Preparation method of nanomotor-hydrogel system for gene-targeted therapy
A targeted therapy and hydrogel technology, applied in nanotechnology, nanotechnology, nanomedicine, etc., can solve the problem of difficulty in entering cells, achieve low cytotoxicity, good gene targeted therapy effect, and increase the effect of retention time.
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[0026] A preparation method of an injectable high cell uptake nanomotor-hydrogel system for gene-targeted therapy of the present invention, comprising the following steps:
[0027] Step 1. First drop the platinum nanoparticle solution on the substrate and dry it;
[0028] Step 2. Then soak the substrate in polyethyleneimine solution, take out the substrate, wash it with ultrapure water several times, then soak the substrate in sodium polystyrene sulfonate solution, take out the substrate, and wash it with ultrapure water repeatedly;
[0029] Step 3. Repeat step 2 repeatedly, assemble polyethyleneimine and sodium polystyrene sulfonate on the surface of platinum nanoparticles, and assemble folic acid-modified polyethyleneimine on the outermost layer to obtain nanocarriers;
[0030] Step 4. Use ultrasound to disperse the nano-carrier in mold-free sterile water, and connect the small molecule interfering RNA to the nano-carrier through electrostatic interaction to obtain a nanomo...
Embodiment 1
[0034] Drop 3 mg / mL platinum nanoparticle solution on the substrate and dry it; then soak the substrate in 3 mg / mL polyethyleneimine solution for 5 min, take out the substrate, wash it with ultrapure water for 3 times, and then put The substrate was soaked in 3 mg / mL sodium polystyrene sulfonate solution for 5 min, the substrate was taken out, and washed 3 times with ultrapure water; the steps were repeated 15 times to assemble polyethyleneimine and polystyrene sulfonate on the surface of platinum nanoparticles. Sodium acid, and folic acid-modified polyethylenimine was assembled on the outermost layer to obtain nanocarriers; the nanocarriers were dispersed in mold-free sterile water (concentration 3 mg / mL) by ultrasound, and mixed with 5 mM small interfering RNA in React in an ice bath for 1 hour to obtain nanomotors; mix 40 mg / mL chitosan solution and 17 mg / mL dialdehyde starch solution (containing 3 mg / mL nanomotors) to prepare an injectable high Cellular uptake of nanomotor...
Embodiment 2
[0038] Drop 1 mg / mL platinum nanoparticle solution on the substrate and dry it; then soak the substrate in 2 mg / mL polyethyleneimine solution for 5 min, take out the substrate, wash it with ultrapure water for 3 times, and then put The substrate was soaked in 2 mg / mL sodium polystyrene sulfonate solution for 5 min, the substrate was taken out, and washed 3 times with ultrapure water; the steps were repeated 10 times to assemble polyethyleneimine and polystyrene sulfonate on the surface of platinum nanoparticles. Sodium acid, and folic acid-modified polyethylenimine was assembled on the outermost layer to obtain nanocarriers; the nanocarriers were dispersed in mold-free sterile water (concentration 3 mg / mL) by ultrasound, and mixed with 5 mM small interfering RNA in React in an ice bath for 1 hour to obtain nanomotors; mix 40 mg / mL chitosan solution and 20 mg / mL dialdehyde starch solution (containing 3 mg / mL nanomotors) to prepare an injectable high Cellular uptake of nanomotor...
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