2013•Zhongguo shiyan fangjixue zazhiRequires access

Simultaneous Determination of Rutin,Quercetin and Quercitroside in Incarvillea mairei by HPLC-DAD

Liu De-ju

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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.

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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.

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Available 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.

Key concepts: Rutin, Quercetin, Chemistry, Chromatography, Phosphoric acid, High-performance liquid chromatography, Antioxidant, Biochemistry

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