High-throughput assay for simultaneous quantification of the plasma concentrations of morphine, fentanyl, midazolam and their major metabolites using automated SPE coupled to LC-MS/MS

被引:55
作者
Ghassabian, Sussan [1 ]
Moosavi, Seyed Mojtaba [1 ]
Valero, Yarmarly Guerra [1 ]
Shekar, Kiran [2 ]
Fraser, John F. [2 ]
Smith, Maree T. [1 ,3 ]
机构
[1] Univ Queensland, Ctr Integrated Preclin Drug Dev, Brisbane, Qld 4029, Australia
[2] Univ Queensland, Prince Charles Hosp, Crit Care Res Grp, Brisbane, Qld 4029, Australia
[3] Univ Queensland, Sch Pharm, Brisbane, Qld 4029, Australia
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2012年 / 903卷
基金
英国医学研究理事会;
关键词
Morphine; M3G; M6G; Fentanyl; Norfentanyl; Midazolam; (MDZ); 1-OHMDZ; 4-OHMDZ; On-line SPE; LC-MS/MS; TANDEM MASS-SPECTROMETRY; SOLID-PHASE EXTRACTION; SENSITIVE DETERMINATION; DOG PLASMA; MORPHINE-3-GLUCURONIDE; NORFENTANYL; URINE; DRUGS; MORPHINE-6-GLUCURONIDE; BENZODIAZEPINES;
D O I
10.1016/j.jchromb.2012.07.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid LC-MS/MS assay method for simultaneous quantification of morphine, fentanyl, midazolam and their major metabolites: morphine-3-beta-D-glucuronide (M3G), morphine-6-beta-D-glucuronide (M6G), norfentanyl, 1'-hydroxymidazolam (1-OH-MDZ) and 4-hydroxymidazolam (4-OH-MDZ) in samples of human plasma has been developed and validated. Robotic on-line solid phase extraction (SPE) instrumentation was used to elute the eight analytes of interest from polymeric SPE cartridges to which had been added aliquots (150 mu L) of human plasma and aliquots (150 mu L) of a mixture of two internal standards, viz. morphine-d3 (200 ng/mL) and 1'-hydroxymidazolam-d5 (50 ng/mL) in 50 mM ammonium acetate buffer (pH 9.25). Cartridges were washed using 10% methanol in ammonium acetate buffer, pH 9.25 (1 mL, 2 mL/min) before elution with mobile phase comprising 0.1% formic acid in water (A) and acetonitrile (B) with a flow rate of 0.6 mL/min using an 11.5 min run time. The analytes were separated on a C18 X-Terre (R) analytical column. The linear concentration ranges were 0.5-100 ng/mL for fentanyl, norfentanyl and midazolam; 1-200 ng/mL for 4-hydroxymidazolam, 2.5-500 ng/mL for 1'-hydroxymidazolam and 3.5-700 ng/mL for morphine, M3G, and M6G. The method showed acceptable within-run and between-run precision (relative standard deviation (RSD) and accuracy <20%) for quality control (QC) samples spiked at concentrations of 80% and 50% of the ULOQ 3 times higher than the LLOQ and also at the LLOQ. Furthermore, analytes were stable in samples (after mixing with internal standard) for at least 48 h in the autosampler (except for 4-hydroxymidazolam which decreased by 22% after 24 h), 5 h at room temperature and after three cycles of freeze and thaw. No autosampler carry-over was observed and the absolute recovery (the area ratio of analyte in plasma relative to that in ammonium acetate buffer 50 mM, pH 9.25) was in the range 40% (midazolam) to 110% (morphine). The assay was applied successfully to the measurement of the analytes of interest in plasma samples from patients on extracorporeal membrane oxygenation (ECMO). (C) 2012 Published by Elsevier B.V.
引用
收藏
页码:126 / 133
页数:8
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