首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Dispersive solid-phase extraction procedure coupled to UPLC-ESI-MS/MS analysis for the simultaneous determination of thirteen cytotoxic drugs in human urine
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Dispersive solid-phase extraction procedure coupled to UPLC-ESI-MS/MS analysis for the simultaneous determination of thirteen cytotoxic drugs in human urine

机译:分散固相萃取程序结合UPLC-ESI-MS / MS分析,可同时测定人尿中的13种细胞毒性药物

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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.
机译:开发了一种快速简便的分散固相萃取(d-SPE)方法,用于测定13种抑制细胞生长的药物。结合快速和同时的超高效液相色谱/串联质谱法对尿液中的残留物进行鉴定和定量,它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见的类别。将Oasis HLB(R)与C-18混合,获得d-SPE吸附剂,并将其应用于大量样品(10 mL)。电喷雾电离质谱法的采集采用混合周期模式:六个采集窗口处于正电离状态,一个采集窗口处于负电离状态(对于5-氟尿嘧啶)。甲氨蝶呤的最低定量限为0.04 g / L尿液。在两个浓度水平下评估细胞毒性药物的绝对回收率,对于较低和较高水平,细胞毒性药物的绝对回收率分别为67.1%(阿糖胞苷)至102.3%(依托泊苷)和65.3%(阿糖胞苷)至101.2%(甲氨蝶呤)。相对标准偏差始终<12%。这种方法提供了在宽分子量范围内(从130至853 a.m.u.)和复杂基质(例如尿液)中分析药物的机会,而不会失去痕量定量方法必须具备的任何功能。版权所有(c)2016 John Wiley&Sons,Ltd.

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