Ahmad Mahmood, Murtaza Ghulam, Akhtar Naveed, Siddique Faryal, Khan Shujaat Ali
Faculty of Pharmacy and Alternative Medicines, Islamia University of Bahawalpur, Bahawalpur-63100, Pakistan.
Acta Pol Pharm. 2011 Jan-Feb;68(1):115-9.
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.
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。