An automated method for the simultaneous measurement of azole antifungal drugs in human plasma or serum using turbulent flow liquid chromatography-tandem mass spectrometry

被引:24
作者
Couchman, L. [1 ]
Buckner, S. L. [1 ]
Morgan, P. E. [1 ]
Ceesay, M. M. [2 ]
Pagliuca, A. [2 ]
Flanagan, R. J. [1 ]
机构
[1] Kings Coll Hosp NHS Fdn Trust, Dept Clin Biochem, Toxicol Unit, London SE5 9RS, England
[2] Kings Coll Hosp NHS Fdn Trust, Dept Haematol Med, London SE5 9RS, England
关键词
TurboFlow MS/MS; Azole antifungals; Itraconazole; Posaconazole; Voriconazole; Automated sample preparation; INVASIVE FUNGAL-INFECTIONS; CELL TRANSPLANT RECIPIENTS; ORAL POSACONAZOLE; ITRACONAZOLE; PHARMACOKINETICS; VORICONAZOLE; PROPHYLAXIS; SAFETY; HYDROXYITRACONAZOLE; MALIGNANCIES;
D O I
10.1007/s00216-012-6176-3
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Azole antifungal drugs are important in the prophylaxis and treatment of invasive aspergillosis. Therapeutic drug monitoring may be indicated to (1) monitor adherence, (2) guide dosage and (3) minimise the risk of drug-drug interactions and dose-related toxicity. TurboFlow(TM) technology offers online, automated sample preparation. An Aria Transcend(TM) TLX-II coupled with a TSQ Vantage(TM) MS was used. Centrifuged samples (25 mu L) were mixed with internal standard solution (975 mu L) and 30 mu L injected directly onto a C18-P-XL TurboFlow column. Analytes were focussed onto a Phenomenex Gemini Phenyl analytical column and eluted using a methanol/water gradient (flow-rate, 0.8 mL/min). Analytes were monitored in selected reaction monitoring mode (two transitions per analyte, positive mode APCI). Calibration ranges were as follows: itraconazole, hydroxyitraconazole, and posaconazole 0.05-5.0 mg/L; voriconazole and fluconazole 0.1-10 mg/L. Total analysis time was 12 min. TurboFlow column recovery was > 77% for all analytes. Calibration was linear (R (2) > 0.99) for all analytes. Inter- and intra-assay imprecision (% RSD) was < 8% and accuracy (nominal internal quality control values) 90-105% for all analytes. The limit of detection was 0.01 mg/L for all analytes. No matrix effects were observed. This method is simple, robust and suitable for measuring these compounds at concentrations attained during therapy.
引用
收藏
页码:513 / 523
页数:11
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