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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    International archives of occupational and environmental health 65 (1993), S. S151 
    ISSN: 1432-1246
    Keywords: Biological monitoring ; Butoxyacetic acid 2-Butoxyethanol ; Glutamine conjugate ; High performance liquid chromatography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary To determine the fraction of butoxyacetic acid (BAA) which is excreted as the amino acid conjugate N-butoxyacetylglutamine (BAA-GLN), urine samples of six lacquerers exposed to 2-butoxyethanol (BE) were collected before and after work and analysed using an HPLC-method which allows the simultaneous quantification of both BAA species. Whereas the pre-shift samples contained only little or no butoxyethanol-related material, concentrations of BAA and BAA-GLN amounted collectively to up to 7 mmol/l in the samples obtained at the end of work. The ratio BAA-GLN vs. total BAA ranged from 0.16 to 0.64 (mean value 0.48) indicating that a substantial fraction of BAA was eliminated as the amino acid conjugate. The results demonstrate that BAA-GLN is an important metabolite of BE in man. Procedures employed for the biological monitoring of exposure to BE should therefore include the quantification of BAA-GLN, otherwise exposure levels would be underestimated.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An automated gas chromatographic/mass spectrometric assay is described for the antiepileptic drug valproic acid (VPA) and 14 of its metabolites in plasma or urine. Quantitative analysis of the parent drug and its biotransformation products was carried out with the aid of trimethylsilyl derivatives, and was performed by selected ion monitoring gas chromatography/mass spectrometry (normally of [M - CH3]+ species) using an HP 5790 mass selective detector (MSD) quadrupole mass spectrometer. The analysis was fully automated, in that simple injection, data acquisition, integration, quantification and report functions were carried out during unattended operation by an HP 59970C ChemStation™ computer system. The method exhibits good accuracy and high precision, with correlation coefficients greater than 0.990 for all standard curves. Replicate analyses of pooled plasma samples over a 4 month period exhibited an inter-day variation of less than 15% for the parent drug and ten of its metabolites. Moreover, the high dynamic range of the MSD instrument permitted quantification of VPA and minor metabolites thereof (e.g. the hepatotoxic terminal olefin, Δ4-VPA) at levels as disparate as 260 μg ml-1 (VPA) and 14 ng ml-1 (Δ4-VPA) in a single analysis. The high stability and sensitivity of the assay, combined with the fully automated features of the instrumentation, make the method ideally suited to expanded clinical studies and for the routine monitoring of potentially high-risk patients on VPA therapy.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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