Ingredient Analysis

Simultaneous determination of three flavonoids and four phenolic acids in Glechomae Herba by HPLC*

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  • 1. Pharmacy Department, The People’s Hospital of Ganzhou, Ganzhou 341000, China;
    2. Jiangxi Institute for Drug Control, NMPA Key Laboratory of Quality Evaluation of Traditional Chinese Patent Medicine, Jiangxi Province Engineering Research Center of Drug and Medical Device Quality, Nanchang 330029, China

Received date: 2023-03-23

  Online published: 2024-06-21

Abstract

Objective: To develop an HPLC method for simultaneous determination of three flavonoids (luteolin 7-O-β-glucuronyl-(1→2)-O-β-glucuronide, apigenin 7-O-β-glucuronyl-(1→2)-O-β-glucuronide and luteolin) and four phenolic acids (chlorogenic acid, cryptochlorogenic acid, caffeic acid and rosmarinic acid) in Glechomae Herba. Methods: The Waters SunFire C18 column(250 mm×4.6 mm,5 μm) was used, the mobile phase was acetonitrile(A)-0.1% phosphoric acid(B) with gradient elution, at the flow rate of 1.0 mL·min-1, the detection wavelength was 330 nm, and the column temperature was 30 ℃. Results: Seven constituents showed good linear relationships within their own ranges (r≥0.999 6), and the precision (RSD≤0.87%) and stability(RSD≤1.1%) were good. The average recoveries (n=6) were 99.1%-101.1% with the RSDs of 0.59%-1.7%. The contents of chlorogenic acid, cryptochlorogenic acid, caffeic acid, luteolin 7-O-β-glucuronyl-(1→2)-O-β-glucuronide, apigenin 7-O-β-glucuronyl-(1→2)-O-β-glucuronide, rosmarinic acid and luteolin in eighteen batches of samples were 0.046-0.602 mg·g-1, 0.071-0.817 mg·g-1, 0.102-1.159 mg·g-1, 0.728-4.817 mg·g-1, 0.592-4.081 mg·g-1, 0.850-13.060 mg·g-1 and 0.019-0.198 mg·g-1, respectively. Conclusion: This method is specific, accurate and reproducible, and can be used to control the quality of the Glechomae Herba.

Cite this article

LIAO Yuan-yue, YUAN Ming-ming, ZHOU Lei-gang, WU Xi, YU He-yun . Simultaneous determination of three flavonoids and four phenolic acids in Glechomae Herba by HPLC*[J]. Chinese Journal of Pharmaceutical Analysis, 2023 , 43(10) : 1664 -1671 . DOI: 10.16155/j.0254-1793.2023.10.04

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