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无需衍生化步骤直接核磁共振鉴定和定量乳脂组分中共轭亚油酸的几何异构体:克服灵敏度和分辨率障碍

Direct nuclear magnetic resonance identification and quantification of geometric isomers of conjugated linoleic acid in milk lipid fraction without derivatization steps: overcoming sensitivity and resolution barriers.

作者信息

Tsiafoulis Constantinos G, Skarlas Theodore, Tzamaloukas Ouranios, Miltiadou Despoina, Gerothanassis Ioannis P

机构信息

NMR Center, University of Ioannina, Ioannina GR-45 110, Greece.

Department of Chemistry, University of Ioannina, Ioannina GR-45 110, Greece.

出版信息

Anal Chim Acta. 2014 Apr 22;821:62-71. doi: 10.1016/j.aca.2014.03.010. Epub 2014 Mar 12.

Abstract

We report the first successful direct and unequivocal identification and quantification of four minor geometric (9-cis, 11-trans) 18:2, (9-trans, 11-cis) 18:2, (9-cis, 11-cis) 18:2 and (9-trans, 11-trans) 18:2 conjugated linoleic acid (CLA) isomers in lipid fractions of lyophilized milk samples with the combined use of 1D (1)H-NMR, 2D (1)H-(1)H TOCSY and 2D (1)H-(13)C HSQC NMR. The significant sensitivity barrier has been successfully overcome under selective suppression of the major resonances, with over 10(4) greater equilibrium magnetization of the -(CH2)n-(1)H spins compared to that of the (1)H spins of the conjugated bonds of the CLA isomers. The resolution barrier has been significantly increased using reduced (13)C spectral width in the 2D (1)H-(13)C HSQC experiment. The assignment was confirmed with spiking experiments with CLA standard compounds and the method does not require any derivatization steps for the lipid fraction. The proposed method is selective, sensitive and compares favorably with the GS-MS method of analysis.

摘要

我们报告了首次成功地直接且明确地鉴定和定量冻干牛奶样品脂质组分中的四种次要几何异构体(9-顺式,11-反式)18:2、(9-反式,11-顺式)18:2、(9-顺式,11-顺式)18:2和(9-反式,11-反式)18:2共轭亚油酸(CLA)异构体,采用了一维(1)H-NMR、二维(1)H-(1)H TOCSY和二维(1)H-(13)C HSQC NMR联用的方法。在选择性抑制主要共振的情况下,成功克服了显著的灵敏度障碍,与CLA异构体共轭键的(1)H自旋相比,-(CH2)n-(1)H自旋的平衡磁化强度高出10^4倍以上。在二维(1)H-(13)C HSQC实验中使用减小的(13)C谱宽,显著提高了解析度障碍。通过CLA标准化合物的加标实验确认了归属,并且该方法对脂质组分不需要任何衍生化步骤。所提出的方法具有选择性、灵敏性,与气相色谱-质谱联用(GS-MS)分析方法相比具有优势。

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