首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Determination of ionophore coccidiostats in feeding stuffs by liquid chromatography-tandem mass spectrometry. Part II. Application to cross-contamination levels and non-targeted feed.
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Determination of ionophore coccidiostats in feeding stuffs by liquid chromatography-tandem mass spectrometry. Part II. Application to cross-contamination levels and non-targeted feed.

机译:液相色谱-串联质谱法测定饲料中的离子载体抗球虫药。第二部分适用于交叉污染水平和非目标饲料。

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摘要

A fit to purpose multi-analyte method for the official control of six coccidiostats (monensin sodium, salinomycin sodium, narasin, lasalocid sodium, semduramicin sodium and maduramicin ammonium alpha) at cross-contamination concentration levels in poultry, cattle, pig and calf compound feed by liquid chromatography tandem mass spectrometry (LC-MS/MS) has been developed and in-house validated. The corresponding maximum levels have been recently introduced by European legislation. The method developed involved a simple extraction of the coccidiostats from the feed samples followed by centrifugation and filtration of the supernatants for all matrices. For calf feed an additional de-fattening step of the filtrated supernatants with n-hexane was necessary. The resulting supernatants were submitted to chromatographic analysis. The analytes were quantified by a modified approach of the standard additions technique applied to the extracts, hence allowing a workload comparable to matrix-matched standard calibration curves. A further simplification of this technique was reached by applying the same addition levels of the target analytes for different concentration ranging from 0.5x maximum level up to 2.5x maximum level (universal approach). The concentration independent intermediate precision expressed in terms of relative standard deviation varied between 3 and 12% (except for maduramicin ammonium alpha and semduramicin sodium up to 21%) and the recovery rates ranged from 80 to 111%, depending on the target analyte and matrix. The limits of detection (LOD) and limits of quantification (LOQ) were different for the various analyte/matrix/instrument combinations but all LOQs were in the 0.01-0.65 mg kg(-1) range, hence well below the target concentrations of each analyte. Based on the obtained method performance characteristics the method is considered fit for the intended purpose.
机译:用于家禽,牛,猪和小牛复合饲料中交叉污染浓度水平的六种球虫抑菌剂(莫能菌素钠,沙利诺霉素钠,那拉辛,拉沙菌素钠,色拉米菌素钠和马杜拉米菌铵α)的官方控制的多目标分析方法液相色谱串联质谱(LC-MS / MS)的开发和内部验证。欧洲立法最近引入了相应的最高水平。开发的方法涉及从饲料样品中简单提取抗球虫药,然后对所有基质的上清液进行离心和过滤。对于小牛饲料,必须使用正己烷对滤过的上清液进行额外的脱脂步骤。将所得的上清液进行色谱分析。通过对提取物应用标准添加技术的改进方法对分析物进行定量,因此可提供与基质匹配的标准校准曲线相当的工作量。通过对不同浓度的目标分析物采用相同的添加量,从0.5倍最大水平到2.5倍最大水平(通用方法),可以实现该技术的进一步简化。以相对标准偏差表示的与浓度无关的中间精度在3%至12%之间变化(除了马杜菌素铵α和高达21%的Semduramicin钠),回收率在80%至111%之间,具体取决于目标分析物和基质。各种分析物/基质/仪器组合的检测限(LOD)和定量限(LOQ)不同,但所有LOQ均在0.01-0.65 mg kg(-1)范围内,因此远低于每种的目标浓度分析物。基于获得的方法性能特征,该方法被认为适合于预期目的。

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