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Rapid Separation and Determination of Metronidazole Benzoate and Other Antiprotozoal Drugs by Pressurized Capillary Electrochromatography

机译:加压毛细管电粒子术快速分离和测定甲硝唑苯甲酸酯和其他抗丙二醇

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摘要

A novel method for the rapid separation and determination of five polar 5-nitroimidazoles in water from different sources by pressurized capillary electrochromatography has been developed. Compared with the gradient elution mode and the packed nonpolar columns which were usually utilized for the separation of 5-nitroimidazoles, a simple isocratic elution mode and low-cost homemade polar molecularly imprinted polymer monolith were used in the experiment. Electrochromatographic conditions such as pH of buffer, organic modifier, concentration of buffer, and separation voltage were optimized. At 320 nm UV wavelengths, the five 5-nitroimidazoles could be baseline-separated rapidly in less than 11 min with the separation voltage of +20 kV in 10 mmol/L sodium dihydrogen phosphate-disodium hydrogen phosphate buffer solution (pH 4.82) containing 30% acetonitrile. Under the optimum conditions, the linear ranges of the metronidazole, secnidazole, tinidazole, ornidazole, and metronidazole benzoate were 0.50–100.00, 0.50–100.00, 0.80–500.00, 0.80–100.00, and 5.00–500.00 μg/mL, respectively, and the detection limits of these analytes were 0.11–0.73 μg/mL. Column efficiencies of 43 000, 36 000, 34 000, 14 000, and 29 000 plates/m were obtained for metronidazole, secnidazole, tinidazole, ornidazole, and metronidazole benzoate, respectively. The recoveries of different water samples were about 85.0–95.8%. Additionally, the proposed method has been successfully applied to the rapid separation of 5-nitroimidazoles in the locally available pure milk sample by simple pretreatment.
机译:在水中由加压毛细管电不同来源的5极性5-硝基咪唑类的快速分离和测定的新方法已被开发出来。在梯度洗脱模式和进行通常用于5-硝基咪唑类分离填充非极性柱相比,一个简单的等度洗脱模式和低成本的自制极性分子印迹聚合物在整料实验中使用。如pH缓冲液中,有机改性剂,缓冲液的浓度和分离电压电色谱条件进行了优化。在320nm处的UV波长,五5-硝基咪唑类可以是基线分离在10毫摩尔/ L磷酸二氢钠 - 磷酸氢二钠缓冲液与20千伏的分离电压小于11分钟迅速含有30(pH值4.82) %乙腈。在最佳条件下,甲硝唑,塞克硝唑,替硝唑,奥硝唑,甲硝唑和苯甲酸的线性范围为0.50-100.00,0.50-100.00,0.80-500.00,0.80-100.00,和5.00-500.00微克/毫升,分别与这些分析物的检出限为0.11-0.73微克/毫升。是为甲硝唑,塞克硝唑,替硝唑,奥硝唑,甲硝唑和苯甲酸分别获得43 000柱英法fi ciencies,36 000,34 000,14 000,29 000板/米。不同水样的回收率为约85.0-95.8%。此外,所提出的方法已被成功地应用到本地可用纯牛奶样品中通过简单的预处理的5-硝基咪唑类的快速分离。

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  • 作者

    Sulan Liao; Qilin Weng;

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  • 年度 2018
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  • 原文格式 PDF
  • 正文语种 eng
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