Vieira Gláucia S, Marques Anna S F, Machado Mariana T C, Silva Vanessa M, Hubinger Miriam D
Department of Food Engineering, School of Food Engineering, University of Campinas (UNICAMP), 80, Monteiro Lobato Street, P.O. Box 6121, Campinas, SP 13083-862 Brazil.
Waters Corporation Brazil, 125, Alphaville, São Paulo, SP 06455-020 Brazil.
J Food Sci Technol. 2017 Jun;54(7):2135-2144. doi: 10.1007/s13197-017-2653-1. Epub 2017 Apr 28.
This work aimed to propose two analytical methods for the quantitative and qualitative analysis of major anthocyanins and non-anthocyanin phenolic compounds in jussara () 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.
本研究旨在提出两种采用超高效液相色谱 - 质谱联用技术对巴西棕榈()提取物中的主要花青素和非花青素酚类化合物进行定量和定性分析的方法。对这些方法的选择性、精密度、线性、检测限和定量限进行了评估。分别在4.5分钟和7分钟内实现了5种花青素和22种非花青素多酚的完全分离。检测限范围为0.55至9.24μg/L,浓度的相对标准偏差高达7.0%。在巴西棕榈提取物中,对27种分析物中的13种进行了表征。主要化合物是矢车菊素 - 3 - O - 芸香糖苷,约占总酚类化合物含量的73%(干重提取物中约为23mg/g)。提取物中发现的其他酚类化合物有:矢车菊素 - 3 - O - 葡萄糖苷、天竺葵素 - 3 - O - 葡萄糖苷、槲皮素、芦丁、杨梅素、山奈酚、山奈酚 - 3 - O - 芸香糖苷、木犀草素、芹菜素、儿茶素、鞣花酸和4,5 - 二咖啡酰奎尼酸。