Kim Young Hoon, Jeong Dong Won, Paek In Bok, Ji Hye Young, Kim Youn-Chul, Sohn Dong Hwan, Lee Hye Suk
Drug Metabolism & Bioanalysis Lab., College of Pharmacy and Medicinal Resources Research Institute, Wonkwang University, Shinyongdong, Iksan 570-749, Republic of Korea.
J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Dec 5;844(2):261-7. doi: 10.1016/j.jchromb.2006.07.021. Epub 2006 Aug 8.
A rapid, sensitive and selective liquid chromatography-tandem mass spectrometric (LC-MS/MS) method for the determination of baicalein, baicalin, oroxylin A and wogonin, Scutellaria baicalensis active components in rat plasma was developed. After liquid-liquid extraction with 2-(3,4-dimethoxy-phenyl)-5,7-dihydroxy-chromen-4-one as internal standard, baicalein, baicalin, oroxylin A and wogonin were eluted from an Atlantis C(18) column within 7 min with isocratic mobile phase consisting of methanol and 0.1% formic acid (60:40, v/v). The analytes were detected using an electrospray ionization tandem mass spectrometry in the multiple reaction monitoring (MRM) mode. The standard curves were linear (r=1.000) over the concentration ranges of 5-500 ng/ml for baicalein, wogonin and oroxylin A and 5-5000 ng/ml for baicalin. The coefficients of variation and relative errors of baicalein, wogonin, oroxylin A and baicalin for intra- and inter-assay at three or four quality control (QC) levels were 0.8-6.1% and -4.0 to 5.8%, respectively. The lower limits of quantification for baicalein, wogonin, oroxylin A and baicalin were 5ng/ml using 50 microl of plasma sample. This method was successfully applied to the pharmacokinetic study of baicalein, baicalin, wogonin and oroxylin A after an intravenous administration of Scutellariae radix extract to male Sprague-Dawley rats.
建立了一种快速、灵敏且选择性好的液相色谱 - 串联质谱(LC-MS/MS)方法,用于测定大鼠血浆中黄芩苷、黄芩素、木犀草素A和汉黄芩素这几种黄芩活性成分。以2-(3,4-二甲氧基苯基)-5,7-二羟基色原酮为内标进行液 - 液萃取后,黄芩苷、黄芩素、木犀草素A和汉黄芩素在7分钟内从Atlantis C(18)柱上洗脱,流动相为甲醇和0.1%甲酸(60:40,v/v)的等度洗脱体系。采用电喷雾电离串联质谱在多反应监测(MRM)模式下检测分析物。黄芩苷、汉黄芩素和木犀草素A在5 - 500 ng/ml浓度范围内,黄芩苷在5 - 5000 ng/ml浓度范围内,标准曲线呈线性(r = 1.000)。黄芩苷、汉黄芩素、木犀草素A和黄芩苷在三个或四个质量控制(QC)水平下的批内和批间变异系数及相对误差分别为0.8 - 6.1%和 - 4.0至5.8%。使用50微升血浆样品时,黄芩苷、汉黄芩素、木犀草素A和黄芩苷的定量下限为5 ng/ml。该方法成功应用于雄性Sprague-Dawley大鼠静脉注射黄芩提取物后黄芩苷、黄芩素、汉黄芩素和木犀草素A的药代动力学研究。