Injectable hydrogel system and preparation method thereof
A hydrogel and system technology, applied in the field of injectable hydrogel system and its preparation, can solve the problems of expensive treatment, unstable curative effect, and long time consumption
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Embodiment 1
[0043] Such as figure 1 with figure 2 As shown, weigh 1g of TG-18 and 100mg of rosiglitazone and add them to the solvent to obtain a mixed solution. The volume of the solvent is 10mL, and the volume ratio of DMSO to water in the solvent is 1:4, and then the mixed solution is heated Keep at 65°C for 15 minutes until TG-18 is completely dissolved, and then when the temperature is lowered to room temperature, an injectable hydrogel system will form after 10 minutes.
[0044] In the present embodiment, TG-18 is amphiphile triglyceride monostearate
Embodiment 2
[0046] Such as image 3Shown, the material properties of rosiglitazone hydrogel. Specifically, a, b: prepare blank TG-18 hydrogel and rosiglitazone hydrogel (the preparation process is the same as above), after vacuum freeze drying, the sample is gold-plated and photographed with a scanning electron microscope, and the blank can be observed The TG-18 hydrogel showed a lamellar structure, while the encapsulated rosiglitazone drug showed a fibrous structure in it. c, d: Rheological testing of TG-18 hydrogel and rosiglitazone hydrogel, it is found that when the temperature drops from 65 °C, the elastic modulus G' increases rapidly, and the formation of TG-18 hydrogel The gel temperature was 58.21°C and the rosiglitazone hydrogel was 60.78°C. e: As the shear rate increased, the viscosity of TG-18 hydrogel and rosiglitazone hydrogel decreased significantly, which indicated that both gels had shear-thinning behavior and were suitable for injection (shear rate From 0.1 to 100w / rad...
Embodiment 3
[0049] Such as Figure 4 As shown, specifically a, b: take the eyelid tissue of C57 / B6J mice, use micro scissors to remove the skin, subcutaneous tissue and conjunctiva of the eyelids under a microscope, and obtain simple mouse meibomian glands, and then use collagenase and Dispase The primary meibomian gland epithelial cells of mice were cultured after enzymatic digestion and inoculated on culture dishes; the meibomian gland epithelial cells were co-cultured with TG-18 hydrogel and rosiglitazone hydrogel for 2 days, and then stained with life and death Kit, the cells were stained for life and death and photographed. Green fluorescence showed live cells, and red fluorescence showed dead cells. It was found that neither rosiglitazone hydrogel nor TG-18 hydrogel could induce meibomian gland epithelial Cell death; c: The eyelid tissues of the experimental mice in each group were obtained and stained with HE. The staining observation found that there was no obvious inflammatory ce...
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