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Quantitative determination of flavonoids in red wine by HPLC with fluorescence detector

Zhixiong Hu

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Abstract

In order to establish quantitative determination of quercetin,morin hydrate and kaempferol in red wine by high performance liquid chromatography(HPLC),The experiment adopted Polaris C18(2.0×100mm 3μm)at 60℃,mobile phase A of 0.1mol/L HAc and mobile phase B of acetonitrile.Acetonitrile was used for gradient elution at rate of 0.2ml/min,post-column derivation.The detection excitation wavelength was set at 438nm and emission wavelength at 483nm.The results showed that calibration curves were linear at ranges of 0.25mg/L~4.0mg/L,average recovery between 89.7%~95.1% and RSD 1.37%~-2.98%.This method was simple with good reproducibility and can be used as quality control of quercetin,morin hydrate and kaempferol of natural goods.

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What this paper is about

In order to establish quantitative determination of quercetin,morin hydrate and kaempferol in red wine by high performance liquid chromatography(HPLC),The experiment adopted Polaris C18(2.0×100mm 3μm)at 60℃,mobile phase A of 0.1mol/L HAc and mobile phase B of acetonitrile.Acetonitrile was used for gradient elution at rate of 0.2ml/min,post-column derivation.The detection excitation wavelength was set at 438nm and emission wavelength at 483nm.The results showed that calibration curves were linear at ranges of 0.25mg/L~4.0mg/L,average recovery between 89.7%~95.1% and RSD 1.37%~-2.98%.This method was simple with good reproducibility and can be used as quality control of quercetin,morin hydrate and kaempferol of natural goods.

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Available abstract

In order to establish quantitative determination of quercetin,morin hydrate and kaempferol in red wine by high performance liquid chromatography(HPLC),The experiment adopted Polaris C18(2.0×100mm 3μm)at 60℃,mobile phase A of 0.1mol/L HAc and mobile phase B of acetonitrile.Acetonitrile was used for gradient elution at rate of 0.2ml/min,post-column derivation.The detection excitation wavelength was set at 438nm and emission wavelength at 483nm.The results showed that calibration curves were linear at ranges of 0.25mg/L~4.0mg/L,average recovery between 89.7%~95.1% and RSD 1.37%~-2.98%.This method was simple with good reproducibility and can be used as quality control of quercetin,morin hydrate and kaempferol of natural goods.

Key concepts: Chromatography, Kaempferol, Chemistry, Wine, High-performance liquid chromatography, Quercetin, Reproducibility, Morin

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