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人骨髓抽吸物的死后分析 - SSRIs 和 SNRIs 类药物的定量测定。

Postmortem analysis of human bone marrow aspirate - Quantitative determination of SSRI and SNRI drugs.

机构信息

Laboratory for Forensic Chemistry, Department of Analytical Chemistry, Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387, Kraków, Poland.

Laboratory for Forensic Chemistry, Department of Analytical Chemistry, Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387, Kraków, Poland.

出版信息

Talanta. 2019 Nov 1;204:607-612. doi: 10.1016/j.talanta.2019.06.054. Epub 2019 Jun 14.

Abstract

For the first time the MAE/UHPLC-TOFMS method was developed and used in order to determine the antidepressant drugs within the human bone marrow aspirate in real forensic cases. The following drugs, belonging to the group of selective serotonin (or serotonin-norepinephrine) reuptake inhibitors, were tested in this study: venlafaxine, citalopram, fluoxetine, sertraline and paroxetine. The sample preparation proposed in the present article included several steps: homogenization in ultrasound bath, liquid-liquid extraction, fat removal and evaporation under nitrogen. The extraction involved microwave-assisted extraction, performed for 15 min at 55 °C, with hexane-isoamyl alcohol (99:1, v/v) mixture, as an extraction solvent. Time and temperature of extraction were optimized using the simplex method. The fat removal step was introduced because of the fatty nature of the bone marrow that resulted in insufficiently purified samples, impossible to analyze using HPLC. It was achieved by adding a mixture of ethanol, water and formic acid to samples consisting of hexane and isoamyl alcohol, so that the analytes could diffuse to polar phase and fat could stay in non-polar phase. The method was validated and parameters such as: LOD, LOQ, linearity, matrix effect, recovery were determined. The validation parameters obtained allowed to recognize the method as quantitative. Due to lack of the data on therapeutic and toxic levels of considered drugs in bone marrow, data regarding serum has been used for reference. Under this assumption, the developed method allows for quantification of all mentioned drugs at therapeutic levels. Moreover this method has been used in real cases. Finally four analytes: venlafaxine (104 ng/mL), fluoxetine (84 ng/mL), paroxetine (about 3.6 μg/mL) and citalopram (68 ng/mL) were found in three case samples.

摘要

首次开发并应用 MAE/UHPLC-TOFMS 方法,旨在实际法医案例中检测人骨髓抽吸物中的抗抑郁药物。本研究测试了以下属于选择性 5-羟色胺(或 5-羟色胺-去甲肾上腺素)再摄取抑制剂类的药物:文拉法辛、西酞普兰、氟西汀、舍曲林和帕罗西汀。本文提出的样品制备包括几个步骤:在超声浴中均质化、液液萃取、脂肪去除和氮气蒸发。提取采用微波辅助提取,在 55°C 下进行 15 分钟,使用己烷-异戊醇(99:1,v/v)混合物作为提取溶剂。使用单纯形法优化提取时间和温度。由于骨髓的脂肪性质,样品不够纯净,无法使用 HPLC 进行分析,因此引入了脂肪去除步骤。通过向己烷和异戊醇组成的样品中加入乙醇、水和甲酸混合物来实现,使分析物可以扩散到极性相,而脂肪可以留在非极性相。对方法进行了验证,确定了检测限、定量限、线性、基质效应、回收率等参数。获得的验证参数表明该方法为定量方法。由于缺乏考虑药物在骨髓中的治疗和毒性水平的数据,因此参考了血清数据。基于此假设,开发的方法允许在治疗水平下定量所有提到的药物。此外,该方法已在实际案例中使用。最后在三个案例样本中发现了四种分析物:文拉法辛(104ng/mL)、氟西汀(84ng/mL)、帕罗西汀(约 3.6μg/mL)和西酞普兰(68ng/mL)。

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