Poklis Justin L, Mohs Amanda J, Wolf Carl E, Poklis Alphonse, Peace Michelle R
Department of Pharmacology & Toxicology, Virginia Commonwealth University, Richmond, VA 23298-0613, USA
Department of Forensic Science, Virginia Commonwealth University, Richmond, VA 23284-3079, USA.
J Anal Toxicol. 2016 Oct;40(8):608-616. doi: 10.1093/jat/bkw065. Epub 2016 Jul 29.
In healthcare settings drug diversion and impairment of physicians are major concerns requiring a rapid and efficient method for surveillance and detection. A Direct Analysis in Real Time ion source coupled to a JEOL AccuTOF time-of-flight mass spectrometer (DART-MS) method was developed to screen parenteral pharmaceutical formulations for potential drug diversion. Parenteral pharmaceutical formulations are also known as injectable formulations and are used with intravenous, subcutaneous, intramuscular and intra-articular administration. A library was created using the mass spectra data collected by a DART-MS operated in switching mode at 20, 60 and 90 V settings. This library contained 17 commonly encountered drugs in parenteral pharmaceutical formulations that included the surgical analgesic: fentanyl, hydromorphone and morphine; anesthetic: baclofen, bupivacaine, ketamine, midazolam, ropivacaine and succinylcholine; and a mixture of other drug classes: caffeine, clonidine, dexamethasone, ephedrine, heparin, methadone, oxytocin and phenylephrine. Randomly selected 200 de-identified parenteral pharmaceutical formulations containing one or more drugs were submitted for analysis to the FIRM Toxicology Laboratory at Virginia Commonwealth University Health and were screened using the DART-MS. The drug contents of the de-identified formulations were previously confirmed by a published high performance liquid chromatography (HPLC) method. The drugs in the formulations were rapidly and successfully identified using the generated library. The DART-MS and HPLC results were in complete agreement for all 200 parenteral pharmaceutical formulations.
在医疗环境中,药物转移和医生的药物滥用问题是主要关注点,需要一种快速有效的监测和检测方法。开发了一种与JEOL AccuTOF飞行时间质谱仪联用的实时直接分析离子源(DART-MS)方法,用于筛选肠胃外药物制剂是否存在潜在的药物转移情况。肠胃外药物制剂也称为注射用制剂,用于静脉内、皮下、肌肉内和关节内给药。利用在20、60和90 V设置下以切换模式运行的DART-MS收集的质谱数据创建了一个库。该库包含肠胃外药物制剂中17种常见药物,包括手术镇痛药:芬太尼、氢吗啡酮和吗啡;麻醉药:巴氯芬、布比卡因、氯胺酮、咪达唑仑、罗哌卡因和琥珀酰胆碱;以及其他药物类别的混合物:咖啡因、可乐定、地塞米松、麻黄碱、肝素、美沙酮、催产素和去氧肾上腺素。随机选择200种含有一种或多种药物的匿名肠胃外药物制剂,提交给弗吉尼亚联邦大学健康学院FIRM毒理学实验室进行分析,并使用DART-MS进行筛选。这些匿名制剂中的药物含量先前已通过已发表的高效液相色谱(HPLC)方法得到确认。使用生成的库快速且成功地鉴定了制剂中的药物。对于所有200种肠胃外药物制剂,DART-MS和HPLC的结果完全一致。