Correlation between nuclear magnetic resonance and traditional method to evaluate the lipid oxidation of emulsified chicken meat products with fat replacement by green banana biomass

TBARS公司 化学 脂质氧化 食品科学 背景(考古学) 脂质过氧化 脂肪酸 生物量(生态学) 核磁共振波谱 硫代巴比妥酸 质子核磁共振 抗氧化剂 有机化学 生物 海洋学 地质学 古生物学
作者
Bruna Emygdio Auriema,Juarez Vicente,Mário Geraldo de Carvalho,Rosane Nora Castro,Rosa Helena Luchese,Simone Pereira Mathias
出处
期刊:Journal of Food Processing and Preservation [Wiley]
卷期号:45 (3) 被引量:5
标识
DOI:10.1111/jfpp.15277
摘要

This study aimed to compare the methods of nuclear magnetic resonance (NMR) and thiobarbituric acid reactive substances (TBARS) on the lipid oxidation of chicken mortadella with substitution (0%, 25%, 50%, 75%, and 100%) of chicken skin by green banana biomass (GBB) for 90 days of storage. The NMR method was correlated with the Fourier transform-infrared spectroscopy (FT-IR), medium-infrared spectroscopy, flame ionization gas chromatography (GC-FID), and physical-chemical parameters. During 90 days of storage, TBARS values ranged from 2.16 to 2.56 mg/kg−1. NMR showed appearance of allylic protons and there was an increase of the trans fatty acids content over 90 days in relation to the first day of storage with the decrease of GBB concentration. The lipid content was highly correlated with allylic protons and trans fatty acids content (R2 values ranged from 0.952 to 0.965), revealing that NMR is an efficient methodology with high precision for determination of lipid oxidation. Practical applications Lipid oxidation is one of the main problems found in the processing and storage of emulsified meats, once these products present a high fat content. In this context, the present study suggested the use of green banana biomass as fat replacement in chicken mortadella, and the results showed a reduction in the total fat content as well as a lower concentration of trans fatty acids. In addition, this work presented understanding regarding the NMR method as the most indicated method in relation to the usual method, TBARS, to evaluate lipid oxidation during 90 days of storage.
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