Application of bioactive composite material in periodontal bone defect repair and/or periodontal bone regeneration
A technology of bioactive and composite materials, which is applied in the field of application of bioactive composite materials in periodontal bone defect repair and/or periodontal bone regeneration, which can solve the problems of complex surgery, slow degradation, easy to cause inflammation, etc., and achieve simplification The operation steps and preparation process are simple, and the effect of shortening the operation time
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[0043] The preparation method of the present invention will be further described in detail in conjunction with specific examples below. It should be understood that the following examples are only for illustrating and explaining the present invention, and should not be construed as limiting the protection scope of the present invention. All technologies realized based on the above contents of the present invention are covered within the scope of protection intended by the present invention.
[0044] The experimental methods used in the following examples are conventional methods unless otherwise specified; the reagents and materials used in the following examples can be obtained from commercial sources unless otherwise specified.
[0045] Biological testing methods are as follows:
[0046] 1. Cell culture
[0047] To evaluate the effect of bioactive nanoparticles on osteoblasts and fibroblasts, we chose mouse osteoblast cell line MC3T3-El, mouse fibroblast cell line L929 and...
preparation example 1
[0060] Preparation Example 1: Preparation of Bioactive Nanoparticles and Biological Test Results
[0061] 0.2 mL of 3-methacryloxypropyltrimethoxysilane and 0.6 mL of isoamyl acetate were added to 40 mL of pure water. The pH of the solution was adjusted to 10. After ultrasonication for 15 minutes, nitrogen gas was introduced for 20 minutes to remove the oxygen in the reaction bottle. The mixture system was heated to 70° C., 10 mg of potassium persulfate was added, and the polymerization reaction was continued for 20 hours to terminate the reaction. Then the centrifuge was centrifuged at a speed of 10,000 rpm for 15 minutes to collect a white precipitate, which was washed three times with ethanol. The nanoparticles are dispersed in water to form a colloidal solution. 300mL saturated Ca(OH) 2 The solution is added to the colloidal solution of the above particles, Ca(OH) 2 The molar ratio to nanoparticles is 50:1. After the system was stirred at 25° C. for 24 hours, the preci...
preparation example 2
[0064] Preparation Example 2: Preparation of Bioactive Nanoparticles
[0065] At room temperature, 4.48 mL of silica dispersion (Ludox TM40) with a solid content of 40% and 4 mL of 3-methacryloxypropyltrimethoxysilane were added to 150 mL of pure water, and stirred for 24 hours to form an emulsion. Nitrogen gas was introduced into the emulsion, and after deoxygenation for 30 minutes, the temperature of the system was raised to 70° C., and 25 mg of potassium persulfate was added to initiate polymerization, and the polymerization reaction continued for 24 hours. The emulsion was centrifuged at 11,000 rpm for 15 minutes to collect a white precipitate, which was washed three times with ethanol. 100 mL of saturated CaCl 2 solution was added to the colloidal solution of the above particles, CaCl 2 The molar ratio to nanoparticles is 100:1. After the system was stirred at 15° C. for 48 hours, the precipitate was collected by centrifugation, washed with pure water, and dried to obt...
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