Preparation method and application of electropositive polymer fluorescent carbon quantum dots with gene vector function
A technology of carbon quantum dots and gene carriers, which is applied in the field of preparation of fluorescent carbon quantum dots, can solve the problems of unstable fluorescence properties and low quantum yields, and achieve the effects of improving quantum yields, wide sources, and high quantum yields
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specific Embodiment approach 1
[0031] Specific embodiment one: the preparation method of the polymer fluorescent carbon quantum dot of the positive gene carrier function of this embodiment, comprises the following steps:
[0032] 1. Add organic acid and cationic high molecular polymer to deionized water, ultrasonically dissolve at room temperature to form a uniform mixed solution; wherein the mass ratio of organic acid and cationic high molecular polymer is 1: (1 ~ 5), organic The mass ratio of acid and deionized water is 1:(10~20);
[0033] 2. Put the mixed solution obtained in step 1 into the reaction kettle, and after heating and reacting at 180-200°C for 5-12 hours, the color of the mixed solution turns dark brown;
[0034] 3. Add 2 times the volume of deionized water to the dark brown solution obtained in step 2, centrifuge at a high speed to remove the bottom solid, and retain the solution;
[0035] 4. Then add 2 to 3 times the volume of deionized water to the solution obtained in step 3, mix well an...
specific Embodiment approach 2
[0036] Embodiment 2: This embodiment differs from Embodiment 1 in that the organic acid molecule in Step 1 is folic acid, ethylenediaminetetraacetic acid, histidine, phthalic acid or ascorbic acid. Others are the same as in the first embodiment.
specific Embodiment approach 3
[0037] Specific embodiment three: the difference between this embodiment and specific embodiment one or two is: the cationic high molecular polymer described in step one is polyethyleneimine, chitosan, polyvinylpyridine, poly(dimethylamino) Ethyl methacrylate, cationic polyacrylamide, polydiallyldimethylammonium chloride, polyamidine or polyvinylamine. Others are the same as in the first or second embodiment.
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