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Rapid determination of trace semicarbazide in flour products by high-performance liquid chromatography based on a nucleophilic substitution reaction

机译:基于亲核取代反应的高效液相色谱法快速测定面粉产物中痕量氨基脲氨基脲

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摘要

Semicarbazide, a toxic food contaminant, widely exists in food products and it originates from the thermal degradation of a food additive of azodicarbonamide or a metabolite of nitrofurazone abused in meat specimens. Many previous methods for semicarbazide determination usually required expensive instruments, difficult-to-prepare monoclonal antibodies, and a long operation time. In this study, a high-performance liquid chromatography method was developed for the rapid determination of trace semicarbazide coupling with a nucleophilic substitution reaction firstly using 4-nitrobenzoyl chloride as derivatization reagent. The derivatization reaction was mild at room temperature for 1 min in neutral solution. Then, semicarbazide derivative was separated and quantified by high-performance liquid chromatography with ultraviolet detection under optimal separation conditions at lambda(max) = 261 nm. The proposed method offered the detection limit of 1.8 mu g/L and was successfully applied for the rapid determination of trace semicarbazide in flour products. Semicarbazide in positive real samples could be actually found and quantified in the range of 0.47-7.53 mg/kg. The recoveries were 76.6-119% with relative standard deviations of 0.5-9.1% (n = 3). This developed method was rapid, reliable, and convenient for the determination of trace semicarbazide in food.
机译:氨基脲是一种有毒食品污染物,广泛存在于食品中,并且它起源于氮杂喹甲酰胺食品添加剂的热降解或滥用肉类标本中的硝基脲的代谢物。以前的许多用于近氨基脲确定的方法通常需要昂贵的仪器,难以准备单克隆抗体,以及长的操作时间。在该研究中,开发了一种高效液相色谱法,用于快速测定与亲核偶联反应首先使用4-硝基苯甲酰氯作为衍生物化试剂的痕量氨基脲偶联。衍生化反应在室温下温和1分钟以中性溶液。然后,通过在Lambda(MAX)= 261nm的最佳分离条件下,通过高效液相色谱分离和定量氨基脲衍生物并定量紫外线检测。所提出的方法提供了1.8μg/ l的检出限,并成功地应用于在面粉产品中快速测定痕量氨基脲。氨基脲在阳性真实样品中可以实际上发现并量化在0.47-7.53mg / kg的范围内。回收率为76.6-119%,相对标准偏差为0.5-9.1%(n = 3)。这种开发方法快速,可靠,方便地测定食物中痕量氨基脲。

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