Biochip and preparation method thereof
A technology of biological chips and biological substances, which is applied in the fields of biochemical equipment and methods, biological testing, and microbial determination/inspection, etc., to achieve the effects of simple preparation process, wide application range and low cost
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Embodiment 1
[0038] Embodiment 1, the preparation of HeLa cell chip
[0039] Prepare the ink-jet ink soluble ink containing 2nm gold nanoparticles, the specific preparation method is as follows:
[0040] 1) First prepare a polymer-protected stable gold nanoparticle dispersion with a particle size of 2nm, remove excess polymer protective agent by dialysis, freeze-dry, and prepare a 10% mass concentration with double-distilled water after autoclaving Gold nanoparticles solution. Before adding the polymer dispersant, the toxic effect of gold nanoparticles on HeLa cells was detected by MTT colorimetry, and the results are shown in figure 1 . Depend on figure 1 It can be seen that with the increase of co-cultivation time, the percentage of cell viability decreased. It is proved that gold nanoparticles have a strong ability to inhibit the growth of cells and a great toxicity to cells. According to the principle of chip selection, it was demonstrated that gold nanoparticles can be used.
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Embodiment 2
[0044] Embodiment 2, preparation of K-562 cell chip template
[0045] Prepare the ink-jet ink soluble ink containing silver nanoparticles with a particle size of 10nm, the specific preparation method is as follows:
[0046] 1) First prepare the silver nanoparticle dispersion of the stable particle size 10nm of macromolecule protection, after dialysis removes excess macromolecule protective agent, freeze-dry, be mixed with the mass concentration of 18% with double distilled water after autoclaving solution of silver nanoparticles. Before adding the polymer dispersant, the toxic effect of silver nanoparticles on K-562 cells was detected by MTT colorimetry, and the results are shown in figure 1 . Prove that silver nanoparticles can be used.
[0047] 2) Add 2 mL of hexanediol as a co-solvent in 0.80 g of butylene and styrene copolymer (macromolecule dispersant), after dissolving completely, add the silver nanoparticle solution with a mass concentration of 18% prepared above 4 ...
Embodiment 3
[0050] Embodiment 3, the preparation of ESF cell chip template
[0051] Prepare the inkjet ink soluble ink containing platinum nanoparticles with a particle size of 25nm, the specific preparation method is as follows:
[0052] 1) First prepare the stable particle diameter 25nm platinum nanoparticle dispersion of macromolecule protection, dialyze to remove excess polymer protective agent, freeze-dry, and prepare the mass concentration of 8% with double distilled water after autoclaving Platinum nanoparticles solution. Before adding the polymer dispersant, the toxic effect of platinum nanoparticles on ESF cells was detected by MTT colorimetry, and the results are shown in figure 1 . Prove that platinum nanoparticles can be used.
[0053] 2) First add 2 mL of glycerol to 0.80 g of gelatin and glutaraldehyde cross-linked compound (polymer dispersant). After the dissolution is complete, add 4.0 mL of platinum nanoparticle solution with a mass concentration of 8% to the solution ...
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