首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of limonin, dictamnine, obacunone and fraxinellone in rat plasma by a validated UHPLC-MS/MS and its application to a pharmacokinetic study after oral administration of Cortex Dictamni extract
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Simultaneous determination of limonin, dictamnine, obacunone and fraxinellone in rat plasma by a validated UHPLC-MS/MS and its application to a pharmacokinetic study after oral administration of Cortex Dictamni extract

机译:经验证的UHPLC-MS / MS同时测定大鼠血浆中柠檬苦素,三氢嘧啶,奥沙酮和六甲酮的含量,并将其用于口服给予地皮提取物后的药代动力学研究

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A rapid and selective ultra high performance liquid chromatography-tandem mass spectrometry method was developed for the simultaneous determination of four major ingredients in Cortex Dictamni extract, including limonin, dictamnine, obacunone and fraxinellone in rats plasma. Nimodipine was used as the internal standard. Following extraction by methyl tert-butyl ether, the analytes were separated on a Thermo Syncronis C_(18) column by a gradient elution within a runtime of 9min. The mobile phase consisted of A (methanol) and B (2mmol/L ammonium acetate in water). The detection was accomplished by using positive ion electrospray ionization in multiple reaction monitoring mode. The method was linear for all analytes over investigated range with all correlation coefficients greater than 0.998. The lower limits of quantification were 9.18ng/mL for limonin, 12.0ng/mL for dictamnine, 16.05ng/mL for obacunone and 4.59ng/mL for fraxinellone. The intra- and inter-day precision (RSD%) was within 10% and the accuracy (RE%) ranged from -12.9% to 9.7%. This rapid and sensitive method was fully validated and successfully applied to the pharmacokinetic study of limonin, dictamnine, obacunone and fraxinellone in the rat plasma after oral administration of Cortex Dictamni extract.
机译:建立了一种快速选择性的超高效液相色谱-串联质谱法,用于同时测定大鼠血浆中柠檬皮素,三氢嘧啶、,豆酮和六甲新酮中的柠檬皮提取物中的四种主要成分。尼莫地平用作内标。用甲基叔丁基醚萃取后,分析物在Thermo Syncronis C_(18)色谱柱上通过梯度洗脱在9分钟内进行分离。流动相由A(甲醇)和B(水中2mmol / L乙酸铵)组成。通过在多个反应监控模式下使用正离子电喷雾电离来完成检测。对于所有研究范围内的所有分析物,该方法都是线性的,所有相关系数均大于0.998。柠檬苦素的定量下限为9.18ng / mL,三丁胺的定量下限为12.0ng / mL,奥巴酮的定量下限为16.05ng / mL,而六氢新萘酮的定量下限为4.59ng / mL。日内和日间精度(RSD%)在10%以内,精度(RE%)在-12.9%至9.7%之间。该快速灵敏的方法得到了充分验证,并成功应用于口服皮质酮地卡那提取物后大鼠血浆中柠檬苦素,十氢丁胺,奥巴康酮和六甲新酮的药代动力学研究。

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