2009ZhongcaoyaoRequires access

Determination of rutin,quercetin,kaempferol,and isorhamnetin in extract of Ginkgo biloba leaves by HPLC with solid phase extraction

Lin Han

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Abstract

Objective To determine four flavonol components as markers,rutin,quercetin,kaempferol,and isorhamnetin for quality control of extract of Ginkgo biloba(EGb)by a validated high performance liquid chromatographic(HPLC)method with solid phase extraction.Methods The four flavonols of EGb were extracted with Waters Sep-Park-C18 solid-phase extraction column.Separation was achieved using a Kromasil C18 column(250 mm×4.6 mm,5 μm)at 40 ℃ with a step linear gradient using methanol∶0.1% formic acid at a flow rate of 1.0 mL/min,wavelength was 360 nm,sample amount was 20 μL.Results The limits of quantitation for rutin,quercetin,kaempferol,and isorhamnetin were 20,6,5,and 5 mg/mL,respectively.This method was linear over concentration ranges of 14—198,15—205,3—40 and 3—41 mg/L for rutin,quercetin,kaempferol,and isorhamnetin,respectively.The solid phase extraction recoveries for rutin,quercetin,kaempferol,and isorhamnetin were 93.7%—104.7%.The precision of intra-day and inter-day were less than 2% and 3% for all compounds,repectively.Conclusion The vali-dated method is simple,accurate,and able to provide the basis for the quality control of flavonols in EGb.

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Objective To determine four flavonol components as markers,rutin,quercetin,kaempferol,and isorhamnetin for quality control of extract of Ginkgo biloba(EGb)by a validated high performance liquid chromatographic(HPLC)method with solid phase extraction.Methods The four flavonols of EGb were extracted with Waters Sep-Park-C18 solid-phase extraction column.Separation was achieved using a Kromasil C18 column(250 mm×4.6 mm,5 μm)at 40 ℃ with a step linear gradient using methanol∶0.1% formic acid at a flow rate of 1.0 mL/min,wavelength was 360 nm,sample amount was 20 μL.Results The limits of quantitation for rutin,quercetin,kaempferol,and isorhamnetin were 20,6,5,and 5 mg/mL,respectively.This method was linear over concentration ranges of 14—198,15—205,3—40 and 3—41 mg/L for rutin,quercetin,kaempferol,and isorhamnetin,respectively.The solid phase extraction recoveries for rutin,quercetin,kaempferol,and isorhamnetin were 93.7%—104.7%.The precision of intra-day and inter-day were less than 2% and 3% for all compounds,repectively.Conclusion The vali-dated method is simple,accurate,and able to provide the basis for the quality control of flavonols in EGb.

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Available abstract

Objective To determine four flavonol components as markers,rutin,quercetin,kaempferol,and isorhamnetin for quality control of extract of Ginkgo biloba(EGb)by a validated high performance liquid chromatographic(HPLC)method with solid phase extraction.Methods The four flavonols of EGb were extracted with Waters Sep-Park-C18 solid-phase extraction column.Separation was achieved using a Kromasil C18 column(250 mm×4.6 mm,5 μm)at 40 ℃ with a step linear gradient using methanol∶0.1% formic acid at a flow rate of 1.0 mL/min,wavelength was 360 nm,sample amount was 20 μL.Results The limits of quantitation for rutin,quercetin,kaempferol,and isorhamnetin were 20,6,5,and 5 mg/mL,respectively.This method was linear over concentration ranges of 14—198,15—205,3—40 and 3—41 mg/L for rutin,quercetin,kaempferol,and isorhamnetin,respectively.The solid phase extraction recoveries for rutin,quercetin,kaempferol,and isorhamnetin were 93.7%—104.7%.The precision of intra-day and inter-day were less than 2% and 3% for all compounds,repectively.Conclusion The vali-dated method is simple,accurate,and able to provide the basis for the quality control of flavonols in EGb.

Key concepts: Rutin, Isorhamnetin, Kaempferol, Quercetin, Chromatography, Chemistry, Flavonols, High-performance liquid chromatography

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Determination of rutin,quercetin,kaempferol,and isorhamnetin in extract of Ginkgo biloba leaves by HPLC with solid phase extraction — Research Paper | ScholarLens