Hector Goicoechea

Prof. Hector Goicoechea

Laboratorio de Desarrollo Analítico y Quimiometría (LADAQ), Cátedra de Química Analítica I, Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral, Ciudad Universitaria, Santa Fe S3000ZAA, Argentina
orcid

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 2014 in Talanta
Verified
Journal Article
Closed access
LCLuciana Vera Candioti
Luciana Vera Candioti
MZMaría M. De Zan
María M. De Zan
MCMaría S. Cámara
María S. Cámara
Hector GoicoecheaHector Goicoechea
Hector Goicoechea

1 May 2022 in Analytica Chimica Acta
Verified
Journal Article
Closed access
SGSofía A. Gegenschatz
Sofía A. Gegenschatz
FCFabricio Alejandro Chiappini
Fabricio Alejandro Chiappini
CTCarla M. Teglia
Carla M. Teglia
APArsenio Muñoz de la Peña
Arsenio Muñoz de la Peña
Hector GoicoecheaHector Goicoechea
Hector Goicoechea



1 January 2011 in Talanta
Verified
Journal Article
Closed access
Hector GoicoecheaHector Goicoechea
Hector Goicoechea
MCM.J. Culzoni
M.J. Culzoni
GGGil García
Gil García
MGM. Martínez Galera
M. Martínez Galera

15 January 2010 in The Analyst
Verified
Journal Article
Closed access
PDF file
Hector GoicoecheaHector Goicoechea
Hector Goicoechea
AOAlejandro C. Olivieri
Alejandro C. Olivieri
RTRomà Tauler
Romà Tauler
Correlation constrained multivariate curve resolution-alternating least-squares is shown to be a feasible method for processing first-order instrumental data and achieve analyte quantitation in the presence of unexpected interferences. Both for simulated and experimental data sets, the proposed method could correctly retrieve the analyte and interference spectral profiles and perform accurate estimations of analyte concentrations in test samples. Since no information concerning the interferences was present in calibration samples, the proposed multivariate calibration approach including the correlation constraint facilitates the achievement of the so-called second-order advantage for the analyte of interest, which is known to be present for more complex higher-order richer instrumental data. The proposed method is tested using a simulated data set and two experimental data systems, one for the determination of ascorbic acid in powder juices using UV-visible absorption spectral data, and another for the determination of tetracycline in serum samples using fluorescence emission spectroscopy.