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作 者:秦红岩[1] 魏玉辉[1] 赵刚[1,2] 杜玮[1,2] 文洁[2] 武新安[1]
机构地区:[1]兰州大学第一医院药剂科,兰州市730000 [2]兰州大学药学院,兰州市730000
出 处:《中国药房》2008年第36期2814-2815,共2页China Pharmacy
摘 要:目的:建立以高效液相色谱(HPLC)法测定大鼠血浆中炎琥宁含量的方法,并对其药动学进行研究。方法:色谱柱为VP-ODS C18 Column(150mm×4.6mm,5μm),流动相为甲醇-1%醋酸-三乙胺(65∶35∶0.02),内标物为安定,流速为1.0mL·min-1,检测波长为251nm,温度为40℃。用甲醇沉淀蛋白后取上清液过0.45μm微孔滤膜进样分析,采用DAS1.0软件进行药动学参数估算。结果:炎琥宁进样浓度分别在0.05~1.0μg·mL-1(r=0.9999)和1.0~10.0μg·mL-1(r=0.9998)范围内与各自峰面积积分值之比呈良好线性关系;平均回收率为90.12%,RSD=0.508%(n=3)。大鼠静脉注射4mg·kg-1炎琥宁后,其tmax、Cmax、t1/2α和AUC0~240分别为(5.03±1.2)min、(1.09±7.5)mg·L-1、(0.95±4.4)min和(18.14±1.1)mg·min·L-1。结论:炎琥宁在大鼠体内的药动学过程符合二室模型。OBJECTIVE: To determine plasma level of Potassium sodium in rat by a reversed phase high performance chromatographic method(RP- HPLC) and to study its pharmaeokinetics.METHODS: The plasma was deproteinized with methanol that contained an internal standard (diazepamum) and was separated.The plasma samples were chromatographed on VP- ODS C18(150 mm × 4.6 mm, 5 μm) column with a mobile phase consisting of methanol - 1% acetic acid- triethylamine (65 : 35 : 0.02) and detected at 251 nm.The flow - rate was 1.0 mL · min^- 1 and the column temperature was set at 40 ℃ . After deproteinization of plasma, supernatant was taken to be filtered through 0.45 μm microporous membrane for analysis.The pharmacokinetics parameters were calculated using DAS 1.0 Software. RESULTS: The linear calibration curve of Potassium sodium in plasma at a concentration range from 0.05 to 1.0 μg · ml^-1(r = 0.999 9) and 1.0 to 10.0μg · ml^- 1( r = 0.999 8).The average recovery of Potassium sodium was 90.12% (RSD = 0. 508%, n = 3).The pharmacokinetie parameters of Potassium sodium in rats after iv. at a dose of 4 mg · kg^- 1 were as follows: tmax, Cmax,t1/ 2α and AUC0-240 were 5.03± 1.2 min, 1.09± 7.5 mg · L^-1, (0.95± 4.4) rain and(18.14± 1.1) mg · min· L^- 1, respectively.CONCLUSION: The pharmaeokinetics of Potassium sodium in rats fits the two- compartment model.
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