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Technical Briefs |
Univ. of Florida College of Med., Dept. of Pathol., Immunol., and Lab. Med., P.O. Box 100275, Gainesville, FL 32610-0275
a author for correspondence: fax 352-846-1586, e-mail goldberg.pathology@mail.health.ufl.edu
Benzodiazepines are used therapeutically as antidepressant, anxiolytic, anticonvulsant, hypnotic, muscle relaxant, and preanesthetic agents. Moreover, benzodiazepines are often abused for their euphoric effects. Consequently, benzodiazepines are commonly detected in toxicological analyses.
Immunoassays of benzodiazepines are plagued by several factors that make reliable detection difficult. Complicated metabolic pathways, including N-dealkylation, C-hydroxylation, and glucuronidation, effectively reduce the parent compound to more polar, and thus easily excreted, metabolites. Some of these metabolites are pharmacologically active; in some cases, they are present in higher concentrations and have a longer elimination half-life than the parent compound (1)(2). Many, especially the glucuronide conjugates, which appear at high concentrations in the urine, do not readily cross-react with commercial immunoassays. In contrast, other benzodiazepine metabolites demonstrate high cross-reactivity, depending on the immunoassay utilized (3).
In the US, 13 benzodiazepines of various potencies are commonly prescribed. Therapeutic daily doses have substantially decreased with the newer generation of benzodiazepines (2). Variations in dosage and in ultimate excretion patterns complicate the ability to accurately detect benzodiazepine use (4).
Accumulated research findings indicate pretreating urine
Acknowledgments
References
The following articles in journals at HighWire Press have cited this article:
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D. Borrey, E. Meyer, L. Duchateau, W. Lambert, C. Van Peteghem, and A. De Leenheer Enzymatic Hydrolysis Improves the Sensitivity of Emit Screening for Urinary Benzodiazepines Clin. Chem., November 1, 2002; 48(11): 2047 - 2049. [Full Text] [PDF] |
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