Solid-phase UV spectroscopic multisensor for the simultaneous determination of caffeine, dimenhydrinate and acetaminophen by using partial least squares multicalibration

被引:25
作者
Cañada, MJA
Reguera, MIP
Díaz, AM
Capitán-Vallvey, LF
机构
[1] Univ Jaen, Dept Phys & Analyt Chem, Fac Expt Sci, E-23071 Jaen, Spain
[2] Univ Granada, Dept Analyt Chem, Fac Sci, E-18071 Granada, Spain
关键词
solid-phase spectroscopy; PLS multicalibration; flow-through sensor; pharmaceuticals;
D O I
10.1016/S0039-9140(99)00065-X
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A straightforward flow-through multisensor was developed for the fast simultaneous determination of caffeine (CF), dimenhydrinate (DMH) and acetaminophen (AAP) based on the integration of their retention and UV detection. A diode array spectrophotometer was used to monitor the inherent UV full-spectra in the range 245-310 nm of the analytes retained on C-18 bonded phase beads packed in a flow cell, without requiring additional reagents or derivatization processes. The extensively overlapped spectra of the analytes retained on the solid support could be resolved by partial least squares (PLS) regression. After collecting the response of the multisensor, its active microzone was regenerated by using methanol as the eluting agent, leaving it ready for the next determination. The proposed multisensor has been satisfactorily applied for the analysis of synthetic and real samples with different nominal contents of these active principles. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:691 / 701
页数:11
相关论文
共 14 条
[1]  
[Anonymous], 1989, MULTIVARIATE CALIBRA
[2]   SPECTROPHOTOMETRIC METHOD FOR THE ANALYSIS OF PLUTONIUM AND NITRIC-ACID USING PARTIAL LEAST-SQUARES REGRESSION [J].
CAREY, WP ;
WANGEN, LE ;
DYKE, JT .
ANALYTICAL CHEMISTRY, 1989, 61 (15) :1667-1669
[3]   Resolution of phenol, o-cresol, m-cresol and p-cresol mixtures by excitation fluorescence using partial least-squares (PLS) multivariate calibration [J].
delOlmo, M ;
Diez, C ;
Molina, A ;
deOrbe, I ;
Vilchez, JL .
ANALYTICA CHIMICA ACTA, 1996, 335 (1-2) :23-33
[4]   NONLINEAR MULTIVARIATE CALIBRATION USING PRINCIPAL COMPONENTS REGRESSION AND ARTIFICIAL NEURAL NETWORKS [J].
GEMPERLINE, PJ ;
LONG, JR ;
GREGORIOU, VG .
ANALYTICAL CHEMISTRY, 1991, 63 (20) :2313-2323
[5]   PARTIAL LEAST-SQUARES METHODS FOR SPECTRAL ANALYSES .1. RELATION TO OTHER QUANTITATIVE CALIBRATION METHODS AND THE EXTRACTION OF QUALITATIVE INFORMATION [J].
HAALAND, DM ;
THOMAS, EV .
ANALYTICAL CHEMISTRY, 1988, 60 (11) :1193-1202
[6]   EVALUATION OF MULTICOMPONENT KINETIC-ANALYSIS DATA BY A PARTIAL LEAST-SQUARES CALIBRATION METHOD [J].
HAVEL, J ;
JIMENEZ, F ;
BAUTISTA, RD ;
LEON, JJA .
ANALYST, 1993, 118 (11) :1355-1360
[7]  
MERAS ID, 1993, ANALYST, V118, P807
[8]   MEASUREMENT OF CAUSTIC AND CAUSTIC BRINE SOLUTIONS BY SPECTROSCOPIC DETECTION OF THE HYDROXIDE ION IN THE NEAR-INFRARED REGION, 700-1150 NM [J].
PHELAN, MK ;
BARLOW, CH ;
KELLY, JJ ;
JINGUJI, TM ;
CALLIS, JB .
ANALYTICAL CHEMISTRY, 1989, 61 (13) :1419-1424
[9]   PLS-NIR determination of total sugar, glucose, fructose and sucrose in aqueous solutions of fruit juices [J].
Rambla, FJ ;
Garrigues, S ;
delaGuardia, M .
ANALYTICA CHIMICA ACTA, 1997, 344 (1-2) :41-53
[10]   CROSS-VALIDATORY CHOICE AND ASSESSMENT OF STATISTICAL PREDICTIONS [J].
STONE, M .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1974, 36 (02) :111-147