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首页> 外文期刊>Journal of the Iranian Chemical Society >Determination of trace amounts of nystatin in water and vaccine samples using sodium dodecyl sulfate-coated iron oxide magnetic nanoparticles followed by high-performance liquid chromatography-ultraviolet detection
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Determination of trace amounts of nystatin in water and vaccine samples using sodium dodecyl sulfate-coated iron oxide magnetic nanoparticles followed by high-performance liquid chromatography-ultraviolet detection

机译:使用十二烷基硫酸钠涂层的氧化铁磁性纳米粒子然后高性能液相色谱 - 紫外线检测测定水和疫苗样品中痕量的黄芪蛋白。

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摘要

In this work, magnetic solid-phase extraction based on sodium dodecyl sulfate-coated Fe3O4 nanoparticles has been successfully applied for extraction and preconcentration of trace amounts of nystatin from water and vaccine samples prior to high-performance liquid chromatography-ultraviolet detection. Various experimental parameters affecting extraction and recovery of the analyte, such as the amount of sodium dodecyl sulfate, pH of the sample solution, salt concentration, extraction time, sample volume and desorption conditions, were systematically studied and optimized. Under optimized conditions, nystatin was quantitatively extracted. Proper linear range with good coefficient of determination, (R (2) > 0.99) and limit of detection and quantification (based on signal-to-noise ratios of 3 and 10) of 2.0 and 5.0 A mu g L-1, over the investigated concentration range (5-700 A mu g L-1), were obtained, respectively. The intra-day and inter-day relative standard deviations at 50 A mu g L-1 level of NYS were 1.4 and 4.5% based on six replicate determinations. The accuracy of the method was evaluated by recovery measurements on spiked samples. Suitable recoveries of 96-102 and 26-44% were achieved (at spiked levels of 50, 300 and 500 A mu g L-1) for water and vaccine samples, respectively.
机译:在这项工作中,基于十二烷基硫酸钠涂覆的Fe3O4纳米颗粒的磁性相萃取已经成功地应用于在高效液相色谱 - 紫外线检测之前从水和疫苗样品中萃取和前染料的痕量Nystatin的萃取和前浓缩。系统研究和优化了影响分析物的萃取和回收分析物的萃取和回收的实验参数,例如产硫酸钠钠,盐浓度,提取时间,样品体积和解吸条件的量。在优化条件下,大量提取乳腺素。适当的线性范围具有良好的测定系数,(R(2)> 0.99)和检测和定量限制(基于3和10的信噪比)为2.0和5.0 a mu g l-1,通过分别获得研究的浓度范围(5-700a mu g L-1)。基于六个重复测定,在50 a mu g l-1液位下的日期和日间相对标准偏差为1.4和4.5%。通过对尖刺样品的恢复测量评估该方法的准确性。为水和疫苗样品分别达到了96-102和26-44%的合适回收率(以50,300和500μmg1-1),水和疫苗样品。

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