Determination of Oxytetracycline from Salmon Muscle and Skin by Derivative Spectrophotometry
Author
dc.contributor.author
Toral Ponce, María
Author
dc.contributor.author
Sabay, Tamara
Author
dc.contributor.author
Orellana, Sandra L.
Author
dc.contributor.author
Richter Duk, Pablo
Admission date
dc.date.accessioned
2015-09-24T20:06:00Z
Available date
dc.date.available
2015-09-24T20:06:00Z
Publication date
dc.date.issued
2015
Cita de ítem
dc.identifier.citation
Journal of AOAC International Vol. 98, No. 3, 2015
en_US
Identifier
dc.identifier.other
DOI: 10.5740/jaoacint.14-027
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/133835
General note
dc.description
Artículo de publicación ISI
en_US
Abstract
dc.description.abstract
A method was developed for the identification and quantification of oxytetracycline residues present in salmon muscle and skin using UV-Vis derivative spectrophotometry. With this method, it was possible to reduce the number of steps in the procedure typically required for instrumental analysis of a sample. The spectral variables, order of the derivative, scale factor, smoothing factor, and analytical wavelength were optimized using standard solutions of oxytetracycline dissolved in 900 mg/L oxalic acid in methanol. The matrix effect was significant; therefore, quantification for oxytetracycline residues was carried out using drug-free salmon muscle and skin samples fortified with oxytetracycline. The LOD and LOQ were found to be 271 and 903 mu g/kg, respectively. The precision and accuracy of the method were validated using drug-free salmon muscle and skin tissues fortified at three different concentrations (8, 16, and 32 mg/kg) on 3 different days. The recoveries at all fortified concentrations were between 90 and 105%, and RSDs in all cases were less than 6.5%. This method can be used to screen out compliant samples and thereby reduce the number of suspect positive samples that will require further confirmatory analysis.