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两种品牌美洛昔康片在健康巴基斯坦男性受试者中的生物等效性研究。

Bioequivalence study of two brands of meloxicam tablets in healthy human Pakistani male subjects.

作者信息

Ahmad Mahmood, Murtaza Ghulam, Akhtar Naveed, Siddique Faryal, Khan Shujaat Ali

机构信息

Faculty of Pharmacy and Alternative Medicines, Islamia University of Bahawalpur, Bahawalpur-63100, Pakistan.

出版信息

Acta Pol Pharm. 2011 Jan-Feb;68(1):115-9.

Abstract

Meloxicam is a cyclooxygenase-2, preferential inhibitor non-steroidal anti-inflammatory drug (NSAID) and belongs to an enolic acid (oxicam) class used for the treatment of osteoarthritis and rheumatoid arthritis. The purpose of this single dose randomized cross-over study was to assess bioequivalence of two brands of oral meloxicam tablets (Xobix manufactured by Hilton Pharma (Pvt.) Ltd. as a reference and tablet Melfax by AGP (Pvt.) Ltd. as a test) in 18 healthy male volunteers in local population of Pakistan. The data obtained were subjected to non-compartment model pharmacokinetic analysis. The value of C(max) calculated in present study was 1.051 +/- 3.762 microg/mL for reference formulation and 1.023 +/- 4.102 microg/mL (the mean +/- SEM) for test sample. The value of T(max) was 3.125 +/- 1.004 h for reference standard and 3.750 +/- 1.469 h (the mean +/- SEM) for test sample. The area under the curve from zero to infinity (AUC(0-72)) was 28.667 +/- 0.414 microg x h/mL for reference standard and 28.367 +/- 0.333 microg x h/mL for test sample (the mean +/- SEM). The t1/2 values were 13.694 +/- 0.568 h and 13.319 +/- 0.567 h (the mean +/- SEM) for reference formulation and for test sample, respectively. The test formulation was found to be bioequivalent to reference formulation based on the pharmacokinetic parameters.

摘要

美洛昔康是一种环氧化酶-2选择性抑制剂非甾体抗炎药(NSAID),属于烯醇酸(昔康)类,用于治疗骨关节炎和类风湿关节炎。这项单剂量随机交叉研究的目的是评估两种品牌的口服美洛昔康片(希尔顿制药(私人)有限公司生产的Xobix作为参比制剂,AGP(私人)有限公司生产的Melfax片作为受试制剂)在巴基斯坦当地18名健康男性志愿者中的生物等效性。所获得的数据进行了非房室模型药代动力学分析。本研究中计算的参比制剂的C(max)值为1.051±3.762μg/mL,受试样品的C(max)值为1.023±4.102μg/mL(平均值±标准误)。参比标准品的T(max)值为3.125±1.004小时,受试样品的T(max)值为3.750±1.469小时(平均值±标准误)。从零到无穷大的曲线下面积(AUC(0 - 72)),参比标准品为28.667±0.414μg·h/mL,受试样品为28.367±0.333μg·h/mL(平均值±标准误)。参比制剂和受试样品的t1/2值分别为13.694±0.568小时和13.319±0.567小时(平均值±标准误)。根据药代动力学参数,受试制剂被发现与参比制剂生物等效。

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