In-house validation of an ELISA method for screening of semicarbazide in eggs
Language English Country England, Great Britain Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Validation Study
PubMed
18608512
DOI
10.1080/02652030701883203
PII: 793150938
Knihovny.cz E-resources
- MeSH
- Chromatography, Liquid methods MeSH
- Enzyme-Linked Immunosorbent Assay methods MeSH
- Mass Spectrometry methods MeSH
- Carcinogens analysis MeSH
- Food Contamination analysis MeSH
- Drug and Narcotic Control MeSH
- Chickens MeSH
- Nitrofurazone MeSH
- Drug Residues analysis MeSH
- Semicarbazides analysis MeSH
- Eggs analysis MeSH
- Animals MeSH
- Check Tag
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Validation Study MeSH
- Names of Substances
- carbamylhydrazine MeSH Browser
- Carcinogens MeSH
- Nitrofurazone MeSH
- Semicarbazides MeSH
An enzyme-linked immunosorbent assay (ELISA) method is described for the semi-quantitative determination of semicarbazide (SEM), the marker residue for the banned nitrofuran drug, nitrofurazone, in chicken eggs. The sample homogenate is subjected to acid hydrolysis and derivatisation with o-nitrobenzaldehyde, followed by ethyl acetate/hexane extraction and detection by ELISA. The ELISA procedure has been validated using 0.3, 1.0 and 3 microg kg(-1) of SEM in fortified samples. Detection capability (CC(ss)) was based on the acceptance of 5% false compliant results for a given concentration level according to Commission Decision 2002/657/EC and was determined to be 0.3 microg kg(-1) with a respective limit of detection of 0.13 microg kg(-1). A validated LC-MS/MS method was used for the analysis of incurred egg samples and the results compared with ELISA. A good correlation between the results obtained from ELISA and LC-MS/MS within the concentration range 0.12-20.3 microg kg(-1) was observed in samples collected from chickens fed with a medicated ration of nitrofurazone (r = 0.992, n = 14). Validated ELISA enabled reliable monitoring of SEM levels in eggs collected from incurred chickens over a 90-day period.
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