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September 1995, Volume 1 No. 2
ARTICLE 6
Simultaneous determination
of retinol, carotenoids and tocopherols in human serum by high
pressure liquid chromatography
Tee E-Siong and Khor Swan-Choo
Division of Human
Nutrition, Institute for Medical Research, 50588 Kuala Lumpur,
Malaysia
ABSTRACT
The determination of serum
vitamins having antioxidant properties has gained in importance in
recent years. This is mainly due to the observation that an inverse
correlation exists between blood levels of these vitamins, including
retinol, carotenoids and tocopherol, and diet-related chronic
diseases such as coronary heart disease and cancers. This laboratory
has been carrying out a series of studies into the nutritional and
analytical aspects of retinol and carotenoids. A simple
reversed-phase HPLC method has been developed in an effort to
improve methodologies for the separation and quantitation of
carotenoids and retinol in foods and biological specimens,
especially blood serum. As an extension to these studies, trials
were carried out to determine the feasibility of analysing
tocopherols using the same chromatographic procedure. With the
addition of another detector wavelength, the same procedure detected
and quantitated 3 major tocopherols simultaneously with retinol and
five carotenoids. Within-day and between-day precision of the
procedure was satisfactory. Trials carried out were able to improve
recovery of the vitamins. Experiments conducted also showed that the
addition of ascorbic acid to the extracting ethanol was beneficial
for the analytical procedure. The presence of peroxide in ethyl
acetate used in the chromatography mobile phase caused drastic
destruction to the vitamins analysed. The addition of ascorbic acid
during sample preparation was able to inhibit this destruction. The
method was used for the analysis of sera from 65 apparently healthy
Malaysians with a mean age of 52.8 years (range 24-76 years). Mean
retinol concentration of the group was 69.8 ± 18.8 µg/dl. The mean
β-carotene concentration of the subjects studied was 33.8 ±
24.3 µg/dl, while the mean total carotenoid concentration was 180.2
± 3.0 µg/dl. The most abundant carotenoid in the serum samples
studied was lutein, comprising about one-third of all carotenoids
quantitated. The concentrations of δ- and γ-tocopherols in the
serum samples studied were too low to be identified with certainty
and quantitated accurately. The mean α-tocopherol level was 1840 ±
528 μg/dl. For retinol, α-tocopherol and most of the carotenoids
determined, there was no statistically significant difference in the
mean levels between male and female subjects as well as among the
three different ethnic groups. Results obtained in this study were
very similar to those previously reported by this laboratory. It is
hoped that more data on the serum concentrations of these vitamins
can become available for various population groups, including during
various disease conditions.
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