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Development of selective comprehensive two-dimensional liquid chromatography with parallel first-dimension sampling and second-dimension separation—application to the quantitative analysis of furanocoumarins in apiaceous vegetables
- Larson, Elliot D., Groskreutz, Stephen R., Harmes, David C., Gibbs-Hall, Ian C., Trudo, Sabrina P., Allen, Robert C., Rutan, Sarah C., Stoll, Dwight R.
- Analytical and bioanalytical chemistry 2013 v.405 no.13 pp. 4639-4653
- absorbance, beverages, celery, chemometrics, comprehensive two-dimensional liquid chromatography, factor analysis, functional foods, high performance liquid chromatography, least squares, parsley, parsnips, psoralens, quantitative analysis, value added
- Various implementations of two-dimensional high-performance liquid chromatography are increasingly being developed and applied to the analysis of complex materials, including those encountered in the analysis of foods, beverages, and nutraceuticals. Previously, we introduced the concept of selective comprehensive two-dimensional liquid chromatography (sLC × LC) as a hybrid between the more conventional, but extreme opposite sampling modes of heartcutting (LC–LC) and fully comprehensive (LC × LC) 2D separation. The sLC × LC approach breaks the link between first dimension (¹D) sampling time and second dimension (²D) analysis time that is faced in LC × LC and allows very rapid (as low as 1 s) sampling of highly efficient¹D separations, while at the same time allowing efficient²D separations on the timescale of tens of seconds. In this paper, we improve upon our previous sLC × LC work by demonstrating the ability to perform the processes of¹D sampling and²D separation in parallel. This significantly improves the flexibility of the technique and allows targeted analysis of analytes that elute close together in time in the¹D separation. To demonstrate the value of this added capability, we have developed a sLC × LC method using multi-wavelength ultraviolet absorbance detection for the quantitative analysis of six target furanocoumarin compounds in extracts of celery, parsley, and parsnips. We show that²D separations of¹D effluent containing the target compounds of interest reveal the presence of unanticipated interferent peaks that would otherwise compromise the quantitative accuracy of the method. We also demonstrate the application of the chemometric method iterative key set factor analysis with alternating least-squares to sLC × LC to mathematically resolve target compounds that are only slightly separated chromatographically but not sufficiently resolved for accurate quantitation.