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HPLC-UV analysis of ginkgolide A,B,C
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DOI   10.11656/j.issn.1672-1519.2024.09.18
Key Words   ginkgolides;HPLC;methodology validation
Author NameAffiliationE-mail
HU Zheming Modern Chinese Medicine Discovery and Preparation Technology Engineering Center of the Ministry of Education, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China  
PI Ziyue Modern Chinese Medicine Discovery and Preparation Technology Engineering Center of the Ministry of Education, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China  
JOHN OSILAMA THOMAS Modern Chinese Medicine Discovery and Preparation Technology Engineering Center of the Ministry of Education, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China  
GUO Pan Modern Chinese Medicine Discovery and Preparation Technology Engineering Center of the Ministry of Education, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China guopan@tjutcm.edu.cn 
Abstract
    [Objective] To establish and methodologically validate an HPLC-UV method for the determination of ginkgolides A,B,and C. The method was validated by the HPLC-UV method. [Methods] The investigation included detection wavelength,eight different mobile phase systems and their ratios,injection volume,flow rate and column temperature. The method validation examined the specificity, precision,accuracy,linear range,repeatability,system suitability,spiked recovery and stability. [Results] The separation was carried out on an Agilent TC-5 C18 column at a detection wavelength of 220 nm with a mobile phase of water-methanol(70∶30) at an injection volume of 20 μL,a column temperature of 30 ℃,and a flow rate of 1.0 mL/min. The linearity of the method was good,and the peaks of the chromatograms did not interfere with each other. [Conclusion] The method is accurate,effective,economical,easy to obtain and simple to operate,and can provide a reference for the determination of other ginkgolides.

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