Fabrizi Giovanni, Fioretti Marzia, Mainero Rocca Lucia
Italian Workers' Compensation Authority, Department of Occupational and Environmental Medicine, Epidemiology and Hygiene, Chemical Agents Laboratory, Via Fontana Candida 1, 00040, Monte Porzio Catone, Rome, Italy.
Biomed Chromatogr. 2016 Aug;30(8):1297-308. doi: 10.1002/bmc.3684. Epub 2016 Feb 12.
A fast and easy tailored dispersive solid-phase extraction (d-SPE) procedure has been developed for the determination of 13 cytostatic drugs. Combined with a rapid and simultaneous ultra performance liquid chromatography/tandem mass spectrometry method for residue identification and quantification in urine, it has been fully validated and tested to study a realistic situation in working environment. The target compounds were chosen from the most common classes used in hospitals. The d-SPE adsorbent was obtained mixing Oasis HLB® with C18 and applied to a large volume of sample (10 mL). The electrospray ionization-mass spectrometry acquisition was conducted in a mixed period mode: six acquisition windows were in positive ionization and one in negative (for 5-fluorouracil). The lowest limit of quantification was found at 0.04 μg/L urine for methotrexate. The absolute recovery of cytotoxic drugs was assessed at two concentrations levels and ranged from 67.1% (cytarabine) to 102.3% (etoposide) and from 65.3% (cytarabine) to 101.2% (methotrexate) for the lower and higher levels, respectively, with the relative standard deviation always <12%. This method gives the opportunity to analyze drugs in a wide molecular weight range (from 130 to 853 a.m.u.) and in a complex matrix, such as urine, without losing any of the features that a method intended for trace quantification must have. Copyright © 2016 John Wiley & Sons, Ltd.
已开发出一种快速简便的定制分散固相萃取(d-SPE)方法,用于测定13种细胞毒性药物。结合快速同步超高效液相色谱/串联质谱法对尿液中的残留物进行鉴定和定量,该方法已得到充分验证和测试,以研究工作环境中的实际情况。目标化合物选自医院中最常用的类别。d-SPE吸附剂是通过将Oasis HLB®与C18混合获得的,并应用于大量样品(10 mL)。电喷雾电离质谱采集采用混合周期模式:六个采集窗口为正离子模式,一个为负离子模式(用于5-氟尿嘧啶)。甲氨蝶呤在尿液中的最低定量限为0.04 μg/L。在两个浓度水平评估了细胞毒性药物的绝对回收率,较低和较高水平分别为67.1%(阿糖胞苷)至102.3%(依托泊苷)以及65.3%(阿糖胞苷)至101.2%(甲氨蝶呤),相对标准偏差始终<12%。该方法能够在宽分子量范围(130至853原子质量单位)内以及复杂基质(如尿液)中分析药物,而不会丧失痕量定量方法应具备的任何特性。版权所有© 2016 John Wiley & Sons, Ltd.