4.6 Article

HPLC-DAD-Q-TOF-MS/MS analysis and HPLC quantitation of chemical constituents in traditional Chinese medicinal formula Ge-Gen Decoction

Journal

JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
Volume 80, Issue -, Pages 192-202

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpba.2013.03.008

Keywords

Ge-Gen Decoction products; Chemical constituents; HPLC-Q-TOF-MS/MS; Quality control

Funding

  1. Ministry of Education, the New Teachers' Fund for Doctor Stations [20110096120011]
  2. Program for Excellent Scientific and Technological Innovation Team of Jiangsu Higher Education
  3. Priority Academic Program Development of Jiang Su Higher Education institutions (PAPD)

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Ge-Gen Decoction (GGD) is a classical formula of traditional Chinese medicine. It is generally used for treating common cold, fever and influenza in China and South East Asia. In this study, a systematic method was established for the qualitative and quantitative analysis of the major constituents in GGD. For qualitative analysis, a method of liquid chromatography coupled with electrospray ionization quadrupole time-of-flight tandem mass spectrometry (Q-TOF MS/MS) was developed for identification of multi-constituents. Based on the UV spectra, retention time and MS spectra, sixty compounds in GGD extract were identified or tentatively characterized by comparing with reference substances or literatures. According to the qualitative results, a new quantitative analysis method of GGD was established by HPLC-DAD. Fourteen representative compounds unequivocally identified were chosen as marker components which were derived from five herbs in GGD excluding Zingiberis Rhizoma Recens and Jujubae Fructus. The analytical method was validated through intra- and inter-day precision, repeatability and stability, and the R.S.D. was less than 3.18%, 4.48%, 336% and 3.54%, respectively. The LODs and the LOQs for the analytes were less than 1.06 and 3.12 mu g mL(-1), respectively. The overall recoveries ranged from 94.8% to 105.6%, with the R.S.D. ranging from 0.68% to 3.23%. Then the new method was applied to determine twelve batches of GGD commercial products of three dosage forms. The results indicated that the new approach was applicable in the routine analysis and quality control of GGD products. The study might provide a basis for quality control of GGD, and further study of GGD in vivo. (C) 2013 Elsevier B.V. All rights reserved.

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