2001
DOI: 10.1016/s0021-9673(00)01110-9
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Determination of RS,E/Z-tocotrienols by HPLC

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Cited by 40 publications
(32 citation statements)
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“…Structurally, tocopherols and tocotrienols are very similar. The main difference is that tocopherols have a long saturated carbon side chain with chiral centers, while tocotrienols have three unsaturated bonds in the carbon side chain with one chiral center 39 . This unique property promotes the efficient metabolic function of tocotrienols, which allows tocotrienols to penetrate tissues with saturated fatty layers more readily when compared with tocopherols.…”
Section: Tocotrienolsmentioning
confidence: 99%
“…Structurally, tocopherols and tocotrienols are very similar. The main difference is that tocopherols have a long saturated carbon side chain with chiral centers, while tocotrienols have three unsaturated bonds in the carbon side chain with one chiral center 39 . This unique property promotes the efficient metabolic function of tocotrienols, which allows tocotrienols to penetrate tissues with saturated fatty layers more readily when compared with tocopherols.…”
Section: Tocotrienolsmentioning
confidence: 99%
“…Analysis of stereoisomer ratios of a-tocopherol from feedstuffs and muscle Total a-tocopherol from feedstuffs (three samples each of grass and silage; four samples of concentrate) and muscle (four samples from each of the P, SiP, SiPC and C groups and four samples from each country) was extracted and separated as described above and collected using an Agilent fraction collector (Agilent Technologies, 1200 series, Analyt FC). a-Tocopherol was derivatised following modifications of the method of Riss et al (1994) by Drotleff and Ternes (2001). The a-tocopherol fractions in n-hexane were transferred to 2 ml Eppendorf tubes and evaporated to dryness under nitrogen.…”
Section: Measurement Of A-tocopherol In Feed and Musclementioning
confidence: 99%
“…It is also possible to separate simultaneously the four tocopherols into their 2R and 2S isomers using a simple isocratic method (hexane plus 0.05% ethanol or propanol) by HPLC on a Chiralcel OD-H column. The same column was also used in the determination of tocotrienols stereoisomers [136]. Stereochemistry of natriuretic factor ␥-CEHC was assessed by chiral HPLC on a S,S Whelk O 1 column [137] while simultaneous separation of ␣-and ␥-CEHC enantiomers was accomplished on a Chiradex column in a study regarding the change of CEHCs serum levels after a single dose of vitamin E supplement [138].…”
Section: Chiral Chromatography Of Vitamin E Moleculesmentioning
confidence: 99%