Optimization of an HPLC method for determination of luteolin-7-O-glucoside in Flos Lonicerae Japonicae
Lin Rui-chao
Abstract
Lin Rui-chao
Abstract
Objective:To develop an HPLC method for the determination of luteolin-7-O-glucoside in Flos Lonicerae Japonicae.Method:An Agilent ZORBAX SB-phenyl column(4.6 mm×250 mm,5 μm) was adopted;The mobile phase was acetonitrile-0.5% acetic acid with gradient elution mode at a flow rate of 1 mL·min-1;The detecting wavelength was 350 nm,the column was 25 ℃,and the injection volume was 10 μL.Results:The calibration curve was linear in the range of 0.09-0.91 μg of luteolin-7-O-glucoside with correlation coefficient of 0.9999;The average recovery(n=6) was 103.1% with RSD of 2.1%;The limit of detection(S/N=3) was 3.48 ng and the limit of quantification(S/N=10) was 8.70 ng.Conclusion:This method is accurate,and can be used to determine the content of luteolin-7-O-glucoside in Flos Lonicerae Japonicae.
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Objective:To develop an HPLC method for the determination of luteolin-7-O-glucoside in Flos Lonicerae Japonicae.Method:An Agilent ZORBAX SB-phenyl column(4.6 mm×250 mm,5 μm) was adopted;The mobile phase was acetonitrile-0.5% acetic acid with gradient elution mode at a flow rate of 1 mL·min-1;The detecting wavelength was 350 nm,the column was 25 ℃,and the injection volume was 10 μL.Results:The calibration curve was linear in the range of 0.09-0.91 μg of luteolin-7-O-glucoside with correlation coefficient of 0.9999;The average recovery(n=6) was 103.1% with RSD of 2.1%;The limit of detection(S/N=3) was 3.48 ng and the limit of quantification(S/N=10) was 8.70 ng.Conclusion:This method is accurate,and can be used to determine the content of luteolin-7-O-glucoside in Flos Lonicerae Japonicae.
Key concepts: Chemistry, Flos, Chromatography, Luteolin, Calibration curve, High-performance liquid chromatography, Detection limit, Glucoside