Gel-poly(lactide-co-glycolide) (PLGA) two-phase gradient transition cartilage-bone repair material and preparation thereof
A gradient transition and bone repair technology, applied in bone implants, medical science, prostheses, etc., can solve the problems that the multiphase gradient scaffold cannot realize the continuous gradient of the components in the transition zone, and is easy to fall off and separate, so that it is not easy to separate and fall off , Simple preparation process, good biocompatibility effect
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Embodiment 1
[0016] 1. Weigh 0.11g of gelatin microspheres with a diameter of 350-450μm and place them in a columnar template with a diameter of 6mm, then press them into a glass mold with a tapered tip (5mm in diameter, 2mm in height), and drop 100μL A solution with a ratio of ethanol to water of 8 / 2 was cross-linked at 37°C for 15 minutes to obtain a gelatin skeleton.
[0017] 2. Immerse the gelatin skeleton in 7% poly(lactide- co -glycolide) (PLGA) in dichloromethane solution, soak for 12 hours, and remove the gas in the pores in a vacuum oven to ensure that the solution enters completely. Take out the stent, blot the surface solution dry, separate the phases in the refrigerator (-20°C) for 12 hours, and replace with ethanol for 12 hours. Finally, the gelatin skeleton was washed away in water at 37° C. to obtain a poly(lactide-lactide- co - glycolide) (PLGA) porous scaffold. The scaffolds were dried in a vacuum oven and stored at -20 °C.
[0018] 3. Weigh 8.9mg of carboxymethyl chit...
Embodiment 2
[0021] 1. Weigh 0.15g of gelatin microspheres with a diameter of 350~450μm and place them in a columnar template with a diameter of 6mm, then press them into a glass mold with a tapered tip (5mm in diameter, 3mm in height), and drop 100μL A solution with a ratio of ethanol to water of 8 / 2 was cross-linked at 37°C for 30 minutes to obtain a gelatin skeleton.
[0022]2. Immerse the gelatin skeleton in 6% poly(lactide- co -glycolide) (PLGA) in dichloromethane solution, soak for 12 hours, and remove the gas in the pores in a vacuum oven to ensure that the solution enters completely. Take out the stent, blot the surface solution dry, separate the phases in the refrigerator (-20°C) for 12 hours, and replace with ethanol for 12 hours. Finally, the gelatin skeleton was washed away in water at 37° C. to obtain a poly(lactide- co - glycolide) (PLGA) porous scaffold. The scaffolds were dried in a vacuum oven and stored at -20°C.
[0023] 3. Weigh 5.6 mg of carboxymethyl chitosan modi...
Embodiment 3
[0026] 1. Weigh 0.11g of gelatin microspheres with a diameter of 350-450μm and place them in a columnar template with a diameter of 6mm, then press them into a glass mold with a tapered tip (5mm in diameter, 2mm in height), and drop 100μL A solution with a ratio of ethanol to water of 8 / 2 was cross-linked at 37°C for 15 minutes to obtain a gelatin skeleton.
[0027] 2. Immerse the gelatin skeleton in 9% poly(lactide- co -glycolide) (PLGA) in dichloromethane solution, soak for 12 hours, and remove the gas in the pores in a vacuum oven to ensure that the solution enters completely. Take out the stent, blot the surface solution dry, separate the phases in the refrigerator (-20°C) for 12 hours, and replace with ethanol for 12 hours. Finally, the gelatin skeleton was washed away in water at 37° C. to obtain a poly(lactide-lactide- co - glycolide) (PLGA) porous scaffold. The scaffolds were dried in a vacuum oven and stored at -20°C.
[0028] 3. Weigh 12 mg of carboxymethyl chito...
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