两种5mg孟鲁司特钠咀嚼片的相对生物利用度:单剂量、随机、开放标签、2期交叉比较在健康的韩国成年男性志愿者中。

Arzneimittel-Forschung-Drug Research Pub Date : 2012-03-01 Epub Date: 2012-01-19 DOI:10.1055/s-0031-1298004
H T Kim, Y-K Song, S D Lee, Y Park, C-K Kim
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引用次数: 5

摘要

孟鲁司特钠,半胱氨酸白三烯受体1特异性拮抗剂,已在韩国上市,用于支气管哮喘和过敏性鼻炎的治疗。本研究的目的是比较孟鲁司特5毫克咀嚼片的试验配方和参考配方在韩国健康男性志愿者中的药代动力学和相对生物利用度,以满足KFDA对新仿制配方销售的监管标准。本研究设计为单剂量、两种治疗、两期交叉试验,有32名健康志愿者参加。每个受试者被随机分配接受试验制剂(东国孟鲁司特钠咀嚼片5mg®)或参考制剂(Singulair咀嚼片5mg®)。嚼片20次,用水240 mL吞下。采用经验证的UPLC-MS/MS方法测定孟鲁司特给药后24 h的血浆浓度,并通过对数转换AUC0-24 h和Cmax的平均比值统计分析,评估两种制剂之间的生物等效性。没有检测到周期或序列效应。试验制剂的AUC0-24 h为1 835 ng·h/mL,参比制剂的AUC0-24 h为1 930 ng·h/mL。AUC0-∞分别为1 917和2 015 ng·h/mL。检测品和参比品(分别为247和283 ng/mL)的Cmax分别为2.25和2.72 h。然后逐渐降低,被试产品和参比产品的平均终端t1/2分别为5.25和5.30 h。对数变换后的AUC0-24 h比值的90% ci为0.92-0.99,对照制剂的Cmax为0.83-0.91。本研究未报告不良事件。这项单剂量研究发现,试验产品和参考产品在这些禁食的健康韩国男性志愿者中符合生物等效性的监管标准。
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Relative bioavailability of two 5-mg montelukast sodium chewable tablets: a single dose, randomized, open-label, 2-period crossover comparison in healthy korean adult male volunteers.

Montelukast sodium, cysteinyl leukotriene receptor 1 specific antagonist, has been marketed in Korea for the treatment of bronchial asthma and allergic rhinitis. The aim of this study was to compare the pharmacokinetics and relative bioavailability of a test and reference formulation of montelukast 5-mg chewable tablets in healthy Korean male volunteers to meet KFDA regulatory criteria for marketing of the new generic formulation. This study was designed as a single-dose, 2-treatment, and 2-period crossover trial with 32 healthy volunteers. Each subject was randomly assigned to receive the test (Dong-Kook Montelukast Sodium Chewable Tablet 5 mg®) or reference (Singulair Chewable Tablet 5 mg®) formulation. The tablet was chewed 20 times, and then swallowed with 240 mL of water. Plasma concentrations of montelukast up to 24 h after the dose were determined using a validated UPLC-MS/MS method, and the bioequivalence between the 2 formulations was assessed by statistical analysis of mean ratios of log-transformed AUC0-24 h and Cmax. No period or sequence effects were detected. The AUC0-24 h was 1 835 ng·h/mL for the test formulation, and 1 930 ng·h/mL for the reference formulation. The respective values of AUC0-∞ were 1 917 and 2 015 ng·h/mL. The Cmax of the test and reference products (247 and 283 ng/mL, respectively) reached at 2.25 and 2.72 h, respectively. Then, they gradually decreased with the mean terminal t1/2 of 5.25 and 5.30 h for the test and reference products, respectively. The 90% CIs for the ratio of log-transformed AUC0-24 h and Cmax for the test and reference formulations were 0.92-0.99 and 0.83-0.91, respectively. No adverse events were reported in this study. This single dose study found that the test and reference products met the regulatory criteria for bioequivalence in these fasting healthy Korean male volunteers.

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