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采用高效液相色谱-蒸发光散射检测法和质谱检测法同时对牛膝中8种三萜类化合物进行定性和定量分析。

Simultaneous qualification and quantification of eight triterpenoids in radix achyranthis bidentatae by high-performance liquid chromatography with evaporative light scattering detection and mass spectrometric detection.

作者信息

Li Juan, Li Ping, Li Hui-Jun, Song Yue, Bi Zhi-Ming, Li Yan-Jing

机构信息

Key Laboratory of Modern Chinese Medicines, Ministry of Education and Department of Pharmacognosy, China Pharmaceutical University, Tongjia Lane, Nanjing, China.

出版信息

J Sep Sci. 2007 Apr;30(6):843-50. doi: 10.1002/jssc.200600341.

DOI:10.1002/jssc.200600341
PMID:17536729
Abstract

An HPLC with evaporative light scattering detection (ELSD) and ESI-MS was established for the simultaneous determination of eight triterpenoids in Radix Achyranthis Bidentatae. The optimal chromatographic conditions were achieved on a Zorbax C18 column by linear gradient elution with 0.08% v/v aqueous formic acid and ACN as the mobile phase at the flow rate of 0.8 mL/min. Temperature for the detector drift tube was set at 101 degrees C and the nitrogen flow rate was 2.8 L/min. The identities of the analytes were accomplished by comparing retention times and mass data with those of reference compounds. The validation of the method included tests of linearity, sensitivity, repeatability, recovery, and stability. All the calibration curves of the eight triterpenoids showed good linear regression (R2 >0.997) within the test ranges. The method provides desirable repeatability with overall intra- and interday variations of less than 4.9%. The obtained recoveries varied between 93.6 and 98.1% while the RSDs were below 3.9% (n = 3). The analysis results indicate that the content of investigated triterpenoids in Radix Achyranthis Bidentatae from different locations was greatly diverse, and the triterpenoids could be used as chemical markers for the discrimination of genuine and ungenuine crude drugs.

摘要

建立了一种采用蒸发光散射检测(ELSD)和电喷雾电离质谱(ESI-MS)的高效液相色谱法,用于同时测定牛膝中8种三萜类化合物。在Zorbax C18柱上,以0.08%(v/v)甲酸水溶液和乙腈为流动相,通过线性梯度洗脱,流速为0.8 mL/min,实现了最佳色谱条件。将检测器漂移管温度设定为101℃,氮气流量为2.8 L/min。通过将分析物的保留时间和质量数据与参考化合物的进行比较来鉴定分析物。该方法的验证包括线性、灵敏度、重复性、回收率和稳定性测试。8种三萜类化合物的所有校准曲线在测试范围内均显示出良好的线性回归(R2>0.997)。该方法具有良好的重复性,日内和日间总体变化小于4.9%。获得的回收率在93.6%至98.1%之间,相对标准偏差低于3.9%(n = 3)。分析结果表明,不同产地牛膝中所研究的三萜类化合物含量差异很大,这些三萜类化合物可作为鉴别正品和伪品药材的化学标志物。

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