Enzyme inhibition method for detecting carbamates
A technology of carbamates and dithiodinitrobenzoic acid, applied in the field of chemistry, can solve problems such as no mention of urethane, limited, etc., and achieve the effect of simple steps, simple and fast methods, and less equipment
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0047] (1) Add 5mL EC standard solution (20g / L, excess) (0.1mol / L, pH9.0 phosphate buffer solution) into the test tube;
[0048] (2) Add 50-200ul acetylcholinesterase (13mg / mL) and 50-200ul DTNB (10mg / mL), and react in a water bath at 30-40°C for 10-30min;
[0049] (3) Add 50-200ul of thioacetylcholine iodide (10mg / mL), mix well and immediately use a 1cm cuvette at a wavelength of 412nm for colorimetry, and use a buffer without EC as a control. Record the change value of absorbance with time for 3 minutes △A 0 and △A 1 . A 0 =0.3830, △A 1 =0.3910, excess EC has no inhibitory effect on acetylcholinesterase.
Embodiment 2
[0051] (1) Add 5mL EC standard solution (20g / L, excess) (prepared in 0.1mol / L, pH9.0 phosphate buffer) to the test tube, then add 20-200ul bromine preparation (bromine water-sodium hydroxide solution) Oxidize for 10-20 minutes, and reduce with 60-600ul 5-15% sodium nitrite; in the bromine water-sodium hydroxide solution used, the mass fraction of bromine is 3%, and the concentration of sodium hydroxide is 0.001mol / L.
[0052] (2) Add 50-200ul acetylcholinesterase (13mg / mL) and 50-200ul DTNB (10mg / mL), and react in a water bath at 30-40°C for 10-30min;
[0053] (3) Add 50-200ul of thioacetylcholine iodide (10mg / mL), mix well and immediately use a 1cm cuvette at a wavelength of 412nm for colorimetry, and use a buffer without EC as a control. Record the change value of absorbance with time for 3 minutes A 0 and △A 1 . A 0 =0.3830, △A 1 =-0.0063, the inhibition rate of excess EC oxidized by bromine preparations was significantly increased, reaching 101.64%.
Embodiment 3
[0055] (1) Add 5ml of EC standard solution (2mg / L) into the test tube, then add 20-200ul oxidant (bromine preparation) to oxidize for 10-20min, and reduce with 60-600ul 5-15% sodium nitrite; the bromine preparation is bromine water -sodium hydroxide solution; in the bromine water-sodium hydroxide solution adopted, the mass fraction of bromine is 5%, and the concentration of sodium hydroxide is 0.002mol / L.
[0056] (2) Add 50-200ul acetylcholinesterase (13mg / mL) and 50-200ul DTNB (10mg / mL), and react in a water bath at 30-40°C for 10-30min;
[0057] (3) Add 50-200ul of thioacetylcholine iodide (10mg / mL), mix well and immediately use a 1cm cuvette at a wavelength of 412nm for colorimetry, and use a buffer without EC as a control. Record the change value of absorbance with time for 3 minutes A 0 and △A 1 . A 0 =0.3830, △A 1 =0.23635, 2mg / L EC standard solution oxidized by oxidant, the inhibition rate can reach 38.29%
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com