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Determination of rutin and quercetin in A.hendersonii Hook f. by HPLC

Hong Xia Zheng

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Abstract

OBJECTIVE To develop a method for determining rutin and quercetin in A.hendersonii Hook f.METHODS HPLC method was adopted.Agilent Zorbax SB-C18(250 mm ×4.6 mm,5 μm)column and methanol–0.04% phosphoric acid (40:60) as mobile phase were used.The flow rate was 1.0 ml·min-1 and the detection wavelength was 360 nm.The column temperature was 35℃.RESULTS The peak areas vs the concentrations of rutin and quercetin showed good correlation in the ranges of 0.01–0.20 μg and 0.007–0.099 μg(r=0.9999 and 0.9998),respectively.The average recoveries was 102.1% for quercetin (RSD=2.0%,n=6) and 99.5% for rutin (RSD=1.4%,n=6),respectively.CONCLUSION The method is simple,rapid and accurate.It can be used for the quality control of A.hendersonii Hook f..

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OBJECTIVE To develop a method for determining rutin and quercetin in A.hendersonii Hook f.METHODS HPLC method was adopted.Agilent Zorbax SB-C18(250 mm ×4.6 mm,5 μm)column and methanol–0.04% phosphoric acid (40:60) as mobile phase were used.The flow rate was 1.0 ml·min-1 and the detection wavelength was 360 nm.The column temperature was 35℃.RESULTS The peak areas vs the concentrations of rutin and quercetin showed good correlation in the ranges of 0.01–0.20 μg and 0.007–0.099 μg(r=0.9999 and 0.9998),respectively.The average recoveries was 102.1% for quercetin (RSD=2.0%,n=6) and 99.5% for rutin (RSD=1.4%,n=6),respectively.CONCLUSION The method is simple,rapid and accurate.It can be used for the quality control of A.hendersonii Hook f..

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Available abstract

OBJECTIVE To develop a method for determining rutin and quercetin in A.hendersonii Hook f.METHODS HPLC method was adopted.Agilent Zorbax SB-C18(250 mm ×4.6 mm,5 μm)column and methanol–0.04% phosphoric acid (40:60) as mobile phase were used.The flow rate was 1.0 ml·min-1 and the detection wavelength was 360 nm.The column temperature was 35℃.RESULTS The peak areas vs the concentrations of rutin and quercetin showed good correlation in the ranges of 0.01–0.20 μg and 0.007–0.099 μg(r=0.9999 and 0.9998),respectively.The average recoveries was 102.1% for quercetin (RSD=2.0%,n=6) and 99.5% for rutin (RSD=1.4%,n=6),respectively.CONCLUSION The method is simple,rapid and accurate.It can be used for the quality control of A.hendersonii Hook f..

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

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