2006Lishizhen Medicine and Materia Medica ResearchRequires access

Quantitative Determination of Hyperoside and Quercitrin and Luteolin in Polygonum aviculare by HPLC

Wang A-li

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Abstract

ObjectiveThe purpose is to determine the content of hyperoside,quercitrin and luteolin in polygonum aviculare by HPLC.MethodsThe analysis of hyperoside and quercitrin was carried out on Shimadzu C_(18)column(150 mm×4.6 mm,5 μm).The mobile phase was methanol-0.2%phosphate(45∶55).The flow-rate was 1.0 ml·min~(-1)and wave-length was 350 nm.Temperature was room temperature.The analysis of luteolin was carried out on Shimadzu C_(18)column(150 mm×4.6 mm,5 μm).The mobile phase was methanol-0.2% phosphate(50∶50).The flow-rate was 1.0 ml·min~(-1)and wave-length was 254 nm.Temperature was room temperature.ResultsThe method was simple and had a good linear relationship.The linear range of hyperoside was 0.50~2.50 μg and gave a correlation(r) of 0.999 8.The recovery was 95.13%.RSD was 2.91%.The linear range of quercitrin was(0.40)~2.00 μg and gave a correlation(r) of 0.999 6.The recovery was 96.49%.RSD was 2.77%.The linear range of luteolin was(0.40)~2.00 μg and gave a correlation(r) of 0.999 6.The recovery was 95.75%,RSD 2.49%.ConclusionThe method is easy and fast to determine the content of hyperoside,quercitrin and luteolin from polygonum aviculare.

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ObjectiveThe purpose is to determine the content of hyperoside,quercitrin and luteolin in polygonum aviculare by HPLC.MethodsThe analysis of hyperoside and quercitrin was carried out on Shimadzu C_(18)column(150 mm×4.6 mm,5 μm).The mobile phase was methanol-0.2%phosphate(45∶55).The flow-rate was 1.0 ml·min~(-1)and wave-length was 350 nm.Temperature was room temperature.The analysis of luteolin was carried out on Shimadzu C_(18)column(150 mm×4.6 mm,5 μm).The mobile phase was methanol-0.2% phosphate(50∶50).The flow-rate was 1.0 ml·min~(-1)and wave-length was 254 nm.Temperature was room temperature.ResultsThe method was simple and had a good linear relationship.The linear range of hyperoside was 0.50~2.50 μg and gave a correlation(r) of 0.999 8.The recovery was 95.13%.RSD was 2.91%.The linear range of quercitrin was(0.40)~2.00 μg and gave a correlation(r) of 0.999 6.The recovery was 96.49%.RSD was 2.77%.The linear range of luteolin was(0.40)~2.00 μg and gave a correlation(r) of 0.999 6.The recovery was 95.75%,RSD 2.49%.ConclusionThe method is easy and fast to determine the content of hyperoside,quercitrin and luteolin from polygonum aviculare.

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Available abstract

ObjectiveThe purpose is to determine the content of hyperoside,quercitrin and luteolin in polygonum aviculare by HPLC.MethodsThe analysis of hyperoside and quercitrin was carried out on Shimadzu C_(18)column(150 mm×4.6 mm,5 μm).The mobile phase was methanol-0.2%phosphate(45∶55).The flow-rate was 1.0 ml·min~(-1)and wave-length was 350 nm.Temperature was room temperature.The analysis of luteolin was carried out on Shimadzu C_(18)column(150 mm×4.6 mm,5 μm).The mobile phase was methanol-0.2% phosphate(50∶50).The flow-rate was 1.0 ml·min~(-1)and wave-length was 254 nm.Temperature was room temperature.ResultsThe method was simple and had a good linear relationship.The linear range of hyperoside was 0.50~2.50 μg and gave a correlation(r) of 0.999 8.The recovery was 95.13%.RSD was 2.91%.The linear range of quercitrin was(0.40)~2.00 μg and gave a correlation(r) of 0.999 6.The recovery was 96.49%.RSD was 2.77%.The linear range of luteolin was(0.40)~2.00 μg and gave a correlation(r) of 0.999 6.The recovery was 95.75%,RSD 2.49%.ConclusionThe method is easy and fast to determine the content of hyperoside,quercitrin and luteolin from polygonum aviculare.

Key concepts: Quercitrin, Hyperoside, Luteolin, Chromatography, Chemistry, High-performance liquid chromatography, Quercetin, Biochemistry

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