Dominion Diagnostics, 211 Circuit Drive, North Kingstown, RI 02852, USA.
CLS Diagnostics, 750 Union Street, Franklin, MA 02038, USA.
J Anal Toxicol. 2022 Aug 13;46(7):757-764. doi: 10.1093/jat/bkab113.
Norbuprenorphine interferences were observed in urine drug testing LC-MS-MS confirmation methods used to assess patient compliance with prescribed buprenorphine for chronic pain and opioid use disorder. The interferences were observed in the norbuprenorphine MS-MS transitions, m/z 414.4/83.1 and 414.4/187.2, at and near the norbuprenorphine retention time at multiple laboratories using different sample preparation procedures and chromatographic conditions. When the interferences were present, a norbuprenorphine result could not be reported. Upon investigation, the interferences were correlated with prescribed quetiapine (Seroquel, Seroquel XR), a second-generation antipsychotic medication approved for the treatment of schizophrenia, bipolar disorder and more recently as an adjunct treatment for major depressive disorder. In addition to the approved indications, quetiapine is prescribed off-label for other conditions including insomnia and anxiety disorders. Off-label prescribing has increased in recent years, thereby exacerbating this analytical issue. Here, we present the study of four quetiapine metabolites found to have significant direct or potential interferences in norbuprenorphine quantitation. The four metabolites were putatively identified as two hydroxyquetiapine acids differing in the site of hydroxylation and a quetiapine sulfoxide acid diastereomer pair. As a result of this study, interference-free norbuprenorphine MS-MS transitions, m/z 414.4/340.2 and 414.4/326.1, were found that were selective for norbuprenorphine while maintaining an acceptable 10 ng/mL lower limit of quantitation.
在用于评估慢性疼痛和阿片类药物使用障碍患者遵医嘱使用丁丙诺啡的尿液药物检测 LC-MS-MS 确证方法中,观察到了去甲丁丙诺啡的干扰。在多个实验室使用不同的样品制备程序和色谱条件下,在去甲丁丙诺啡保留时间附近和处,在去甲丁丙诺啡 MS-MS 跃迁 m/z 414.4/83.1 和 414.4/187.2 处观察到了干扰。当存在干扰时,无法报告去甲丁丙诺啡的结果。经调查,这些干扰与处方喹硫平(Seroquel,Seroquel XR)有关,喹硫平是一种第二代抗精神病药物,用于治疗精神分裂症、双相情感障碍,最近也被批准作为治疗重度抑郁症的辅助治疗药物。除了批准的适应症外,喹硫平还被开处用于治疗其他疾病,包括失眠和焦虑症。近年来,非适应证用药有所增加,从而加剧了这一分析问题。在这里,我们介绍了四种喹硫平代谢物的研究结果,这些代谢物被发现对去甲丁丙诺啡的定量有显著的直接或潜在干扰。这四种代谢物被推测为两种羟喹硫平酸,它们在羟化部位不同,以及一对喹硫平亚砜酸非对映异构体。由于这项研究,找到了无干扰的去甲丁丙诺啡 MS-MS 跃迁 m/z 414.4/340.2 和 414.4/326.1,它们对去甲丁丙诺啡具有选择性,同时保持可接受的 10ng/mL 定量下限。