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小叶女贞果实花青素组分鉴定及色谱纯化技术
引用本文:王二雷,陈晶晶,赵叶辉,刘静波.小叶女贞果实花青素组分鉴定及色谱纯化技术[J].农业工程学报,2016,32(4):302-308.
作者姓名:王二雷  陈晶晶  赵叶辉  刘静波
作者单位:1. 吉林大学食品科学与工程学院营养与功能食品研究室,长春,130062;2. 吉林亚泰生物药业股份有限公司,长春,130031
基金项目:国家自然科学基金面上项目(31271907)
摘    要:为提高小叶女贞果实的食用、药用价值,该文系统研究了果实中花青素种类构成及提取物的制备技术。试验采用紫外可见光谱法、高效液相色谱-质谱串联法、酸水解制备苷元等技术对小叶女贞果实花青素含量、单体种类进行了测定,并借助提取、萃取、柱层析等技术研究了花青素提取物的分离纯化过程。研究结果如下:测得每100 g小叶女贞果实中含花青素总量为(499±18.42)mg,从中鉴定出2种花青素单体,分别为矢车菊素-3-O-葡萄糖苷和牵牛花色素-3-O-葡萄糖苷,并以后者为主要存在形式;获得了纯天然、简单易行的花青素提取物制备技术,主要包括酸化乙醇提取、乙酸乙脂萃取、Amberlite XAD-7HP大孔树脂层析分离步骤,最终制得的花青素提取物纯度为35%、得率为0.6%。该研究为后期制备高纯度牵牛花素-3-O-葡萄糖苷单体提供了良好原料基础,为深入研究小叶女贞果实花青素功能活性及其在食品、药品领域潜在应用提供了参考。

关 键 词:提取  萃取  柱层析  小叶女贞  花青素
收稿时间:2015/9/23 0:00:00
修稿时间:2015/12/29 0:00:00

Identification of anthocyanins in Ligustrum quihoui Carr and chromatographic separation techniques
Wang Erlei,Chen Jingjing,Zhao Yehui and Liu Jingbo.Identification of anthocyanins in Ligustrum quihoui Carr and chromatographic separation techniques[J].Transactions of the Chinese Society of Agricultural Engineering,2016,32(4):302-308.
Authors:Wang Erlei  Chen Jingjing  Zhao Yehui and Liu Jingbo
Institution:1. Laboratory of Nutrition and Functional Food, College of Food Science and Engineering, Jilin University, Changchun 130062, China,1. Laboratory of Nutrition and Functional Food, College of Food Science and Engineering, Jilin University, Changchun 130062, China,2. Jilin Yatai Biological Pharmacy Co., Ltd., Changchun 130031, China and 1. Laboratory of Nutrition and Functional Food, College of Food Science and Engineering, Jilin University, Changchun 130062, China
Abstract:Abstract: As one kind of important hedge materials, Ligustrum quihoui Carr. has been widely used in landscaping. Currently, a number of researchers are engaged in the identification of the chemical structure for the leaves of Ligustrum quihoui Carr.. However, the chemical ingredients in the fruits have not been well studied up till now, especially the study on the anthocyanins is rare. In order to promote the application of Ligustrum quihoui Carr. on food and medicine fields, the present research focuses on the determination of anthocyanin content and monomer composition of Ligustrum quihoui Carr. fruits. The study adopted the combined techniques of ultraviolet-visible spectroscopy spectrum (UV-vis), reversed phase high-performance liquid chromatography (RP-HPLC), high-performance liquid chromatography - diode array detector - electrospray ionization - tandem mass spectrometry (HPLC-DAD-ESI-MS/MS) and acid hydrolysis, as well as the preparation process of anthocyanin extracts using extraction, concentration, partition, column chromatography and freeze-drying technologies. The UV-vis spectrum results verified the existence of anthocyanins in the fruit part, and the total anthocyanin content was 499±18.42 mg per 100 g fresh fruits, which was determined by the pH differential method. Two glycosylated anthocyanin monomers (cyanidin-3-O-glucoside and petunidin-3-O-glucoside) were successfully identified from the fruits of Ligustrum quihoui Carr. by means of RP-HPLC, HPLC-DAD-ESI-MS/MS technologies, and then testified through the identification of anthocyanin aglycones prepared by acid hydrolysis of anthocyanin glycosides. We also found that, petunidin-3-O-glucoside was the dominating form in the fruits of Ligustrum quihoui Carr., which could become a new focus of our further research. A natural and simple preparation process of anthocyanin extracts was obtained by the combined chromatographic separation techniques. A kind of safe and cheap extractant was employed to extract anthcoyanin glycosides instead of the use of harmful methanol, acetone, trifluoroacetic acid etc., which was composed of 70% ethanol (v/v) and 0.1 mol/L HCl with a mixing proportion of 9:1 (v/v). After the anthocyanin extracts were filtered and concentrated, ethyl acetate was used to remove fat-soluble impurities from the anthocyanin extracts in the partition process, and the extraction was carried out for 3 times. Because of the existence of lots of water-soluble impurities (reducing sugars, proteins and polar flavonoids) in anthocyanin extracts, the aqueous anthocyanin extracts were loaded onto a column (2.6 cm × 50 cm) of cation-exchange resin (Amberlite XAD-7HP, particle size: 20-60 meshes), washed by deionized water (containing 0.01% HCl, v/v) to remove water-soluble ingredients, and then eluted by 40% aqueous ethanol (containing 0.01% HCl, v/v) to collect anthocyanin eluents, concentrated and freeze-dried; finally the extract was obtained with a purity of 35% and a yield of 0.6%. In view of the current purity of anthocyanin extracts, it was estimated that there were still many impurities mixed with the anthocyanin extracts, which needed a further separation using gel chromatography, high-speed countercurrent chromatography, preparative-HPLC etc. Because of the simplicity of anthocyanin profiles and high content of petunidin-3-O-glucoside monomer in Ligustrum quihoui Carr. fruit, it was promising to separate high-purity petunidin-3-O-glucoside monomer from the anthocyanin extracts using the combined purification techniques in our next experiments. The present research can promote the comprehensive development of the Ligustrum quihoui Carr. fruit, and meanwhile lay a foundation for further research on the bio-activity of anthocyanins in Ligustrum quihoui Carr. fruit and its potential application in food and medicine fields.
Keywords:extraction  partitions  column chromatography  Ligustrum quihoui Carr  anthocyanins
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