Performance evaluation of preprocessing techniques utilizing expert information in multivariate calibration

被引:20
作者
Sharma, Sandeep [1 ]
Goodarzi, Mohammad [1 ]
Ramon, Herman [1 ]
Saeys, Wouter [1 ]
机构
[1] Katholieke Univ Leuven, BIOSYST MeBioS, B-3001 Louvain, Belgium
关键词
Pure component spectrum; Glucose; Extended Multiplicative Signal Correction; Spectral Interference Subtraction; External Parameter Orthogonalization; Generalized Least Squares Weighting; MULTIPLICATIVE SIGNAL CORRECTION; SCATTER-CORRECTION; SOLUBLE SOLIDS; SPECTRA; SPECTROSCOPY; ROBUSTNESS; PREDICTION;
D O I
10.1016/j.talanta.2013.12.053
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Partial Least Squares (PLS) regression is one of the most used methods for extracting chemical information from Near Infrared (NIR) spectroscopic measurements. The success of a PLS calibration relies largely on the representativeness of the calibration data set. This is not trivial, because not only the expected variation in the analyte of interest, but also the variation of other contributing factors (interferents) should be included in the calibration data. This also implies that changes in interferent concentrations not covered in the calibration step can deteriorate the prediction ability of the calibration model. Several researchers have suggested that PLS models can be robustified against changes in the interferent structure by incorporating expert knowledge in the preprocessing step with the aim to efficiently filter out the spectral influence of the spectral interferents. However, these methods have not yet been compared against each other. Therefore, in the present study, various preprocessing techniques exploiting expert knowledge were compared on two experimental data sets. In both data sets, the calibration and test set were designed to have a different interferent concentration range. The performance of these techniques was compared to that of preprocessing techniques which do not use any expert knowledge. Using expert knowledge was found to improve the prediction performance for both data sets. For data set-1, the prediction error improved nearly 32% when pure component spectra of the analyte and the interferents were used in the Extended Multiplicative Signal Correction framework. Similarly, for data set-2, nearly 63% improvement in the prediction error was observed when the interferent information was utilized in Spectral Interferent Subtraction preprocessing. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:105 / 112
页数:8
相关论文
共 30 条
[1]   Extended multiplicative signal correction in vibrational spectroscopy, a tutorial [J].
Afseth, Nils Kristian ;
Kohler, Achim .
CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 2012, 117 :92-99
[2]   Molar absorptivities of glucose and other biological molecules in aqueous solutions over the first overtone and combination regions of the near-infrared spectrum [J].
Amerov, AK ;
Chen, J ;
Arnold, MA .
APPLIED SPECTROSCOPY, 2004, 58 (10) :1195-1204
[3]   STANDARD NORMAL VARIATE TRANSFORMATION AND DE-TRENDING OF NEAR-INFRARED DIFFUSE REFLECTANCE SPECTRA [J].
BARNES, RJ ;
DHANOA, MS ;
LISTER, SJ .
APPLIED SPECTROSCOPY, 1989, 43 (05) :772-777
[4]   Pretreatments by means of orthogonal projections [J].
Boulet, Jean-Claude ;
Roger, Jean-Michel .
CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 2012, 117 :61-69
[5]   A comparison of methods for testing differences in predictive ability [J].
Cederkvist, HR ;
Aastveit, AH ;
Næs, T .
JOURNAL OF CHEMOMETRICS, 2005, 19 (09) :500-509
[6]  
Codgill R.P., 2005, JNIR SPEC, V13, P119
[7]   Near-infrared spectra of Penicillium camemberti strains separated by extended multiplicative signal correction improved prediction of physical and chemical variations [J].
Decker, M ;
Nielsen, PV ;
Martens, H .
APPLIED SPECTROSCOPY, 2005, 59 (01) :56-68
[8]   LINEARIZATION AND SCATTER-CORRECTION FOR NEAR-INFRARED REFLECTANCE SPECTRA OF MEAT [J].
GELADI, P ;
MACDOUGALL, D ;
MARTENS, H .
APPLIED SPECTROSCOPY, 1985, 39 (03) :491-500
[9]   Towards better understanding of feature-selection or reduction techniques for Quantitative Structure-Activity Relationship models [J].
Goodarzi, Mohammad ;
Funar-Timofei, Simona ;
Vander Heyden, Yvan .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2013, 42 :49-63
[10]   MULTICOMPONENT DETERMINATION OF CHLORINATED HYDROCARBONS USING A REACTION-BASED CHEMICAL SENSOR .1. MULTIVARIATE CALIBRATION OF FUJIWARA REACTION-PRODUCTS [J].
HENSHAW, JM ;
BURGESS, LW ;
BOOKSH, KS ;
KOWALSKI, BR .
ANALYTICAL CHEMISTRY, 1994, 66 (20) :3328-3336