Yuling Long, Wenpeng Zhang, Fang Wang, Zilin Chen. Simultaneous determination of three curcuminoids in Curcuma longa L. by high performance liquid chromatography coupled with electrochemical detection[J]. Journal of Pharmaceutical Analysis, 2014, (5): 325-330. doi: 10.1016/j.jpha.2013.10.002
Citation:
Yuling Long, Wenpeng Zhang, Fang Wang, Zilin Chen. Simultaneous determination of three curcuminoids in Curcuma longa L. by high performance liquid chromatography coupled with electrochemical detection[J]. Journal of Pharmaceutical Analysis, 2014, (5): 325-330. doi: 10.1016/j.jpha.2013.10.002
Yuling Long, Wenpeng Zhang, Fang Wang, Zilin Chen. Simultaneous determination of three curcuminoids in Curcuma longa L. by high performance liquid chromatography coupled with electrochemical detection[J]. Journal of Pharmaceutical Analysis, 2014, (5): 325-330. doi: 10.1016/j.jpha.2013.10.002
Citation:
Yuling Long, Wenpeng Zhang, Fang Wang, Zilin Chen. Simultaneous determination of three curcuminoids in Curcuma longa L. by high performance liquid chromatography coupled with electrochemical detection[J]. Journal of Pharmaceutical Analysis, 2014, (5): 325-330. doi: 10.1016/j.jpha.2013.10.002
Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Wuhan University, Ministry of Education, and Wuhan University School of Pharmaceutical Sciences, Wuhan 430071, China
Funds:
The National Scientific Foundation of China
Doctroral Fund of Ministry of Education of China
Innovation Seed Fund and Translational Medical Research Fund of Wuhan University School of Medicine
A novel method for analysis of three active components curcumin, demethoxycurcumin and bisdemethoxycurcumin in Curcuma longa L. was developed by HPLC coupled with electrochemical detection. Three curcuminoids were well separated on a C18 column and detected with high sensitivity. A mobile phase containing acetonitrile and 10 mM Na2HPO4-H3PO4 (pH 5.0) (50:50, v/v) was used. Good linearity was obtained in the range of 0.208-41.6, 0.197-39.4, and 0.227-114μM for curcumin, demethoxycurcumin and bisdemethoxycurcumin respectively. The limit of detection reached up to 10 ? 8 M, which was lower than that by UV detection. The relative standard deviations (RSDs) ranged from 1.06%to 1.88%for intra-day precision and from 4.30%to 5.79%for inter-day precision, respectively. The proposed method has been applied in real herb sample and recoveries ranging from 86.3%to 111%were obtained.