Volume 4, Issue 3 pp. 173-188
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DIRECT DETERMINATION OF TRANS-OCTADECENOIC ACID IN DIET COMPOSITES USING A COMBINATION OF SILVER ION-HIGH PERFORMANCE LIQUID CHROMATOGRAPHY AND CAPILLARY GAS CHROMATOGRAPHY

K.M. PHILLIPS

Corresponding Author

K.M. PHILLIPS

Department of Biochemistry Virginia Polytechnic Institute and State University Blacksburg, VA 24061–0308

1Corresponding author. (TEL) 540–231–9960, (FAX) 540–231–9070, [email protected]Search for more papers by this author
R.D. LUGOGO

R.D. LUGOGO

Department of Biochemistry Virginia Polytechnic Institute and State University Blacksburg, VA 24061–0308

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R.F. HARRIS

R.F. HARRIS

Department of Biochemistry Virginia Polytechnic Institute and State University Blacksburg, VA 24061–0308

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M.-T. TARRAGÓ-TRANI

M.-T. TARRAGÓ-TRANI

Department of Biochemistry Virginia Polytechnic Institute and State University Blacksburg, VA 24061–0308

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J.A. BAILEY

J.A. BAILEY

Department of Biochemistry Virginia Polytechnic Institute and State University Blacksburg, VA 24061–0308

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K.K. STEWART

K.K. STEWART

Department of Biochemistry Virginia Polytechnic Institute and State University Blacksburg, VA 24061–0308

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First published: 04 May 2007
Citations: 7

ABSTRACT

Silver ion-high performance liquid chromatography (Ag-HPLC) and capillary gas chromatography (GC) were combined to quantify total trans-octadecenoic acid (18:1t) in diet composites and oils. The 18:1 cis and trans fatty acid methyl esters (FAME) of saponified and methylated (BF3/methanol) oils and food composite total lipid extracts were separated by Ag-HPLC (ChromSpher5 Lipids column); total 18:1t in the trans fraction was quantified by GC (105m × 0.25mm SP-2560 capillary column). Positional isomers 18:1c and 18:1t which coeluted in direct GC were clearly separated by preparatory Ag-HPLC. Quantitative recovery of 18:1t from a standard mixture of FAME, an oil, and a diet composite was obtained for additions of 4–57 mg. The analytical range for total 18:1t was 1.6–260 mg/mL per aliquot of total lipid extract or oil. Relative standard deviations were < 6% for food composites and < 3% for oils and pure standards.

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