盐酸曲马多胶囊在汉族健康人体内的药动学研究

夏东亚;王彦慧;郭涛

中国药学杂志 ›› 2008, Vol. 43 ›› Issue (20) : 1582-1584.

中国药学杂志 ›› 2008, Vol. 43 ›› Issue (20) : 1582-1584.
论著

盐酸曲马多胶囊在汉族健康人体内的药动学研究

  • 夏东亚;王彦慧,;郭涛
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Pharmacokinetics of Tramadol Hydrochloride in Chinese Han Healthy Volunteers

  • XIA Dong-ya1,WANG Yan-hui1,2,GUO Tao1
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摘要

目的研究盐酸曲马多胶囊在汉族健康人体内的药动学。方法选择10名健康受试者口服盐酸曲马多胶囊100 mg后,于不同时间点分别从受试者静脉取血4 mL,用高效液相色谱荧光检测法测定血浆中盐酸曲马多浓度。用3P97药动学软件进行房室模型判断并计算药动学参数。结果口服盐酸曲马多胶囊后,曲马多的药-时曲线符合一级吸收二室模型,tmax为(2.4±0.7)h,ρmax为(401.4±77.9)μg·L-1,t1/2α为(2.1±1.8)h,t1/2β为(6.6±1.2)h,AUC0-36为(4 249±1 290)μg·h·L-1,AUC0-∞(4 370±1 347)μg·h·L-1。结论健康受试者单剂量po盐酸曲马多胶囊的药动学参数与文献报道基本一致。不同性别受试者药动学参数的差异无统计学意义。

Abstract

OBJECTIVE To investigate the pharmacokinetics of tramadol hydrochloride in Chinese Han healthy volunteers.METHODS 10 Healthy volunteers were given with a single oral dose(100 mg) of Tramadol Hydrochloride Capsule.Blood samples were collected from vein at certain sampling times.Tramadol hydrochloride in plasma were determined by HPLC-fluorescence method,and the pharmacokinetic parameters were calculated by 3P97 software.RESULTS The plasma concentration-time curves of tramadol were fitted to a two-compartment model with a first order absorption.The main pharmacokinetic parameters were as follows: tmax(2.4±0.7) h,ρmax(401.4±77.9) μg·L-1,t1/2α(2.1±1.8)h,t1/2β(6.6±1.2)h,AUC0-36(4 249±1 290)μg·h·L-1,AUC0-∞(4 370±1 347)μg·h·L-1.CONCLUSION The pharmacokinetic parameters of tramadol in healthy volunteers after an oral single dose of tramadol hydrochloride capsule is concordant with that of the literature.There is no significant difference in the pharmacokinetic parameters between female and male subjects.

关键词

盐酸曲马多 / 高效液相色谱法 / 药动学 / 血药浓度

Key words

tramadol hydrochloride / HPLC / pharmacokinetics / plasma concentration

引用本文

导出引用
夏东亚;王彦慧;郭涛. 盐酸曲马多胶囊在汉族健康人体内的药动学研究[J]. 中国药学杂志, 2008, 43(20): 1582-1584
XI Dong-y;WNG Yn-hui;GUO To. Pharmacokinetics of Tramadol Hydrochloride in Chinese Han Healthy Volunteers [J]. Chinese Pharmaceutical Journal, 2008, 43(20): 1582-1584

参考文献

[1] CHEN X Q,JIN Y Y,TANG G. New Pharmaceutics(新编药物学)[M] . 16th ed. Bejing: People’s Medical Publishing House,2007: 178-179. [2] ZHU Y M. Effect and pharmacokinetics of tarmadol [J] . F Med Sci Anesth Resus(国外医学·麻醉学与复苏分册),2001,22(1):56-58. [3] WANG M,WEN A D,ZHAO L,et al. Pharmacokinetics and relative bioequivalence of tramadol hydrochloride in healthy volunters[J] . J Fourth Mil Med Univ(第四军医大学学报),2003,24(20):1902-1904. [4] LI H,WANG N,QIAO Z H,et al. Pharmacokinetics and relative bioavailability of tramadol hydrochloride tablet[J] . Clin J Clin Phamacol(中国临床药理学杂志),1995,11(1):28-32. [5] QARECIA-QUETGLAS E,AZANZA J R,SADABA B,et al. Pharmacokinetics of tramadol enantiomers and their respective phase Ⅰ metabolites in relation to CYP2D6 phenotype[J] . Pharmacol Res,2007,55(1):122-130. [6] ROUINI M R, ARDAKANI Y H, SOLTANI F, et al. Development and validation of a rapid HPLC method for simultaneous determination of tramadol,and its two main metabolites in human plasma[J] . J Chromatogr B,2006,830(2): 207-211.

基金

全军医学科学技术研究“十一五”计划科技攻关课题基金资助项目(No.06G023)

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