Interpretation of oral fluid tests for drugs of abuse

被引:128
作者
Cone, Edward J.
Huestis, Marilyn A.
机构
[1] Johns Hopkins Sch Med, Baltimore, MD USA
[2] NIDA, Chem & Drug Metab Sect, IRP, NIH, Baltimore, MD USA
来源
ORAL-BASED DIAGNOSTICS | 2007年 / 1098卷
关键词
oral fluid; saliva; interpretation; testing; advantages; limitations;
D O I
10.1196/annals.1384.037
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Oral fluid testing for drugs of abuse offers significant advantages over urine as a test matrix. Collection can be performed under direct observation with reduced risk of adulteration and substitution. Drugs generally appear in oral fluid by passive diffusion from blood, but also may be deposited in the oral cavity during oral, smoked, and intranasal administration. Drug metabolites also can be detected in oral fluid. Unlike urine testing, there may be a close correspondence between drug and metabolite concentrations in oral fluid and in blood. Interpretation of oral fluid results for drugs of abuse should be an iterative process whereby one considers the test results in the context of program requirements and a broad scientific knowledge of the many factors involved in determining test outcome. This review delineates many of the chemical and metabolic processes involved in the disposition of drugs and metabolites in oral fluid that are important to the appropriate interpretation of oral fluid tests. Chemical, metabolic, kinetic, and analytic parameters are summarized for selected drugs of abuse, and general guidelines are offered for understanding the significance of oral fluid tests.
引用
收藏
页码:51 / 103
页数:53
相关论文
共 193 条
[1]   Single- and multiple-dose pharmacokinetic and dose-proportionality study of oxymorphone immediate-release tablets [J].
Adams M.P. ;
Ahdieh H. .
Drugs in R & D, 2005, 6 (2) :91-99
[2]   Pharmacokinetics and dose-proportionality of oxymorphone extended release and its metabolites: Results of a randomized crossover study [J].
Adams, MP ;
Ahdieh, H .
PHARMACOTHERAPY, 2004, 24 (04) :468-476
[3]   Positive cannabis results in urine and blood samples after consumption of hemp food products [J].
Alt, A ;
Reinhardt, G .
JOURNAL OF ANALYTICAL TOXICOLOGY, 1998, 22 (01) :80-81
[4]  
[Anonymous], 1999, Analytical determination of nicotine and related compounds and their metabolites
[5]   pH-Metric logP .7. Octanol-, chloroform-, and propylene glycol dipelargonat-water partitioning of morphine-6-glucoronide and other related opiates [J].
Avdeef, A ;
Barrett, DA ;
Shaw, PN ;
Knaggs, RD ;
Davis, SS .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (22) :4377-4381
[6]   Analysis of oxycodol and noroxycodol stereoisomers in biological samples by capillary electrophoresis [J].
Baldacci, A ;
Thormann, W .
ELECTROPHORESIS, 2005, 26 (10) :1969-1977
[7]   Evaluation of urinary dihydrocodeine excretion in human by gas chromatography-mass spectrometry [J].
Balikova, M ;
Maresova, V ;
Habrdova, V .
JOURNAL OF CHROMATOGRAPHY B, 2001, 752 (01) :179-186
[8]   CORRELATION OF PSYCHOTOMIMETIC ACTIVITY OF PHENETHYLAMINES AND AMPHETAMINES WITH 1-OCTANOL-WATER PARTITION-COEFFICIENTS [J].
BARFKNECHT, CF ;
NICHOLS, DE ;
DUNN, WJ .
JOURNAL OF MEDICINAL CHEMISTRY, 1975, 18 (02) :208-210
[9]  
BASELT RC, 1972, CLIN PHARMACOL THER, V13, P64
[10]  
Baselt RC., 2008, Disposition of Toxic Drugs and Chemicals in Man, V8