论文部分内容阅读
采用反相HPLC法测定人血清中氯唑沙宗浓度。线性范围0.26±62.52μg,ml ̄(-1),高、中、低3种浓度回收率分别为97.0%±2.3%,97.1%±3.5%,93.8%±3.0%(n=5),日内、日间RSD均<4.8%。以本法测定8例.怒愿受试者氯唑沙宗血药浓度,并计算分析药代动力学参数,结果单剂量口服800mg氯唑沙宗后,药时曲线呈一室模型。T_(max)=1.63±0.43h,C_(max)=19.71±3.90μg·ml ̄(-1),AUC_(0~∞)=82.20±11.31mg·h·L ̄(-1),Ka=0.92±0.38h ̄(-1),Ke=0.54±0.11h ̄(-1),T_(1/2)=1.31±0.24h,Vd=18.63±3.15L,Cl=9.92±1.55L·h ̄(-1)。
The concentration of chlorzoxazone in human serum was determined by reverse phase HPLC. The linear range was 0.26 ± 62.52μg, ml ~ (-1). The recoveries of high, medium and low concentrations were 97.0% ± 2.3% and 97.1% ± 3.5%, respectively .8% ± 3.0% (n = 5). The intra-day and inter-day RSD were both <4.8%. Eight cases were measured by this method. Anxious to test the concentration of chlorzoxazone blood, and calculate the analysis of pharmacokinetic parameters, the results of a single oral dose of 800mg clozaprazide, the drug curve was a one-compartment model. T max = 1.63 ± 0.43 h, C max = 19.71 ± 3.90 μg · ml -1, AUC 0 ~ ∞ = 82.20 ± 11.31 mg · h · L ~ (-1), Ka = 0.92 ± 0.38h ~ (-1), Ke = 0.54 ± 0.11h ~ (-1), T ~ (1/2) = 1.31 ± 0. 24h, Vd = 18.63 ± 3.15L, Cl = 9.92 ± 1.55L · h ~ (-1).