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借助银离子固相萃取通过气相色谱-火焰离子化检测分析对乳脂肪脂肪酸丙酯进行赋值

Assignment of Milk Fat Fatty Acid Propyl Esters by GC-FID Analysis with the Aid of Ag-ion Solid-phase Extraction.

作者信息

Sasaki Ryo, Umezawa Masatoshi, Tsukahara Satoru, Ishiguro Takashi, Sato Shinichi, Watanabe Yomi

机构信息

Miyoshi Oil & Fat Co., Ltd.

出版信息

J Oleo Sci. 2015;64(12):1251-8. doi: 10.5650/jos.ess15125.

Abstract

The recovery of short-chain fatty acids (FAs) in milk fat (MF) is improved when the analysis of the FA composition of MF by gas chromatography (GC) is conducted with the propyl or butyl ester derivatives, instead of the methyl esters. However, this approach complicates the detection of minor FAs, such as the minor positional isomers of 16:1, which represent <0.2% of the total content. In addition, the standards of these minor esters are not commercially available. In this study, with the aim to identify minor FAs, the fatty acid propyl esters (FAPEs) of MF were fractionated by Ag-ion solid phase extraction (Ag(+)-SPE) and analyzed by GC using a DB-23 capillary column. FAPEs were successfully fractionated mainly according to the degree of unsaturation by adjusting the elution conditions of the Ag(+)-SPE, and the minor FAPEs were easily determined without the aid of standard compounds. For example, by comparison of the GC profile of the saturated Ag(+)-SPE fraction with that of the original MF, minor FAs, such as iso-, anteiso-, and saturated FAs of 15:0 and 17:0, were expected to be eluted in this order. In addition, 16:1 propyl ester was co-eluted with iso 17:0 propyl ester under the GC conditions used in this study, as confirmed by the detection of the corresponding molecular ions (296 and 312, respectively) by GC-MS. Moreover, 9c,11t-conjugated linoleic acid was found to elute between 18:3 and 20:0. To the best of our knowledge, this is the first report suggesting that the peak observed before that of cis-12:1 corresponds to trans-12:1. In conclusion, Ag(+)-SPE fractionation of FAPEs contributed to the identification of minor FAs in MF without the use of standard compounds.

摘要

当采用气相色谱法(GC)分析乳脂肪(MF)的脂肪酸组成时,若使用丙酯或丁酯衍生物而非甲酯,短链脂肪酸(FAs)在乳脂肪中的回收率会提高。然而,这种方法使微量FAs的检测变得复杂,比如16:1的微量位置异构体,其占总含量不到0.2%。此外,这些微量酯的标准品并无商业供应。在本研究中,为了鉴定微量FAs,通过银离子固相萃取(Ag(+)-SPE)对MF的脂肪酸丙酯(FAPEs)进行分离,并使用DB-23毛细管柱通过GC进行分析。通过调整Ag(+)-SPE的洗脱条件,FAPEs主要根据不饱和度成功分离,并且无需标准化合物的辅助就能轻松测定微量FAPEs。例如,通过比较饱和Ag(+)-SPE馏分与原始MF的GC图谱,预计异丁酸、反异丁酸以及15:0和17:0的饱和脂肪酸等微量FAs会按此顺序洗脱。此外,在本研究使用的GC条件下,16:1丙酯与异17:0丙酯共洗脱,这通过GC-MS检测相应的分子离子(分别为296和312)得到证实。而且,发现9c,11t-共轭亚油酸在18:3和20:0之间洗脱。据我们所知,这是首次报道表明在顺式-12:1之前观察到的峰对应反式-12:1。总之,FAPEs的Ag(+)-SPE分离有助于在不使用标准化合物的情况下鉴定MF中的微量FAs。

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