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Target and non-target analytical method for potential hazardous substances in livestock and pet hair using liquid- and gas chromatography quadrupole time-of-flight mass spectrometry.
Seo, Hyung-Ju; Na, Tae Woong; Lee, Seung Hwa; Kim, Ho Jin; Hong, Sunghie; Cho, Hyunjeong.
Afiliação
  • Seo HJ; Experiment Research Institute, National Agricultural Products Quality Management Service, 141, Yongjeon-ro, Gimcheon-si, Gyeongsangbuk-do 39660, Korea. Electronic address: hlhl103@naver.com.
  • Na TW; Experiment Research Institute, National Agricultural Products Quality Management Service, 141, Yongjeon-ro, Gimcheon-si, Gyeongsangbuk-do 39660, Korea. Electronic address: naratw@korea.kr.
  • Lee SH; Experiment Research Institute, National Agricultural Products Quality Management Service, 141, Yongjeon-ro, Gimcheon-si, Gyeongsangbuk-do 39660, Korea. Electronic address: shlee96@korea.kr.
  • Kim HJ; Experiment Research Institute, National Agricultural Products Quality Management Service, 141, Yongjeon-ro, Gimcheon-si, Gyeongsangbuk-do 39660, Korea. Electronic address: rex7878@korea.kr.
  • Hong S; Experiment Research Institute, National Agricultural Products Quality Management Service, 141, Yongjeon-ro, Gimcheon-si, Gyeongsangbuk-do 39660, Korea. Electronic address: cybergus@korea.kr.
  • Cho H; Experiment Research Institute, National Agricultural Products Quality Management Service, 141, Yongjeon-ro, Gimcheon-si, Gyeongsangbuk-do 39660, Korea. Electronic address: hjcho201@korea.kr.
J Chromatogr A ; 1705: 464170, 2023 Aug 30.
Article em En | MEDLINE | ID: mdl-37390765
ABSTRACT
Extraction using acetonitrile and water and quadrupole time-of-flight mass spectrometry (LC and GC-QTOF/MS) techniques were used to screen for potential hazardous substances in livestock and pet hair. In addition, LC-MS/MS and GC-MS/MS techniques were used for verification of the analytical method and quantitative analysis of pesticides, veterinary drugs, mycotoxins and antioxidants in hair. Optimized sample preparation involves extracting 0.05 g of sample with 0.6 mL of ACN and 0.4 mL of distilled water. In addition, the two layers were separated by adding 0.1 g of NaCl. Then, both the ACN and water layers were analyzed by LC-TOF/MS, and the ACN layer was analyzed by GC-TOF/MS. Most of the matrix effects of livestock and pet hair were less than 50%, but some matrices and components showed high results, so matrix matching correction was applied for more precise quantification. Method validation was performed for 394 constituents (293 pesticides, 93 veterinary drugs, 6 mycotoxins and 2 preservatives) in dog, cat, cow and pig hair and chicken and duck feathers. All components showed good linearity (r2 ≥0.98) in the developed assay. The quantification limit of all compounds was set at 0.02 mg/kg, which is the lowest level that satisfies the recovery rate standard. The recovery experiment was repeated 8 times at 3 concentrations. Most of the components were extracted with the ACN layer, and the recovery rate was 63.35-119.98%. In order to confirm the efficiency of extracting harmful substances from actual samples, 30 hairs of livestock and pets were screened.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Praguicidas / Drogas Veterinárias Tipo de estudo: Risk_factors_studies Limite: Animals Idioma: En Revista: J Chromatogr A Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Praguicidas / Drogas Veterinárias Tipo de estudo: Risk_factors_studies Limite: Animals Idioma: En Revista: J Chromatogr A Ano de publicação: 2023 Tipo de documento: Article