Hydrogel tissue filling agent for ophthalmology and preparation method thereof
The technology of hydrogel and filler is applied in the field of ophthalmic hydrogel tissue filler and its preparation, which can solve the problems of low volume swelling and inability to meet the requirements, achieve good tolerance and biocompatibility, and reduce complications Symptoms, excellent swelling ability and the effect of mechanical strength
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2010-01-20
- Estimated Expiration
- Not applicable · inactive patent
Smart Images
Figure 1
Abstract
Description
technical field
[0001] The invention relates to a novel ophthalmic hydrogel tissue filler and a preparation method thereof. Background technique
[0002] Orbital development continues from birth through adolescence, and normal development of the bony orbit is dependent on the presence of a normal eyeball. In clinical work, eyeballs are often enucleated due to severe ocular trauma, intraocular malignant tumors, and blindness and painful eyes caused by various eye diseases. In ophthalmic surgery, the average enucleation rate is 218 / 100,000. After enucleation in adults, post-enucleation syndrome often results. After children enucleate the eyeball, it will not only lead to enucleation syndrome, but also the orbital bone will lose the stimulating effect of the eyeball, resulting in retardation of orbital bone development, and severe facial deformities. Since Mules carried out eye enucleation in 1885 and Frost reported enucleation in 1886, many scholars have conducted a lot of ...
Examples
Embodiment 1
[0024] (1) The bulk polymerization method is adopted, with AIBN as the initiator, allyl MA and EGDM as the crosslinking agent, and NVP and MMA as the monomers to carry out the copolymerization reaction. The total raw material weight is 4g, the monomer composition is NVP / MMA=75 / 25, the amount of crosslinking agent allyMA / EGDM=0.19% / 0.026%, and the amount of initiator is 0.05%. In the triangular grinding mouth flask, according to the predetermined ratio, dissolve the initiator and cross-linking agent in NVP, then add MMA, stir to make all components mix completely. The monomer mixture was filtered, the filtrate was poured into a mold, and reacted in a constant temperature incubator at 80° C. for 24 hours.
[0025] (2) Take the sample synthesized in step (1), fully swell in physiological saline for 72 hours, place in a container with 20% NaOH solution (about 20ml), and react at a constant temperature at 70°C for 1 hour.
[0026] (3) Take the sample treated in step (2), wash it i...
Embodiment 2
[0028](1) The bulk polymerization method is adopted, with BPO as the initiator, allyl MA and EGDM as the crosslinking agent, and NVP and MMA as the monomers to carry out the copolymerization reaction. The total raw material weight is 4g, the monomer composition is NVP / MMA=80 / 20, the crosslinking agent addition allyMA / EGDM=0.38% / 0.052%, and the initiator dosage is 0.2%. In the triangular grinding mouth flask, according to the predetermined ratio, dissolve the initiator and cross-linking agent in NVP, then add MMA, stir to make all components mix completely. The monomer mixture was filtered, and the filtrate was poured into a mold, and reacted in a constant temperature incubator at 90° C. for 12 hours.
[0029] (2) Take the sample synthesized in step (1), fully swell in saline for 72 hours, place it in a container with 30% NaOH solution (about 20ml), and react at a constant temperature at 80°C for 4 hours.
[0030] (3) With step (3) in embodiment 1. The volume swelling degree ...
Embodiment 3
[0032] (1) The bulk polymerization method is adopted, with AIBN as the initiator, allyl MA and EGDM as the crosslinking agent, and NVP and MMA as the examples to carry out the copolymerization reaction. The total raw material weight is 4g, the monomer composition is NVP / MMA=65 / 35, the amount of crosslinking agent added is allyMA / EGDM=0.19% / 0.026%, and the amount of initiator is 0.08%. In the triangular grinding mouth flask, according to the predetermined ratio, dissolve the initiator and cross-linking agent in NVP, then add MMA, stir to make all components mix completely. The monomer mixture was filtered, and the filtrate was poured into a mold, and reacted in a constant temperature incubator at 80° C. for 24 hours.
[0033] (2) Take the sample synthesized in step (1), fully swell in normal saline for 72 hours, place it in a container with 10% NaOH solution (about 20ml), and react at a constant temperature at 60°C for 10 hours.
[0034] (3) With step (3) in embodiment 1. The...