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[Determination of 12 prohibited veterinary drug residues in pig urine by ultra high performance liquid chromatography-tandem mass spectrometry].
Wan, Jian-Chun; Han, Ying; Ma, Xin-Xin; Li, Shi-Xiang; Wu, Hua-Wen; Ji, Li-Hua; Deng, Zhi-Wei; Zhan, Chun-Rui.
Afiliación
  • Wan JC; Technology Center of Nanchang Customs District, Nanchang 330038, China.
  • Han Y; Technology Center of Nanchang Customs District, Nanchang 330038, China.
  • Ma XX; Technology Center of Nanchang Customs District, Nanchang 330038, China.
  • Li SX; Technology Center of Nanchang Customs District, Nanchang 330038, China.
  • Wu HW; Technology Center of Nanchang Customs District, Nanchang 330038, China.
  • Ji LH; Technology Center of Nanchang Customs District, Nanchang 330038, China.
  • Deng ZW; Technology Center of Nanchang Customs District, Nanchang 330038, China.
  • Zhan CR; Technology Center of Nanchang Customs District, Nanchang 330038, China.
Se Pu ; 42(5): 474-480, 2024 Apr 08.
Article en Zh | MEDLINE | ID: mdl-38736391
ABSTRACT
A method was established for the simultaneous detection of 12 prohibited veterinary drugs, including ß2-receptor agonists, nitrofuran metabolites, nitroimidazoles, chlorpromazine, and chloramphenicol, in pig urine. The sample was pretreated by enzymolysis, acid hydrolysis/derivatization, and liquid-liquid extraction combined with solid-phase extraction. Detection was performed using ultra high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). Ammonium acetate solution (0.2 mol/L, 4.5 mL) and ß-glucuronidase/aryl sulfatase (40 µL) were added to the sample, which was subsequently enzymolized at 37 ℃ for 2 h. Then, 1.5 mL of 1.0 mol/L hydrochloric acid solution and 100 µL of 0.1 mol/L o-nitrobenzaldehyde solution were added to the sample. The mixture was incubated at 37 ℃ for 16 h, and the analytes were extracted with 8 mL of ethyl acetate by liquid-liquid extraction. The lower aqueous phase obtained after extraction was extracted and purified using a mixed cation-exchange solid-phase extraction column. The extracts were combined, the extraction solution was blow-dried with nitrogen, and the residue was redissolved for determination. The samples were analyzed under multiple-reaction monitoring mode with both positive and negative electrospray ionization, and quantified using an isotope internal standard method. The correlation coefficients (r) of the 12 compounds were >0.99. The limits of detection (LODs) and quantification (LOQs) of chloramphenicol were 0.05 and 0.1 µg/L, respectively, and the LODs and LOQs of the other compounds were 0.25 and 0.5 µg/L, respectively. The mean recoveries and RSDs at 1, 2, and 10 times the LOQ were 83.6%-115.3% and 2.20%-12.34%, respectively. The proposed method has the advantages of high sensitivity, good stability, and accurate quantification; thus, it is suitable for the simultaneous determination of the 12 prohibited veterinary drug residues in pig urine.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Residuos de Medicamentos / Drogas Veterinarias / Espectrometría de Masas en Tándem Límite: Animals Idioma: Zh Revista: Se Pu Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Residuos de Medicamentos / Drogas Veterinarias / Espectrometría de Masas en Tándem Límite: Animals Idioma: Zh Revista: Se Pu Año: 2024 Tipo del documento: Article País de afiliación: China