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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 gelsemine and koumine in rat plasma by UPLC‐MS/MS and application to pharmacokinetic study after oral administration of Gelsemium elegans Gelsemium elegans Benth extract
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Simultaneous determination of gelsemine and koumine in rat plasma by UPLC‐MS/MS and application to pharmacokinetic study after oral administration of Gelsemium elegans Gelsemium elegans Benth extract

机译:UPLC-MS / MS同时测定大鼠血浆中的甲基喹啉和koumine及其在口服胶杆胶质杆菌露胶胶质杆菌胶质杆菌瘦虫草中的药代动力学研究

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摘要

Abstract A simple, rapid and sensitive method using UPLC‐MS/MS was established and validated for simultaneous determination of gelsemine and koumine in rat plasma after oral administration of Gelsemium elegans Benth extract. Plasma was performed with methanol precipitation and berberine was chosen as the internal standard. Plasma samples were separated on an Acquity UPLC? BEH C 18 column (3.0 × 50?mm, 1.7?μm) with gradient elution using acetonitrile and 0.1% formic acid aqueous solution as the mobile phase at a flow rate of 0.4?mL/min. Multiple reaction monitoring mode in positive ion mode was utilized for detection. The calibration curves were linear over the range of 0.2–100?ng/mL for gelsemine and 0.1–50?ng/mL for koumine, with the lower limits of quantification 0.2 and 0.1?ng/mL, respectively. The intra‐ and inter‐precision and accuracy were well within the acceptable ranges. The developed method was successfully applied to an in vivo pharmacokinetic study in rat after oral administration of 10?mg/kg Gelsemium elegans Benth extract.
机译:摘要建立了一种简单,快速,敏感的方法,用于同时测定大鼠血管胶质杆菌提取物的大鼠血浆中的蜕变和koumine。用甲醇沉淀进行等离子体,并选择Berberine作为内标。在Acquity UPLC上分离等离子体样品? BEH C 18柱(3.0×50×50μm,1.7≤μm),使用乙腈和0.1%甲酸水溶液的梯度洗脱,以0.4Ω×ml / min的流速。利用阳性离子模式中的多反应监测模式进行检测。校准曲线在0.2-100Ω·Ng / ml的范围内,对于koumine的0.1-50×ng / ml,分别为0.2和0.1Ω·ng / ml的下限。在可接受的范围内,具有精确度和精度和精度良好。在口服给药10μmg/ kg凝胶杆菌提取物中,成功地应用于大鼠体内药代动力学研究的体内药代动力学研究。

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