首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Simultaneous quantification of paeoniflorin, nobiletin, tangeretin, liquiritigenin, isoliquiritigenin, liquiritin and formononetin from Si-Ni-San extract in rat plasma and tissues by liquid chromatography-tandem mass spectrometry
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Simultaneous quantification of paeoniflorin, nobiletin, tangeretin, liquiritigenin, isoliquiritigenin, liquiritin and formononetin from Si-Ni-San extract in rat plasma and tissues by liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法同时定量测定大鼠血浆和组织中Si-Ni-San提取物中的eon药苷,诺比林汀,橘皮苷,异黄体素,异异黄体素,异黄体素和福乐菌素

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摘要

In this study, a sensitive and reliable liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated for the determination of seven bioactive components including paeoniflorin, nobiletin, tangeretin, liquiritigenin, isoliquiritigenin, liquiritin and formononetin in rat plasma and tissues after oral administration of Si-Ni-San extract using astragaloside IV as internal standard (IS). The plasma and tissue samples were extracted by solid-phase extraction. Chromatographic separation was accomplished on a C18 column with a multiple-step gradient elution. The quantification was obtained by scanning with multiple reaction monitoring via an electrospray ionization source that was operated by switching between the positive and negative modes in two MS/MS scan segments. Full validation of the assay was implemented. In conclusion, this method demonstrated good linearity and specificity. The lower limits of quantification for the analytes were 7.5 ng/mL. Intra- and inter-day precisions (RSD) were 12.5% and accuracy (RE) ranged from -10.2 to 7.3%. The average recoveries of the analytes from rat plasma and tissues were 65.2% and 58.6%, respectively. The validated method was further applied to the determination of actual rat plasma and tissues after oral administration of Si-Ni-San extract. The results provided a meaningful basis for the clinical application of this prescription.
机译:在这项研究中,建立了灵敏可靠的液相色谱-串联质谱(LC-MS / MS)方法,并已用于测定大鼠血浆中的七种生物活性成分,包括pa药苷,诺比列汀,坦格列汀,脂质体生成素,异寡糖蛋白生成素,脂质体和formononetin使用黄芪甲苷IV作为内标(IS)口服Si-Ni-San提取物后的组织和组织。通过固相提取来提取血浆和组织样品。色谱分离是在C18色谱柱上完成的,采用多步梯度洗脱。定量是通过电喷雾电离源在多个反应监测下进行扫描而获得的,电喷雾电离源通过在两个MS / MS扫描段中在正负模式之间切换来操作。对测定进行了完全验证。总之,该方法表现出良好的线性和特异性。分析物的定量下限为<7.5 ng / mL。日内和日间精度(RSD)小于12.5%,精度(RE)介于-10.2至7.3%之间。从大鼠血浆和组织中分析物的平均回收率分别> 65.2%和58.6%。经验证的方法可进一步应用于口服Si-Ni-San提取物后测定实际大鼠血浆和组织。结果为该处方的临床应用提供了有意义的依据。

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