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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Preconcentration of trace amounts of methadone in human urine, plasma, saliva and sweat samples using dispersive liquid-liquid microextraction followed by high performance liquid chromatography
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Preconcentration of trace amounts of methadone in human urine, plasma, saliva and sweat samples using dispersive liquid-liquid microextraction followed by high performance liquid chromatography

机译:使用分散液-液微萃取和高效液相色谱法对人尿,血浆,唾液和汗液样品中痕量美沙酮进行预浓缩

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摘要

A simple, rapid and efficient method for the preconcentration of methadone was developed using dispersive liquid-liquid microextraction (DLLME) followed by high performance liquid chromatography with ultra violet detection (HPLC-UV). The extraction method is based on the fast injection of a mixture of extracting and disperser solvents into the aqueous solution to form a cloudy ternary component solvent (aqueous solution:extracting solvent:disperser solvent) system. The extraction parameters such as nature and volume of extracting and disperser solvents, pH of sample, and extraction time were studied for optimization. Under the optimal conditions (extracting solvent: chloroform, 250 μL; disperser solvent: methanol, 2.5 mL and pH of sample: 10.0) a linear calibration curve was obtained in the range of 0.5-5000 ng mL ~(-1) with r ~2 = 0.9995. To demonstrate analytical performance, figures of merits of the proposed method in four different biological matrices (urine, plasma, saliva and sweat) spiked with methadone were investigated. The limits of detection and quantification in these matrices were ranged from 4.90 to 24.85 ng mL ~(-1) and 16.32 to 82.75 ng mL ~(-1), respectively. The extraction recoveries were above 97% and the preconcentration factors of methadone in distilled water, urine, plasma, saliva, and sweat samples were 196.52, 10.03, 9.93, 1.97 and 1.99, respectively. While the precision for inter-day was ≤6.43 (n = 5), it was ≤2.26 (n = 5) for intra-day assay. Finally, the method was successfully applied in the determination of methadone in the human urine, plasma, saliva and sweat samples.
机译:建立了一种简单,快速,高效的美沙酮预浓缩方法,方法是使用分散液-液微萃取(DLLME),然后进行高效液相色谱和紫外检测(HPLC-UV)。提取方法基于将提取和分散溶剂的混合物快速注入水溶液中,以形成浑浊的三元组分溶剂(水溶液:提取溶剂:分散溶剂)体系。研究了萃取参数,如萃取剂和分散剂的性质和体积,样品的pH值以及萃取时间,以优化工艺。在最佳条件下(萃取溶剂:氯仿,250μL;分散剂:甲醇,2.5 mL,样品的pH:10.0),在0.5〜5000 ng mL〜(-1)范围内获得线性校正曲线,r〜 2 = 0.9995。为了证明分析性能,研究了该方法在美沙酮加标的四种不同生物基质(尿液,血浆,唾液和汗液)中的优缺点。这些基质中的检测和定量限分别为4.90至24.85 ng mL〜(-1)和16.32至82.75 ng mL〜(-1)。提取回收率高于97%,美沙酮在蒸馏水,尿液,血浆,唾液和汗液样品中的富集系数分别为196.52、10.03、9.93、1.97和1.99。日间精度为≤6.43(n = 5),而日内分析精度为≤2.26(n = 5)。最终,该方法成功地用于人尿,血浆,唾液和汗液中美沙酮的测定。

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