Preparation method of bone repair scaffold with drug sustained release and antibacterial effects
A technology of antibacterial effect and bone repair, applied in medical science, prosthesis, etc., can solve the problems of PLLA brittleness, non-union, unfavorable cell adhesion and proliferation, etc., and achieve the effect of accelerating bone repair, promoting proliferation and differentiation
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[0017] The invention provides a preparation method of a bone repair scaffold with slow drug release and antibacterial effect, which comprises the following steps:
[0018] First, mix MBG powder with PLLA powder, ultrasonically disperse, ball mill, and dry to obtain a composite powder, which is subjected to selective laser sintering to obtain a PLLA / MBG bone scaffold; mesoporous bioactive glass (MBG) is an inorganic material, which After compounding with PLLA polymer, the hydrophobic properties of the polymer can be significantly improved, and the biocompatibility can be improved. As a bone scaffold material, it can provide good mechanical properties and an environment for cell migration and adhesion, and the MBG degradation product is non-toxic and non-toxic. Harmful, can be metabolized by the human body. In the implementation process, the mass ratio of MBG powder to PLLA powder is 1:(5-10), and the particle size of the composite powder is 50-100 microns, so that MBG has enoug...
Embodiment
[0022] According to the mass ratio of 1:10, MBG powder and PLLA powder were mixed, dispersed by ultrasonic, and ball-milled into a composite powder with an average particle size of about 100 microns, which was then dried for use, and then selectively laser sintered into a diameter of about 5 mm and a height of about 5 mm. 10mm cylindrical PLLA / MBG bone scaffold; then, immerse the PLLA / MBG bone scaffold in a 6g / L chitosan hydrogel solution for 1 hour, then put it into an oven to dry at 37°C, take it out, rinse it with ultrapure water, and then rinse it with ultrapure water. Put into 5% NaOH solution for 30min, and then rinsed with ultrapure water for 3 times to obtain PLLA / MBG / CS scaffold; then immerse PLLA / MBG / CS scaffold in 2g / L Slit3 solution for 1 hour at 37℃ , then take out -20°C freeze and dry to obtain a PLLA / MBG / CS scaffold loaded with Slit3, cut out a small section of the PLLA / MBG / CS scaffold to expose the cross section, and detected by electron microscope, the MBG pore...
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