Detection method of water body genetic toxicity of urban drinking water
A genotoxicity and detection method technology, applied in the field of detection and analysis, can solve the problems of high long-term maintenance cost of experimental animals, low sensitivity or positive accuracy ratio, time-consuming long-term test methods, etc. time consuming effect
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Embodiment 1
[0024] (1) adopt detection step of the present invention:
[0025] (1) First wash the 4021 reverse osmosis membrane with pure water at a washing speed of 8L / min; take 100L of a surface source water, and during reverse osmosis treatment, the water sample is processed at a speed of 80-100mL / min for reverse osmosis treatment. The pressure is 0.1MPa, and 3.8L of reverse osmosis concentrated water is obtained;
[0026] (2) Collect 3.8 L of concentrated water obtained by reverse osmosis, filter it through a 0.45 μm glass cellulose membrane, and then enrich it with an HLB column. Use 5mL of n-hexane / dichloromethane (1:1, volume ratio) and 10mL methanol / dichloromethane (1:9, volume ratio) as eluents for elution. Dry the eluent and replace the solvent with DMSO, set the volume to 5mL to obtain the sample to be tested, and store it at -20°C;
[0027] (3) The samples to be tested are subjected to genotoxicity experiments
[0028] ①Ames experiment: The plate incorporation method was us...
Embodiment 2
[0043] This specific embodiment adopts the following steps:
[0044] (1) First wash the 4021 reverse osmosis membrane with pure water at a washing speed of 8L / min; take 100L of factory water from a certain water plant, and during reverse osmosis treatment, the water sample is processed at a rate of 80-100mL / min for reverse osmosis treatment. The pressure of the membrane is 0.1MPa, and 3.8L of concentrated reverse osmosis water is obtained;
[0045] (2) Collect 3.8 L of concentrated water obtained by reverse osmosis, filter it through a 0.45 μm glass cellulose membrane, and then enrich it with an HLB column. Use 5mL of n-hexane / dichloromethane (1:1, volume ratio) and 10mL methanol / dichloromethane (1:9, volume ratio) as eluents for elution. Dry the eluent and replace the solvent with DMSO, set the volume to 5mL to obtain the sample to be tested, and store it at -20°C;
[0046] (3) The samples to be tested are subjected to genotoxicity experiments
[0047] ①Ames experiment: Th...
Embodiment 3
[0052] This specific embodiment adopts the following steps:
[0053] (1) First wash the 4021 reverse osmosis membrane with pure water at a rate of 8L / min; take 100L of water from a certain pipe network, and during reverse osmosis treatment, feed water samples at a rate of 80-100mL / min for reverse osmosis treatment. The pressure is 0.1MPa, and 3.8L of reverse osmosis concentrated water is obtained;
[0054] (2) Collect 3.8 L of concentrated water obtained by reverse osmosis, filter it through a 0.45 μm glass cellulose membrane, and then enrich it with an HLB column. Use 5mL of n-hexane / dichloromethane (1:1, volume ratio) and 10mL methanol / dichloromethane (1:9, volume ratio) as eluents for elution. Dry the eluent and replace the solvent with DMSO, set the volume to 5mL to obtain the sample to be tested, and store it at -20°C;
[0055] (3) Recombinant Escherichia coli-SOS effect experiment was carried out on the sample to be tested: After the preserved recombinant Escherichia c...
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