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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Simultaneous determination of triterpenoid saponins in dog plasma by a validated UPLC-MS/MS and its application to a pharmacokinetic study after administration of total saponin of licorice.
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Simultaneous determination of triterpenoid saponins in dog plasma by a validated UPLC-MS/MS and its application to a pharmacokinetic study after administration of total saponin of licorice.

机译:经验证的UPLC-MS / MS同时测定狗血浆中的三萜类皂苷及其在甘酚总皂苷施用后的药代动力学研究。

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摘要

A rapid and sensitive ultra performance liquid chromatography-tandem mass spectrometry method was developed for simultaneous determination of eight constituents, uralsaponin C, uralsaponin F, 22?acetoxyl-glycyrrhizin, 24-hydroxy-licorice-saponin E2, licorice-saponin G2, licorice-saponin E2, glycyrrhizin, and licorice-saponin J2, from total saponin of licorice (TSL) in dog plasma. Ardisiacrispin A was used as the internal standard (IS). The separation was performed on Thermo Syncronic C(18) column (100mm?.1mm, 1.7糾) at a flow rate of 0.4mLmin(-1), and acetonitrile/methanol (3:1, v/v)-0.1% formic acid was used as mobile phase. The detection was performed on a triple quadrupole tandem mass spectrometer by multiple reaction monitoring (MRM) via electrospray ionization (ESI) source with negative ionization mode. All calibration curves had good linearity (r>0.991) over the concentration range from 2.03-405ngmL(-1) to 2.63-2625ngmL(-1) for all components. The intra- and inter-day precision was within 15% and the accuracy ranged from -14.08% to 13.8%. The method was successfully applied to pharmacokinetic study of eight triterpenoid saponins in dog plasma after oral administration of TSL.
机译:开发了一种快速和敏感的超高效液相色谱 - 串联质谱法,用于同时测定八种成分,尿素己素C,尿素己素F,22〜乙酰氧基甘草蛋白,24-羟基 - 甘草 - 皂苷E2,甘草 - 皂苷G2,甘草 - Saponin E2,Glycyrrhizin和甘草-SaponinJ2,从狗血浆中的甘草(TSL)的总皂苷。 Ardisiacrispin A被用作内标(是)。以0.4mLmin(-1)的流速,在热校长C(18)柱(100mmβ1mm,1.7℃)上进行分离,乙腈/甲醇(3:1,v / v)-0.1%甲状腺酸被用作流动相。通过具有负电离模式的电喷雾电离(ESI)源对三重四极杆串联质谱仪进行检测。所有校准曲线在所有组件的2.03-405ngml(-1)到2.63-2625ngmm(-1)的浓度范围内都具有良好的线性度(r> 0.991)。日内和日间精度在15%以内,精度从-14.08%到13.8%。在口服TSL后,该方法已成功应用于八个三萜皂苷的八个三萜类皂苷的药代动力学研究。

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