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Enantiomeric separation of triacylglycerols containing fatty acids with a ring (cyclofatty acids).
- Source :
-
Journal of chromatography. A [J Chromatogr A] 2020 Jul 05; Vol. 1622, pp. 461103. Date of Electronic Publication: 2020 Apr 17. - Publication Year :
- 2020
-
Abstract
- Triacylglycerols (TAGs) containing cyclofatty acids (cycloFAs) from two oilseeds of Sterculia foetida and Hydnocarpus wightiana were analysed using both reversed-phase (RP18) and chiral phase columns. TAGs were identified using high-resolution electrospray ionization mass spectrometry in the positive ion mode. Fifty-five molecular species of TAGs have been identified in sterculic oil, 27 of which contained at least one cyclopropenyl-FA (e.g., malvalic or sterculic acids). The structures of regioisomers and enantiomers were determined for five major TAGs with cyclopropenyl-FAs. One hundred thirty-six TAGs were identified in chaulmoogra oil, 71 of which contained at least one cyclopentenyl-FA (e.g., gorlic, chaulmoogric, and hydnocarpic acids, etc.). Furthermore, in three molecular species, regioisomers and enantiomers were identified using HPLC on a chiral phase column. Eight molecular species of TAGs were prepared through organic synthesis to facilitate the identification of enantiomers. Retention times of fatty acid-containing triacylglycerols with one ring and one double bond are very similar to triacylglycerols with a dienoic fatty acid, but elution times are shorter. For example, dimalvaloylpalmitate elutes earlier than dilinoleylpalmitate. The order of elution of TAGs on the chiral column differs. In TAGs with 2 degrees of unsaturation (ring and double bond, e.g. PStP-StPP-PPSt), the order of elution is symmetric-asymmetric-asymmetric TAGs. TAGs with 4 degrees of unsaturation (one ring and three double bonds or two rings and two double bonds) present a different pattern. When TAGs contain two rings and two double bonds, the order of elution TAGs is asymmetric-symmetric-asymmetric (StStP-StPSt-PStSt); when TAGs contain a ring and 3 double bonds, the elution order is symmetric-asymmetric-asymmetric TAGs (OStO-StOO-OOSt). In species with a higher degree of unsaturation (e.g., 5), the elution order of the TAGs is asymmetric-asymmetric-symmetric (e.g. CCO-OCC-COC).<br />Competing Interests: Declaration of Competing Interest The authors declare no competing financial interest.<br /> (Copyright © 2020 Elsevier B.V. All rights reserved.)
- Subjects :
- Chromatography, High Pressure Liquid
Chromatography, Reverse-Phase
Cyclopropanes analysis
Fatty Acids chemistry
Fatty Acids isolation & purification
Fatty Acids, Monounsaturated analysis
Plant Oils chemistry
Spectrometry, Mass, Electrospray Ionization
Sterculia chemistry
Stereoisomerism
Fatty Acids analysis
Triglycerides chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3778
- Volume :
- 1622
- Database :
- MEDLINE
- Journal :
- Journal of chromatography. A
- Publication Type :
- Academic Journal
- Accession number :
- 32317104
- Full Text :
- https://doi.org/10.1016/j.chroma.2020.461103