首页> 美国卫生研究院文献>EXCLI Journal >Determination of tricyclic antidepressants in human urine samples by the three-step sample pretreatment followed by HPLC-UV analysis: an efficient analytical method for further pharmacokinetic and forensic studies
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Determination of tricyclic antidepressants in human urine samples by the three-step sample pretreatment followed by HPLC-UV analysis: an efficient analytical method for further pharmacokinetic and forensic studies

机译:通过三步样品预处理然后进行HPLC-UV分析测定人尿液样品中的三环类抗抑郁药:一种有效的分析方法可用于进一步的药代动力学和法医学研究

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摘要

In this work, an efficient sample pretreatment method has been developed by combining salt induced-homogenous liquid-liquid extraction, dispersive solid phase extraction, and dispersive liquid-liquid microextraction based on the solidification of floating organic droplet for the extraction of some widely used tricyclic antidepressant (TCA) drugs (nortriptyline, amitriptyline, desipramine, clomipramine, and imipramine) in human urine samples before their determination by high performance liquid chromatography-ultraviolet detection. In brief, the target analytes are first isolated from urine samples into acetonitrile (ACN) separated by adding a salt. Then the obtained ACN phase is treated with a mixture of appropriate sorbents to remove interferences. Afterward, the purified ACN is mixed with menthol as an extractant and rapidly injected into alkaline HPLC-grade water as a preconcentration step. Next, the obtained solution is placed in an ice bath and menthol collects on top of the solution after solidification. The solidified drop is then withdrawn and injected into separation system after dissolving in 10 µL ACN. Under the optimum experimental conditions, extraction recoveries and enrichment factors of the selected drugs ranged from 69-84 % and 345-420, respectively. The limits of detection and quantification were obtained at the ranges of 0.22-0.31, and 0.71-1.1 µg L-1, respectively. The relative standard deviations of the proposed method were ≤ 6 % for intra- (n=6) and inter-day (n=4) precisions at a concentration of 10 µg L-1 (each drug). Finally, the suggested approach was applied to determine of TCA drugs in different patients' urine samples. The method could be applied in further TCAs pharmacokinetic and forensic studies.
机译:在这项工作中,已经开发了一种有效的样品预处理方法,该方法结合了盐诱导的均相液-液萃取,分散固相萃取和基于漂浮有机液滴固化的分散液-液微萃取,以萃取一些广泛使用的三环高效液相色谱-紫外检测法测定人尿液样品中的抗抑郁药(去甲替林,阿米替林,地昔帕明,氯米帕明和丙咪嗪)。简而言之,首先将目标分析物从尿液样品中分离成乙腈(ACN),方法是加入盐将其分离。然后将获得的ACN相用适当的吸附剂混合物处理,以消除干扰。然后,将纯化的ACN与薄荷醇作为萃取剂混合,并作为预浓缩步骤迅速注入碱性HPLC级水中。接下来,将获得的溶液置于冰浴中,并在固化后将薄荷醇收集在溶液的顶部。然后将固化的液滴溶解在10 µL ACN中后取出并注入到分离系统中。在最佳实验条件下,所选药物的提取回收率和富集因子分别为69-84%和345-420。检出限和定量限分别在0.22-0.31和0.71-1.1 µg L -1 范围内。对于浓度为10 µg L -1

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