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Carboxyl Fe3O4 magnetic nanoparticle-based SPE and HPLC method for the determination of six tetracyclines in water

机译:基于羧基Fe3O4磁性纳米粒子的SPE和HPLC方法,用于测定水中六条四环素的方法

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A novel carboxyl Fe3O4 magnetic nanoparticle-based solid-phase extraction combined with high-performance liquid chromatography was developed for the analysis of oxytetracycline, tetracycline, demeclocycline, metacycline, chlortetracycline, and doxycycline in water samples. Driven by the electrostatic interaction and the strong chelation between tetracyclines and iron ions, tetracyclines in samples were adsorbed onto the adsorbents. The adsorbed analytes were subsequently eluted with oxalic acid and separated with a C-18 column under gradient condition with a mobile phase consisting of methanol, acetonitrile, and oxalic acid at a flow rate of 0.5 mL/min. The detection was performed at variable ultraviolet wavelengths. Under optimized conditions, the developed method gave an enrichment factor of 33.3, linearity ranges of 5.00-1000 g/L, detection limits of (2.86-5.19) x 10(-2) g/L, quantification limits of (9.54-17.3) x 10(-2) g/L, recoveries of 76.2-98.0%, and intra- and inter-day RSDs of 0.132-15.5% and 2.28-14.5% for these tetracyclines. The established method was successfully applied for the determination of these six tetracyclines in tap water, river water, pond water, and lake water samples.
机译:开发了一种新的羧基Fe3O4磁性纳米颗粒基固相萃取,用于分析水样中的催产素,四环素,Demeclincline,Metalycline,Chlortorcycline和催生物的分析。由静电相互作用和四环素和铁离子之间的强螯合的驱动,将样品中的四环素吸附到吸附剂上。随后用草酸洗脱吸附的分析物并在梯度条件下用C-18柱分离,其流动相以0.5ml / min的流速由甲醇,乙腈和草酸组成。在可变紫外波长下进行检测。在优化条件下,发育方法具有33.3的富集因子,线性范围为5.00-1000g / L,检测限为(2.86-5.19)×10( - 2)G / L,量化限制(9.54-17.3) X 10(-2)G / L,回收率为76.2-98.0%,以及这些四环素的日内和日内的历史记录,2.28-14.5%。成熟的方法已成功地应用于自来水,河水,池塘水和湖水样品中这六个四环素的测定。

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