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HPLC Determination of Extractable and Unextractable Proanthocyanidins in Plant Materials

机译:高效液相色谱法测定植物材料中可提取和不可提取的原花色素

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This study developed a method for the determination of extractable and unextractable proanthocyanidins.Extractable proanthocyanidins were separated according to their degree of polymerization using normal phase HPLC.Unextractable proanthocyanidins were measured after acid-catalyzed depolymerization as flavan-3-ols(terminal units)and benzylthioethers(external units).Electrospray ionization mass spectrometry(ESI-MS)was used for the identification of proanthocyanidins in the samples.Hubaux-Vos detection limits were 0.01-0.15 ng/injection for extractable proanthocyanidins,with recovery rates from 69 to 91%.Detection limits for unextractable proanthocyanidin derivatives were 0.002-0.035 ng/injection with 80% recovery.The developed method was applied to the analysis of several fruit and berry samples.Results showed great variation in the proportion of unextractable proanthocyanidins in total proanthocyanidin content between samples,being highest in the green variety of table grape(63%)and lowest in the apple cultivar'Valkeakuulas'(4.1%).The method reported herein is reliable and gives valuable information on the nature of proanthocyanidins in plant-derived foods.
机译:本研究建立了一种可萃取和不可萃取原花青素的测定方法,采用正相HPLC根据其聚合度对可萃取原花青素进行分离,酸催化解聚后以黄烷-3-醇(末端单元)和苄基硫醚的形式测定了不可萃取原花青素。使用电喷雾电离质谱(ESI-MS)鉴定样品中的原花青素,Hubaux-Vos的检出限为0.01-0.15 ng /进样可萃取原花青素,进样率从69%到91%。不可萃取原花青素衍生物的检出限为0.002-0.035 ng /进样,回收率为80%。该方法用于几种水果和浆果样品的分析,结果表明样品之间不可萃取原花青素在总原花青素含量中的比例差异很大,在鲜食葡萄的绿色品种中最高(63%)和低在苹果品种'Valkeakuulas'(4.1%)中向西。本文报道的方法可靠,并且提供了有关植物性食品中原花青素性质的有价值的信息。

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