Chromatographic Resolution of 7 of 8 Stereoisomers of Vitamin K1 on an Amylose Stationary Phase Using Supercritical Fluid Chromatography

In a previous report, it was shown that the trans -isomers of the 2′–3′ double bond on the side chain of vitamin K 1 (phylloquinone) represented 88.65 % of a specific sample, while the cis -isomer represented 11.35 %. However, the side chain contains 2 chiral centers, indicating there are 8 possible...

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Bibliographic Details
Published inChromatographia Vol. 76; no. 9-10; pp. 549 - 552
Main Authors Berger, Terry A., Berger, Blair K.
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer-Verlag 01.05.2013
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Summary:In a previous report, it was shown that the trans -isomers of the 2′–3′ double bond on the side chain of vitamin K 1 (phylloquinone) represented 88.65 % of a specific sample, while the cis -isomer represented 11.35 %. However, the side chain contains 2 chiral centers, indicating there are 8 possible stereoisomers. Seven of these 8 stereoisomers were partially resolved in 20 min, on a RegisPack 4.6 × 250 mm, 5 μm column, using 5 % methanol in CO 2 , at 2 mL/min, 30 °C, 150 bar. This is the first reported separation of these enantiomers by supercritical fluid chromatography, and, apparently, the first separation, by any technique, on a widely available commercial chiral stationary phase. The chiral separation produced one dominant peak, accounting for approximately 58 % of the total area, most likely due to 2′,3′- trans -4 R ,11 R -philloquinone. Three other peaks each accounted for 9.7, 13.4, and 10.3 % of the total area, for a total of an additional ±33.4 %. These 4 peaks account for ≈91.4 % of the total area, in near agreement with the achiral findings for the separation of the trans -isomers. Three smaller, broad, poorly quantified peaks, collectively accounted for 8.1 % of the total area. Mass balance suggests these 3 small peaks are all cis -enantiomers, leaving approximately 3.2 % of the total area, representing the 4th cis -enantiomer, unaccounted for, and likely a co-elution with one of the 4 larger peaks.
ISSN:0009-5893
1612-1112
DOI:10.1007/s10337-013-2428-4