An injectable-porous-drug-loaded polymethyl methacrylate-based composite scaffold bone graft material and its preparation method
A polymethyl methacrylate and composite stent technology, which is used in medical science, prosthesis, etc., can solve the problems of mismatching mechanical properties with natural bone, high polymerization reaction temperature, and shedding of surrounding tissue, so as to reduce the cost of treatment. , the matching of mechanical characteristics, the effect of improving the success rate
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2018-01-12
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Abstract
Description
Technical field
[0001] The invention belongs to the field of organic functional material preparation, and specifically relates to an injectable-porous-drug-loaded polymethyl methacrylate-based composite scaffold bone graft material and a preparation method thereof. Background technique
[0002] Bone transplantation has been dedicated to repairing large-scale bone defects caused by trauma, tumor, infection, etc., in order to restore the body's function and beauty. It is one of the most common transplant operations. Bone transplantation is divided into autologous bone transplantation, allogeneic bone transplantation and artificial bone replacement material transplantation according to the source of the graft. Autologous bone transplantation is the gold standard for bone repair and bone reconstruction. However, due to the limited sources, it will cause secondary trauma and cannot provide initial stability. Its clinical application is greatly restricted. Allogeneic bone grafts are e...
Examples
Embodiment 1
[0042] (1) Dissolve chitosan (CS) in a 0.1mol / L hydrochloric acid solution at room temperature to prepare a CS hydrochloric acid solution with a mass concentration of 2%. After the dissolution is complete, stir in an ice bath for 15 minutes.
[0043] (2) At the same time, dissolve sodium glycerophosphate (GP) in distilled water to prepare a 50% mass concentration GP solution, and place it in an ice bath for 15 minutes.
[0044] (3) Under constant stirring, slowly drop 0.5 mL of GP solution into 4.5 mL of CS hydrochloric acid solution, keep the solution free of turbidity, and stir for 20 minutes to obtain a uniformly mixed CS-GP solution.
[0045] (4) Add 25mg of gentamicin sulfate (GM) and 300mg of hydroxyapatite (HA) to the well-mixed CS-GP solution, and ultrasonic treatment to make it evenly mixed to obtain CS-GP / Nano-HA / GM mixture.
[0046] (5) Place the CS-GP / Nano-HA / GM mixed solution in a 37°C incubator, and form a CS-GP / Nano-HA / GM gel after 5 minutes.
[0047] (6) The CS-GP / Nano-...
Embodiment 2
[0050] (1) Dissolve chitosan (CS) in a 0.1mol / L hydrochloric acid solution at room temperature to prepare a CS hydrochloric acid solution with a mass concentration of 2%. After the dissolution is complete, stir in an ice bath for 15 minutes.
[0051] (2) At the same time, dissolve sodium glycerophosphate (GP) in distilled water to prepare a 50% mass concentration GP solution, and place it in an ice bath for 15 minutes.
[0052] (3) Under constant stirring, slowly drop 0.5 mL of GP solution into 4.5 mL of CS hydrochloric acid solution, keep the solution free of turbidity, and stir for 20 minutes to obtain a uniformly mixed CS-GP solution.
[0053] (4) Add 25mg vancomycin (VM) and 300mg hydroxyapatite (HA) to the well-mixed CS-GP solution, and ultrasonic treatment to make it evenly mixed to obtain a CS-GP / Nano-HA / VM mixed solution .
[0054] (5) Place the CS-GP / Nano-HA / VM mixed solution in a 37°C incubator and form a gel after 5 minutes.
[0055] (6) The CS-GP / Nano-HA / VM gel is freeze-dr...
Embodiment 3
[0058] (1) Dissolve chitosan (CS) in a 0.1mol / L hydrochloric acid solution at room temperature to prepare a CS hydrochloric acid solution with a mass concentration of 2%. After the dissolution is complete, stir in an ice bath for 15 minutes.
[0059] (2) At the same time, dissolve sodium glycerophosphate (GP) in distilled water to prepare a 50% mass concentration GP solution, and place it in an ice bath for 15 minutes.
[0060] (3) Under constant stirring, slowly drop 0.5 mL of GP solution into 4.5 mL of CS hydrochloric acid solution, keep the solution free of turbidity, and stir for 20 minutes to obtain a uniformly mixed CS-GP solution.
[0061] (4) Add 25mg of gentamicin sulfate (GM) and 300mg of hydroxyapatite (HA) to the well-mixed CS-GP solution, and ultrasonic treatment to make it evenly mixed to obtain CS-GP / Nano-HA / GM mixture.
[0062] (5) Place the CS-GP / Nano-HA / GM mixed solution in a 37°C incubator, and form a CS-GP / Nano-HA / GM gel after 5 minutes.
[0063] (6) Mix the powder ...