Evaluation of flow injection analysis for determination of cholinesterase activities in biological material

• Published in: Chemico-biological interactions 2010-09, Vol.187 (1), p.225-228
• Main Authors: Cabal, Jiri, Bajgar, Jiri, Kassa, Jiri
• Format: Article
• Language: English
• Subjects: Acetylcholinesterase; Acetylcholinesterase - blood; Acetylcholinesterase - metabolism; Animals; Apparatus; Cholinesterase Inhibitors - pharmacology; Dithionitrobenzoic Acid - metabolism; Enzyme Assays - instrumentation; Enzyme Assays - methods; Flow Injection Analysis - instrumentation; Flow Injection Analysis - methods; Flow system; Kinetics; Membranes, Artificial; Monitoring; Optimalization; Rats
• ISSN: 0009-2797; 1872-7786
• DOI: 10.1016/j.cbi.2010.02.027

The method for automatic continual monitoring of acetylcholinesterase (AChE) activity in biological material is described. It is based on flexible system of plastic pipes mixing samples of biological material with reagents for enzyme determination; reaction product penetrates through the semipermeable membrane and it is spectrophotometrically determined (Ellman's method). It consists of sampling (either in vitro or in vivo), adding the substrate and flowing to dialyzer; reaction product (thiocholine) is dialyzed and mixed with 5,5′-dithio-bis-2-nitrobenzoic acid (DTNB) transported to flow spectrophotometer. Flowing of all materials is realised using peristaltic pump. The method was validated: time for optimal hydratation of the cellophane membrane; type of the membrane; type of dialyzer; conditions for optimal permeation of reaction components; optimization of substrate and DTNB concentrations (linear dependence); efficacy of peristaltic pump; calibration of analytes after permeation through the membrane; excluding of the blood permeation through the membrane. Some examples of the evaluation of the effects of AChE inhibitors are described. It was demonstrated very good uniformity of peaks representing the enzyme activity (good reproducibility); time dependence of AChE inhibition caused by VX in vitro in the rat blood allowing to determine the half life of inhibition and thus, bimolecular rate constants of inhibition; reactivation of inhibited AChE by some reactivators, and continual monitoring of the activity in the whole blood in vivo in intact and VX-intoxicated rats. The method is simple and not expensive, allowing automatic determination of AChE activity in discrete or continual samples in vitro or in vivo. It will be evaluated for further research of cholinesterase inhibitors.