Toxicology experiment device and method for evaluating toxicity of pesticide by using toxicology experiment device
A technology of experimental device and evaluation method, which can be used in material inspection products, testing pharmaceutical preparations, etc., can solve the problems of complex detection process and unstable reliability of detection results, and achieve the effect of high reliability and simple structure.
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Embodiment 1
[0053] Example 1 is a 10-day sediment acute toxicity test. In this experiment, the lethality of third-instar chironomus larvae and the inhibition rate of acetylcholinesterase (AChE) in sediments containing harmful components such as pesticides were used as the basic indicators for evaluating the toxicity of pesticides. According to the Bt protein concentration of different samples of sediments, the experimental The subjects were divided into 5 groups, and there were 3 control groups: a blank control group, a solvent control control group and a negative control group. Blank control is to carry out toxicological experiment without adding any compound; Solvent control control group is to only add the solvent (for example ethanol or acetone) of dissolving target compound to beaker and carry out toxicological experiment, the purpose is to examine the influence of solvent on test organism; and The negative control group is to add the protein solution extracted from ordinary cotton, ...
Embodiment 2
[0063] Embodiment 2 is a 4-day water acute toxicity test. The basic principle and steps of embodiment 2 are the same as in embodiment 1, but the difference is that the time of the experiment is only 4 days, and the main substrate is a water body. During the experiment, it is not necessary to change the water in the beaker. The experiment includes the following steps:
[0064] Step 1: After stirring the sediment samples to be tested, divide them into 5 groups and divide them into 300mL beakers. Add 10g of treated clean sand to each beaker, then add 200mL of water samples, and let stand After a period of time (usually standing overnight) until the upper layer of water is clarified; another set of blank control, a solvent control control group and a negative control group are set.
[0065] Step 2, add 10 third-instar chironomus larvae into each beaker.
[0066] Step 3: Control the experimental temperature at 23±1°C, and keep the light / dark ratio of 16 / 8.
[0067] Step 4: Feed 1...
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