Early warning method for paralytic saxitoxin in bivalve mollusks
A shellfish toxin, bivalve mollusk technology, applied in the direction of instruments, measuring devices, scientific instruments, etc., can solve problems such as the inability to realize easy-to-operate, economical, sensitive, accurate and efficient early monitoring and early warning, and achieve economical and economical toxin extraction. , rapid detection, easy operation effect
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Embodiment 1
[0017] Example 1: Establish a method
[0018] Early warning methods for paralytic shellfish toxins in bivalve shellfish include the following steps:
[0019] 1) Feeding 40 bivalve shellfish under laboratory detoxification conditions for one week;
[0020] 2) The poisonous algae producing paralytic shellfish toxin were fed continuously for 5 days at the same concentration every day, and 10 were sampled at 4 different time periods on the 0th day, 1 day, 3 days and 5 days. Store the digestive glands separate from the remaining tissue at -20 °C when sampling;
[0021] 3) Add 0.1% of the formic acid solution homogenization to the tissues obtained in step 2) according to the ratio of 1:2 (tissue weight / g: reagent / mL), after 24 h of maceration at 4 °C, centrifuge at 12000 r / min for 10 min and aspirate the supernatant.
[0022] 4) Add the supernatant obtained in step 3) to the pre-activated well Purification is performed in the HLB solid phase extraction column.
[0023] 5) The purified li...
Embodiment 2
[0030] Example 2: Ezo scallops are detected as samples
[0031] Taking Ezo scallops as an example, the detection is carried out according to the method of Example 1.
[0032] 1. Feed 40 Ezo scallops for one week under laboratory detoxification conditions;
[0033] 2. Ezo scallops were continuously fed at a daily concentration of 3000 cell / mL with paralyzing shellfish toxin-producing algae for 5 days, and 10 scallops were sampled on the 0th, 1st, 3rd and 5th days of feeding, respectively. Store the digestive glands separate from the remaining tissue at -20 °C when sampling;
[0034] 3. Add 0.1% of the formic acid solution to the sample tissue obtained in step 2 according to the ratio of 1:2 (tissue weight / g: reagent / mL), homogenize with a tissue homogenizer, and extract the supernatant after 24h at 4 °C, centrifuge at 12000 revolutions for 10 min.
[0035]4. Add the supernatant obtained in step 3 to activate it with 6mL methanol and 6mL of water in advance Purification is performe...
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