空腹和进食条件下两种配方的孟鲁司特钠片剂在健康中国志愿者中的药代动力学和生物等效性。

IF 1.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Xiali Rao, Xinghong Wu, Jiawei Hu, Zhaoming Huang
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引用次数: 0

摘要

孟鲁司特钠是一种白三烯 1 型受体拮抗剂,可用于预防和治疗哮喘。然而,孟鲁司特钠片剂(10 毫克)在中国健康受试者中的药代动力学仍不清楚。在此,我们进行了一项单剂量、随机、开放标签、2序列和2期交叉(治疗间有7天的冲洗期)研究,以比较在空腹和进食条件下,中国健康受试者服用单剂量10毫克时,试验产品与参比品的药代动力学和生物等效性。研究人员在规定的时间点采集血样,采用经过验证的液相色谱-串联质谱法分析血浆中孟鲁司特的浓度。结果表明,最大血浆药物浓度、从时间 0 到终点的浓度-时间曲线下面积以及从时间 0 到无穷大的浓度-时间曲线下面积的试验/参照物几何平均比值的 90% 置信区间值在 80%-125% 范围内。此外,试验制剂和参比制剂均安全且耐受性良好,未出现严重不良反应。这些结果表明,在空腹和进食条件下,试验用孟鲁司特钠片剂和参比制剂在中国健康受试者中表现出相似的生物等效性、安全性和耐受性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacokinetics and Bioequivalence of Two Formulations of Montelukast Sodium Tablets in Healthy Chinese Volunteers Under Fasting and Fed Conditions.

Montelukast sodium is a leukotriene type 1 receptor antagonist that can be used for the prophylaxis and treatment of asthma. However, the pharmacokinetics of montelukast sodium tablets (10 mg) remain unclear in healthy Chinese subjects. Here, a single-dose randomized, open-label, 2-sequence, and 2-period crossover (7-day washout period between treatments) study was performed to compare the pharmacokinetics and bioequivalence between the test products and the reference at a single dose of 10 mg among healthy Chinese subjects under fasting and fed conditions. Blood samples were collected at specified time points to analyze the plasma concentrations of montelukast by a validated liquid chromatography-tandem mass spectrometry method. The results showed that the 90% confidence interval values of the geometric mean ratio of test/reference for the maximum plasma drug concentration, area under the concentration-time curve from time 0 to the end, and area under the concentration-time curve from time 0 to infinity were within the range of 80%-125%. Moreover, both the test and reference formulations were safe and well tolerated, with no occurrence of severe adverse events. These results demonstrate that both the test montelukast sodium tablets and the reference showed similar bioequivalence, safety, and tolerability among healthy Chinese subjects under fasting and fed conditions.

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来源期刊
CiteScore
3.70
自引率
10.00%
发文量
154
期刊介绍: Clinical Pharmacology in Drug Development is an international, peer-reviewed, online publication focused on publishing high-quality clinical pharmacology studies in drug development which are primarily (but not exclusively) performed in early development phases in healthy subjects.
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