Dendritic macromolecule-copolymer cell capturing material as well as preparation method and application thereof
A technology of copolymers and macromolecules, applied in the field of dendrimer-copolymer cell capture materials and their preparation, can solve the problems of high separation efficiency, large cell damage, poor specificity and sensitivity, etc., so as to improve the capture efficiency and increase the Contact chance, the effect of enhancing the amount of modification
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Embodiment 1
[0021] Example 1 : Synthesis of three-dimensional network-like superhydrophilic dendrimers with aminophenylboronic acid as "bait"-copolymer cell capture material
[0022] Dissolve acrylamide, methylene acrylamide, and PEG-6000 in PBS solution at a mass ratio of 1:1:1.5, add 50 μL of the above solution, 0.5-5.0 μL of methyl methacrylate, and tetramethylmethacrylate to each well of a 96-well plate. 0.6 μL of ethylenediamine, 2.5 μL of 10% ammonium persulfate solution, 50 ° C, shaking reaction for 1 h, a milky white colloidal solid was obtained, which was washed with PBS solution. The copolymer base material was irradiated with ultraviolet rays for 10 minutes, and then washed with PBS, and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) was added to the material with a mass ratio of 1:1. ) and N-hydroxysuccinimide (NHS) in PBS, after activation for 0.5h, add 0.5-10.0μL of PAMAM dendrimers (ethylenediamine core), react at 37°C for 2-6h, wash with PBS net. Ami...
Embodiment 2
[0023] Example 2 : Application of superhydrophilic dendrimers-copolymer materials with three-dimensional network structure in capturing human glioma cells U251
[0024] Add 100 μL of human glioma cell U251 suspension to the 96-well plate containing aminophenylboronic acid-modified dendrimer-copolymer material, and the cell density is 10 5 -10 6 , in an incubator (37°C, 5% CO 2 ) after incubating for 5-90 min, the supernatant was sucked and washed three times with PBS, and the cell capture efficiency was calculated. Add 10 μg / mL DAPI dye to the captured cells, wash them after staining at room temperature for 15 min, and observe with a fluorescence microscope.
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