Ana Maria Contento Salcedo

Prof. Dr. Ana Maria Contento Salcedo

orcid

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

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

Representative Publications

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1 December 1995 in Talanta
Verified
Journal Article
Closed access
JNJ.J.Berzas Nevado
J.J.Berzas Nevado
CCC.Guiberteau Cabanillas
C.Guiberteau Cabanillas
ASAna Maria Contento Salcedo
Ana Maria Contento Salcedo

1 January 1999 in Analytica Chimica Acta
Verified
Journal Article
Closed access
JNJ.J. Berzas Nevado
J.J. Berzas Nevado
CCC. Guiberteau Cabanillas
C. Guiberteau Cabanillas
ASAna Maria Contento Salcedo
Ana Maria Contento Salcedo

1 January 2015 in Talanta
Verified
Journal Article
Closed access
GDGema M. Durán
Gema M. Durán
ASAna Maria Contento Salcedo
Ana Maria Contento Salcedo
ÁRÁngel Ríos
Ángel Ríos

1 August 1998 in Talanta
Verified
Journal Article
Closed access
JNJ.J Berzas Nevado
J.J Berzas Nevado
JFJ Rodrı́guez Flores
J Rodrı́guez Flores
CCC Guiberteau Cabanillas
C Guiberteau Cabanillas
MLM.J Villaseñor Llerena
M.J Villaseñor Llerena
ASAna Maria Contento Salcedo
Ana Maria Contento Salcedo

1 May 2000 in Journal of Chromatographic Science
Verified
Journal Article
Open access
PDF file
JNJ. J. Berzas Nevado
J. J. Berzas Nevado
MLM. J. Villasenor Llerena
M. J. Villasenor Llerena
ASAna Maria Contento Salcedo
Ana Maria Contento Salcedo
ENE. Aguas Nuevo
E. Aguas Nuevo
A simple and fast capillary gas chromatographic method with flame ionization detection is proposed for the simultaneous determination of fluoxetine, fluvoxamine, and clomipramine without a prederivatization. The reported method is the first one that allows the determination of three selective serotonin reuptake inhibitors. Optimal conditions for the quantitative separation were investigated: column head pressure (80 kPa), injector and detector temperatures (260 and 250°C), time and temperature for the splitless step (0.75 min and 60°C), size of sample (2 μL), and oven temperature program, providing analysis times shorter than 10 min. Aspects such as the stability of the solutions, linearity, accuracy, and precision are examined in order to validate this method. Peak purity and detection and quantitation limits are also assesed using mass selective detection. The scope of the validated method is tested in the analysis of pharmaceutical preparations, with recoveries between 97.5 and 102.5% with regard to their nominal contents.

1 July 2000 in Analytica Chimica Acta
Verified
Journal Article
Closed access
JNJ.J. Berzas Nevado
J.J. Berzas Nevado
ASAna Maria Contento Salcedo
Ana Maria Contento Salcedo
MLM.J. Villaseñor Llerena
M.J. Villaseñor Llerena
ENE. Aguas Nuevo
E. Aguas Nuevo