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作 者:刘史佳[1] 黄国栋[2] 孙冰婷 戴国梁[1] 刘芳[1] 殷俊刚 李长印[1] 冯丽雯[2] 俞景梅[1] 居文政[1]
机构地区:[1]南京中医药大学附属医院临床药理科,南京210029 [2]南京中医药大学药学院,南京210046
出 处:《中国临床药学杂志》2017年第1期10-14,共5页Chinese Journal of Clinical Pharmacy
基 金:国家自然科学基金青年科学基金(编号81403174;81503300);国家自然科学基金(编号81470197);江苏省自然基金(编号BK20161602)
摘 要:目的评价米格列奈片在健康人体内的生物等效性。方法 24名健康成年男性志愿者采用随机分组自身交叉对照试验设计,单剂量口服10 mg米格列奈片后,用LC-MS/MS法测定血浆中药物浓度。结果米格列奈片和米格列奈钙片的主要药动学参数:t1/2(1.69±0.16)和(1.65±0.28)h;tmax[0.25(0.17~0.5)]和[0.33(0.25~1.50)]h;ρmax(1 165.1±357.50)和(1 081.0±338.41)μg·L^(-1);AUC_(0→τ)(1 489.6±336.85)和(1 378.3±309.56)μg·h·L^(-1);AUC0→∞(1 497.2±339.73)和(1 386.1±311.58)μg·h·L^(-1);AUC_(0→12h)/AUC_(0→∞)(99.51±0.16)%和(99.44±0.24)%;以AUC_(0→12h)计算受试制剂的相对生物利用度为(108.6±10.9)%。结论 2种米格列奈制剂生物等效。AIM To evaluate the bioequivalence of two kinds of mitiglinide preparations in healthy volunteers. METHODS A total of 20 healthy male volunteers were enrolled in a randomized crossover study in which the subjects were randomly assigned to receive single oral dose of 10 mg mitiglinide tablets. The plasma concentrations of mitiglinide were determined by LC-MS/MS. RESULTS The main pharmacokinetic parameters of test and reference preparations were as follows : t1/2(1.69±0.16) and (1.65±0.28)h;tmax[0.25(0.17~0.5)] and [0.33(0.25~1.50)]h;ρmax(1165.1±357.50) and (1081.0±338.41)μg·L-1;AUC0→τ,(1489.6±336.85) and (1378.3±309.56)μg·h·L-1;AUC0→∞(1497.2±339.73) and (1386.1±311.58)μg·h·L-1;AUC0→12h/AUC0→∞(99.51±0.16)% and (99.44±0.24)%;The relative bioavailability of mitiglinide tables to reference preparation was (108.6±10.9)%. CONCLUSION Test preparation and reference preparation of mitiglinide are bioequivalent.
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