Limitation of using silver ion solid‐phase extraction for animal lipids with a low trans content

Abstract

AbstractSilver ion solid‐phase extraction (Ag+‐SPE) was reported to provide effective separations compared to other Ag+ techniques but at a fraction of cost and time. Ag+‐SPE cartridges resolved fatty acid methyl esters (FAMEs) with different number and/or geometric configuration of double bonds. Here we attempted to determine the trans fatty acids (FA) contained in a low total trans FA sample, horse lipids; lamb was used as a control having a markedly higher total trans content. Gas chromatographic assessment of the fractions showed a good separation of the cis and trans monounsaturated FA (MUFA) fractions, but the relative high content of contaminants that coeluted with these FA impaired the identification of the latter in horse lipids. In lamb trans MUFA isomers could be identified since their abundance relative to impurities was greater. Several attempts were made to remove the contaminants from the SPE cartridges including an extensive prewash with acetone and hexane, a prewash with solvents that would elute the cis MUFA fraction, and a complete prewash of all solvents used in the fractionation, hexane, acetone, and acetonitrile. The prewash using all elution solvents removed most contaminants but subsequently impaired the separation of trans and cis MUFA fractions. The same samples were subjected to Ag+‐HPLC fractionation that showed no impurities demonstrating that they were derived from the Ag+‐SPE separation. The trans MUFA fraction collected from Ag+‐HPLC allowed for the identification of the trans 16:1 and 18:1 FA in horse lipids and is recommended for samples with low trans levels.Practical applications: The commercially available silver ion solid‐phase extraction (Ag+‐SPE) cartridges contain appreciable amounts of contaminants that can interfere with the subsequent GC‐FID elution of low levels of trans fatty acid methyl esters (FAMEs), especially when contaminants are leaked by the SPE tube in quantities comparable to the trans MUFA content. The contaminants could not be quantitatively removed by prewashing the cartridges with acetone and hexane. Acetonitrile removed most contaminants but altered the Ag+‐SPE tube ability to resolve the trans and cis MUFA fractions. Ag+‐HPLC fractionation is recommended for isolation of low levels of trans MUFA, since the washing and conditioning of the chromatographic column can be extended as needed.Ag+‐SPE cartridges are used to separate FAMEs based on number and geometric configuration of double bonds to aid in the identification of complex GC separations.