2009
DOI: 10.1016/j.chroma.2009.04.003
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Newly identified degradation products of ceftiofur and cephapirin impact the analytical approach for quantitative analysis of kidney

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Cited by 29 publications
(31 citation statements)
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“…The resulting hydroxy acid undergoes cyclization to the cephapirin lactone (PIR-4, m/z 364.0420) and the hydrolysis of the ␤-lactam ring in the latter yields PIR-6 (hydrolyzed cephapirin lactone, m/z 382.0526). These compounds, together with PIR-7 (methoxy desacetylcephapirin, m/z 396.0682) and PIR-8 (desacetylcephapirin methyl ester, m/z 396.0682), were detected previously in chicken muscle and bovine milk and kidney [17][18][19]. The formation of PIR-7 and PIR-8 can be tentatively rationalized as the degradation of PIR-5 affected by the sample preparation procedure, in which MeOH is used.…”
Section: Cephapirinmentioning
confidence: 77%
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“…The resulting hydroxy acid undergoes cyclization to the cephapirin lactone (PIR-4, m/z 364.0420) and the hydrolysis of the ␤-lactam ring in the latter yields PIR-6 (hydrolyzed cephapirin lactone, m/z 382.0526). These compounds, together with PIR-7 (methoxy desacetylcephapirin, m/z 396.0682) and PIR-8 (desacetylcephapirin methyl ester, m/z 396.0682), were detected previously in chicken muscle and bovine milk and kidney [17][18][19]. The formation of PIR-7 and PIR-8 can be tentatively rationalized as the degradation of PIR-5 affected by the sample preparation procedure, in which MeOH is used.…”
Section: Cephapirinmentioning
confidence: 77%
“…The limited number of papers published regarding antibiotics in matrices such as meat or milk constitutes a demonstration. Among them, the simulated degradation at physiological temperatures of the cephalosporins ceftiofur and cephapirin in kidney extract has been described [17]. TPs and metabolites of the ␤-lactam antibiotics amoxicillin, cephapirin and ceftiofur, have also been studied in chicken meat [18].…”
Section: Introductionmentioning
confidence: 99%
“…In general, the QuEChERS method seemed to provide slightly better results than the SPE counterpart, and recovery values were only lower than 80% for LEX. The PIR recovery of the SPE method was rather poor, probably due to a degradation underwent by this cephalosporin when was in contact for a long time with meat samples as some studies have described [37].…”
Section: Accuracymentioning
confidence: 92%
“…Issues pertaining to the lack of stability in milk and tissues of certain βLs has been reported in literature [39]. The degradation products of two cephalosporins, ceftiofur and cephapirin, in kidney extract and in acidic and basic solutions was described in recent work by Berendsen et al [277].…”
Section: β-Lactamsmentioning
confidence: 99%
“…Hence, it is common to analyse diaminopoyrimidines together with SA [276][277][278][279][280][281]. Recent review papers by Wang et al [10] and Samanidou et al [318] provide an excellent overview of SAs in foodstuff of animal origin.…”
Section: Sulphonamidesmentioning
confidence: 99%