首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of total florfenicol residues as florfenicol amine in bovine tissues and eel by liquid chromatography-tandem mass spectrometry using external calibration
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Determination of total florfenicol residues as florfenicol amine in bovine tissues and eel by liquid chromatography-tandem mass spectrometry using external calibration

机译:用外部校准,通过液相色谱 - 串联质谱法测定牛肉组织中氟苯尼醇的总氟苯尼醇残基

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A reliable liquid chromatography-tandem mass spectrometry method was developed to determine total florfenicol residues in bovine tissues and eel. Florfenicol and its metabolites (florfenicol amine, monochloroflorfenicol, florfenicol oxamic acid, and florfenicol alcohol) were analyzed as the marker residue, florfenicol amine, as defined by several regulatory agencies. After hydrolysis with hydrochloric acid, samples were defatted and subjected to solid-supported liquid extraction and Oasis MCX-cartridge cleanup before analysis. The method was validated for florfenicol and its metabolites at two levels in eel and bovine muscle, fat, and liver. Excellent recoveries were obtained (93-104%), with relative standard deviations of < 6% for all compounds. Negligible matrix effects and minimal analyte loss during sample preparation enabled accurate quantification by external calibration using solvent standards. No interfering peaks were observed around the retention time of florfenicol amine, indicating the high selectivity of the method. Retention times in the spiked samples corresponding to that of the calibration standard in solvent did not exceed +/- 0.1 min. Ion ratios from the spiked sample were within +/- 10% (relative) of the calibration standards. Calibration curves were linear in the range of 0.5 to 100 ng/mL, with coefficients of determination higher than 0.998. The limits of quantification and limits of detection of the proposed method were estimated to be 0.01 mg/kg and 0.0005 mg/kg, respectively, in all food samples. Thus, the developed method is considered reliable and suitable for regulatory use.
机译:开发了可靠的液相色谱 - 串联质谱法以确定牛组织和鳗鱼中的总氟芬醇残基。分析了弗洛林比酚及其代谢物(Florfenicol胺,单氯氟乙烯酸,弗洛林比醇和弗洛林尼醇酒精)作为标记物残留物,氟苯纤维胺,由几种监管机构定义。用盐酸水解后,在分析之前,样品被脱落并进行固体支持的液体萃取和OASIS MCX盒清理。该方法在鳗鱼和牛肌肉,脂肪和肝脏中的两种水平验证了弗洛芬辛及其代谢物。获得优异的回收率(93-104%),所有化合物的相对标准偏差为<6%。可忽略的矩阵效应和样品制备过程中的最小分析物损耗使使用溶剂标准通过外部校准能够精确定量。在氟苯辛酚胺的保留时间周围没有观察干扰峰,表明该方法的高选择性。对应于溶剂中校准标准的尖刺样品中的保留时间不超过+/- 0.1分钟。来自尖刺样品的离子比在校准标准的+/- 10%(相对)内。校准曲线在0.5至100ng / ml的范围内是线性的,测定系数高于0.998。在所有食物样品中,估计所提出的方法的定量限制和检测的检测限估计分别为0.01mg / kg和0.0005mg / kg。因此,显影方法被认为是可靠的并且适合于监管使用。

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