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A Fast and Validated High Throughput Bar Adsorptive Microextraction (HT-BAµE) Method for the Determination of Ketamine and Norketamine in Urine Samples

机译:快速高效的高通量棒吸附微萃取(HT-BAµE)方法测定尿样中的氯胺酮和去甲氯胺酮

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摘要

We developed, optimized and validated a fast analytical cycle using high throughput bar adsorptive microextraction and microliquid desorption (HT-BAμE-μLD) for the extraction and desorption of ketamine and norketamine in up to 100 urine samples simultaneously, resulting in an assay time of only 0.45 min/sample. The identification and quantification were carried out using large volume injection-gas chromatography-mass spectrometry operating in the selected ion monitoring mode (LVI-GC-MS(SIM)). Several parameters that could influencing HT-BAµE were assayed and optimized in order to maximize the recovery yields of ketamine and norketamine from aqueous media. These included sorbent selectivity, desorption solvent and time, as well as shaking rate, microextraction time, matrix pH, ionic strength and polarity. Under optimized experimental conditions, suitable sensitivity (1.0 μg L ), accuracy (85.5–112.1%), precision (≤15%) and recovery yields (84.9–105.0%) were achieved. Compared to existing methods, the herein described analytical cycle is much faster, environmentally friendly and cost-effective for the quantification of ketamine and norketamine in urine samples. To our knowledge, this is the first work that employs a high throughput based microextraction approach for the simultaneous extraction and subsequent desorption of ketamine and norketamine in up to 100 urine samples simultaneously.
机译:我们开发,优化和验证了使用高通量条形吸附微萃取和微液体解吸(HT-BAμE-μLD)的快速分析周期,可同时提取和解吸多达100个尿液样品中的氯胺酮和去甲酮胺,从而使分析时间仅为0.45分钟/样品。使用在选定的离子监测模式下运行的大体积进样气相色谱-质谱法(LVI-GC-MS(SIM))进行鉴定和定量。分析并优化了一些可能影响HT-BAµE的参数,以最大程度地从水性介质中回收氯胺酮和去甲氯胺酮。这些包括吸附剂的选择性,解吸溶剂和时间,以及振荡速率,微萃取时间,基质pH,离子强度和极性。在优化的实验条件下,获得了合适的灵敏度(1.0μgL),准确度(85.5–112.1%),精确度(≤15%)和回收率(84.9–105.0%)。与现有方法相比,此处描述的分析周期对于尿液样品中的氯胺酮和去甲氯胺酮的定量要快得多,对环境友好且具有成本效益。据我们所知,这是采用基于高通量的微萃取方法进行的第一项工作,该方法可同时提取和随后同时分离多达100个尿液样品中的氯胺酮和去甲氯胺酮。

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