Varying the temperature of a polymeric C18 high performance liquid chromatography [HPLC) column caused significant changes in elution profiles of carotenoid and chlorophyll (chl) pigment mixtures.High temperature operation (60°C) was optimal for carotenoid separations, including the separation of zeaxanthin from lutein.Chlorophyll and chlorophyll derivative separations were optimal at a column temperature between 10 and 30°C.A protocol is presented that achieves quantifiable resolution of all taxonomically important pigments tested by running the analysis at 2 temperatures: 10 and 60°C.Of particular significance was the ability to separate divinyl chl a from monovinyl chl a, chl c, from chl c,, and partial separation of chl c, and MG 2,4-divinyl phaeoporphorin a, monomethyl ester.An example is given of the utility in separating chl c pigments, and lutein and zeaxanthin in natural phytoplankton samples.
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Heukelem et al. (1994) studied this question.
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