Quantitative determination of Tri‐, Di‐,monooleins and free oleic acid by the thin layer chromatography‐flame lonization detector system using internal standards and boric acid impregnated chromarod

Publisher Website
Google Scholar
Abstract
The separation conditions for hydrolysates of triglycerides by lipase and their quantitative determination are discussed for a thin layer chromatography‐flame ionization detector system utilizing internal standards. The complete separation of glyceride hydrolysis mixtures (triolein 1,3‐diolein, 1,2‐diolein, 1‐monoolein and oleic acid) was achieved on a 3% boric acid‐impregnated Chromarod S‐II by development with benzene/chloroform/acetic acid (70∶30∶2, v/v/v) (mobile phase A) or hexane/ ether/acetic acid (70∶30∶1, v/v/v) (mobile phase B). Mobile phase B had an advantage over mobile phase A in terms of free space to add internal standards for simultaneous quantitation and was employed.p‐Hydroxybenzoic acid andp‐carboethoxy benzyl alcohol, which appeared between 1,2‐diolein and 1‐moloolein, were adopted as the internal standards. The calibration curves relating internal standards to each glyceride were all approximated by the equations Y=aXb giving high correlations. The method was applied to hydrolysis of triolein by pancreatic lipase.