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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Determination of 5-nitroimidazole residues in milk by capillary electrochromatography with packed C-18 silica beds
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Determination of 5-nitroimidazole residues in milk by capillary electrochromatography with packed C-18 silica beds

机译:装有C-18硅胶床的毛细管电色谱法测定牛奶中的5-硝基咪唑残留量

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This work presents a novel methodology for analysing 5-nitroimidazole residues in milk samples by capillary electrochromatography using lab-made packed columns, produced by carrying out a high pressure packing procedure using acetone as driving solvent and C-18 silica uncapped particles (5 mu m particle size) as packing material. Column frits resulted from sintering the proper stationary phase by heating the packed material for 20 s with a nichrome ribbon (80% Ni-20% Cr, 28 cm x 2 mm x 0.2 mm, electric resistance 1.3 Omega) connected to a 7 V AC power supply. Lab-made C-18 silica packed capillaries (40 cmx50 mu m i.d.) were employed for the determination of 5-nitroimidazole drugs. Milk samples were treated by a salting-out assisted liquid-liquid extraction followed by a solid phase extraction with Oasis (R) HLB cartridges prior to their injection. Samples were hydrodynamically injected into the column for 120 s at 11.5 bar. Afterwards eight 5-nitroimidazole compounds were separated in isocratic mode under an applied voltage of 27 kV and a temperature of 30 degrees C. The selected mobile phase consisted of a mixture 60:40 acetonitrile:ammonium acetate (2.5 mM, pH=5). Separation was monitored at 320 nm and it was performed in less than 15 min. The method was characterized in terms of linearity (R-2 >= 0.993) and precision (repeatability, RSD <= 12.2% and reproducibility, RSD <= 14.5%), obtaining detection limits lower than 29 mu g/L for all compounds under study. (C) 2015 Elsevier B.V. All rights reserved.
机译:这项工作提出了一种新的方法,该方法使用实验室制造的填充柱通过毛细管电色谱法分析牛奶样品中的5-硝基咪唑残留物,该色谱柱是通过使用丙酮作为驱动溶剂和C-18二氧化硅未封端的颗粒(5μm)进行高压填充而制得的粒径)作为包装材料。通过将填充的材料与连接到7 V AC的镍铬合金带(80%Ni-20%Cr,28 cm x 2 mm x 0.2 mm,电阻1.3 Omega)一起加热20 s,从而烧结适当的固定相而产生柱状熔块。电源。使用实验室制造的C-18硅胶填充的毛细管(40 cmx50μmi.d.)测定5-硝基咪唑药物。在进样之前,先通过盐析辅助液-液萃取处理牛奶样品,然后使用Oasis®HLB柱进行固相萃取。在11.5 bar下将样品以流体动力学方式注入色谱柱中120 s。然后,在27 kV施加电压和30摄氏度的温度下,以等度模式分离出8种5-硝基咪唑化合物。选定的流动相由60:40乙腈:乙酸铵(2.5 mM,pH = 5)组成。在320 nm处监测分离,并在不到15分钟的时间内完成分离。该方法具有线性(R-2> = 0.993)和精密度(重复性,RSD <= 12.2%和重现性,RSD <= 14.5%)的特点,所有化合物的检测限均低于29μg / L研究。 (C)2015 Elsevier B.V.保留所有权利。

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