YI Xiao-lan, YANG Hua, ZHANG Fei-fei, et al. Multi-component Fingerprint Chromatogram of Shenxuebao Mixture by HPLC[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(1): 57-60.
YI Xiao-lan, YANG Hua, ZHANG Fei-fei, et al. Multi-component Fingerprint Chromatogram of Shenxuebao Mixture by HPLC[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(1): 57-60. DOI: 10.13422/j.cnki.syfjx.2016010057.
建立生血宝合剂的多成分HPLC指纹图谱。方法: 采用Thermo Syncronis-C18色谱柱(4.6 mm×150 mm
5μm)
流动相乙腈(A)-0.1%磷酸溶液(B)梯度洗脱(0~15 min
2%A;15~30 min
2%~15%A;30~50 min
15%~25%A;50~60 min
25%A);检测波长230 nm
柱温30℃
流速0.8~1.0 mL·min-1
进样体积5μL
分析时间60 min。结果: 在同一色谱条件下可同时检测出芍药苷等成分
确认了14个共有峰
方法学考察结果较好
10批生血宝合剂指纹图谱的相似度均>0.9。结论: 该方法简便、重复性好
为生血宝合剂的综合质量评价提供了科学依据。
Abstract
Objective: To conduct a qualitative analysis for the quality of Shengxuebao mixture by HPLC
in order to achieve the quality control of the overall accuracy of Shengxuebao mixture
and establish a multi-component fingerprint chromatogram of Shenxuebao mixture by HPLC. Method: Thermo Syncronis-C18 column(4.6 mm×150 mm
5μm) was eluted with the mobile phase of acetonitrile(A) and 0.1% phosphoric acid(B) in a gradient mode(0-15 min
2%A;15-30 min
2%-15%A;30-50 min
15%-25%A;50-60 min
25%A). Detection wavelength was set at 230 nm;column temperature was 30℃;the flow rate was 0.8-1.0 mL·min-1 and analytic time was 60 min. Injection volume was 5μL. Result: Under the same chromatogram condition
paeoniflorin and other condittuents were determined
and 14 peaks were identified on the HPLC fingerprint. The methodological results were satisfactory. The similarity of the 10 batches of Shenxuebao mixture was above 0.9. Conclusion: The method is simple and highly reproducible
and can provide scientific basis for the quality control of Shenxuebao mixture.