Iqbal Yasir, Ponnampalam Eric N, Suleria Hafiz A R, Cottrell Jeremy J, Dunshea Frank R
School of Agriculture and Food, Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, VIC 3010, Australia.
Animal Production Sciences, Agriculture Victoria Research, Department of Jobs, Precincts and Regions, Bundoora, VIC 3083, Australia.
Antioxidants (Basel). 2021 Jun 8;10(6):932. doi: 10.3390/antiox10060932.
Chicory and lucerne are used as specialised forages in sheep or dairy production systems in some parts of the world. Recently, these plants are gaining attention as raw materials in the search for natural antioxidants for use in animal feeds, human foods and nutraceutical formulations. The antioxidant potential of these plants is credited to polyphenols, a subgroup of phytochemicals. Therefore, phenolic characterisation is an essential step before their use as ingredients in animal feeds, human food or nutraceutical preparations. In this study, we performed qualitative and quantitative analysis of polyphenols in chicory and lucerne. Profiling of polyphenols from chicory and lucerne was performed by LC-ESI/QTOF-MS with a total of 80 phenolic compounds identified in chicory and lucerne. The quantification of polyphenols was achieved by high performance liquid chromatography, coupled with a photo diode array (HPLC-PDA). Chicoric acid was the major phenolic acid found in chicory, with the highest concentration (1692.33 ± 0.04 µg/g DW) among all the polyphenols quantified in this study. 2-hydroxybenzoic acid was the major phenolic acid found in lucerne, with the highest concentration of 1440.64 ± 0.04 µg/g DW. Total phenolic, flavonoids and total tannin contents were measured, and the antioxidant potential was determined by 2,2-Diphenyl-1-picrylhydrazyl, Ferric Reducing Antioxidant Power, 2,2-Azino-bis-3-ethylbenzothiazoline-6-sulfonic Acid, Hydroxyl (OH) Radical Scavenging Activity, Chelating Ability of Ferrous Ion (Fe) and Reducing Power (RPA) assays. Both chicory (8.04 ± 0.33 mg AAE/g DW) and lucerne (11.29 ± 0.25 mg AAE/g DW) showed high values for Hydroxyl (OH) Radical Scavenging Activity. The current study allowed us to draw a profile of polyphenols from chicory and lucerne. They provided a molecular fingerprint useful for the application of these plant materials in human foods, animal feeds and pharmaceutical formulations.
在世界某些地区,菊苣和苜蓿被用作绵羊或奶牛生产系统中的专用饲料。最近,这些植物作为寻找用于动物饲料、人类食品和营养制剂的天然抗氧化剂的原材料而受到关注。这些植物的抗氧化潜力归因于多酚,多酚是植物化学物质的一个亚组。因此,在将它们用作动物饲料、人类食品或营养制剂的成分之前,酚类物质的表征是必不可少的一步。在本研究中,我们对菊苣和苜蓿中的多酚进行了定性和定量分析。通过LC-ESI/QTOF-MS对菊苣和苜蓿中的多酚进行了分析,共鉴定出菊苣和苜蓿中的80种酚类化合物。多酚的定量分析是通过高效液相色谱结合光电二极管阵列(HPLC-PDA)实现的。菊苣酸是菊苣中发现的主要酚酸,在本研究中定量的所有多酚中浓度最高(1692.33±0.04μg/g干重)。2-羟基苯甲酸是苜蓿中发现的主要酚酸,最高浓度为1440.64±0.04μg/g干重。测定了总酚、黄酮类化合物和总单宁含量,并通过2,2-二苯基-1-苦基肼、铁还原抗氧化能力、2,2-联氮-双-3-乙基苯并噻唑啉-6-磺酸、羟基(OH)自由基清除活性、亚铁离子(Fe)螯合能力和还原能力(RPA)测定法测定了抗氧化潜力。菊苣(8.04±0.33mg AAE/g干重)和苜蓿(11.29±0.25mg AAE/g干重)的羟基(OH)自由基清除活性均显示出较高的值。当前的研究使我们能够描绘出菊苣和苜蓿中多酚的概况。它们提供了一个分子指纹,有助于这些植物材料在人类食品、动物饲料和药物制剂中的应用。