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首页> 外文期刊>Chromatographia >Head-Column Field-Amplified Sample Stacking in Binary-System Capillary Electrophoresis: The Need for the Water Plug
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Head-Column Field-Amplified Sample Stacking in Binary-System Capillary Electrophoresis: The Need for the Water Plug

机译:二元系统毛细管电泳中头柱场放大的样品堆叠:对水塞的需求

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Strategies to improve the sensitivity of drug monitoring in microliter amounts of biological fluids by capillary electrokinetic methods are currently being explored in our laboratory. Head-column field-amplified sample stacking is the most effective method of sensitivity enhancement - this approach is robust and highly reproducible when applied correctly. For analysis of opioids as standards or in plasma extracts by binary capillary electrophoresis with ethylene glycol, the data presented in this work unambiguously demonstrate that the water plug initially inserted at the column inlet is essential for establishing a steady current during separation, and thus the highest reproducibility. Internal calibration shows that RSD imprecision values otherwise up to approximately 30% are reduced to values significantly below 10%. The water plug also results in higher detector responses at elevated solute levels (>=100ng mL~(-1)) and leads to increased sensitivity when the sample (standards and extracts of body fluids) is dissolved in water. The water plug does not, however, furnish higher sensitivity in the analysis of opioids as standards or in plasma extracts that are prepared in the optimized sample solvent or buffer. The optimum length of the water plug cannot, furthermore, be obtained merely by dipping the capillary inlet into water (insertion of water by capillary action). The water zone obtained in this way must be elongated by approximately 0.6mm by deliberate hydrodynamic introduction of additional water from a different vial. These head-column field-amplified sample-stacking conditions are shown in operation on two different commercial instruments. As an illustration, data are presented depicting the analysis of dihydrocodeine and nordihydrocodeine in plasma and urine specimens of individuals to which dihydrocodeine was administered.
机译:目前正在我们实验室中探索通过毛细管电动方法提高微升量生物液体中药物监测灵敏度的策略。头柱场放大的样品叠加是提高灵敏度的最有效方法-如果正确应用,此方法是可靠且可高度重现的。对于使用阿片类药物作为标准品或使用乙二醇进行二元毛细管电泳分析血浆提取物中的阿片类药物,这项工作中提供的数据明确表明,最初插入色谱柱入口的水塞对于分离过程中建立稳定的电流至关重要,因此最高重现性。内部校准表明,否则RSD的不精确值可降低到大约10%以下,否则可达30%。当样品(标准液和体液提取物)溶于水时,水塞在较高的溶质水平(> = 100ng mL〜(-1))下也会导致更高的检测器响应,并导致灵敏度提高。但是,在分析作为标准品的阿片类药物或在优化的样品溶剂或缓冲液中制备的血浆提取物时,水塞不能提供更高的灵敏度。此外,仅通过将毛细管入口浸入水中(通过毛细管作用插入水)就不能获得水塞的最佳长度。通过故意通过水力作用从其他样品瓶中引入额外的水,必须将以此方式获得的水区域延长约0.6毫米。在两种不同的商用仪器上运行时,显示了这些头柱场放大的样品堆叠条件。作为说明,所提供的数据描述了在给予双氢可待因的个体的血浆和尿液样本中对双氢可待因和去甲双氢可待因的分析。

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