Department of Analytical Chemistry, Faculty of Chemistry, Gdańsk University of Technology, 11/12 Narutowicza Str., Gdańsk 80-233, Poland.
Department of Forensic Medicine, Faculty of Medicine, Medical University of Gdańsk, 3A Marii Skłodowskiej-Curie Str., Gdańsk 80-210, Poland.
J Anal Toxicol. 2023 Jan 24;46(9):1073-1078. doi: 10.1093/jat/bkac006.
Benzodiazepines (BZDs) and Z-drugs are among the most commonly prescribed pharmaceuticals in the world and are considered standard care for various mental illnesses and for the treatment of sleeping and anxiety disorders, alcohol withdrawal, muscle spasms and epilepsy. Some BZDs are not allowed as pharmaceuticals in many countries, and they are used as designer benzodiazepines (DBZDs). All these compounds are typically screened in routine toxicological analyses for forensic purposes. Knowledge of time-dependent decreases in drug concentrations during storage or transport of samples is of considerable significance and allows forensic toxicologists to achieve reliable data, proper interpretation and high-quality results. The aim of this study was to evaluate changes in the amounts of selected BZDs, DBZDs and Z-drugs in blood samples stored at various temperatures. The study involved BZDs (19), DBZDs (3) and Z-drugs (2) spiked into blank blood. Subsequently, the blood samples were stored at various temperatures (room temperature, 4°C, -20°C and -80°C) for up to 6 months. Analyses were performed at 1- to 2-week intervals using liquid chromatography-tandem mass spectrometry. The stability of compounds was evaluated under four temperature conditions over a 6-month period. Some BZDs were stable at all temperatures tested (e.g., diazepam, oxazepam, nordazepam and prazepam) with a degradation rate of only 0-10%. The highest instability was observed for analyte samples kept at room temperature, and the losses in content for some compounds, e.g., lorazepam and chlordiazepoxide, were almost 100%. For other compounds, the stability was clearly different at each tested temperature. To the best of our knowledge, this is one of the first such comprehensive study of the long-term stability of BZDs covering a wide range of different storage temperatures.
苯二氮䓬类药物(BZDs)和 Z 类药物是世界上最常用的处方药物之一,被认为是各种精神疾病以及治疗睡眠和焦虑障碍、酒精戒断、肌肉痉挛和癫痫的标准疗法。一些国家不允许将某些苯二氮䓬类药物作为药物使用,而是将其用作设计苯二氮䓬类药物(DBZDs)。所有这些化合物通常都在常规毒理学分析中进行筛选,以用于法医目的。了解储存或运输样本过程中药物浓度随时间的下降具有重要意义,可使法医毒物学家获得可靠的数据、正确的解释和高质量的结果。本研究旨在评估储存于不同温度下的血液样本中选定的 BZDs、DBZDs 和 Z 类药物的含量变化。该研究涉及将 BZDs(19 种)、DBZDs(3 种)和 Z 类药物(2 种)掺入空白血液中。随后,将血液样本分别在不同温度(室温、4°C、-20°C 和-80°C)下储存长达 6 个月。使用液相色谱-串联质谱法在 1 周至 2 周的时间间隔内进行分析。在 6 个月的时间内,在四种温度条件下评估了化合物的稳定性。一些 BZDs 在所有测试温度下都稳定(例如,地西泮、奥沙西泮、去甲西泮和普拉西泮),降解率仅为 0-10%。在室温下保存的分析物样本表现出最高的不稳定性,一些化合物(例如,劳拉西泮和氯氮䓬)的含量损失几乎达到 100%。对于其他化合物,在每个测试温度下的稳定性显然不同。据我们所知,这是首次对苯二氮䓬类药物在广泛不同储存温度下的长期稳定性进行的全面研究之一。