HUANG Ming-jun, SUN Yao-zhi, GAO Song, et al. Analysis of Main Components in Danggui Liuhuang Tang Based on LC-MS[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(9): 63-67.
HUANG Ming-jun, SUN Yao-zhi, GAO Song, et al. Analysis of Main Components in Danggui Liuhuang Tang Based on LC-MS[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(9): 63-67. DOI: 10.13422/j.cnki.syfjx.2016090063.
并建立高效液相-质谱(LC-MS)法分析当归六黄汤汤剂中主要成分。方法: HPLC采用Agela Venusil XBP-C18色谱柱(4.6 mm×250 mm
5.0 μm)
流动相乙腈(A)-0.3%甲酸水溶液(B)梯度洗脱(0~10 min
5%~15%A;10~15 min
15%~20%A;15~35 min
20%~25%A;35~50 min
25%~31%A;50~62 min
31%~55%A;62~70 min
55%~60%A;70~75 min
60%~70%A)
柱温30℃
体积流量0.8 mL·min-1;质谱采用电喷雾离子源
正负离子模式下全扫描检测
并通过[M-H]-
[M+H]+等离子信息推断化合物。结果: 建立当归六黄汤汤剂的HPLC分析方法及指纹图谱
并建立当归六黄汤汤剂的LC-MS图谱
指认汤剂中主要的19个特征色谱峰。结论: 当归六黄汤HPLC指纹图谱分析方法稳定可靠
具有较好的重复性;通过建立LC-MS图谱
更加有效的指认了当归六黄汤汤剂中的主要成分。
Abstract
Objective: To establish HPLC fingerprint of Danggui Liuhuang Tang
analyze chromatographic data and analyze main components in Danggui Liuhuang Tang by high performance liquid chromatography and mass spectrometry (LC-MS) method. Method: HPLC was used on Agela Venusil XBP-C18(4.6 mm×250 mm
5.0 μm) column
with acetonitrile (A)-0.3% formic acid (B) as mobile phase for gradient elution (0-10 min
5%-15%A;10-15 min
15%-20%A;15-35 min
20%-25%A;35-50 min
25%-31%A;50-62 min
31%-55%A;62-70 min
55%-60%A;70-75 min
60%-70%A);with column temperature of 30℃
and volume flow rate of 0.8 mL·min-1;electrospray ionization was used for mass spectrometry
and full scan testing was done under cationic-anionic mode. Compounds were estimated through [M-H]-
[M+H]+ plasma information. Result: HPLC analysis and fingerprint were established for Danggui Liuhuang Tang;LC-MS spectra were established for Danggui Liuhuang Tang;19 characteristic chromatographic peaks of the Tang were identified. Conclusion: HPLC fingerprint analysis method of the Danggui Liuhuang Tang is stable and reliable
with good repeatability;the main components of Danggui Liuhuang Tang can be effectively identified through the establishment of LC-MS spectra.