Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12188/21575
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Hajrulai musliu, Zehra | en_US |
dc.contributor.author | Uzunov, Risto | en_US |
dc.contributor.author | Krluku, Maksud | en_US |
dc.contributor.author | Angeleska, Aleksandra | en_US |
dc.contributor.author | Dimitrieska Stojkovikj, Elizabeta | en_US |
dc.contributor.author | Sasanya, James, Jacob | en_US |
dc.date.accessioned | 2022-07-25T22:43:00Z | - |
dc.date.available | 2022-07-25T22:43:00Z | - |
dc.date.issued | 2022-02-24 | - |
dc.identifier.uri | http://hdl.handle.net/20.500.12188/21575 | - |
dc.description.abstract | In this work, an liquid chromatography- tandem mass spectrometry (LC-MS/MS) methodology is proposed for the multi-class multi-residue screening of veterinary drugs, pesticides and mycotoxins in bovine urine, using an LS-MS/MS both in positive and negative mode.The method currently covers 72 analytes belonging to different families such as antibiotics, steroid hormones, β-agonists, lactones, thyreostatics and contaminants such as pesticides and mycotoxins. After comparing different sample preparation procedures, extraction with sodium acetate and phosphate buffer followed by enzymatic hydrolyze with β-glucuronidase and solid phase extraction with OASIS cartridges was selected as the most appropriate methodology. In the validation study were included linearity, limit of detection, limit of quantification, decision limit, detection capability, accuracy and precision of the method. The method was linear with R2>0.99. The limit of quantification were established between 0.19 μg/l and 16.7 μg/l, demonstrating the usefulnes of LC-MS/MS as an ideal tool for compliance monitoring in regulatory laboratories. The results for accuracy, expressed as recovery, were with values from 65 – 115%. Intra-day precision (repeatability) and inter-day precision (reproducibility) were expressed thought coefficient of variation. The CV was from 1.26 to 23.31 % for intra-day precision and from 2.29 to 29.42 % for inter-day precision. The results for accuracy and precision fulfill the criteria prescribed in the Commission Decision 2002/657/EC. The method was successfully applied for routine analysis of bovine urine samples. The routine analysis showed that the target components were not detected in the bovine urine samples. | en_US |
dc.language.iso | en | en_US |
dc.relation | IAEA project Integrated radiometric and complementary techniques for mixed contaminants and residues in food (D52041) | en_US |
dc.subject | veterinary drug residues, pesticide residues, mycotoxins, bovine urine,validation study, LC-MS/MS | en_US |
dc.title | Multi-class, Multi-residue LC-MS/MS Method For Veterinary Drug Residues, Mycotoxins And Pesticide In Urine | en_US |
dc.type | Proceeding article | en_US |
dc.relation.conference | SECOND INTERNATIONAL CONGRESS ON BIOLOGICAL AND HEALTH SCIENCES | en_US |
item.fulltext | With Fulltext | - |
item.grantfulltext | open | - |
crisitem.author.dept | Faculty of Veterinary Medicine | - |
crisitem.author.dept | Faculty of Veterinary Medicine | - |
crisitem.author.dept | Faculty of Veterinary Medicine | - |
Appears in Collections: | Faculty of Veterinary Medicine: Conference papers |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
ICBH 2022 PROCEEDINGS Hajruali-Musliu.pdf | 15.84 MB | Adobe PDF | View/Open |
Page view(s)
103
checked on Jul 24, 2024
Download(s)
41
checked on Jul 24, 2024
Google ScholarTM
Check
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.