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作 者:陈锋杰[1] 张成志[1] 李岑[1] 何海霞[2] 周远大[2] 杨辉[2]
机构地区:[1]重庆医科大学附属第一医院药剂科,重庆400016 [2]重庆医科大学附属第一医院临床药理研究室,重庆400016
出 处:《实用医院临床杂志》2006年第6期85-86,共2页Practical Journal of Clinical Medicine
摘 要:目的建立用高效液相色谱法快速检测盐酸替扎尼定血药浓度的方法。方法取血浆加1mol/L.NaOH.混匀,加氯仿提取吹干,用流动相复溶进样;色谱柱SUNTEK KromasiL C85μm粒径,150×4.6mm;色谱条件:A:乙睛=100:25[A:水-甲酸-氨水(28%):100:5:10(V/V,pH8.50)];流速1.0m1/min;紫外检测波长318nm,内标物为雷尼替丁。结果盐酸替扎尼定的保留时间为6.9min,雷尼替丁的保留时间为8.2min,检测的线性范围0.3867~49.5000ng/ml(r=0.9982)方法回收率大于90.78%(n=5)日内RSD=7.74%,日间RSD=3.79%(n:5)。结论本方法简便快速,定量准确,适用于盐酸替扎尼定人体临床药代动力学和生物利用度的研究.Objective To develop a specific HPLC method for measurement of Tizanidine Hydrochloride in human serum. Methods The plasma protein was mixed with 1 mol/L NaOH. Chloroform was used to extract the materials in the serum. The mobile phase was used as solvention. The chromatography conditions were: SUNTEK Kromasil C18 5μm column, A: acetonitrile = 100:25 ( A: water-Formic Acid-Concentrated Ammonia Solution ( 28%)} = 100:5 : 10 ( V/V, pH 8.50 )) as mobile phase at 1.0 ml · min^-1. Detection wavelength was 318 nm. Ranitidine was the internal standard. Results The retention time of Tizanidine Hydrochloride and internal standard were 6.9 min and 8.2 min respectively. A good linearity was shown in the concentration rang of 0. 3867 - 49. 5000 ng/ml ( r = 0.9982 ) The recovery was more than 90.78%. The intra-day RSD was 7.74% and the inter-day RSD was 3.79% ( n = 5). Conclusion This method is simple, rapid and accurate, and eligible for the study of pharmacokinetic and bioavailability of Tizanidine Hydrochloride.
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