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作 者:戴歌心[1] 罗顺斌[2] 林迦勒[1] 陈连国[2]
机构地区:[1]温州医学院附属第一医院,浙江温州325000 [2]温州医学院药学院,浙江温州325000
出 处:《中国卫生检验杂志》2012年第10期2314-2316,共3页Chinese Journal of Health Laboratory Technology
摘 要:目的:建立大鼠血浆中氯吡格雷羧酸代谢物SR26334检测的高效液相色谱方法,研究SR26334的药代动力学。方法:血浆经高氯酸沉淀,以ZORBAX SB-C18为色谱柱;流动相为乙腈-水-0.1%TFA(三氟乙酸),流速为1.0 ml/min;检测波长为230 nm(0 min~4.5 min)、280 nm(4.5 min~6 min)。结果:SR26334浓度在0.5 mg/L~50 mg/L范围内线性关系良好(r=0.9999);定量下限为0.5 mg/L;低、中、高三个浓度的相对回收率100.34%~101.78%;日内RSD(相对标准偏差)和日间RSD均小于10%。结论:本方法准确可靠、简便快速,适用于大鼠血浆SR26334浓度的测定。Objective: To develop a high performance liquid chromatography method for the determination of SR26334 in rat plasma and study its pharmacokinetics. Methods: The plasma samples were simply pretreated by protein precipitation with perchloric acetate. The analytical column was ZORBAX SB -C18. The mobile phase was acetonitrile - water - 0.1% trifluoroacetic acid and the flow rate was 1.0 ml/min. The UV detection wavelength was 230 nm (0 min-4.5 min) and 280 nm (4.5 min - 6 min). Results: Excellent liner relationship was obtained from the range of 0.5 mg/L to 50 mg/L ( r = 0. 9999) , the lower limit of quantification of SR26334 was 0.5 mg/L. The relative recoveries were 100.34% - 101.78% , the intra - day RSD and inter - day RSD were both less than 10%. Conclusion: The method was accurate, simple, rapid and could be used to determine the SR26334 concen- tration in rat plasma.
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