SPE–UPLC–UV Method for the Determination of Toltrazuril and its Two Metabolite Residues in Chicken and Porcine Tissues

Ultra high performance liquid chromatography with UV detection was developed and validated for the simultaneous determination of residues of toltrazuril and its two metabolites, namely, toltrazuril sulphone and toltrazuril sulphoxide, in edible tissues (chicken and porcine muscle, liver and kidney)....

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Published inChromatographia Vol. 77; no. 23-24; pp. 1705 - 1712
Main Authors Zhaoling, Jiang, Lifang, Zhang, Chong, Zhang, Xiao, Zhang, Feiqun, Xue
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer-Verlag 01.12.2014
Springer Berlin Heidelberg
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Abstract Ultra high performance liquid chromatography with UV detection was developed and validated for the simultaneous determination of residues of toltrazuril and its two metabolites, namely, toltrazuril sulphone and toltrazuril sulphoxide, in edible tissues (chicken and porcine muscle, liver and kidney). Acetonitrile was used to extract analytes from tissues, which were then cleaned using primary secondary amine and Oasis™ MAX solid phase extraction cartridges. Chromatographic separation was performed on a C₁₈column with gradient elution. The analytes were determined using a UV detector. The regression coefficients of matrix-matched calibration curves showed linearity of >0.99. Calibration ranged from 25 to 1,000 μg kg⁻¹for toltrazuril and toltrazuril sulphone, and 37.5–1,500 μg kg⁻¹for toltrazuril sulphoxide. The accuracy was between 80 and 110 %, and the inter and intraday RSDs were lower than 15.2 and 18.3 %, respectively. The limits of detection for toltrazuril, toltrazuril sulphone and toltrazuril sulphoxide were between 10 and 37.5 μg kg⁻¹in all the tissues. The developed method was successfully applied to detect toltrazuril, toltrazuril sulphone and toltrazuril sulphoxide in tissues of medicated chicken.
AbstractList Ultra high performance liquid chromatography with UV detection was developed and validated for the simultaneous determination of residues of toltrazuril and its two metabolites, namely, toltrazuril sulphone and toltrazuril sulphoxide, in edible tissues (chicken and porcine muscle, liver and kidney). Acetonitrile was used to extract analytes from tissues, which were then cleaned using primary secondary amine and Oasis™ MAX solid phase extraction cartridges. Chromatographic separation was performed on a C 18 column with gradient elution. The analytes were determined using a UV detector. The regression coefficients of matrix-matched calibration curves showed linearity of >0.99. Calibration ranged from 25 to 1,000 μg kg −1 for toltrazuril and toltrazuril sulphone, and 37.5–1,500 μg kg −1 for toltrazuril sulphoxide. The accuracy was between 80 and 110 %, and the inter and intraday RSDs were lower than 15.2 and 18.3 %, respectively. The limits of detection for toltrazuril, toltrazuril sulphone and toltrazuril sulphoxide were between 10 and 37.5 μg kg −1 in all the tissues. The developed method was successfully applied to detect toltrazuril, toltrazuril sulphone and toltrazuril sulphoxide in tissues of medicated chicken.
Ultra high performance liquid chromatography with UV detection was developed and validated for the simultaneous determination of residues of toltrazuril and its two metabolites, namely, toltrazuril sulphone and toltrazuril sulphoxide, in edible tissues (chicken and porcine muscle, liver and kidney). Acetonitrile was used to extract analytes from tissues, which were then cleaned using primary secondary amine and Oasis™ MAX solid phase extraction cartridges. Chromatographic separation was performed on a C₁₈column with gradient elution. The analytes were determined using a UV detector. The regression coefficients of matrix-matched calibration curves showed linearity of >0.99. Calibration ranged from 25 to 1,000 μg kg⁻¹for toltrazuril and toltrazuril sulphone, and 37.5–1,500 μg kg⁻¹for toltrazuril sulphoxide. The accuracy was between 80 and 110 %, and the inter and intraday RSDs were lower than 15.2 and 18.3 %, respectively. The limits of detection for toltrazuril, toltrazuril sulphone and toltrazuril sulphoxide were between 10 and 37.5 μg kg⁻¹in all the tissues. The developed method was successfully applied to detect toltrazuril, toltrazuril sulphone and toltrazuril sulphoxide in tissues of medicated chicken.
Author Zhaoling, Jiang
Chong, Zhang
Xiao, Zhang
Feiqun, Xue
Lifang, Zhang
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10.1007/s00216-010-3704-x
10.1016/j.jchromb.2011.04.021
10.1016/j.chroma.2012.07.001
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Keywords Toltrazuril sulphone
Chicken and porcine tissues
Toltrazuril
Toltrazuril sulphoxide
SPE–UPLC–UV
Language English
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Snippet Ultra high performance liquid chromatography with UV detection was developed and validated for the simultaneous determination of residues of toltrazuril and...
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SubjectTerms acetonitrile
Analytical Chemistry
Chemistry
Chemistry and Materials Science
chickens
Chromatography
cleaning
detection limit
kidneys
Laboratory Medicine
liver
metabolites
muscles
Pharmacy
Proteomics
Short Communication
solid phase extraction
swine
tissues
toltrazuril
ultra-performance liquid chromatography
Title SPE–UPLC–UV Method for the Determination of Toltrazuril and its Two Metabolite Residues in Chicken and Porcine Tissues
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