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.
%0 Journal Article
%1 RN232
%A Toral, M.I.
%A Sabay, T.
%A Orellana, S.L.
%A Richter, P.
%D 2015
%J Journal of Aoac International
%K antibiotics, aquaculture, detection, dqcauchile fluorescence liquid-chromatography, performance residues, samples tetracycline
%N 3
%P 559-565
%R 10.5740/jaoacint.14-027
%T Determination of Oxytetracycline from Salmon Muscle and Skin by Derivative Spectrophotometry
%U /brokenurl#<Go to ISI>://WOS:000356903400004
%V 98
%X 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.
@article{RN232,
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.},
added-at = {2019-12-04T03:57:35.000+0100},
author = {Toral, M.I. and Sabay, T. and Orellana, S.L. and Richter, P.},
biburl = {https://www.bibsonomy.org/bibtex/2e11cf569da4abb79d796b4ad66d18ff9/dqcauchile},
doi = {10.5740/jaoacint.14-027},
interhash = {ab5046823e0b27734656e7889edd9ebe},
intrahash = {e11cf569da4abb79d796b4ad66d18ff9},
issn = {1060-3271},
journal = {Journal of Aoac International},
keywords = {antibiotics, aquaculture, detection, dqcauchile fluorescence liquid-chromatography, performance residues, samples tetracycline},
number = 3,
pages = {559-565},
timestamp = {2019-12-04T03:58:17.000+0100},
title = {Determination of Oxytetracycline from Salmon Muscle and Skin by Derivative Spectrophotometry},
type = {Journal Article},
url = {/brokenurl#<Go to ISI>://WOS:000356903400004},
volume = 98,
year = 2015
}