A kind of hydroxyapatite nanorod with surface grafted egcg and its preparation method and application
A technology of hydroxyapatite and surface grafting, which is applied in the field of nanomaterials, can solve the problems of limited clinical application and poor bioavailability, and achieve the effects of increasing the application range, supporting bone growth, and improving stability
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Embodiment 1
[0036] The preparation method of a kind of hydroxyapatite surface grafting EGCG of the present embodiment, the specific preparation steps are as follows:
[0037] (1) Octadecylamine (1.0 g, 2.0 g, 3 g, 4 g, 6 g, 12 g) was dissolved in oleic acid (12 ml), and the heating temperature was 100°C. Add 48ml ethanol and stir to mix, then add 25ml Ca(NO 3 ) 2 .4H 2 O (0.25mol / L) solution, after stirring for 10min, add 25ml Na 3 PO 4 ·12H 2 O (0.15mol / L) aqueous solution, stirred for about 10min. Then transfer to a 150ml polytetrafluoroethylene hydrothermal reactor, seal the reactor, react at 150°C for 10h, and cool the autoclave to room temperature. Centrifuged, washed several times with cyclohexane, ethanol and water, and dried to obtain samples OA-OM-HA-1, OA-OM-HA-2, OA-OM-HA-3, OA-OM-HA-4, respectively , OA-OM-HA-6, OA-OM-HA-12, select the appropriate size OA-OM-HA-4 for subsequent experiments.
[0038] (2) Disperse 50 mg of OA-OM-HA-4 nanorods in 20 mL of cyclohexane, and...
Embodiment 2
[0042] The preparation method of a kind of hydroxyapatite surface grafting EGCG of the present embodiment, the specific preparation steps are as follows:
[0043] (1) The preparation of OA-OM-HA is the same as that of Example 2.
[0044] (2) Disperse 50 mg of OA-OM-HA-4 nanorods in 20 mL of acetone, and add phosphoethanolamine solution (50 mg in 20 mL of deionized water) in an ice bath with vigorous stirring at 1000 r / min, and react for 12 h. Centrifuged, washed three times with deionized water, and dried to obtain the sample HA-NH 2 .
[0045] (3) EGCG (0.05 mM) was dissolved in 3 ml of dry DMSO and added to a single-necked flask. Next, 1,1'-carbonyldiimidazole (0.05 mM) was added and the reaction was allowed to 2 Atmosphere and stirring in the dark for 24h. Then, the HA-NH 2 (20 mg) was added to the above solution and the reaction was allowed to proceed in the dark at room temperature for 24 h. After centrifugation, the product was washed several times with DMSO and ab...
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