Dispersive solid-phase extraction procedure coupled to UPLC-ESI-MS/MS analysis for the simultaneous determination of thirteen cytotoxic drugs in human urine

被引:31
作者
Fabrizi, Giovanni [1 ]
Fioretti, Marzia [1 ]
Rocca, Lucia Mainero [1 ]
机构
[1] Italian Workers Compensat Author, Chem Agents Lab, Dept Occupat & Environm Med Epidemiol & Hyg, Via Fontana Candida 1, I-00040 Rome, Italy
关键词
UPLC-MS; MS; dispersive SPE; antineoplastic drugs; urine analysis; occupational exposure; TANDEM MASS-SPECTROMETRY; HANDLING ANTINEOPLASTIC DRUGS; CYTOSTATIC DRUGS; SURFACE CONTAMINATION; HOSPITAL PERSONNEL; ANTICANCER DRUGS; NURSES; CYCLOPHOSPHAMIDE; EXPOSURE; HEALTH;
D O I
10.1002/bmc.3684
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 (R) with C-18 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 g/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 (c) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:1297 / 1308
页数:12
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