2007Lishizhen Medicine and Materia Medica ResearchRequires access

Determination of Puerarinin Content in Guangxi Radix puerariae thomsonii by HPLC

Dongping Wei

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Abstract

ObjectiveTo determine the content of puerarin from Guangxi Radix puerariae thomsonii by HPLC.Methods The isolation was conducted on a phenomenex gemini C18 column(250 rmm ×4.6 mm,5 μm),the mobile phase consisted of acetonitnle(A)-0.4% phosphoric and(B) in a gradient model,the flow rate wes 1.0 ml/min,the detection wavelength was 250 nm and the column temporature was 30℃.ResultsThe content of puerarin showed good linearity in the range of 800 ng~2400 ng,the regression equation was A=7.682×104C +5.885×104,r=0.999 3(n=5),and the average recovery was 99.49%,RSD was 0.75%(n=5).ConclusionThis method is simple,rapid,accurate and reliable.It can be used for quality control of Guangxi Radix puerariae thomsonii.

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ObjectiveTo determine the content of puerarin from Guangxi Radix puerariae thomsonii by HPLC.Methods The isolation was conducted on a phenomenex gemini C18 column(250 rmm ×4.6 mm,5 μm),the mobile phase consisted of acetonitnle(A)-0.4% phosphoric and(B) in a gradient model,the flow rate wes 1.0 ml/min,the detection wavelength was 250 nm and the column temporature was 30℃.ResultsThe content of puerarin showed good linearity in the range of 800 ng~2400 ng,the regression equation was A=7.682×104C +5.885×104,r=0.999 3(n=5),and the average recovery was 99.49%,RSD was 0.75%(n=5).ConclusionThis method is simple,rapid,accurate and reliable.It can be used for quality control of Guangxi Radix puerariae thomsonii.

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Available abstract

ObjectiveTo determine the content of puerarin from Guangxi Radix puerariae thomsonii by HPLC.Methods The isolation was conducted on a phenomenex gemini C18 column(250 rmm ×4.6 mm,5 μm),the mobile phase consisted of acetonitnle(A)-0.4% phosphoric and(B) in a gradient model,the flow rate wes 1.0 ml/min,the detection wavelength was 250 nm and the column temporature was 30℃.ResultsThe content of puerarin showed good linearity in the range of 800 ng~2400 ng,the regression equation was A=7.682×104C +5.885×104,r=0.999 3(n=5),and the average recovery was 99.49%,RSD was 0.75%(n=5).ConclusionThis method is simple,rapid,accurate and reliable.It can be used for quality control of Guangxi Radix puerariae thomsonii.

Key concepts: Chromatography, Puerarin, Radix (gastropod), High-performance liquid chromatography, Chemistry, Content determination, Phosphoric acid, Recovery rate

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