Producing method of functional quantum point used for specific recognizating tumor cell
A technology of tumor cells and quantum dots, applied in biological testing, material inspection products, etc., can solve problems such as non-specific staining, and achieve the effects of safe raw materials, safe and simple operation, and convenient preparation
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[0025] Example 1:
[0026] 1. Preparation of quantum dots
[0027] (1) Prepare a solution of AOT and n-heptane
[0028] Prepare 30 mL of 0.1M AOT in n-heptane solution.
[0029] (2) Configuration of reverse micelle system
[0030] Add CdCl to the above solution 2 The concentration of the aqueous phase in the system is 0.1M. Join CdCl 2 After the aqueous solution is dissolved, use ultrasonic dispersion for 30 minutes until the system is clear and transparent, thus obtaining a reversed-phase micromicelle system.
[0031] (3) Reaction to generate CdS quantum dots
[0032] At room temperature, bubbling nitrogen into the reversed-phase micromicelle system for 5 minutes to remove the oxygen in the system, and then under the condition of magnetic stirring, add sufficient H into the micromicelle system. 2 S gas. When the color of the system no longer changes, the reaction is complete and the quantum dots have been successfully prepared.
[0033] 2. Surface modification of thioglycolic aci...
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[0042] Example 2:
[0043] The greatest creativity of the method of the present invention lies in the step of functional modification of the surface of the quantum dots (that is, the connection of the quantum dots and folic acid). This step is:
[0044] After surface of the prepared quantum dots with sulfhydryl-containing small molecule compounds, wash 3-5 times with acetone, wash, centrifuge, and dry alternately; then, disperse 5 mg of quantum dot powder in 5-10 mL PBS, and add 20 -30 μL of 0.05M NHS in DMSO solution and the same volume of 0.05M EDC in DMSO solution, stirring for 30-60 minutes, adding 20-30 μL of 0.05M folic acid in DMSO solution, stirring, and reacting for 12-24 hours. Finally, the reactant was dialyzed with deionized water for 5-8 hours to remove unreacted small molecules.
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