天然产物研究与开发
天然產物研究與開髮
천연산물연구여개발
NATURAL PRODUCT RESEARCH AND DEVELOPMENT
2011年
5期
894-897
,共4页
珠芽蓼%牡荆素%槲皮苷%槲皮素%RP-HPLC
珠芽蓼%牡荊素%槲皮苷%槲皮素%RP-HPLC
주아료%모형소%곡피감%곡피소%RP-HPLC
采用RP-HPLC法建立了同时测定珠芽蓼中牡荆素、槲皮苷、槲皮素三种黄酮的方法,色谱柱为kromasil C18(250 mm×4.6mm,5μm),以甲醇-水(含0.25%磷酸)为流动相梯度洗脱,流速1 mL/min,检测波长360 nm.结果表明,牡荆素、槲皮苷和槲皮素质量浓度在8~40、5~50 μg/mL和5.33~52 μg/mL范围内与色谱峰面积均呈良好的线形关系,平均回收率分别为100.3%、98.9%和100.4%,日内稳定性偏差分别为0.78%,0.51%和0.38%,日间稳定性偏差为2.6%,1.9%和2.1%.该方法简单、准确,可为珠芽蓼的质量控制提供科学依据.
採用RP-HPLC法建立瞭同時測定珠芽蓼中牡荊素、槲皮苷、槲皮素三種黃酮的方法,色譜柱為kromasil C18(250 mm×4.6mm,5μm),以甲醇-水(含0.25%燐痠)為流動相梯度洗脫,流速1 mL/min,檢測波長360 nm.結果錶明,牡荊素、槲皮苷和槲皮素質量濃度在8~40、5~50 μg/mL和5.33~52 μg/mL範圍內與色譜峰麵積均呈良好的線形關繫,平均迴收率分彆為100.3%、98.9%和100.4%,日內穩定性偏差分彆為0.78%,0.51%和0.38%,日間穩定性偏差為2.6%,1.9%和2.1%.該方法簡單、準確,可為珠芽蓼的質量控製提供科學依據.
채용RP-HPLC법건립료동시측정주아료중모형소、곡피감、곡피소삼충황동적방법,색보주위kromasil C18(250 mm×4.6mm,5μm),이갑순-수(함0.25%린산)위류동상제도세탈,류속1 mL/min,검측파장360 nm.결과표명,모형소、곡피감화곡피소질량농도재8~40、5~50 μg/mL화5.33~52 μg/mL범위내여색보봉면적균정량호적선형관계,평균회수솔분별위100.3%、98.9%화100.4%,일내은정성편차분별위0.78%,0.51%화0.38%,일간은정성편차위2.6%,1.9%화2.1%.해방법간단、준학,가위주아료적질량공제제공과학의거.
To develop a 8ensitive and specific reversed-phase high perfonnance liquid chromatography ( RP-HPLC) method for simultaneous detennination of three flavoniods in Polygonum viviparum,the HPLC separation was performed on a Kromasil C18 column (250 mm ×4.6 mm,5 μm) and detected with DAD at 360 nm.The gradient elution was carried out with methano-H2O (containing 0.25% phosphoric acid) as the mobile phase at a flow rate of 1 mL/min.The results indicated that the calibration cunre8 for viterxin,quercetin and quercitrin were linear over the ranges of 8-40 μg/mL,5-50 μg/mL and 5.33 -52 μg/mL,their assay recoveries were 100.3%,98.9%and 100.4%,their intraday repeatability were 0.78%,0.51% and 0.38%,and interday repeatability were 2.6%,1.9% and 2.1%,respectively.This method was simple,accurate and sensitive,so it could be used for the quality control of P.viviparum.<英文关键词>=Key words:Polygonum viviparum ; viterxin ; quercetin ; quercitrin ; RP-HPLC