Abbott propoxyphene assay: evaluation and comparison of TDx FPIA and GC/MS methods.

Details

Serval ID
serval:BIB_F57C1EAF9A8B
Type
Article: article from journal or magazin.
Collection
Publications
Title
Abbott propoxyphene assay: evaluation and comparison of TDx FPIA and GC/MS methods.
Journal
Journal of Analytical Toxicology
Author(s)
Kintz P., Mangin P.
ISSN
0146-4760[print], 0146-4760[linking]
Publication state
Published
Issued date
1993
Volume
17
Number
4
Pages
222-224
Language
english
Abstract
This study evaluated the capability of the Abbott TDx assay to test for propoxyphene in urine and various biological samples, including tissues obtained from three fatal overdoses, by comparison to gas chromatography/mass spectrometry (GC/MS). First, within-run and between-run precision were determined using three control samples (200, 400, and 900 ng/mL) tested over a two-week period. Within-run coefficients of variation (CV) for the three controls were 1.4, 2.2, and 2.5%, respectively; the between-run CVs were 2.5, 3.1, and 4.0%, respectively. The cross-reactivity with norpropoxyphene, the major metabolite of propoxyphene, was concentration dependent and in the range of 29.3 to 92.6%. Propoxyphene and its metabolite were assayed in biological samples the same day using the Abbott TDx and GC/MS. Tissue preparations were analyzed by TDx without specimen pretreatment other than homogenization and dilution with saline. The TDx results were in accordance with the results obtained by GC/MS.
Keywords
Dextropropoxyphene/analysis, Dextropropoxyphene/urine, Evaluation Studies as Topic, Fluorescence Polarization Immunoassay, Gas Chromatography-Mass Spectrometry, Humans, Reagent Kits, Diagnostic
Pubmed
Create date
18/10/2010 15:02
Last modification date
20/08/2019 17:22
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