Suppr超能文献

合成多酚类抗氧化剂对食用油中活性羰基化合物形成的抑制活性。

Inhibitory Activity on the Formation of Reactive Carbonyl Species in Edible Oil by Synthetic Polyphenol Antioxidants.

机构信息

Department of Food Science and Technology, School of Food Science and Pharmaceutical Engineering, Nanjing Normal University, 2 Xuelin Road, Nanjing, Jiangsu 210023, People's Republic of China.

Spice and Beverage Research Institute, Chinese Academy of Tropical Agricultural Sciences, Wanning, Hainan 571533, People's Republic of China.

出版信息

J Agric Food Chem. 2021 Aug 18;69(32):9025-9033. doi: 10.1021/acs.jafc.0c07248. Epub 2021 Jan 17.

Abstract

Food lipids play an important role in food quality, and their attributes contribute to texture, flavor, and nutrition. However, high-temperature processing leads to lipid peroxidation, degradation, and the formation of reactive carbonyl species (RCS), such as acrolein (ACR), glyoxal (GO), and methylglyoxal (MGO). We investigated the changes in the peroxidation value (POV), Rancimat induction time, formation and total amount of RCS, and inhibitory effects of synthetic polyphenol antioxidants on ACR/GO/MGO in plant oils during heating processing through an accelerated oxidation test using Rancimat. With increasing temperature and heating time, the amounts of ACR, GO, and MGO in oil increased and the level of ACR was about several times higher than that of GO and MGO. We also found that some amounts of ACR, GO, and MGO were produced at the initial stage before reaching the peak value of POV, even before oil oxidative rancidity, and the common antioxidant butyl hydroxyanisole (BHA)/butylated hydroxytoluene (BHT) could not remove them once they were generated. This is first time to purify PG-ACR-MGO and elucidate the structure based on analysis of their high resolution mass spectrometry and H, C, and two-dimensional nuclear magnetic resonance. We further found that PG rather than BHT and BHA efficiently trapped ACR, OG, and MGO to form adducts in oil and roasted beef burgers with corn oil. Additionally, after incubation at 80 °C, the trapping order of PG was as follows: ACR, MGO, and GO, and the adduct of PG-ACR was formed within 1 min; after 10 min, PG-MGO was generated; and three adducts formed at 15 min. However, PG could not trap ACR, GO, or MGO to form adducts at room temperature. This study provided novel knowledge to advance our understanding of the ability of synthetic polyphenol antioxidants to scavenge RCS simultaneously, such as ACR, MGO, and GO. Our findings demonstrated that PG, as an inhibitor of RCS, is suitable for medium- and high-temperature food processing but not for normal-temperature storage.

摘要

食品脂质在食品质量中起着重要作用,其特性有助于形成食品的质地、风味和营养。然而,高温加工会导致脂质过氧化、降解,并形成反应性羰基化合物(RCS),如丙烯醛(ACR)、乙二醛(GO)和甲基乙二醛(MGO)。我们通过使用 Rancimat 进行加速氧化试验,研究了在加热过程中植物油脂的过氧化值(POV)、Rancimat 诱导时间、RCS 的形成和总量以及合成多酚抗氧化剂对 ACR/GO/MGO 的抑制作用的变化。随着温度和加热时间的增加,油中 ACR、GO 和 MGO 的含量增加,ACR 的水平约为 GO 和 MGO 的数倍。我们还发现,在达到 POV 峰值之前的初始阶段,甚至在油氧化酸败之前,就已经产生了一些 ACR、GO 和 MGO,而且一旦生成,常见的抗氧化剂丁基羟基茴香醚(BHA)/叔丁基对羟基茴香醚(BHT)也无法去除它们。这是首次纯化 PG-ACR-MGO 并基于其高分辨率质谱和 H、C 和二维核磁共振分析阐明其结构。我们进一步发现,PG 而不是 BHA 和 BHT 能够有效地在油和玉米油烤牛肉汉堡中捕获 ACR、OG 和 MGO 并形成加合物。此外,在 80°C 孵育后,PG 的捕获顺序如下:ACR、MGO 和 GO,PG-ACR 的加合物在 1 分钟内形成;10 分钟后生成 PG-MGO;15 分钟时生成三种加合物。然而,PG 不能在室温下捕获 ACR、GO 或 MGO 以形成加合物。本研究为深入了解合成多酚抗氧化剂同时清除 RCS(如 ACR、MGO 和 GO)的能力提供了新的知识。我们的研究结果表明,PG 作为 RCS 的抑制剂,适用于中高温食品加工,但不适用于常温储存。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验