A comprehensive normal-phase × reversed-phase (NP-LC×RP-LC) liquid chromatography system was developed, and applied for analysis of the intact carotenoid composition of red chili peppers, with photodiode array and mass spectrometry detection. A micro-bore cyano column (250x1.0 mm, 5 μm d.p.) was chosen for the first dimension (1D) separation, interfaced to a second dimension (2D) C18 column (30x4.6 mm, 2.7 μm d.p.) packed with fused-core particles. Subsequently, two columns of the same stationary phase were coupled serially for second dimension separation, and operated under ultra high pressure LC conditions (UHPLC), within a cycle time of 1.50 or 1.00 min, and equal modulation times. Performances of the three different set-ups were evaluated, in terms of peak capacity values (nc), and afterwards corrected by taking into account both the under-sampling, and the orthogonality effects. After these adjustments, the peak capacity values were estimated as follows: nc 727, for the NP-LC×RP-LC system, nc 377, for the NP-LC×RP-UHPLC system with a 1.50 min modulation time, nc 984, for the NP-LC×RP-UHPLC system, with a 1.00 min modulation time. A total of 33 compounds were separated into 10 different chemical classes in the two-dimensional space, and identified by accurate IT-TOF (ion trap-time of flight) MS detection.

Ultra high pressure in the second dimension of a comprehensive two-dimensional liquid chromatographic system for carotenoid separation in red chili peppers.

CACCIOLA, FRANCESCO;DONATO, Paola Agata Eustochia;GIUFFRIDA, Daniele;DUGO, Paola;MONDELLO, Luigi
2012-01-01

Abstract

A comprehensive normal-phase × reversed-phase (NP-LC×RP-LC) liquid chromatography system was developed, and applied for analysis of the intact carotenoid composition of red chili peppers, with photodiode array and mass spectrometry detection. A micro-bore cyano column (250x1.0 mm, 5 μm d.p.) was chosen for the first dimension (1D) separation, interfaced to a second dimension (2D) C18 column (30x4.6 mm, 2.7 μm d.p.) packed with fused-core particles. Subsequently, two columns of the same stationary phase were coupled serially for second dimension separation, and operated under ultra high pressure LC conditions (UHPLC), within a cycle time of 1.50 or 1.00 min, and equal modulation times. Performances of the three different set-ups were evaluated, in terms of peak capacity values (nc), and afterwards corrected by taking into account both the under-sampling, and the orthogonality effects. After these adjustments, the peak capacity values were estimated as follows: nc 727, for the NP-LC×RP-LC system, nc 377, for the NP-LC×RP-UHPLC system with a 1.50 min modulation time, nc 984, for the NP-LC×RP-UHPLC system, with a 1.00 min modulation time. A total of 33 compounds were separated into 10 different chemical classes in the two-dimensional space, and identified by accurate IT-TOF (ion trap-time of flight) MS detection.
2012
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/2327759
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