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Determination of Colistin B in Chicken Muscle and Egg Using Ultra-High-Performance Liquid Chromatography-Tandem Mass Spectrometry

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dc.rights.license CC BY eng
dc.contributor.author Kumar, Harsh cze
dc.contributor.author Kumar, Dinesh cze
dc.contributor.author Nepovimová, Eugenie cze
dc.contributor.author Oulkar, Dasharath cze
dc.contributor.author Kumar, Anil cze
dc.contributor.author Azad, Ramiz Mohammad Rafi cze
dc.contributor.author Budakoti, Subodh Kumar cze
dc.contributor.author Upadhyay, Navneet Kumar cze
dc.contributor.author Verma, Rachna cze
dc.contributor.author Kuča, Kamil cze
dc.date.accessioned 2026-07-21T06:18:04Z
dc.date.available 2026-07-21T06:18:04Z
dc.date.issued 2021 eng
dc.identifier.issn 1660-4601 eng
dc.identifier.uri http://hdl.handle.net/20.500.12603/2737
dc.description.abstract Colistin, an imperative member of the polymyxin group, is a cationic peptide antibiotic. Itis also known as polymyxin E, but this peptide antibiotic has been forbidden for human consumption due to its high toxicity. Regrettably, this antibiotic is utilized as a feed additive and veterinary drug for animals. Due to the toxicity of colistin, the presence of its residue in the animal system represents a threat to human health regarding the consumption of meat, especially chicken. A novel method was proposed for quantifying colistin B in chicken muscles and eggs using ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). In this method, extraction of colistin B from samples was achieved by mixing the sample with acidified methanol:water (1/1, v/v), followed by centrifugation and filtration by a membrane filter excluding solid-phase extraction (SPE) clean up, as well as evaporation steps. The analysis was conducted by optimized liquid chromatography-tandem mass spectrometry (LC-MS/MS), and method performance was assessed in terms of the limit of quantitation, specificity, selectivity, precision, linearity and recovery in coherence with the guidelines of SANTE and the Commission Decision 2002/657/EC. The result obtained from the study showed the limit of quantitation (LOQ) as 10 mu g Kg(-1) for muscles and 5 mu g Kg(-1) for eggs, with acceptable recoveries along with precision. The linearity was plotted in the range of 5-25 mu g L-1 (solvent) for egg and 10-50 mu g Kg(-1) (matrix-matched) for muscles. The result of average recoveries showed the value of 70-94% (3.3-12% relative standard deviation (RSD)) for chicken muscles and 88-107% (2.5-18.6% RSD) for egg samples, which meets the criteria for acceptability of method according to both SANTE and 2002/657/EC guidelines. This proposed protocol provides a cost-effective solution for food testing labs by reducing the cost of the sample preparation by 60% along with the time required for SPE cleanup. Further, the optimized method was also tested on real samples collected from nearby provinces in Solan city, Himachal Pradesh, India, and three out of 20 muscles were found to have colistin B in the range of 50-560 mu g Kg(-1). eng
dc.format p. "Article Number: 2651" eng
dc.language.iso eng eng
dc.publisher MDPI eng
dc.relation.ispartof INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, volume 18, issue: 5 eng
dc.subject chicken eng
dc.subject colistin eng
dc.subject ultra-high-performance liquid chromatography eng
dc.subject mass spectrometry eng
dc.title Determination of Colistin B in Chicken Muscle and Egg Using Ultra-High-Performance Liquid Chromatography-Tandem Mass Spectrometry eng
dc.type article eng
dc.identifier.obd 43877571 eng
dc.identifier.wos 000628175100001 eng
dc.identifier.doi 10.3390/ijerph18052651 eng
dc.publicationstatus postprint eng
dc.peerreviewed yes eng
dc.source.url https://www.mdpi.com/1660-4601/18/5/2651/htm cze
dc.relation.publisherversion https://www.mdpi.com/1660-4601/18/5/2651/htm eng
dc.rights.access Open Access eng


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