Analysis of Fatty Acids by Gas Liquid Chromatography

互联网2014-02-13

971

The fatty acids (FA) of animal, plant, and microbial origin are predominantly unbranched aliphatic chains with an even number of carbon atoms and a single carboxyl group. FA can be classified as saturated, monounsaturated, or polyunsaturated (Fig. 1 ). Saturates have all single carbon-to-carbon bonds. Monounsaturates contain a single cis double bond, whereas polyunsaturates have two or more. A list of the commonly occurring natural FA in animal tissues is shown in Table 1 . In general, FA do not exist as free carboxylic acids in living cells. In animals, they are mainly esterified into membrane phospholipids (phosphoglycerides and sphingolipids) and cytosolic neutral lipids (triglycerides and cholesteryl esters). In order to analyze the FA components of cell lipids, they must first be converted into nonpolar, volatile derivatives before they can be separated and quantified by the rapid and highly sensitive technique of gas liquid chromatography (GLC).

Fig. 1. Structural classification of fatty acids.

Table 1 Nomenclature of Some Common Natural Fatty Acids

Common name	Synonym ^a	Abbreviation ^b
Myristic	Tetradecanoic	14:0
Palmitic	Hexadecanoic	16:0
Stearic	Octadecanoic	18:0
Arachidic	Eicosanoic	20:0
Behenic	Docosanoic	22:0
Lignoceric	Tetracosanoic	24:0
Cerotic	Hexacosanoic	26:0
Palmitoleic	7-Hexadecenoic	16:1 n-9
Oleic	9-Octadecenoic	18:1 n-9
Gadoleic	11-Eicosenoic	20:1 n-9
Erucic	13-Docosenoic	22:1 n-9
Nervonic	15-Tetracosenoic	24:1 n-9
Linoleic	9,12-Octadecadienoic	18:2 n-6
Alpha-linolenic	9,12,15-Octadecatrienoic	18:3 n-3
Gamma-linolenic	6,9,12-Octadecatrienoic	18:3 n-6
Arachidonic	5,8,11,14-Eicosatetraenoic	20:4 n-6
Adrenic	7,10,13,16-Docosatetraenoic	22:4 n-6
Timnodonic	5,8,11,14,17-Eicosapentaenoic	20:5 n-3
Clupanodonic	4,7,10,13,16,19-Docosahexaenoic	22:6 n-3
^a Double bonds numbered from the carboxyl end of the molecule.

^a Abbreviated fatty acid formulae showing the number of carbon atoms (e.g., 12,18,22), the number of double bonds (e.g., 0,1,4), and the position of the first double bond in relation to the n-carbon or methyl end of the molecule (e.g., n-3,n-6).

关于丁香通

公司信息

个人用户

企业机构

无忧采购轻松科研

提问

扫一扫

实验小助手

扫码领资料

反馈

TOP

打开小程序