1. Comparison of methaqualone excretion patterns using Abuscreen ONLINE and EMIT II immunoassays and GC/MS.
- Author
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Brenner C, Hui R, Passarelli J, Wu R, Brenneisen R, Bracher K, ElSohly MA, Ghodoussi VD, and Salamone SJ
- Subjects
- Adult, Cross Reactions, Enzyme Multiplied Immunoassay Technique, Female, Humans, Hypnotics and Sedatives administration & dosage, Hypnotics and Sedatives metabolism, Male, Methaqualone administration & dosage, Methaqualone metabolism, Sensitivity and Specificity, Time Factors, Gas Chromatography-Mass Spectrometry, Hypnotics and Sedatives urine, Immunoassay, Methaqualone urine
- Abstract
A study was performed to compare the ONLINE and EMIT II immunoassays with gas chromatographic/mass spectrometric (GC/MS) analysis of methaqualone metabolites on urine using samples obtained from a clinical study. Urine was collected over a 72 h period from six healthy adults (4 male, 2 female) after oral dosing with 200 mg methaqualone (MTQ). Each urine sample was analyzed by ONLINE and EMIT II. The samples were then analyzed by GC/MS, hydrolyzed with beta-glucuronidase and again analyzed by GC/MS. Both immunoassays showed greater than 600 ng/ml concentrations of drug in each sample by the second void and remained highly positive for the rest of the 72 h. Unhydrolyzed samples analyzed by GC/MS showed both low concentrations of MTQ as well as its five major hydroxylated metabolites. The hydrolyzed samples analyzed by GC/MS showed high concentrations of the hydroxylated metabolites with the 2'-hydroxy and 3'-hydroxy metabolites being present at the highest concentrations, the 4'-hydroxy metabolite at a lower amount and the 6-hydroxy and 2-hydroxy metabolites at the lowest concentrations. The GC/MS data coupled with the antibody cross-reactivity data indicate that the major species in clinical samples that cross-react in both immunoassays are the conjugated forms of the hydroxylated metabolites of MTQ. Therefore when confirming by GC/MS after an immunoassay screen it would be prudent to confirm for the major hydroxylated metabolites as glucuronides of MTQ instead of the parent drug.
- Published
- 1996
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