Preparation method of core-shell magnetic conductive polymer microspheres and application thereof
A conductive polymer and polymer technology, applied in the direction of DNA preparation, recombinant DNA technology, etc., can solve the problems of unfriendly environment and increased production cost
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Embodiment 1
[0055] Example 1: Core-shell Fe 3 O 4 / PANI composite microsphere preparation
[0056] Add 0.1g Fe into a 100mL three-necked flask 3 O 4 , 40mL 0.1mol / L hydrochloric acid, ultrasonic dispersion at room temperature for 5 minutes, sealed and placed in a 5 ℃ constant temperature box for 12 hours, magnetic separation to remove the aqueous hydrochloric acid solution, retaining the magnetic core; then add 15mL absolute ethanol, 0.1 g Re-distilled aniline, ultrasonically disperse for 5 minutes, and place it in a thermostat at 5°C for 12 hours.
[0057] Place the flask in an ultrasonic cleaner, and control the water temperature of the ultrasonic cleaner to 5-10°C. Dissolve 0.25mL of 12mol / L hydrochloric acid in 45mL of distilled water, then add 0.28g of ammonium persulfate to dissolve, slowly add the oxidant solution dropwise to control the dropping time to 0.5h; the reaction is maintained and stirred with the assistance of ultrasound for 3h.
[0058] Solid-liquid magnetic separation, water...
Embodiment 2
[0059] Example 2: Core-shell Fe 3 O 4 / PPy composite microsphere preparation
[0060] Replace the aniline in Example 1 with pyrrole, and use 0.40g FeCl for 0.28g ammonium persulfate 3 ·6H 2 O instead, other operations remain unchanged, you can get Fe 3 O 4 / PPy sample.
Embodiment 3
[0061] Example 3: Using Fe 3 O 4 / PANI composite microspheres to separate and purify E.coli DH5α plasmid DNA
[0062] Take 10mg de-doped Fe 3 O 4 / PANI magnetic ball is placed in a 1.5mL sterile centrifuge tube, sonicated with 1mL 70% (v / v) ethanol solution, sterilized twice, then transferred to another sterile centrifuge tube, and then added 40μL E.coli DH5α The crude plasmid DNA extract and 1mL Tris-HCl (10mmol / L, pH 7.8) buffer, shake well, and place it at room temperature for 20 minutes until the DNA is adsorbed on the surface of the magnetic ball. Collect the magnetic ball under a magnetic field and discard the supernatant. Wash the magnetic balls twice with 1 mL of 70% ethanol solution, magnetically separate, discard the supernatant, and place the magnetic balls adsorbing DNA at room temperature to volatilize the ethanol.
[0063] Add 0.4mL of 2mol / L NaCl solution to the centrifuge tube containing the magnetic ball, shake well, place at room temperature for 30 minutes until D...
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