Determination of opiates and cocaine in urine by high pH mobile phase reversed phase UPLC-MS/MS

被引:109
作者
Berg, Thomas [1 ]
Lundanes, Elsa [2 ]
Christophersen, Asbjorg S. [1 ]
Strand, Dag Helge [1 ]
机构
[1] Norwegian Inst Publ Hlth, Div Forens Toxicol & Drug Abuse, Oslo, Norway
[2] Univ Oslo, Fac Math & Nat Sci, Dept Chem, Oslo, Norway
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2009年 / 877卷 / 04期
关键词
UPLC; LC-MS/MS; Opiates; Opioids; Cocaine; High pH mobile phase; Reversed phase; Forensic toxicology; PERFORMANCE LIQUID-CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; PRESERVED ORAL FLUID; LC-MS-MS; QUANTITATIVE-ANALYSIS; ILLICIT DRUGS; WHOLE-BLOOD; METABOLITES; HEROIN; PLASMA;
D O I
10.1016/j.jchromb.2008.12.052
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A fast and selective ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the determination of opiates (morphine, codeine, 6-monoacetylmorphine (6-MAM), pholcodine. oxycodone, ethylmorphine), cocaine and benzoylecgonine in urine has been developed and validated. Sample preparation was performed by solid phase extraction (SPE) on a mixed mode cation exchange (MCX) cartridge. For optimized chromatographic performance with repeatable retention times, narrow and symmetrical peaks, and focusing of all analytes at the Column inlet at gradient start, a basic mobile phase consisting of 5 mM ammonium bicarbonate, pH 10.2, and methanol (MeOH) was chosen. Positive electrospray ionization (ESI+) MS/MS detection was performed with a minimum of two multiple reaction monitoring (MRM) transitions for each analyte. Deuterium labelled-internal standards were used for six of the analytes. Between-assay retention time repeatabilities (n = 10 series, 225 injections in total) had relative standard deviation (RSD) values within 0.1-0.6%. Limit of detection (LOD) and limit of quantification (LOQ) values were in the range 0.003-0.051 mu M (0.001-0.02 mu g/mL) and 0.01-0.16 mu M (0.003-0.06 mu g/mL), respectively. The RSD values of the between-assay repeatabilities of concentrations were <= 10% at five concentration levels for all analytes, except for pholcodine. Specificity was investigated by determination of the retention times of 96 drugs and internal standards in total. Co-eluting compounds were in all cases separated by the MS/MS detection. No or only minor matrix effects were observed. Total run time, including injection and equilibration time was 5.7 min. The method has been routinely used at the Norwegian Institute of Public Health (NIPH) since August 2007 for qualitative detection of opiates, cocaine and benzoylecgonine in more than 2000 urine samples with two replicates of each sample. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:421 / 432
页数:12
相关论文
共 33 条
  • [21] Current role of liquid chromatography-mass spectrometry in clinical and forensic toxicology
    Maurer, Hans H.
    [J]. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2007, 388 (07) : 1315 - 1325
  • [22] Validated assay for the determination of markers of illicit heroin in urine samples for the control of patients in a heroin prescription program
    Musshoff, F
    Trafkowski, J
    Madea, B
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2004, 811 (01): : 47 - 52
  • [23] Differences in preparative loadability between the charged and uncharged forms of ionizable compounds
    Neue, UD
    Wheat, TE
    Mazzeo, JR
    Mazza, CB
    Cavanaugh, JY
    Xia, F
    Diehl, DM
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2004, 1030 (1-2) : 123 - 134
  • [24] Drug screening of preserved oral fluid by liquid chromatography-tandem mass spectrometry
    Oiestad, Elisabeth Leere
    Johansen, Unni
    Christophersen, Asbjorg Solberg
    [J]. CLINICAL CHEMISTRY, 2007, 53 (02) : 300 - 309
  • [25] The quantitative analysis of heroin, methadone and their metabolites and the simultaneous detection of cocaine, acetylcodeine and their metabolites in human plasma by high-performance liquid chromatography coupled with tandem mass spectrometry
    Rook, EJ
    Hillebrand, MJX
    Rosing, H
    van Ree, JM
    Beijnen, JH
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2005, 824 (1-2): : 213 - 221
  • [26] Simultaneous quantification of opiates, cocaine, and metabolites in hair by LC-APCI-MS/MS
    Scheidweiler, KB
    Huestis, MA
    [J]. ANALYTICAL CHEMISTRY, 2004, 76 (15) : 4358 - 4363
  • [27] SNYDER LR, 1978, J CHROMATOGR SCI, V16, P223, DOI 10.1093/chromsci/16.6.223
  • [28] SWARTZ ME, 2005, J CHROMATOGR RELAT T, P1253
  • [29] A high-throughput multicomponent screening method for diuretics, masking agents, central nervous system (CNS) stimulants and opiates in human urine by UPLC-MS/MS
    Thorngren, John-Olof
    Ostervall, Fredrik
    Garle, Mats
    [J]. JOURNAL OF MASS SPECTROMETRY, 2008, 43 (07): : 980 - 992
  • [30] Simultaneous assay of morphine, morphine-3-glucuronide and morphine-6-glucuronide in human plasma using normal-phase liquid chromatography-tandem mass spectrometry with a silica column and an aqueous organic mobile phase
    Weng, ND
    Lee, JW
    Jiang, XY
    Wehling, M
    Hulse, JD
    Lin, PP
    [J]. JOURNAL OF CHROMATOGRAPHY B, 1999, 735 (02): : 255 - 269