Time shift correction in second-order liquid chromatographic data with iterative target transformation factor analysis

被引:32
作者
Comas, E [1 ]
Gimeno, RA [1 ]
Ferré, J [1 ]
Marcé, RM [1 ]
Borrull, F [1 ]
Rius, FX [1 ]
机构
[1] Univ Rovira & Virgili, Dept Analyt & Organ Chem, Tarragona 43005, Spain
关键词
HPLC; time shift; ITTFA; time window; selectivity; GRAM;
D O I
10.1016/S0003-2670(02)00769-9
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
When the generalized rank annihilation method (GRAM) is applied to liquid chromatographic data with diode-array detection, an important problem is the time shift of the peak of the analyte in the test sample. This problem leads to erroneous predictions. This time shift can be corrected if a time window is selected so that the chromatographic profile of the analyte in the test sample is trilinear with the peak of the analyte in the calibration sample. In this paper we present a new method to determine when this condition is met. This method is based on the curve resolution with iterative target transformation factor analysis (ITTFA). The calibration and test matrices are independently decomposed into profiles and spectra, and aligned before GRAM is applied. Here we study two situations: first, when the calibration matrix has one analyte and second, when it has two analytes. When the calibration matrix has two analytes, we selectively determine the time window for the analyte to be quantified. There were considerably fewer prediction errors after correction. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:163 / 173
页数:11
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