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作 者:李珂珂[1] 吕青志[1] 赵娟娟[1] 张晓帆[1] 关景欣[1]
出 处:《中国药师》2012年第11期1565-1567,共3页China Pharmacist
基 金:烟台市科技发展计划项目(编号:2010326)
摘 要:目的:建立测定人血浆中氯诺昔康浓度的方法。方法:采用高效液相色谱法,以美洛昔康为内标,血浆样品以直接蛋白沉淀法处理,色谱柱为Agilent C_(18)(250mm×4.6mm,5μm),以甲醇-水(含0.05%三乙胺,用HCl调节pH至6.0)(55:45)为流动相,流速为1.0 ml·min^(-1),柱温为室温,检测波长为378nm,进样量为20μl。结果:氯诺昔康血药浓度在2~500 ng·ml^(-1)浓度范围内线性关系良好(r=0.995 0);高、中、低3种浓度的方法回收率为96.29%~104.00%,提取回收率>92.0%,日内、日间RSD分别为2.57%~6.41%和1.73%~6.62%。结论:本方法灵敏度、准确度及回收率均能达到人体血药浓度测定的要求,也可用于临床人体药动学的研究。Objective:To establish a method for the determination of lornoxicam in human plasma.Method:HPLC was adopted. The plasma samples were extracted by direct protein precipitation using meloxicam as the internal standard.The determination was performed on an Agilent C_(18)(250 mm×4.6 mm,5μm) column with the mobile phase consisting of methanol-water(containing 0.05% triethylamine,pH adjusted to about 6.0 by HCl)(55:45) with the flow rate of 1.0 ml ? min^(-1) at room temperature.The detection wavelength was set at 378 nm and the injection volume was 20 |xl.Result;The linear range of lornoxicam was from 2 to 500 ng ? ml^(-1) (r = 0.995 0).The method recovery was 96.29%-104.00%and the extraction recovery was above 92.0%.The intra- and inter-day RSD was 2.57%-6.41%and 1.73%-6.62%,respectively.Conclusion:The sensitivity,accuracy and recovery of the method all meet the standard of plasma concentration monitoring,which can be used in the clinical pharmacokinetic study.
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