首页> 美国卫生研究院文献>Journal of Food Science and Technology >Determination of anthocyanins and non-anthocyanin polyphenols by ultra performance liquid chromatography/electrospray ionization mass spectrometry (UPLC/ESI–MS) in jussara (Euterpe edulis) extracts
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Determination of anthocyanins and non-anthocyanin polyphenols by ultra performance liquid chromatography/electrospray ionization mass spectrometry (UPLC/ESI–MS) in jussara (Euterpe edulis) extracts

机译:超浓缩液相色谱/电喷雾电离质谱(UPLC / ESI–MS)测定菊苣(Euterpe edulis)提取物中的花色苷和非花色苷多酚

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摘要

This work aimed to propose two analytical methods for the quantitative and qualitative analysis of major anthocyanins and non-anthocyanin phenolic compounds in jussara (Euterpe edulis) extracts, using ultra performance liquid chromatography-mass spectrometry. These methods were evaluated for selectivity, precision, linearity, detection and quantification limits. The complete separation of 5 anthocyanins and 22 non-anthocyanins polyphenols was achieved in 4.5 and 7 min, respectively. Limits of detection ranged from 0.55 to 9.24 µg/L, with relative standard deviation for concentration up to 7.0%. In jussara extract, 13 of the 27 analytes were characterized. The dominant compound was cyanidin-3-O-rutinoside, representing about 73% of the total phenolic compounds content (approximately 23 mg/g of extract in dry weight). Other phenolic compounds found in the extract were: cyanidin-3-O-glucoside, pelargonidin-3-O-glucoside, quercetin, rutin, myricetin, kaempferol, kaempferol-3-O-rutinoside, luteolin, apigenin, catechin, ellagic acid and 4,5-dicaffeoylquinic acid.
机译:这项工作旨在提出两种分析方法,采用超高效液相色谱-质谱法对菊苣(Euterpe edulis)提取物中的主要花色苷和非花青素酚类化合物进行定量和定性分析。对这些方法的选择性,精密度,线性,检测和定量限进行了评估。分别在4.5分钟和7分钟内完成了5种花色素苷和22种非花色素苷多酚的完全分离。检测限范围为0.55至9.24 µg / L,相对标准偏差为7.0%。在jussara提取物中,对27种分析物中的13种进行了表征。占主导地位的化合物是花青素3-O-芸香糖苷,约占酚类化合物总含量的73%(以干重计约为23 mg / g提取物)。提取物中发现的其他酚类化合物为:花青素3-O-葡糖苷,pelargonidin-3-O-葡糖苷,槲皮素,芦丁,杨梅素,kaempferol,kaempferol-3-o-rutinoside,木犀草素,芹菜素,儿茶素,鞣花酸和4,5-二咖啡酰奎宁酸。

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