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 in | Chromatographia Vol. 77; no. 23-24; pp. 1705 - 1712 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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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. |
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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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CitedBy_id | crossref_primary_10_1016_j_jpba_2018_11_020 crossref_primary_10_1016_j_jchromb_2017_10_016 crossref_primary_10_2754_avb202190040383 crossref_primary_10_1007_s10337_023_04281_0 crossref_primary_10_1007_s12161_019_01669_3 crossref_primary_10_1002_jssc_201700017 crossref_primary_10_22159_ijpps_2022v14i5_44179 |
Cites_doi | 10.1016/j.aca.2004.08.017 10.1080/19440049.2013.794306 10.1111/j.1365-2885.2008.01039.x 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 |
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References | Varenina I, Bilandžić N, Cvetnić Ž et al (2012) Egmond aan Zee, Nizozemska, pp 533–538 MoloneyMClarkeLO’MahonyJGadajAO’KennedyRDanaherMJ Chromatogr A20121253941041:CAS:528:DC%2BC38XhtFGlurbM10.1016/j.chroma.2012.07.001 Xiujuan F (2005) Nanjing Agricultural University, Nanjing Dirikolu L, Yohn R, Garrett EF, Chakkath T, Ferguson DC (2008) J Vet Pharmacol Therap 32:280–288. doi:10.1111/j.1365-2885.2008.01039.x EMEA (1998) The European Agency for the Evaluation of Medicinal Products, Europe EMEA (2004) The European Agency for the Evaluation of Medicinal Products MulderPPJBalzer-RutgersPTe BrinkeEMAnal Chim Acta20055293313371:CAS:528:DC%2BD2MXnsVynsg%3D%3D10.1016/j.aca.2004.08.017 ClarkeLMoloneyMO’MahonyJO’KennedyRDanaherMFood Addit Contam Part A Chem Anal Control Expo Risk Assess2013309589691:CAS:528:DC%2BC3sXlvFyqsbk%3D10.1080/19440049.2013.794306 EMEA (2000) The European Agency for the Evaluation of Medicinal Products Martinez-VillalbaAMoyanoEMartinsCPGalceranMTAnal Bioanal Chem2010397289329011:CAS:528:DC%2BC3cXltV2ktLw%3D10.1007/s00216-010-3704-x China TMOA (2005) China, The Ministry of Agriculture EMEA (1999) The European Agency for the Evaluation of Medicinal Products, Europe AiLSunHWangFChenRGuoCJ Chromatogr B Analyt Technol Biomed Life Sci2011879175717631:CAS:528:DC%2BC3MXntFSmsbs%3D10.1016/j.jchromb.2011.04.021 FurrMOQuanceJKennedyTVet Ther200012452511:STN:280:DC%2BD1MnivVGmsw%3D%3D 2759_CR6 A Martinez-Villalba (2759_CR13) 2010; 397 2759_CR8 2759_CR9 M Moloney (2759_CR10) 2012; 1253 2759_CR14 PPJ Mulder (2759_CR7) 2005; 529 L Clarke (2759_CR11) 2013; 30 L Ai (2759_CR12) 2011; 879 MO Furr (2759_CR5) 2000; 1 2759_CR2 2759_CR1 2759_CR4 2759_CR3 |
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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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