Muñoz-Muñoz Ana Celia, Pekol Teresa, Schubring Dana, Johnson Charlene, Andrade Lawrence
Dominion Diagnostics, 211 Circuit Drive, North Kingstown, RI 02852, USA.
J Anal Toxicol. 2018 Jan 1;42(1):6-16. doi: 10.1093/jat/bkx065.
Novel opioid interferences were observed during the development of a high-resolution liquid chromatography-mass spectrometry urine drug testing method for 47 analytes from multiple drug classes. The interferences affected both analytes and internal standards and were only observed when the method was challenged with patient samples. Some interferences were attributable to isomeric opioid metabolites not previously reported while others were due to interference from in-source dissociations or 13C isotopic contributions from known opioid metabolites not typically monitored as analytes. Based on patient drug profiles, known and inferred metabolism, accurate mass, retention time and MS/MS spectrum, the putative identity of each interference was assigned and later confirmed, when possible, using an authentic standard. Opioids are some of the most frequently monitored analytes in urine drug testing laboratories. Because of the potential for co-purification, co-chromatography and spectral similarity, it is anticipated that the reported opioid metabolite interferences could be present with other method conditions and instrument platforms. The objectives of this work are to raise awareness of these interferences and emphasize the importance of evaluating patient samples for potential interferences during method development.
在开发一种用于检测多种药物类别中47种分析物的高分辨率液相色谱 - 质谱尿液药物检测方法的过程中,观察到了新型阿片类干扰。这些干扰影响分析物和内标,并且仅在该方法用患者样本进行测试时才被观察到。一些干扰归因于先前未报道的异构阿片类代谢物,而其他干扰则是由于源内解离或来自通常不作为分析物监测的已知阿片类代谢物的13C同位素贡献所导致的干扰。根据患者药物谱、已知和推断的代谢、精确质量、保留时间和MS/MS谱图,确定了每种干扰的推定身份,并在可能的情况下使用真实标准品进行了后续确认。阿片类药物是尿液药物检测实验室中最常监测的一些分析物。由于存在共纯化、共色谱和光谱相似性的可能性,预计所报道的阿片类代谢物干扰可能在其他方法条件和仪器平台中出现。这项工作的目的是提高对这些干扰的认识,并强调在方法开发过程中评估患者样本潜在干扰的重要性。