Simultaneous Determination of Rutin,Quercetin and Quercitroside in Incarvillea mairei by HPLC-DAD
Liu De-ju
Abstract
Liu De-ju
Abstract
Objective:To establish an HPLC-DAD method for simultaneous determination of rutin,quercetin and quercitroside in Incarvillea mairei.Method: A Dikma Diamonsil C18column(4.6 mm×150 mm,5 μm) was used.The column temperature was set at 30 ℃;the investigated compounds were separated with gradient mobile phase consisting of methanol(A)-0.5% phosphoric acid(B);the flow rate was 1.0 mL·min-1 and the detection wavelength was kept at 254 nm.Result: The good separation of three flavonoids was achieved within 10 min.The linearity was achieved in the range of 0.30-1.0 mg(r=0.999 8) for rutin,0.030-0.10 mg(r=0.999 8) for quercetin and 0.010-0.033 mg(r=0.999 5) for quercitrosid.The average recoveries were 100.95%(RSD 0.98%),99.51%(RSD 1.54%) and 102.84%(RSD 3.53%) respectively.Conclusion: The method is simple,rapid and accurate,which can be able to detect rutin,quercetin and quercitroside simultaneously,and can be used for quality control of I.mairei.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective:To establish an HPLC-DAD method for simultaneous determination of rutin,quercetin and quercitroside in Incarvillea mairei.Method: A Dikma Diamonsil C18column(4.6 mm×150 mm,5 μm) was used.The column temperature was set at 30 ℃;the investigated compounds were separated with gradient mobile phase consisting of methanol(A)-0.5% phosphoric acid(B);the flow rate was 1.0 mL·min-1 and the detection wavelength was kept at 254 nm.Result: The good separation of three flavonoids was achieved within 10 min.The linearity was achieved in the range of 0.30-1.0 mg(r=0.999 8) for rutin,0.030-0.10 mg(r=0.999 8) for quercetin and 0.010-0.033 mg(r=0.999 5) for quercitrosid.The average recoveries were 100.95%(RSD 0.98%),99.51%(RSD 1.54%) and 102.84%(RSD 3.53%) respectively.Conclusion: The method is simple,rapid and accurate,which can be able to detect rutin,quercetin and quercitroside simultaneously,and can be used for quality control of I.mairei.
Key concepts: Rutin, Quercetin, Chemistry, Chromatography, Phosphoric acid, High-performance liquid chromatography, Antioxidant, Biochemistry