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Confirmatory and quantitative analysis of beta-lactam antibiotics in bovine kidney tissue by dispersive solid-phase extraction and liquid chromatography-tandem mass spectrometry

机译:分散固相萃取-液相色谱-串联质谱法对牛肾组织中β-内酰胺类抗生素的确证和定量分析

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A simple, rapid, rugged, sensitive, and specific method for the confirmation and quantitation of 10 beta-lactam antibiotics in fortified and incurred bovine kidney tissue has been developed. The method uses a simple solvent extraction, dispersive solid-phase extraction (dispersive SPE) cleanup, and liquid chromatography-tandem mass spectrometry (LC/MS/MS) for confirmation and quantitation. Dispersive-SPE greatly simplifies and accelerates sample cleanup and improves overall recoveries compared with conventional SPE cleanup. The beta-lactam antibiotics tested were as follows: deacetylcephapirin (an antimicrobial metabolite of cephapirin), amoxicillin, desfuroylceftiofur cysteine disulfide (DCCD, an antimicrobial metabolite of ceftiofur), ampicillin, cefazolin, penicillin G, oxacillin, cloxacillin, naficillin, and dicloxacillin. Average recoveries of fortified samples were 70% or better for all beta-lactams except DCCD, which had an average recovery of 58%. The LC/MS/MS method was able to demonstrate quantitative recoveries at established tolerance levels and provide confirmatory data for unambiguous analyte identification. The method was also tested on 30 incurred bovine kidney samples obtained from the USDA Food Safety and Inspection Service, which had previously tested the samples using the approved semiquantitative microbial assay. The results from the quantitative LC/MS/MS analysis were in general agreement with the microbial assay for 23 samples although the LC/MS/MS method was superior in that it could specifically identify which beta-lactam was present and quantitate its concentration, whereas the microbial assay could only identify the type of beta-lactam present and report a concentration with respect to the microbial inhibition of a penicillin G standard. In addition, for 6 of the 23 samples, LC/MS/ MS analysis detected a penicillin and a cephalosporin beta-lactam, whereas the microbial assay detected only a penicillin beta-lactam. For samples that do not fall into the "general agreement" category, the most serious discrepancy involves two samples where the LC/MS/MS method detected a violative level of a cephalosporin beta-lactam (deacetylcephapirin) in the first sample and a possibly violative level of desfuroylceftiofur in the second, whereas the microbial assay identified the two samples as having only violative levels of a penicillin beta-lactam.
机译:已经开发出一种简单,快速,坚固,灵敏且特定的方法,用于确认和定量强化和患病的牛肾组织中的10种β-内酰胺类抗生素。该方法使用简单的溶剂萃取,分散固相萃取(分散SPE)净化和液相色谱-串联质谱(LC / MS / MS)进行确认和定量。与传统的SPE净化相比,分散型SPE极大地简化并加速了样品净化,并提高了总体回收率。所测试的β-内酰胺抗生素如下:脱乙酰头孢菌素(头孢氨苄的抗菌代谢产物),阿莫西林,去呋喃头孢噻呋半胱氨酸二硫化物(DCCD,头孢噻呋的抗菌代谢产物),氨苄西林,头孢唑啉,青霉素G,氧氟西林,双氧氟西林,除DCCD外,所有β-内酰胺的强化样品平均回收率为70%或更高,DCCD的平均回收率为58%。 LC / MS / MS方法能够证明已建立的耐受水平下的定量回收率,并提供了用于明确分析物鉴定的确证数据。还对30种从美国农业部食品安全和检验局获得的牛肾样品进行了测试,该样品先前已使用批准的半定量微生物测定法进行了测试。 LC / MS / MS定量分析的结果与23种样品的微生物检测结果基本一致,尽管LC / MS / MS方法具有优越性,因为它可以特异性鉴定存在的β-内酰胺并定量其浓度,而微生物测定法只能鉴定存在的β-内酰胺的类型,并报告有关青霉素G标准品对微生物的抑制作用的浓度。此外,对于23个样本中的6个,LC / MS / MS分析检测到了青霉素和头孢菌素β-内酰胺,而微生物检测仅检测到了青霉素β-内酰胺。对于不属于“一般协议”类别的样品,最严重的差异涉及两个样品,其中LC / MS / MS方法检测到第一个样品中头孢菌素β-内酰胺(去乙酰头孢菌素)的违规水平,并且可能违规。在第二次检测中,呋喃西林的水平达到了十氢呋喃头孢噻呋的水平,而微生物测定法则将这两个样品鉴定为仅具有违规水平的青霉素β-内酰胺。

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