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一项通过核磁共振氢谱(¹H NMR)光谱法和固相微萃取-气相色谱/质谱联用(SPME-GC/MS)对富含或未富含单酚、二酚或三酚衍生物的初榨亚麻籽油进行体外消化的全球研究。这些化合物的抗氧化效率。

A Global Study by H NMR Spectroscopy and SPME-GC/MS of the in Vitro Digestion of Virgin Flaxseed Oil Enriched or not with Mono-, Di- or Tri-Phenolic Derivatives. Antioxidant Efficiency of These Compounds.

作者信息

Alberdi-Cedeño Jon, Ibargoitia María L, Guillén María D

机构信息

Food Technology, Faculty of Pharmacy, Lascaray Research Center, University of the Basque Country (UPV-EHU), Paseo de la Universidad nº 7, 01006 Vitoria-Gasteiz, Spain.

出版信息

Antioxidants (Basel). 2020 Apr 15;9(4):312. doi: 10.3390/antiox9040312.

Abstract

The effect of enriching virgin flaxseed oil with dodecyl gallate, hydroxytyrosol acetate or gamma-tocopherol on its in vitro digestion is studied by means of proton nuclear magnetic resonance and solid phase microextraction followed by gas chromatography/mass spectrometry. The extent and pattern of the lipolysis reached in each sample is analyzed, as is the bioaccessibility of the main oil components. None of the phenolic compounds provokes inhibition of the lipase activity and all of them reduce the lipid oxidation degree caused by the in vitro digestion and the bioaccessibility of oxidation compounds. The antioxidant efficiency of the three tested phenols is in line with the number of phenolic groups in its molecule, and is dose-dependent. The concentration of some minor oil components such as terpenes, sesquiterpenes, cycloartenol and 24-methylenecycloartenol is not modified by in vitro digestion. Contrarily, gamma-tocopherol shows very low in vitro bioaccessibility, probably due to its antioxidant behavior, although this increases with enrichment of the phenolic compounds. Oxidation is produced during in vitro digestion even in the presence of a high concentration of gamma-tocopherol, which remains bioaccessible after digestion in the enriched samples of this compound.

摘要

通过质子核磁共振和固相微萃取结合气相色谱/质谱法,研究了用没食子酸十二酯、羟基酪醇乙酸酯或γ-生育酚富集初榨亚麻籽油对其体外消化的影响。分析了每个样品中达到的脂解程度和模式,以及主要油成分的生物可及性。酚类化合物均未引起脂肪酶活性的抑制,且所有酚类化合物均降低了体外消化引起的脂质氧化程度以及氧化化合物的生物可及性。三种测试酚的抗氧化效率与其分子中的酚羟基数量一致,且呈剂量依赖性。一些次要油成分如萜类、倍半萜类、环阿屯醇和24-亚甲基环阿屯醇的浓度不受体外消化的影响。相反,γ-生育酚的体外生物可及性非常低,这可能归因于其抗氧化行为,尽管随着酚类化合物的富集其生物可及性会增加。即使在高浓度γ-生育酚存在的情况下,体外消化过程中仍会发生氧化,在该化合物的富集样品中消化后γ-生育酚仍具有生物可及性。

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