Method for extracting and purifying microcystic toxins LR and RR by taking cyanobacterial bloom in Dian Lake as raw material
A technology of microcystin and cyanobacteria water, applied in the field of analytical chemistry, can solve the problems of strong liver toxicity, inability to carry out large-scale production, and increase of production cost
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[0051] 1. Use No. 25 plankton net (pore size: 63 μm) to fish fresh algae samples from Dianchi Lake, filter the algae samples with a 60-mesh sieve (pore size: 230 μm) in the laboratory to remove larger groups and impurities; then use a 200-mesh sieve ( Pore size: 76μm) to remove smaller algae to increase the dominance of Microcystis in algal samples.
[0052] 2. Freeze and thaw the treated algae samples three times, and store them in a -20°C low-temperature refrigerator for later use.
[0053] 3. Use a vacuum freeze dryer to dehydrate the algal samples. Weigh about 80 grams of dry algae powder and soak it in 5L, 5% acetic acid solution, and shake it with an ultrasonic instrument. After soaking for 1 hour, centrifuge at a speed of 5000 rpm for 20 minutes, and take the supernatant.
[0054] 4. The supernatant was passed through the activated C18 solid-phase extraction column at a rate of 10 mL per minute to enrich the microcystins therein. The amount of cartridge used depends o...
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