In this study, acetone was used to extract the astaxanthin from Antarctic krill. The silica gel column chromatography was optimised for separating astaxanthin diester, astaxanthin monoester, and free astaxanthin. A suitable developing solvent was selected. Samples were identified by a thin layer chromatography and the three-dimensional structures were confirmed by Chiralpak IC column. The contents of astaxanthin in different forms were quantified using C30-HPLC. The results showed that a gradient elution through silica gel column chromatography with different ratios of acetone-petroleum ether could completely separate free astaxanthin, astaxanthin monoester and diester. V (n-hexane)∶V (acetone)∶V (acetic acid)=8∶2∶0.2 was the optimum developing solvent for thin layer chromatography. Astaxanthin from Antarctic krill included three optical isomers: 3S,3′S, 3S,3′R, and 3R,3′R. The proportions of 3R,3′R in astaxanthin diesters and monoesters were more than 70%, and the proportion of 3S,3′S was the lowest. The total astaxanthin content in Antarctic krill was 18.9 mg/kg, of which the astaxanthin contents of astaxanthin diester, astaxanthin monoester, and free astaxanthin were 12.0, 6.1 and 0.8 mg/kg, respectively.
CONG Xinyuan
,
SUN Weihong
,
ZHANG Huizhen
,
LENG Kailiang
,
XING Lihong
,
MIAO Junkui
,
LIU Xiaofang
. Additives and Contaminants, 2006,23(11):1 056-1 063.Separation, structure identification and content analysis of different forms of astaxanthin in Antarctic krill[J]. Food and Fermentation Industries, 2019
, 45(2)
: 174
-178
.
DOI: 10.13995/j.cnki.11-1802/ts.017586
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