Randomly taken postmortem urine samples (170) were analyzed by the Emit-dau system for their barbiturate and benzodiazepine content. Of the samples, 23% and 25% were found positive for barbiturate and benzodiazepine, respectively. The percentages of the positive samples were reduced by a heating process to 9% and 11%, respectively. TLC and Emit-st were used for reference procedures. The relative high percentage (above 30%) of the urine samples analyzed exhibited elevated lysozyme activity and protein value. It was found that the disturbing proteins in the Emit-dau system contained not only endogene lysozyme but other thermolabile fractions with higher molecular weight.
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http://dx.doi.org/10.1007/BF02116218 | DOI Listing |
Detection, identification and measurement of dextropropoxyphene and its principal plasma metabolite, nordextropropoxyphene, can be important in the diagnosis of acute poisoning. A combination of thin-layer chromatography (TLC) and gas-liquid chromatography (GLC) of solvent or solid-phase extracts of urine or gastric contents usually serves to detect these and many other compounds, and an homogeneous enzyme immunoassay (EMIT-DAU) is also available for dextropropoxyphene. Measurement of dextropropoxyphene by GLC is complicated by the instability of this compound under certain conditions.
View Article and Find Full Text PDFA investigation was conducted to determine the specificity of the EMIT DAU method of drugs of abuse analysis. Drug-free urine, from healthy volunteers, was individually spiked at 1000, 100, 10, and 1 microgram/mL concentrations with each of 162 different drug substances. These spiked samples were analyzed with the EMIT DAU assay for amphetamines, barbiturates, benzodiazepine metabolites, cocaine metabolites, methadone, opiates, and propoxyphene.
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