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首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Simultaneous determination of linarin, naringenin and formononetin in rat plasma by LC-MS/MS and its application to a pharmacokinetic study after oral administration of Bushen Guchi Pill
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Simultaneous determination of linarin, naringenin and formononetin in rat plasma by LC-MS/MS and its application to a pharmacokinetic study after oral administration of Bushen Guchi Pill

机译:LC-MS / MS法同时测定大鼠血浆中柠檬苦素,柚皮素和福乐菌素的含量及其在口服补肾固池丸后的药代动力学研究中的应用

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摘要

A sensitive and reproducible liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed and validated for the simultaneous determination of linarin, naringenin and formononetin in rat plasma after addition of sulfamethoxazole as the internal standard (IS). Separation was carried out on a Diamonsil C-18 column (150x4.6 mm, 5 mu m) with liner gradient elution using methanol (A) and 0.5 parts per thousand formic acid aqueous solution (B). Detection was performed on a triple-quadrupole linear ion trap mass spectrometer with the negative ion electrospray ionization in multiple-reaction monitoring (MRM) mode. The MRM transitions were m/z 591.2283.2, 271.0150.9, 266.9252.0 and 252.0155.9 for linarin, naringenin, formononetin and IS, respectively. All analytes showed good linearity within the concentration range (r>0.9973). The lower limits of quantitation of linarin, naringenin and formononetin were 0.64, 1.07 and 1.04 ng/mL, respectively. Intra-day and inter-day precisions of the investigated components exhibited an RSD within 9.96%, and the accuracy (relative error) ranged from -11.25 to 9.38% at all quality control levels. The developed method was successfully applied to a pharmacokinetic study of linarin, naringenin and formononetin in rats after oral administration of Bushen Guchi Pill. Copyright (c) 2014 John Wiley & Sons, Ltd.
机译:建立了灵敏且可重现的液相色谱串联质谱法(LC-MS / MS),并验证了以磺胺甲恶唑为内标(IS)后可同时测定大鼠血浆中的柠檬苦素,柚皮苷和formononetin的方法。在Diamonsil C-18色谱柱(150x4.6 mm,5μm)上进行分离,并使用甲醇(A)和每千份甲酸水溶液(B)0.5份进行线性梯度洗脱。检测是在三重四极杆线性离子阱质谱仪上进行的,其中负离子电喷雾电离为多反应监测(MRM)模式。 Linarin,naringenin,formononetin和IS的MRM过渡分别为m / z 591.2283.2、271.0150.9、266.9252.0和252.0155.9。所有分析物在浓度范围内均表现出良好的线性(r> 0.9973)。藤黄素,柚皮苷和福乐菌素的定量下限分别为0.64、1.07和1.04 ng / mL。被调查组件的日内和日间精确度均显示RSD在9.96%之内,并且在所有质量控制水平下,准确度(相对误差)在-11.25至9.38%之间。所开发的方法已成功地应用于口服补肾固chi丸后大鼠体内的连皮苷,柚皮苷和formononetin的药代动力学研究。版权所有(c)2014 John Wiley&Sons,Ltd.

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