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作 者:张硕[1] 王宏韬[2] 宋衍芹[3] 黄山[4] 岳旺[1] 毛兴荣
机构地区:[1]青岛大学医学院药学系/临床药理研究所,青岛266021 [2]青岛大学医学院科研科,山东青岛266021 [3]青岛市市立医院,青岛266071 [4]青岛科技大学化工学院药学系,青岛266042 [5]四川奇力药物研究所,成都610031
出 处:《现代生物医学进展》2007年第9期1310-1312,共3页Progress in Modern Biomedicine
摘 要:目的:评价受试酮洛芬缓释片与参比酮洛芬片的生物等效性。方法:采用反相高效液相色谱法测定24名健康男性志愿受试者交叉单剂量口服受试酮洛芬缓释片与参比酮洛芬片150mg后血浆中酮洛芬的浓度,用3p97程序进行数据处理。结果:口服受试和参比酮洛芬制荆后的AUC_(0-(?))分别是38.94±9.15μg·h·ml^(-1)、38.04±6.90μg·h·ml^(-1);AUC_(0-(?))分别是44.50±8.09μg·h·ml^(-1)、42.99±8.36μg·h·ml^(-1);T_(max)分别是3.87±0.55 h、1.96±0.60h;C_(max)分别是5.78±1.11μg·ml^(-1)、11.62±2.10μg·ml^(-1);t_(1/2)(Ke)分别是5.88±1.16h、1.70±1.40h。结论:受试酮洛芬缓释片与参比酮洛芬片具有生物等效性。Objective: To study the pharmacokinetic profile and relative bioavailability of ketoprofen sustained release tablet in healthy volunteers. Methods: A single oral dose of test ketoprofen sustained release tablets and conventional ketoprofen tablets were given to 24 healthy male volunteers according to an open randomized two way crossover design. Ketoprofen concentrations in plasma were determined by HPLG method. The data were analyzed by 3p97 program. Results: The main pharmacokinetic parameters after a single oral dose of test tablets and conventional tablets were as follows: AUC0→t was 38.94± 9.15μg·h·ml^-1 and 38.04± 6.90μg·h·ml^-1,AUG0→∞ was 44.50± 8.09μg·h·ml^-1 and 42.99± 8.36μg·h·ml^-1,Tmax was 3.87± 0.55h and 1.96± 0.60 h, Gmax was 5.78± 1.11μg·ml^-1 and 11.62± 2.10μg·ml^-1, t1/2 Ke) was 5.88±1.16h and 1.70±1.40h, respectively. Conclusion: The two preparations of ketoprofen are of bioequivalence by analysis of variance.
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