Xia Yu, Sun Mingyang, Li Ren, Liu Yue
Department of Pharmacy, Peking University People's Hospital, Beijing, China.
Department of Clinical Pharmacy, Hankun Hospital, Beijing, China.
Biomed Chromatogr. 2019 Jul;33(7):e4519. doi: 10.1002/bmc.4519. Epub 2019 Mar 26.
A rapid, sensitive and reliable quantitative method based on ultra-high performance liquid chromatography coupled with Q-Exactive Orbitrap tandem mass spectrometry was developed for simultaneous determination of berberine, berberrubine, palmatine, jatrorrhizine, columbamine, baicalin, baicalein and wogonin in rat plasma after oral administration with Yan-Ke-Ning-Tablet (YKNT). After precipitation with acetonitrile, the plasma samples were separated on a reverse-phase C column with 1 mm ammonium acetate containing 0.2% acetic acid-acetonitrile as mobile phase. Calibration curves showed good linearity (r > 0.9983) over the tested concentration ranges of 0.5-200 ng/mL for berberine, berberrubine, palmatine, jatrorrhizine and columbamine, and 1-300 ng/mL for baicalin, baicalein and wogonin. The precision (relative standard deviation) at three different concentration levels was <12.15% and the accuracy (relative error) ranged from -8.24 to 10.85%. No matrix effects were observed with matrix effect value ranging from 89.23 to 107.68%. The extraction recovery was in the range of 82.34-92.31%. The validated assay was further successfully applied to the pharmacokinetic study of these components after oral administration of YKNT. The present study provides the pharmacokinetic profiles of major bioactive components found in YKNT, and provides valuable information regarding the chemical components that were absorbed into plasma, which will be helpful for understanding the therapeutic effects of YKNT.
建立了一种基于超高效液相色谱- Q-Exactive Orbitrap串联质谱的快速、灵敏、可靠的定量方法,用于同时测定大鼠口服咽可宁片(YKNT)后血浆中黄连素、小檗红碱、巴马汀、药根碱、黄连碱、黄芩苷、黄芩素和汉黄芩素的含量。血浆样品经乙腈沉淀后,采用含0.2%乙酸的1 mM醋酸铵-乙腈作为流动相,在反相C柱上进行分离。校准曲线在0.5-200 ng/mL的黄连素、小檗红碱、巴马汀、药根碱和黄连碱以及1-300 ng/mL的黄芩苷、黄芩素和汉黄芩素的测试浓度范围内显示出良好的线性(r > 0.9983)。三个不同浓度水平的精密度(相对标准偏差)<12.15%,准确度(相对误差)在-8.24至10.85%之间。基质效应值在89.23至107.68%之间,未观察到基质效应。提取回收率在82.34-92.31%范围内。经过验证的分析方法进一步成功应用于口服YKNT后这些成分的药代动力学研究。本研究提供了YKNT中主要生物活性成分的药代动力学概况,并提供了有关吸收到血浆中的化学成分的有价值信息,这将有助于理解YKNT的治疗效果。