Wu Yu-Tse, Lin Lie-Chwen, Tsai Tung-Hu
Institute of Traditional Medicine, School of Medicine, National Yang-Ming University, Taipei 112, Taiwan.
Biomed Chromatogr. 2006 Oct;20(10):1076-81. doi: 10.1002/bmc.644.
An optimized high-performance liquid chromatographic method coupled with tandem mass spectrometric detection (LC-MS/MS) was developed for the simultaneous determination of honokiol and magnolol in Magnolia officinalis. Honokiol and magnolol were separated from the extracts using a reversed-phase C(18) column with a mobile phase consisted of acetonitrile and water (75:25, v/v) at a flow-rate of 0.8 mL/min. Selected reaction monitoring (SRM) mode was used for all sample quantification by the precursor-ion/product ion pair m/z 265 --> m/z 224 for honokiol and m/z 265 --> m/z 247 for magnolol. Validation data showed that this method has good linearity (r(2) > 0.995) over the concentration range of 0.0025-0.5 microg/mL for honokiol and magnolol, and both intra- and inter-day variability were acceptable within 15% at the lowest concentrations for this method. This proposed method provides excellent specificity, higher sensitivity and shorter run time than conventional methods and was applied successfully to determine the contents of honokiol and magnolol in M. officinalis.
建立了一种优化的高效液相色谱-串联质谱检测法(LC-MS/MS),用于同时测定厚朴中厚朴酚与和厚朴酚的含量。采用反相C(18)柱从提取物中分离厚朴酚与和厚朴酚,流动相为乙腈和水(75:25,v/v),流速为0.8 mL/min。所有样品定量均采用选择反应监测(SRM)模式,厚朴酚的前体离子/产物离子对为m/z 265 --> m/z 224,和厚朴酚的前体离子/产物离子对为m/z 265 --> m/z 247。验证数据表明,该方法在厚朴酚与和厚朴酚浓度范围为0.0025 - 0.5 μg/mL时具有良好的线性关系(r(2) > 0.995),且在该方法最低浓度下,日内和日间变异系数均在15%以内,可接受。该方法具有良好的特异性,与传统方法相比灵敏度更高、运行时间更短,并成功应用于厚朴中厚朴酚与和厚朴酚含量的测定。