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鱼油来源的ω-3脂肪酸酯的分析规模高效液相色谱法。

Analytical-scale high-performance liquid chromatography of omega-3 fatty acid esters derived from fish oils.

作者信息

Beebe J M, Brown P R, Turcotte J G

机构信息

Department of Chemistry, University of Rhode Island, Kingston 02881.

出版信息

J Chromatogr. 1989 May 12;468:225-33. doi: 10.1016/s0021-9673(00)96319-2.

Abstract

Fish oil triglycerides were transesterified to their corresponding methyl and ethyl esters. The esters were separated by reversed-phase high-performance liquid chromatography on a 10-cm column of 5-microns octadecylsilyl silica, using a ternary mobile phase of acetonitrile-tetrahydrofuran-water (9:5:11). The separation of principal saturated and unsaturated C14-C22 fatty acid esters was accomplished in 60 min. For the polyenoic acid esters, detection limits of ca. 26 micrograms were observed, and baseline resolution of the important critical pair of esters of the omega 3 fatty acids, eicosapentaenoic acid (C20:5 omega 3) and docosahexaenoic acid (C22:6 omega 3) was achieved. However, to obtain baseline resolution of the esters from minor fatty acid esters, a urea crystallization procedure was required prior to chromatographic analysis. The influence on the reversed-phase chromatographic retention of four different ester moieties on the fatty acids were also studied. The n-alkyl esters exhibited an increase in ln k' with increasing chain length and with increasing lipophilic character of the alkyl ester moieties; however, with the aromatic benzyl derivatives there was a decrease in ln k' compared with the alkyl esters.

摘要

鱼油甘油三酯被酯交换为相应的甲酯和乙酯。这些酯在一根10厘米长、填充5微米十八烷基硅烷硅胶的反相高效液相色谱柱上进行分离,使用乙腈 - 四氢呋喃 - 水(9:5:11)的三元流动相。主要饱和及不饱和C14 - C22脂肪酸酯在60分钟内完成分离。对于多烯酸酯,检测限约为26微克,并且实现了ω - 3脂肪酸中重要的关键酯对——二十碳五烯酸(C20:5 ω - 3)和二十二碳六烯酸(C22:6 ω - 3)酯的基线分离。然而,为了从小脂肪酸酯中获得酯的基线分离,在色谱分析之前需要进行尿素结晶程序。还研究了四种不同酯部分对脂肪酸反相色谱保留的影响。正烷基酯的ln k'随链长增加以及烷基酯部分亲脂性增加而增大;然而,与烷基酯相比,芳基苄基衍生物的ln k'有所降低。

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