A three-dimensionally printed strontium-containing mesoporous bioglass scaffold loaded with soybean isoflavones and its preparation method
A technology of soybean isoflavones and bioglass, applied in the field of biomedical materials, to achieve the effects of treating osteoporosis, excellent in vivo osteogenic activity, and good biocompatibility
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Embodiment 1
[0037] Example 1: Preparation of a three-dimensionally printed strontium-containing mesoporous bioglass scaffold loaded with soybean isoflavones
[0038] A method for preparing a three-dimensionally printed strontium-containing mesoporous bioglass support loaded with soybean isoflavones according to the present invention comprises the following steps:
[0039] Step 1, preparing strontium-containing bioactive glass powder, passing through a 400-mesh sieve to make its size smaller than 37 μm, dissolving soybean isoflavones in phosphate buffer saline (phosphate buffer saline, PBS) to obtain 100 mg / ml soybean isoflavones solution, soak strontium-containing mesoporous bioglass powder in a PBS solution containing 100 mg / ml for 24 hours, load soybean isoflavones into the mesoporous pores of Sr-MBG; dry and store the powder for later use;
[0040] For the preparation method of strontium-containing bioactive glass powder, please refer to the literature Zhang J, Zhao S, Zhu Y, et al.Thr...
Embodiment 2
[0045] Example 2: Adhesion of MC3T3-E1 cells on a three-dimensionally printed strontium-containing mesoporous bioglass scaffold loaded with soybean isoflavones
[0046] MC3T3-E1 cells (mouse embryonic osteoblast precursor cells) were purchased from the Cell Bank of the Chinese Academy of Sciences.
[0047] Three-dimensionally printed strontium-containing mesoporous bioglass scaffold material samples were soaked in 75% medical alcohol for 4 hours, and then sterilized under ultraviolet light for 24 hours. At the same time, 1ml of α-MEM containing 10% FBS was added to the 24-well plate for culture The substrate was pre-wetted for 24 hours, the medium was replaced, and then the sterilized scaffold material was transferred into a 24-well plate. Then, will contain 1×10 5 200 μl of culture medium of MC3T3-E1 cells was added dropwise to each sample, and incubated at 37°C, 5% CO 2 Atmosphere CO 2 Cultivate in an incubator, and after 8 hours the cells basically adhere to the wall, ad...
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