首页> 美国卫生研究院文献>Journal of Analytical Toxicology >Identification of Drugs in Parenteral Pharmaceutical Preparations from a Quality Assurance and a Diversion Program by Direct Analysis in Real-Time AccuTOFTM-Mass Spectrometry (DART-MS)
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Identification of Drugs in Parenteral Pharmaceutical Preparations from a Quality Assurance and a Diversion Program by Direct Analysis in Real-Time AccuTOFTM-Mass Spectrometry (DART-MS)

机译:通过实时AccuTOFTM-质谱(DART-MS)直接分析从质量保证和转移计划中识别肠胃外药物制剂中的药物

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摘要

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 AccuTOFTM 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.
机译:在医疗机构中,药物转移和医师的损伤是主要问题,需要一种快速有效的方法进行监视和检测。开发了直接实时离子源与JEOL AccuTOF TM 飞行时间质谱仪(DART-MS)结合的方法,以筛选用于潜在药物转移的肠胃外药物制剂。肠胃外药物制剂也称为可注射制剂,并与静脉内,皮下,肌内和关节内给药一起使用。使用DART-MS在20、60和90 V设置下以切换模式操作收集的质谱数据创建库。该药库包含17种肠胃外药物制剂中常见的药物,包括外科手术镇痛药: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。随机选择的200种含一种或多种药物的非确定性肠胃外药物制剂提交弗吉尼亚州联邦健康大学FIRM毒理学实验室进行分析,并使用DART-MS进行筛选。先前已通过公开的高效液相色谱(HPLC)方法确认了脱鉴定制剂的药物含量。使用生成的库可以快速,成功地识别制剂中的药物。所有200种肠胃外药物制剂的DART-MS和HPLC结果完全一致。

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