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Automated detection of organophosphate warfare gases (nerve agents) in air based on micro-SIA - lab-on-valve system
Ondřej Pavlíček, Miroslav Polášek, Martin Foltýn, Jiří Cabal
Language English Country Czech Republic
Document type Research Support, Non-U.S. Gov't, Evaluation Study
NLK
Free Medical Journals
from 2003 to 2013
Freely Accessible Science Journals
from 2003 to 2013
ROAD: Directory of Open Access Scholarly Resources
from 2002
- MeSH
- Butyrylcholinesterase MeSH
- Chemical Warfare Agents MeSH
- Cholinesterase Inhibitors analysis MeSH
- Equipment Design MeSH
- Automation, Laboratory instrumentation MeSH
- Organophosphorus Compounds analysis MeSH
- Flow Injection Analysis * methods instrumentation statistics & numerical data MeSH
- Sarin * analysis MeSH
- Sequence Analysis methods MeSH
- Spectrophotometry methods MeSH
- Equipment and Supplies MeSH
- Air Pollution * analysis statistics & numerical data MeSH
- Publication type
- Evaluation Study MeSH
- Research Support, Non-U.S. Gov't MeSH
Equipment for fast and accurate detection of organophosphate nerve agents is developed and tested. The method is based on the spectrophotometric monitoring of the enzyme activity of butyrylcholinesterase after its contact with air in a special absorption unit (a “scrubber”) developed for the purpose. The scrubber was made from a glass tube filled with glass beads (diam. 3 mm) and filled with approx. 5 ml of butyrylcholinesterase in a phosphate buffer of pH 7.4. The air sample was bubbled through this solution for 20 s at a flow rate of 80 l hour-1. Thereafter 8 microl of the enzyme solution were aspirated into the micro-SIA-LOV analyzer and the activity of the enzymes were evaluated by using Ellman’s reagent, i.e. 2.5 mmol l-1 butyrylthiocholine iodide and 0.25 mmol 5,5’-dithiobis (2-nitrobenzoic acid). The absorbance of the coloured reaction product was measured at 412 nm after the reaction time of 60 s. The residue of the absorption liquid was washed away from the absorber and the system was washed with the enzyme solution prior to next analysis. The contaminated air caused partial inhibition of the enzyme activity of the absorption liquid. The activity of the contaminated sample was compared with the activity of the unaffected enzyme (blank measurement). The analysis was controlled by two PCs. The effect of the concentration of analyte in the absorption liquid on the enzyme activity was tested for 10-5-10-9 mol l-1 sarin. A single analysis (including the absorption step) took <130 s.
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Literatura
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- $a Equipment for fast and accurate detection of organophosphate nerve agents is developed and tested. The method is based on the spectrophotometric monitoring of the enzyme activity of butyrylcholinesterase after its contact with air in a special absorption unit (a “scrubber”) developed for the purpose. The scrubber was made from a glass tube filled with glass beads (diam. 3 mm) and filled with approx. 5 ml of butyrylcholinesterase in a phosphate buffer of pH 7.4. The air sample was bubbled through this solution for 20 s at a flow rate of 80 l hour-1. Thereafter 8 microl of the enzyme solution were aspirated into the micro-SIA-LOV analyzer and the activity of the enzymes were evaluated by using Ellman’s reagent, i.e. 2.5 mmol l-1 butyrylthiocholine iodide and 0.25 mmol 5,5’-dithiobis (2-nitrobenzoic acid). The absorbance of the coloured reaction product was measured at 412 nm after the reaction time of 60 s. The residue of the absorption liquid was washed away from the absorber and the system was washed with the enzyme solution prior to next analysis. The contaminated air caused partial inhibition of the enzyme activity of the absorption liquid. The activity of the contaminated sample was compared with the activity of the unaffected enzyme (blank measurement). The analysis was controlled by two PCs. The effect of the concentration of analyte in the absorption liquid on the enzyme activity was tested for 10-5-10-9 mol l-1 sarin. A single analysis (including the absorption step) took <130 s.
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