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单剂量口服复方缬沙坦分散片的人体药动学研究
引用本文:斯陆勤,黄建耿,宫福海,李高.单剂量口服复方缬沙坦分散片的人体药动学研究[J].中国药房,2008,19(29):2269-2272.
作者姓名:斯陆勤  黄建耿  宫福海  李高
作者单位:华中科技大学同济医学院药学院,武汉市,430030
摘    要:目的:研究单剂量口服复方缬沙坦分散片的药动学特征。方法:采用高效液相色谱法测定人血浆中氢氯噻嗪与缬沙坦的浓度,由DAS软件计算药动学参数。结果:氢氯噻嗪低、中、高剂量主要药动学参数t1/2分别为(12.56±3.66)、(11.47±5.47)、(11.20±5.03)h,Cmax分别为(72.00±19.68)、(169.96±52.17)、(203.66±61.41)ng.mL-1,AUC0~48分别为(592.87±179.44)、(1155.45±252.03)、(1410.99±331.82)ng.h.mL-1,AUC0~∞分别为(779.76±201.42)、(1246.89±307.03)、(1482.14±332.20)ng.h.mL-1;缬沙坦低、中、高剂量主要药动学参数t1/2分别为(7.29±3.10)、(8.56±2.22)、(8.62±2.86)h,Cmax分别为(2.12±0.65)、(6.76±2.08)、(6.71±2.59)ng.mL-1,AUC0~48分别为(18.16±4.52)、(41.77±10.86)、(51.77±27.45)ng.h.mL-1,AUC0~∞分别为(19.07±5.56)、(42.60±11.18)、(53.49±26.93)ng.h.mL-1。结论:复方缬沙坦分散片体内为线性动力学过程,缬沙坦与氢氯噻嗪合用时,氢氯噻嗪与缬沙坦的药动学无相互影响。

关 键 词:复方缬沙坦分散片  药动学  高效液相色谱法  氢氯噻嗪  缬沙坦

Pharmacokinetics of Valsartan and Hydrochlorothiazide in Healthy Volunteers after Single Administration of Its Compound Dispersible Tablets
SI Lu-qin,HUANG Jian-geng,GONG Fu-hai,LI Gao.Pharmacokinetics of Valsartan and Hydrochlorothiazide in Healthy Volunteers after Single Administration of Its Compound Dispersible Tablets[J].China Pharmacy,2008,19(29):2269-2272.
Authors:SI Lu-qin  HUANG Jian-geng  GONG Fu-hai  LI Gao
Institution:(School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China)
Abstract:OBJECTIVE: To study the pharmacokinetics of hydrochlorothiazide and valsartan in healthy volunteers after single administration of its compound dispersible tablets. METHODS: Plasma concentrations of hydrochlorothiazide and valsartan were determined by HPLC and their pharmacokinetic parameters were calculated with DAS software. RESULTS: The pharmacokinetic parameters of hydrochlorothiazide at low, medium and high doses were as follows: t 1/2 were (12.56±3.66), (11.47± 5.47) and (11.20± 5.03) h, respectively; Cmax were (72.00± 19.68), (169.96± 52.17) and (203.66± 61.41)ng · mL^- 1, respectively; AUC0-48 were (592.87± 179.44), (1 155.45±252.03) and (1 410.99±331.82) ng·h·mL^-1. respectively; AUC0-∞ were (779.76±201.42), (1 246.89±307.03) and (1 482.14±332.20) ng·h·mL^-1, respectively. The pharmacokinetic parameters of valsartan at low, medium and high doses were as follows: t 1/ 2 were (7.29± 3.10), (8.56 ± 2.22) and (8.62±2.86)h, respectively; Cmax were (2.12±0.65), (6.76±2.08) and (6.71±2.59)ng · mL^-1, respectively; AUC0-48 were (18.16±4.52), (41.77±10.86) and (51.77±27.45) ng·h·mL^-1 respectively; AUC0-∞ were (19.07± 5.56), (42.60 ± 11.18) and (53.49 ± 26.93) ng·h·mL^-1 respectively. CONCLUSION : The pharmacokinetics for compound valsartan dispersible tablet fitted linear kinetics process. There is no interaction in pharmacokinetics between hydrochlorothiazide and valsartan when they used in combination.
Keywords:Compound valsartan dispersible tablets  Pharmacokinetics  HPLC  Hydrochlorothiazide  Valsartan
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