Unambiguous detection of astaxanthin and astaxanthin fatty acid esters in krill (Euphausia superba Dana)
Autor: | Karsten Putzbach, Manfred Krucker, Petra Hentschel, Graeme J. Nicholson, Marc David Grynbaum, Klaus Albert, Jens Rehbein |
---|---|
Rok vydání: | 2005 |
Předmět: |
chemistry.chemical_classification
Magnetic Resonance Spectroscopy Chromatography Chemistry Fatty Acids Fatty acid Fatty acid ester Filtration and Separation Atmospheric-pressure chemical ionization Xanthophylls Carotenoids High-performance liquid chromatography Mass Spectrometry Analytical Chemistry chemistry.chemical_compound Liquid chromatography–mass spectrometry Astaxanthin Animals Solid phase extraction Derivatization Chromatography High Pressure Liquid Euphausiacea |
Zdroj: | Journal of Separation Science. 28:1685-1693 |
ISSN: | 1615-9314 1615-9306 |
DOI: | 10.1002/jssc.200500152 |
Popis: | HPLC atmospheric pressure chemical ionization (APCI)/MS, GC MS, HPLC diode array detection (DAD), and NMR were used for the identification of astaxanthin and astaxanthin fatty acid esters in krill (Euphausia superba Dana). Matrix solid phase dispersion was applied for the extraction of the carotenoids. This gentle and expeditious extraction technique for solid and viscous samples leads to distinct higher enrichment rates than the conventional liquid-liquid extraction. The chromatographic separation was achieved employing a C30 RP column that allows the separation of shape-constrained geometrical isomers. A methanol/tert-butylmethyl ether/water gradient was applied. (all-E) Astaxanthin and the geometrical isomers were identified by HPLC APCI/MS, by coelution with isomerized authentical standard, by UV spectroscopy (DAD), and three isomers were unambiguously assigned by microcoil NMR spectroscopy. In this method, microcoils are transversally aligned to the magnetic field and have an increased sensitivity compared to the conventional double-saddle Helmholtz coils, thus enabling the measurement on small samples. The carotenol fatty acid esters were saponified enzymatically with Lipase type VII from Candida rugosa. The fatty acids were detected by GC MS after transesterification, but also without previous derivatization by HPLC APCI/MS. C14:0, C16:0, C16:1, C18:1, C20:0, C20:5, and C22:6 were found in astaxanthin monoesters and in astaxanthin diesters. (all-E) Astaxanthin was identified as the main isomer in six fatty acid ester fractions by NMR. Quantitation was carried out by the method of internal standard. (13-cis) Astaxanthin (70 microg/g), 542 microg/g (all-E) astaxanthin, 36 microg/g unidentified astaxanthin isomer, 62 microg/g (9-cis) astaxanthin, and 7842 microg/g astaxanthin fatty acid esters were found. |
Databáze: | OpenAIRE |
Externí odkaz: |