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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of imperatorin and its metabolite xanthotoxol in rat plasma by using HPLC-ESI-MS coupled with hollow fiber liquid phase microextraction
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Simultaneous determination of imperatorin and its metabolite xanthotoxol in rat plasma by using HPLC-ESI-MS coupled with hollow fiber liquid phase microextraction

机译:高效液相色谱-电喷雾质谱联用中空纤维液相微萃取同时测定大鼠血浆中欧前胡素及其代谢物黄嘌呤醇

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The objective of the present study was to develop a new method for the simultaneous quantitation of imperatorin and its metabolite xanthotoxol in rat plasma. The samples were prepared with hollow fiber liquid phase microextraction (HF-LPME). The optimized extraction procedure was acquired by assessing extraction solvent, length of the fiber, agitation rate, extraction temperature and time. A comparison of sample pretreatment ways between HF-LPME and deproteinization with methanol was performed, which demonstrated less ion suppression and better sensitivity of HF-LPME. Analytes were separated on a C_(18) column with a gradient elution consisted of methanol and water containing 1 mmol/L ammonium acetate. The detection was accomplished by electrospray ionization (ESI) source operating in the positive ionization mode. Selected-multiple-reaction monitoring (SMRM) scanning was employed, which guar- anteed a higher sensitivity compared with MRM mode. Calibration curves were linear over investigated ranges with correlation coefficients greater than 0.9979. Precision varied from 0.26% to 14%, and the accuracy varied within ±5.5%. The developed method was successfully applied to the pharmacokinetic research of imperatorin and its metabolite xanthotoxol after oral administration of imperatorin to rats.
机译:本研究的目的是开发一种同时定量大鼠血浆中欧前胡素及其代谢物黄嘌呤醇的新方法。用中空纤维液相微萃取(HF-LPME)制备样品。通过评估萃取溶剂,纤维长度,搅拌速率,萃取温度和时间来获得优化的萃取程序。进行了HF-LPME和甲醇脱蛋白之间样品前处理方式的比较,结果表明离子抑制较少,HF-LPME的灵敏度更高。在C_(18)色谱柱上分离分析物,梯度洗脱由甲醇和含1 mmol / L乙酸铵的水组成。该检测是通过以正电离模式运行的电喷雾电离(ESI)源完成的。采用了选择多反应监测(SMRM)扫描,与MRM模式相比,它保证了更高的灵敏度。校准曲线在研究范围内呈线性,相关系数大于0.9979。精度从0.26%到14%不等,精度在±5.5%以内。所开发的方法成功地应用于大鼠体内口服欧前胡素和欧前胡素及其代谢产物黄嘌呤醇的药代动力学研究。

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