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氟啶酸在健康人体内药动学研究
引用本文:罗顺德 蔡鸿生. 氟啶酸在健康人体内药动学研究[J]. 中国医院药学杂志, 1991, 11(1): 13-15
作者姓名:罗顺德 蔡鸿生
作者单位:湖北医学院临床药学研究室 430060(罗顺德,蔡鸿生,张先州),湖北医学院临床药学研究室 430060(尹武华)
摘    要:本文用尿药浓度法,研究了6名志愿者单剂量口服氟啶酸片、胶囊剂后的药物动力学。结果表明,氟啶酸片剂,胶囊剂具有相同的药物学特征及生物等效性。其药动学参数分别是:k(hr~(-1)):0.1048、0.1039;t1/2(hr):6.92,7.08;Au~(0-42)(mg):460.78,462.51;排泄率:76.80%,77.09%。氟啶酸片的相对生物利用度为99.62%。

关 键 词:氟啶酸  尿药浓度  药动学

Pharmacokinetic Study on Enoxacin in Healthy Chinese Volunteers
Luo Shun-de,Cai Hong-Sheng,Zhang Zhuang,Li Da-Juen. Pharmacokinetic Study on Enoxacin in Healthy Chinese Volunteers[J]. Chinese Journal of Hospital Pharmacy, 1991, 11(1): 13-15
Authors:Luo Shun-de  Cai Hong-Sheng  Zhang Zhuang  Li Da-Juen
Affiliation:Luo Shun-de,Cai Hong-Sheng,Zhang Zhuang,Li Da-Juen Department of Clinical Pharmaceutical Research,Hubei Medical College,wuchang 430060
Abstract:The concentration of enoxacin in urine of six healthy chinese volunteers wasdetermined after the tablet or the capsule was orally given by single-dose. thepharmacokinetic parameters were calculated from the urine drug concentration cur-ves the result showed that the parameters of enoxacin tablet and capsule were K(hr~(-1)) 0. 1048,0.1039; t1/2(hr)6.92, 7.08; Au~(0-24)(mg)460. 78,462.51 and eliminative ra-te(cumulative)6.80%,77.09% respectively. the relative bioavailability of the tabletwas 99.6%
Keywords:Enoxacin  Drug levels in urine  pharmaeokineties  
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