Volledig geautomatiseerde bepaling van desmethyldiazepam in ratteserum met behulp van gerobotiseerde vaste-fase extractie en hogeprestatie vloeistofchromatografie met ultraviolet-detectie
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Series / Report no.
Open Access
Type
Report
Language
nl
Date
1993-06-30
Research Projects
Organizational Units
Journal Issue
Title
Volledig geautomatiseerde bepaling van
desmethyldiazepam in ratteserum met behulp van gerobotiseerde vaste-fase
extractie en hogeprestatie vloeistofchromatografie met
ultraviolet-detectie
Translated Title
[Fully automated determination of
desmethyldiazepam in rat serum by robotized solid-phase extraction and
high-performance liquid chromatography with
UV-detection.]
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Abstract
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In this report a study is described on the fully automated determination of desmethyldiazepam in rat serum. Isolation of desmethyldiazepam from rat serum is with robotized solid-phase extraction with a High-Hydrophobic Octadecylsilane sorbent by using the ASPEC (Automatic Sample Preparation with Extraction Columns.) The solid-phase purified extract is, after dilution, injected on a chromatographic system. Subsequent clean-up of the extract is by column-switching. A "heart-cut" of the precolumn eluate containing the relevant part of the extract (desmethyldiazepam and the internal standard prazepam) is directed to the analytical column. Detection is by UV-absorbance detection at 226 nm. The data are collected, stored and processed on an analytical workstation. The extraction recovery (+- standard deviation) is 83,3 +- 1,0)%. The precision is 5,3% at 1,1 mg/l. The method is adapted to a concentration range from 0.05 to 5,0 mg/l starting with 150 mul serum. The resulting method is completed by the introduction of a quality control to assure the quality and the reliability of the results.
In this report a study is described on the fully automated determination of desmethyldiazepam in rat serum. Isolation of desmethyldiazepam from rat serum is with robotized solid-phase extraction with a High-Hydrophobic Octadecylsilane sorbent by using the ASPEC (Automatic Sample Preparation with Extraction Columns.) The solid-phase purified extract is, after dilution, injected on a chromatographic system. Subsequent clean-up of the extract is by column-switching. A "heart-cut" of the precolumn eluate containing the relevant part of the extract (desmethyldiazepam and the internal standard prazepam) is directed to the analytical column. Detection is by UV-absorbance detection at 226 nm. The data are collected, stored and processed on an analytical workstation. The extraction recovery (+- standard deviation) is 83,3 +- 1,0)%. The precision is 5,3% at 1,1 mg/l. The method is adapted to a concentration range from 0.05 to 5,0 mg/l starting with 150 mul serum. The resulting method is completed by the introduction of a quality control to assure the quality and the reliability of the results.
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