On line photochemically induced excitation-emission-kinetic four-way data Analytical application for the determination of folic acid and its two main metabolites in serum by U-PLS and N-PLS/residual trilinearization (RTL) calibration

被引:28
作者
Jimenez Giron, A. [1 ]
Duran-Meras, I. [1 ]
Espinosa-Mansilla, A. [1 ]
Munoz de la Pena, A. [1 ]
Canada Canada, F. [1 ]
Olivieri, A. C. [2 ]
机构
[1] Univ Extremadura, Dept Analyt Chem, E-06071 Badajoz, Spain
[2] Univ Nacl Rosario, Inst Quim Rosario, CONICET, Fac Ciencias Bioquim & Farmaceut,Dept Quim Analit, RA-2000 Rosario, Santa Fe, Argentina
关键词
folic acid; tetrahydrofolic acid; 5-methyltetrahydrofolic acid; photochemically induced fluorescence; four-way data; unfolded partial least-squares/residual trilinearization; N-dimensional partial least-squares/residual trilinearization;
D O I
10.1016/j.aca.2008.05.079
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学]; 081704 [应用化学];
摘要
The determination of folic acid and its two main serum metabolites, 5-methyltetrahydrofolic acid and tetrahydrofolic acid, has been accomplished using four-way data modelled by the third-order multivariate calibration methods unfolded and N-dimensional partial leastsquares (U-PLS and N-PLS), in combination with the separate procedure known as residual trilinearization (RTL). The four-way data were acquired by following the photochemical reaction of these compounds by on line irradiation with a UV lamp. The excitation-emission matrices (EEMs) were recorded as a function of the irradiation time, using a fast scanning spectrofluorimeter. The method achieves selectivity from the different rates at which the corresponding photoproducts of the folic acid derivatives are formed and degraded. Several N-dimensional chemometric algorithms were used and the method was applied to the determination of these compounds in serum samples. The best algorithms to perform the multivariate calibration were U-PLS and N-PLS in combination with the separate residual trilinearization procedure, achieving the second-order advantage. The approach allows minimizing or eliminating traditionally time-consuming sample pre-treatments and can facilitate quantifying an analyte in its native environment. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:94 / 103
页数:10
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