Ethyl Glucuronide Concentrations in Oral Fluid, Blood, and Urine After Volunteers Drank 0.5 and 1.0 g/kg Doses of Ethanol

被引:51
作者
Hoiseth, Gudrun [1 ]
Yttredal, Borghild [1 ]
Karinen, Ritva [1 ]
Gjerde, Hallvard [1 ]
Morland, Jorg [1 ]
Christophersen, Asbjorg [1 ]
机构
[1] Norwegian Inst Publ Hlth, Div Forens Toxicol & Drug Abuse, N-0403 Oslo, Norway
关键词
TANDEM MASS-SPECTROMETRY; GAS-CHROMATOGRAPHY; DRINKING DRIVERS; PHARMACOKINETICS; EXCRETION; SALIVA; DRUGS; SERUM; SULFATE; PLASMA;
D O I
10.1093/jat/34.6.319
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The aim of this study was to investigate the concentrations of ethyl glucuronide (EtG) in oral fluid, blood, and urine after healthy volunteers drank two doses of ethanol, 0.5 (n = 11) and 1.0 g/kg (n = 10), after an overnight fast. Samples of oral fluid, blood, and urine were collected before drinking started and at 1.5, 3.5, 5.5, 8.5, 11.5, and 24 h post-dosing. Following ingestion of low dose of ethanol, the Cmax for EtG was 0.36 mg/L (range 0.28-0.41 mg/L) in blood and 69.8 mg/L (range 47.1-96.5 mg/L) in urine. In oral fluid, the concentrations were < 1% of those in blood, and only three subjects exceeded the limit of quantification for EtG in oral fluid. After ingestion of the high dose of ethanol, the Cmax for EtG was 1.06 mg/L (range 0.8-1.22 mg/L) in blood, 159.9 mg/L (range 97.2-225.5 mg/L) in urine, and 0.032 mg/L (range 0.013- 0.059 mg/L) in oral fluid. The median oral fluid/blood ratio was 0.029 (range 0.012-0.054) for EtG. The detection time for EtG was median 11.5 h (range 3.5-11.5 h) in oral fluid. According to this, the detection time for EtG in oral fluid is therefore only a few hours longer than for ethanol itself and represents limited additional value. © 2010 Publishing Technology.
引用
收藏
页码:319 / 324
页数:6
相关论文
共 41 条
  • [1] Sensitivity, specificity, and efficiency in detecting opiates in oral fluid with the Cozart® opiate microplate EIA and GC-MS following controlled codeine administration
    Barnes, AJ
    Kim, I
    Schepers, R
    Moolchan, ET
    Wilson, L
    Cooper, G
    Reid, C
    Hand, C
    Huestis, MA
    [J]. JOURNAL OF ANALYTICAL TOXICOLOGY, 2003, 27 (07) : 402 - 406
  • [2] Bellavia S, 2000, Acta Odontol Latinoam, V13, P3
  • [3] Validation of a gas chromatography - Ion trap tandem mass spectrometry for simultaneous analyse of cocaine and its metabolites in saliva
    Cognard, Emmanuelle
    Bouchonnet, Stephane
    Staub, Christian
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2006, 41 (03) : 925 - 934
  • [4] Development and validation of a method for the quantitation of Δ9-tetrahydrocannabinol in oral fluid by liquid chromatography electrospray-mass-spectrometry
    Concheiro, M
    de Castro, A
    Quintela, O
    Cruz, A
    López-Rivadulla, M
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2004, 810 (02): : 319 - 324
  • [5] Confirmation by LC-MS of drugs in oral fluid obtained from roadside testing
    Concheiro, Marta
    de Castro, Ana
    Quintela, Oscar
    Cruz, Angelines
    Lopez-Rivadulla, Manuel
    [J]. FORENSIC SCIENCE INTERNATIONAL, 2007, 170 (2-3) : 156 - 162
  • [6] COOK CE, 1993, DRUG METAB DISPOS, V21, P717
  • [7] Comparison of urinary excretion characteristics of ethanol and ethyl glucuronide
    Dahl, H
    Stephanson, N
    Beck, O
    Helander, A
    [J]. JOURNAL OF ANALYTICAL TOXICOLOGY, 2002, 26 (04) : 201 - 204
  • [8] DEGIER JJ, 1980, BRIT J CLIN PHARMACO, V10, P151
  • [9] Review: Pharmacokinetics of illicit drugs in oral fluid
    Drummer, OH
    [J]. FORENSIC SCIENCE INTERNATIONAL, 2005, 150 (2-3) : 133 - 142
  • [10] Foster-Swanson A., 1994, Clinical Chemistry, V40, P1057