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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 >An LC-MS/MS method for determination of 3,6'-disinapoylsucrose in rat plasma and its application to a pharmacokinetic study.
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An LC-MS/MS method for determination of 3,6'-disinapoylsucrose in rat plasma and its application to a pharmacokinetic study.

机译:LC-MS / MS法测定大鼠血浆中3,6'-二inapoyl蔗糖的方法及其在药代动力学研究中的应用。

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摘要

3,6'-Disinapoylsucrose (DSS), a major active component of traditional Chinese medicine Yuan-Zhi (the roots of Polygala tenuifolia), has significant effects for neuroprotection and improving learning memory. In order to explore the pharmacokinetic properties of DSS so as to further understand its in vivo activities, a sensitive LC-MS/MS method was developed for determination of DSS in rat plasma and applied to a pharmacokinetic study in the present study. After treatment by protein precipitation, the plasma sample was separated on a C(18) HPLC column and analyzed by a mass spectrometry under positive electrospray ionization. Multiple-reaction monitoring was employed to measure the ion transition at m/z 777.4 --> 409.2 for DSS and m/z 557.2 --> 309.1 for forsythin as internal standard. The method was linear over the studied concentration range of 0.5-1000.0 ng/mL. The precision and accuracy ranged from 1.4 to 18.4%, and from -3.7 to -9.5%, respectively, for within-day and between-day assay. Extraction recovery was higher than 86.6%. The limits of detection and quantification were 0.3 and 0.5 ng/mL, respectively. The present method was successfully applied to a pharmacokinetic study. DSS was found to have poor oral absorption with only about 0.5% bioavailability.
机译:3,6'-二萘基蔗糖(DSS)是中药元智(远志的根)的主要活性成分,对神经保护和改善学习记忆具有重要作用。为了探索DSS的药代动力学特性,以便进一步了解其体内活性,开发了一种灵敏的LC-MS / MS方法来测定大鼠血浆中的DSS,并将其应用于本研究的药代动力学研究。通过蛋白质沉淀处理后,血浆样品在C(18)HPLC色谱柱上分离,并在正电喷雾电离下通过质谱分析。采用多反应监测以DSS为标准测量m / z 777.4-> 409.2的离子跃迁,以连翘为内标测量m / z 557.2-> 309.1的离子跃迁。该方法在研究的0.5-1000.0 ng / mL的浓度范围内是线性的。日内和日间检测的准确度和准确性分别为1.4%至18.4%和-3.7%至-9.5%。提取回收率高于86.6%。检测限和定量限分别为0.3和0.5 ng / mL。本方法已成功地应用于药代动力学研究。发现DSS口服吸收不良,生物利用度仅为约0.5%。

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