Abstract
The CEDIA dau Benzodiazepine assay has been reformulated to include online hydrolysis of urinary benzodiazepine glucuronide conjugates. The new antibody possesses enhanced cross-reactivities toward the low-dose benzodiazepines, which are excreted at low urinary drug-metabolite concentrations. The screening method was evaluated using lorazepam as the probe benzodiazepine. Four subjects each consumed a 1-mg lorazepam tablet. Sequential urine voids over the same time intervals were collected for the next 48 h. Twelve postdose urine samples were collected from each subject. Positive results were obtained from 5-24 h to 2-35 h using a 200-ng/mL nitrazepam calibration cutoff. There was no practical difference between hydrolyzing online with the supplied E. coli β-glucuronidase or offline with Helix pomatia β-glucuronidase purchased separately. Without hydrolysis, all urine samples tested negative. The cross-reactivities of lorazepam in terms of nitrazepam calibration equivalents, varied from 108 to 178% for lorazepam concentrations between 50 and 2500 ng/mL. Lorazepam glucuronide gave cross- reactivities (expressed as lorazepam base) between 72 and 136% using the online hydrolysis procedure with E. coli β-glucuronidase. Offline hydrolysis with Helix pomatia gave cross-reactivities between 84 and 134%. Without hydrolysis, lorazepam glucuronide gave less than 4% cross-reactivity in the assay.
Original language | English |
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Pages (from-to) | 270-273 |
Number of pages | 4 |
Journal | Journal of Analytical Toxicology |
Volume | 22 |
Issue number | 4 |
DOIs | |
Publication status | Published - 1998 |
Externally published | Yes |
Bibliographical note
Funding Information:We are grateful for the financial support and supply of CEDIA Benzodiazepine kits from Boehringer Mannheim Corporation.
ASJC Scopus Subject Areas
- Analytical Chemistry
- Environmental Chemistry
- Toxicology
- Health, Toxicology and Mutagenesis
- Chemical Health and Safety
PubMed: MeSH publication types
- Journal Article
- Research Support, Non-U.S. Gov't