Method for rapidly detecting on-site catering safety
A safety and catering technology, applied in the direction of testing food, material inspection products, etc., can solve the problems of poor correlation between organisms, existence of uncertainty, inability to detect the synergistic toxicity of different chemical substances, etc., achieving good predictability and versatility. Effect
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Embodiment 1
[0057] Embodiment 1 Determination of zebrafish developmental stage
[0058] 1. Selection of zebrafish
[0059] Take 4-5 pairs of wild-type AB strain zebrafish parents to mate, hatch the embryos, observe the zebrafish at 2dpf-5dpf under a dissecting microscope, pick and transfer the zebrafish with normal development into 6-well plates, 30 per well .
[0060] Note: ① "dpf" in the present invention = day post fertilization", refers to the number of days after fertilization of zebrafish, such as "5dpf" refers to zebrafish five days after fertilization, the same below.
[0061] ② "Microwell plate" in the present invention includes but is not limited to the aforementioned 6-well plate, and others such as 12, 24, 48, 96 or 384-well plates are acceptable, the same below.
[0062] ③ The "number of zebrafish" in the present invention includes but is not limited to the aforementioned 30 zebrafish per well, and different numbers of zebrafish can be put in according to the different spec...
Embodiment 2
[0076] Safety evaluation of embodiment 2 dine-in vegetables
[0077] 1. Selection of zebrafish
[0078] The zebrafish at 2dpf and 5dpf were observed under a dissecting microscope, and the zebrafish with normal development were picked and transferred into 6-well plates, 30 in each well.
[0079] 2. Preparation of test items
[0080] Vegetables A, B and C from different sources were squeezed and crushed, and then added to fish culture water to treat zebrafish.
[0081] 3. Handling of test items
[0082] Set up 4 experimental groups: 1 normal control group, 3 vegetable treatment groups (namely group A, group B and group C). The zebrafish in the normal control group were treated with fish culture water; the zebrafish in the vegetable treatment group were treated with vegetable juices squeezed and crushed from vegetables A, B and C, respectively. The microwell plate was placed in a constant temperature incubator and incubated at 28°C for 45min.
[0083] 4. Evaluation of the im...
Embodiment 3
[0094] Safety Evaluation of Embodiment 3 Hotel Dishes
[0095] 1. Selection of zebrafish
[0096] The zebrafish at 2dpf and 4dpf were observed under a dissecting microscope, and the normally developed zebrafish were picked and transferred into 12-well plates, 10 in each well.
[0097] 2. Preparation of test items
[0098] The dishes provided by different hotels D, E and F were squeezed and added to fish culture water to treat zebrafish.
[0099] 3. Handling of test items
[0100] Set up 4 experimental groups: 1 normal control group, 3 dish treatment groups (namely D group, E group and F group). The zebrafish in the normal control group were treated with pisciculture water; the zebrafish in the dish treatment group were added to the dishes supplied by hotels D, E and F respectively, and the dish juice after squeezing and crushing was processed. The microwell plate was placed in a constant temperature incubator and incubated at 28°C for 60min.
[0101] 4. Evaluation of the ...
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