Institute of Chinese Medical Sciences, University of Macau, Taipa, Macao; Sichuan Provincial Institute for Food and Drug Control, Chengdu, Sichuan, China.
J Chromatogr A. 2010 Jan 29;1217(5):705-14. doi: 10.1016/j.chroma.2009.12.017. Epub 2009 Dec 5.
A microwave-assisted extraction (MAE) and ultra high performance liquid chromatography coupled with diode array detection and time-of-flight mass spectrometry (UHPLC-DAD-TOF-MS) method was developed for simultaneous determination of 14 phenolic compounds in the root of Pueraria lobata (Wild.) Ohwi and Pueraria thomsonii Benth. Operational conditions of MAE were optimized by central composite design (CCD). The optimized result was 65% ethanol as extraction solvent, 17mL of extraction volume, 100 degrees C of extraction temperature and 2min of hold time. A Zorbax SB C(18) (50mmx4.6mm I.D., 1.8microm) and gradient elution were used during the analysis. The chromatographic peaks of 14 investigated compounds in samples were successfully identified by comparing their retention time, UV spectra and TOF mass data with the reference substances. All calibration curves showed good linearity (r>0.9997) within the test ranges. The intra-day and inter-day variations were less than 1.77% and 2.88%, respectively. The developed method was successfully applied to determine the investigated compounds in 10 samples of Radix Puerariae Lobatae and Radix Puerariae Thomsonii, respectively. The result indicated that MAE and UHPLC-DAD-TOF-MS system might provide a rapid method for the quality control of Radix Puerariae.
建立了一种微波辅助提取(MAE)和超高效液相色谱-二极管阵列检测-飞行时间质谱(UHPLC-DAD-TOF-MS)联用方法,用于同时测定野葛和粉葛根中 14 种酚类化合物。通过中心复合设计(CCD)优化 MAE 的操作条件。优化结果为:提取溶剂为 65%乙醇,提取体积为 17mL,提取温度为 100℃,保持时间为 2min。在分析过程中使用了 Zorbax SB C(18)(50mmx4.6mm I.D.,1.8μm)和梯度洗脱。通过比较保留时间、紫外光谱和 TOF 质谱数据与对照品,成功鉴定了样品中 14 种被调查化合物的色谱峰。所有校准曲线在测试范围内均具有良好的线性(r>0.9997)。日内和日间变异分别小于 1.77%和 2.88%。该方法成功应用于 10 份野葛和粉葛根样品中被调查化合物的测定。结果表明,MAE 和 UHPLC-DAD-TOF-MS 系统可能为葛根的质量控制提供一种快速方法。