Chromatographic fingerprint analysis is feasible for comprehensive quality control of taohongsiwu

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Abstract

Background and Objective: Taohongsiwu decoction, a traditional Chinese medicine formula has been widely developed to treat thrombotic diseases for hundreds of years. It contains variations of multi-components, which pose a serious challenge to its quality control. This study aimed to develop a simple and reliable ultra high performance liquid chromatography coupled with diode array detector method to separate and detect the constituents of the decoction. Materials and Methods: A total of 15 compounds was detected and 6 compounds (including ferulic acid, hydroxysafflor yellow a, ligustilide, amygdalin, 5-hydroxymethyl furfuraldehyde and paeoniflorin) were tentatively identified, using high performance liquid chromatography coupled with diode array detector method. Results: The four components (Ferulic acid, hydroxysafflor yellow a, ligustilide, amygdalin) showed good regression (R>0.9996) within test ranges and the recovery method ranged from 101.73-106.44%. Ten batches of taohongsiwu decoction were analyzed. The similarity scores of common peaks from these samples ranged from 0.957-1.000, which indicating that samples were highly correlated. Conclusion: It is concluded that this extraction method was found to be sensitive and simple, so it was feasible for comprehensive quality control of THSWD.

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Han, L., Qiao, O., Wu, H., Wu, S., Zhang, Y., Yao, L., … Peng, D. (2017). Chromatographic fingerprint analysis is feasible for comprehensive quality control of taohongsiwu. International Journal of Pharmacology, 13(5), 488–494. https://doi.org/10.3923/ijp.2017.488.494

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