Bone repair stent material capable of realizing controlled-release of traditional Chinese medicine and preparation method thereof
A scaffold material and bone repair technology, applied in the field of biomedicine, can solve the problems such as the inability of pre-formed bone cement, the inability to provide appropriate physiological space for cell growth, and the difficulty in repairing large areas, achieving broad clinical application prospects for bone repair and excellent biological Active and biocompatible, easy to store effects
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Embodiment 1
[0029]Using absolute ethanol as the medium, the nano-hydroxyapatite powder and Epimedium extract (purchased from Shaanxi Hebo Natural Products Co., Ltd., the main component is icariin) were fully mixed at a weight ratio of 94 / 6, After freeze-drying, it is ready for use. Add 5g of the above powder into the dichloromethane solution in which 5g of polylactic acid has been dissolved, ultrasonically disperse the suspension sufficiently, then add the suspension to 100ml of 1% gelatin solution, and vigorously stir in a water bath at 35°C (1500r / min ) for 5 hours, microporous filtration three times, washed with distilled water for 5 times, and freeze-dried to obtain drug-loaded composite microcapsules with a particle size of 100 to 400 μm; take 5 g of the drug-loaded composite microcapsules and add them to 100 ml of acetic acid solution containing 0.5 to 2 wt % collagen , and add auxiliary materials such as hyaluronic acid 0.5 ~ 1g, and after uniform stirring, use ethylene sulfonic ac...
Embodiment 2
[0031] With absolute ethanol as the medium, the nano-hydroxyapatite powder and drynaria drynaria extract (purchased from Zelang Pharmaceutical Technology Development Co., Ltd.) were fully mixed at a weight ratio of 95 / 5, freeze-dried, and set aside. Add 5g of the above powder into the dichloromethane solution in which 5g of polylactic acid has been dissolved, ultrasonically disperse the suspension sufficiently, then add the suspension to 100ml of 1% gelatin solution, and vigorously stir in a water bath at 35°C (1500r / min ) for 5 hours, microporous filtration three times, washed with distilled water for 5 times, and freeze-dried to obtain drug-loaded composite microcapsules with a particle size of 100 to 400 μm; take 5 g of the drug-loaded composite microcapsules and add them to 100 ml of acetic acid solution containing 0.5 to 2 wt % collagen , and add auxiliary materials such as hyaluronic acid 0.5 ~ 1g, and after uniform stirring, use ethylene sulfonic acid (MES) as a buffer t...
Embodiment 3
[0032] Example 3: Performance Research of Icariin-Chitosan / Hydroxyapatite (CS / HA) Composite Material
[0033] (1) Cytocompatibility of icariin-CS / HA composites
[0034] The biocompatibility of the icariin-CS / HA scaffold was evaluated by material extraction method and direct contact method. Different groups of material extracts and common DMEM were used to culture hBMSCs seeded at low density for 48 hours. Compared with the control group, the CS / HA group did not reduce the proliferation activity of hBMSCs, indicating that the CS / HA composite material itself had no cytotoxicity; 3 Doses of icariin-CS / HA groups reduced the proliferation activity of hBMSCs to varying degrees, which was related to the drug loading dose. After the cells were inoculated at high density, their proliferation activity was inhibited. After culturing hBMSCs for 10 days with the extracts of three kinds of icariin materials, the ALP content in the cells increased significantly by 7-9 times, indicating that...
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