Development and Validation of a Gas Chromatography-Mass Spectrometry Method for the Determination of Fentanyl and Butyryl Fentanyl in Oral Fluid

IF 4.1 Q2 CHEMISTRY, ANALYTICAL Analytical science advances Pub Date : 2024-12-23 DOI:10.1002/ansa.202400038
Nicola Camedda, Sara Dagoli, Luca Anzillotti, Rossana Cecchi
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Abstract

Synthetic opioids are lab-synthesized substances that target the brain's opioid receptors, offering analgesic and sedative effects. Amongst them, fentanyl is one of the most widely used to intervene in chronic pain in moderate to severe cancer situations. Butyryl fentanyl (BF) is a novel synthetic opioid whose use is growing. Its potency is seven times that of morphine and, unlike fentanyl, BF can only be obtained through illegal sources. Fentanyl and its analogues are related to harmful intoxications and an increase in opioid-related mortality in many countries, such as in the United States and Europe in recent years. This work developed and validated an effective and sensitive method based on solid-phase extraction followed by gas chromatography-mass spectrometry (GC-MS) for the determination of fentanyl and BF in oral fluid samples. To the best of our knowledge, it is the first successful attempt to quantify these analytes using GC-MS with a limit of quantification (LOQ) of 1 ng/mL in OF. Intra-day and inter-day percentage coefficient of variation were found within 1%–3% and 1%–14%, respectively, while accuracy ranged from 92% to 102% at four concentration levels (lower LOQ [LLOQ], 3, 20, 40 ng/mL) in accordance with the established criteria. The absolute recovery values were in the range of 80.0%–100.0%. The method was linear for all analytes, with quadratic regression of calibration curves always higher than 0.99. The validated method demonstrated its great potential to detect and quantify fentanyl and its analogue in OF and it can be useful not only in forensic investigations of addiction histories but also in epidemiological studies on the spread of fentanyl and BF among workers and/or drivers.

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气相色谱-质谱联用测定口服液中芬太尼和丁基芬太尼的方法的建立与验证
合成阿片类药物是实验室合成的物质,以大脑的阿片受体为目标,具有镇痛和镇静作用。其中芬太尼是最广泛用于干预中重度癌症患者慢性疼痛的药物之一。丁基芬太尼(BF)是一种新型合成阿片类药物,其应用日益广泛。它的效力是吗啡的七倍,而且与芬太尼不同,BF只能通过非法途径获得。芬太尼及其类似物与有害中毒以及近年来在美国和欧洲等许多国家阿片类药物相关死亡率的增加有关。本工作建立并验证了固相萃取-气相色谱-质谱联用(GC-MS)法测定口服液样品中芬太尼和BF的高效、灵敏方法。据我们所知,这是第一次成功地尝试用GC-MS定量这些分析物,定量限(LOQ)为1 ng/mL。日内和日内百分比变异系数分别在1% ~ 3%和1% ~ 14%之间,在4个浓度水平(低LOQ [LLOQ]、3、20、40 ng/mL)下,准确度为92% ~ 102%。绝对回收率在80.0% ~ 100.0%之间。该方法对所有分析物均具有良好的线性关系,校正曲线的二次回归均大于0.99。经过验证的方法显示了其在检测和量化芬太尼及其类似物在OF中的巨大潜力,它不仅可以用于成瘾史的法医调查,而且可以用于芬太尼和BF在工人和/或司机之间传播的流行病学研究。
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