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中国临床药理学与治疗学 ›› 2020, Vol. 25 ›› Issue (8): 910-915.doi: 10.12092/j.issn.1009-2501.2020.08.010

• 临床药理学 • 上一篇    下一篇

氟康唑胶囊在中国健康受试者的人体生物等效性研究

李智慧1,刘静彦1,邱雯1,陈红2   

  1. 1兰州大学第二医院国家药物临床试验机构,兰州 730030,甘肃; 2成都医学院第二附属医院,核工业四一六医院,中西医结合科,成都 610057,四川
  • 收稿日期:2020-02-10 修回日期:2020-07-09 出版日期:2020-08-26 发布日期:2020-09-03
  • 通讯作者: 陈红,女,本科,主治医师,研究方向:中西医临床医学,临床药理学。 Tel: 18328598250 E-mail: 31375003@qq.com
  • 作者简介:李智慧,女,本科,研究方向:临床药理学。 Tel: 18380140331 E-mail: lzh18380140331@163.com

Bioequivalence of fluconazole capsules in healthy Chinese subjects

LI Zhihui 1, LIU Jingyan 1, QIU Wen 1, CHEN Hong 2   

  1. 1 National Drug Clinical Trial Institution, Lanzhou University Second Hospital, Lanzhou 730030, Gansu, China; 2 Department of Integrated Traditional Chinese and Western Medicine, the Second Affiliated Hospital of Chengdu Medical College, China National Nuclear Corporation 416 Hospital, Chengdu 610057, Sichuan, China
  • Received:2020-02-10 Revised:2020-07-09 Online:2020-08-26 Published:2020-09-03

摘要: 目的:在空腹和餐后给药条件下,评价成都倍特药业有限公司生产的氟康唑胶囊(50 mg)与辉瑞制药有限公司生产的氟康唑胶囊(50 mg)生物等效性。方法:52名中国健康志愿者中进行随机开放双周期两制剂交叉试验,在空腹和餐后条件下单剂量口服50 mg两种氟康唑胶囊。采用液相色谱-串联质谱联用(LC-MS/MS)法测定人血浆中氟康唑的浓度,采用非房室模型药动学参数计算的方法求算药动学参数,并进行统计分析。结果:空腹条件下受试制剂和参比制剂的主要药动学参数如下:Cmax分别为(1.32±0.21) μg/mL和(1.15±0.20) μg/mL;AUC0-t分别为(52.84±7.91) μg·h·mL-1和(51.49±8.15) μg·h·mL-1;AUC0-∞分别为(58.07±9.30) μg·h·mL-1和(56.99±10.13) μg·h·mL-1。餐后条件下受试制剂和参比制剂的主要药动学参数如下:Cmax分别为(1.04±0.14) μg/mL和(1.04±0.15) μg/mL;AUC0-t分别为(50.64±7.08) μg·h·mL-1和(49.91±9.13) μg·h·mL-1;AUC0-∞(56.79±9.26) μg·h·mL-1和(56.06±11.58) μg·h·mL-1;空腹/餐后条件下氟康唑两制剂的主要药动学参数Cmax、AUC0-t、AUC0-∞几何均数比值的90%置信区间均在80.00%~125.00%。结论:两种氟康唑制剂在空腹和餐后给药条件下具有生物等效性。

关键词: 氟康唑, 药动学, 生物利用度, 生物等效性

Abstract: AIM: To compare the bioequivalence of two brands of fluconazole capsules (50 mg) made in Chengdu Brilliant Pharmaceutical Co., Ltd and Pfizer Pharmaceuticals Ltd. (held in France) in healthy volunteers under fasted and fed conditions. METHODS: The study was an open-label, randomized, two way-crossover study involving 52 healthy Chinese volunteers. A single oral test and reference fluconazole capsules (50 mg) were given to the volunteers under fasted and fed conditions. The plasma concentration of fluconazole was determined by LC-MS/MS method. The non-compartment model pharmacokinetic parameter calculation method was applied to calculate pharmacokinetic parameters and perform statistical analysis.RESULTS: The main pharmacokinetic parameters after oral administration of test and reference fluconazole capsules under fasted conditions were as follows, Cmax (1.32±0.21) μg/mL and (1.15±0.20) μg/mL; AUC0-t (52.84±7.91) μg·h·mL-1 and (51.49±8.15) μg·h·mL-1;AUC0-∞ (58.07±9.30) μg·h·mL-1 and (56.99±10.13) μg·h·mL-1, respectively. The main pharmacokinetic parameters after oral administration of test and reference fluconazole capsules under fed conditions were as follows, Cmax (1.04±0.14) μg/mL and (1.04±0.15) μg/mL;AUC0-t (50.64±7.08) μg·h·mL-1 and (49.91±9.13) μg·h·mL-1;AUC0-∞(56.79±9.26) μg·h·mL-1 and (56.06±11.58) μg·h·mL-1, respectively. The 90% confidential intervals of the geometric mean ratios of Cmax, AUC0-t, AUC0-∞ under fasted and fed conditions were all between 80% and 125%. CONCLUSION: The two brands of fluconazole capsules were bioequivalent under fasted and fed conditions.

Key words: fluconazole, pharmacokinetics, bioavailability, bioequivalence

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