High-strength photosensitive hydrogel as well as preparation method and application thereof
A high-intensity light, hydrogel technology, used in the introduction of foreign genetic material, tumor/cancer cells, animal cells, etc. using a carrier, can solve problems such as gel damage and weak hydrogel mechanical properties, and achieve high water absorption. , Significant photosensitivity, simple preparation method
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Embodiment 1
[0031] Polymerize monomer oligoethylene glycol methacrylate (6 mg), 2-vinyl-4,6-diamino-1,3,5-triazine (6 mg), SP (0.6 mg) and crosslinker Ethylene glycol diacrylate (8.4 mg) was added to a 1.5 ml centrifuge tube, and after dissolving the monomer and crosslinker with 210 μl of DMSO, the photoinitiator Irgacure 2959 (0.5 mg) was added. The solvent containing monomer, crosslinking agent and initiator is injected into the closed mold, and the mold is irradiated in a UV curing box for 30 minutes to initiate free radical polymerization. Then the mold was opened to take out the gel, rinsed several times with deionized water and soaked for 7 days, and the deionized water was replaced every 12 hours.
[0032] Cell culture and detachment on the gel surface: The obtained gel was sterilized by immersing in medical alcohol for 4 hours, then put into a 96-well plate, and 200 μl of DMEM medium was added to replace the medical alcohol. Add the L929 cell suspension to the culture plate with ...
Embodiment 2
[0035] Polymerize the monomer oligoethylene glycol methacrylate (6 mg), 2-vinyl-4,6-diamino-1,3,5-triazine (12 mg), SP (0.9 mg) and the crosslinker Ethylene glycol diacrylate (12.6mg) was added to a 1.5ml centrifuge tube, and after 315μl of DMSO was used to dissolve the monomer and crosslinker, the photoinitiator Irgacure 2959 (0.7mg) was added. The solvent containing monomer, crosslinking agent and initiator is injected into the closed mold, and the mold is irradiated in a UV curing box for 30 minutes to initiate free radical polymerization. Then the mold was opened to take out the gel, rinsed several times with deionized water and soaked for 7 days, and the deionized water was replaced every 12 hours.
[0036] Cell culture and detachment on the gel surface: The obtained gel was sterilized by immersing in medical alcohol for 4 hours, then put into a 96-well plate, and 200 μl of DMEM medium was added to replace the medical alcohol. Add the L929 cell suspension to the culture ...
Embodiment 3
[0039] Polymerize monomer oligoethylene glycol methacrylate (6 mg), 2-vinyl-4,6-diamino-1,3,5-triazine (18 mg), SP (1.2 mg) and crosslinker Ethylene glycol diacrylate (16.8mg) was added to a 1.5ml centrifuge tube, and after 420μl of DMSO was used to dissolve the monomer and crosslinker, the photoinitiator Irgacure 2959 (0.9mg) was added. The solvent containing monomer, crosslinking agent and initiator is injected into the closed mold, and the mold is irradiated in a UV curing box for 30 minutes to initiate free radical polymerization. Then the mold was opened to take out the gel, rinsed several times with deionized water and soaked for 7 days, and the deionized water was replaced every 12 hours.
[0040] Cell culture and detachment on the gel surface: The obtained gel was sterilized by immersing in medical alcohol for 4 hours, then put into a 96-well plate, and 200 μl of DMEM medium was added to replace the medical alcohol. Add the L929 cell suspension to the culture plate wi...
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