了随机,开放标签,两次治疗,两个时期,两个序列的交叉研究。在禁食和进食状态下施用单次625 mg / 5 mL口服剂量的纳米晶体制剂(第一部分)。在第二部分和第三部分中,口服625 mg / 5 mL纳米晶制剂或Megace?在进食和禁食状态下分别给予OS 800 mg / 20 mL。给药后长达120小时收集血样用于药代动力学分析。在整个研究过程中评估了耐受性。结果:醋酸甲孕甾酮的纳米晶体制剂在进食和禁食状态下均被快速吸收。在进食状态下,乙酸孕甾酮纳米晶制剂和Megace?的纳米晶制剂的全身暴露相当。操作系统。然而,在禁食状态下,纳米晶体制剂的血浆血浆浓度峰值和血浆乙酸-孕甾酮最后可测量浓度下的血浆浓度-时间曲线下的面积分别比Megace?高6.7倍和1.9倍。操作系统。没有严重不良反应的报道。结论:使用纳米晶制剂给药时,乙酸甲孕酮的全身暴露受食物摄入不足的影响较小。醋酸孕甾酮的纳米晶体制剂可以更有效地治疗恶病质或厌食症患者。

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