首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Determination of chloramphenicol, thiamphenicol, florfenicol and florfenicol amine in poultry, swine, bovine and fish by liquid chromatography-tandem mass spectrometry
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Determination of chloramphenicol, thiamphenicol, florfenicol and florfenicol amine in poultry, swine, bovine and fish by liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法测定家禽,猪,牛和鱼中的氯霉素,甲砜霉素,氟苯尼考和氟苯尼考胺

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摘要

A simple, rapid and sensitive method for confirmatory and quantitative purposes using liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS) was developed and validated for determination of chloramphenicol, thiamphenicol, florfenicol and its metabolite, florfenicol amine, in poultry, swine, bovine and fish muscle. Sample preparation was based on extraction with organic solvent (ethyl acetate: ammonium hydroxide, 98:2) followed by evaporation and fat removal using hexane. The chromatographic separation was carried out with an XTerra C18 column with a gradient elution using water and acetonitrile both with 2 mM of ammonium acetate. Mass spectrometry with electrospray ionization was operated in positive or negative polarity using selected-reaction monitoring (SRM) analysis mode, achieving the requirements of four identification points for each compound. Chloramphenicol-D-5 was added as internal standard. Method validation was performed according to the criteria of Commission Decision 2002/657/EC. Parameters as precision, reproducibility, trueness, CC alpha and CC beta were determined. Trueness values were within the range 82-108% and 84-111% for bovine and fish, respectively. Precision ranged from 1.1% to 10.1% and within-laboratory reproducibility ranged from 4.3 to 18.1%, depending on matrix. The CC alpha and CC beta for bovine muscle, for instance, were established as 0.06 and 0.11 mu g kg(-1), respectively.
机译:建立了一种简单,快速,灵敏的方法用于液相色谱-电喷雾串联电离质谱(LC-ESI-MS / MS)进行确认和定量的目的,并验证了氯霉素,甲砜霉素,氟苯尼考及其代谢产物氟苯尼考胺的测定家禽,猪,牛和鱼的肌肉中。样品制备是基于用有机溶剂(乙酸乙酯:氢氧化铵,98:2)萃取,然后蒸发并使用己烷除去脂肪。用XTerra C18柱进行色谱分离,用水和乙腈均用2mM乙酸铵进行梯度洗脱。使用选择反应监测(SRM)分析模式,以电喷雾电离质谱法在正极或负极上运行,从而满足每种化合物四个识别点的要求。加入氯霉素-D-5作为内标。根据委员会决定2002/657 / EC的标准进行方法验证。确定精度,可再现性,真实性,CC alpha和CC beta等参数。牛和鱼的真实性值分别在82-108%和84-111%的范围内。取决于基质,精密度范围为1.1%至10.1%,实验室内重现性范围为4.3至18.1%。例如,牛肌肉的CC alpha和CC beta分别确定为0.06和0.11μg kg(-1)。

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