Preparation method of multifunctional electrospinning scaffold for bone regeneration
A multi-functional, bone regeneration technology, applied in the direction of electrospinning, tissue regeneration, pharmaceutical formulations, etc., can solve the problems of shortening the transplantation time and success rate of in vitro culture, slow and long-lasting release, etc., and achieves controllable equipment cost and good stability , the effect of simple process
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[0030] A preparation method of a multifunctional electrospun scaffold for bone regeneration described in the present invention (the embodiment of the present invention discloses a preparation method of a three-dimensional multifunctional tissue engineering scaffold with antibacterial, osteogenic and angiogenesis-promoting), specifically The operation steps are as follows:
[0031] (1), prepare lysophosphatidic acid nanoparticles and deferoxamine nanoparticles respectively, and set aside for later use;
[0032] Specifically, the preparation method for preparing lysophosphatidic acid nanoparticles and deferoxamine nanoparticles is: the desolvation method can be selected to prepare albumin-coated lysophosphatidic acid nanoparticles;
[0033] Deferoxamine nanoparticles are prepared by two-step method to prepare lipid nanoparticles or organic solvent volatilization method to prepare nanoparticles such as liposomes;
[0034] In order to ensure sustained release, the prepared lysoph...
Embodiment 1
[0047] Nanoparticle preparation: Lysophosphatidic acid nanoparticles were prepared with lysophosphatidic acid as the active substance, albumin, chitosan, and absolute ethanol as auxiliary materials, with a particle size of about 250nm and a PDI of 0.23; deferoxamine as the active substance, phospholipids, Glycerol, SPAN80, and Tween 80 were used as excipients to prepare deferoxamine lipid nanoparticles, with a particle size of about 280 nm and a PDI of 0.18; the obtained nanoparticle solution was frozen at -80°C and then freeze-dried for 24 hours;
[0048] Preparation of electrospinning solution: Weigh polycaprolactone and polylactic acid copolymers and distribute them as 0.5g and 0.5g; add them into 6ml of hexafluoroisopropanol solvent, and stir evenly on a magnetic stirrer to obtain a polymer solution; Take 4.2ml of the solution, add 20mg of lysophosphatidic acid nanoparticles, add 23mg of zinc oxide nanoparticles, and stir until evenly distributed; at the same time, take 1.8...
Embodiment 2
[0052] Nanoparticle preparation: Lysophosphatidic acid nanoparticles were prepared with lysophosphatidic acid as the active substance, albumin, chitosan, and absolute ethanol as auxiliary materials, with a particle size of about 120nm and a PDI of 0.18; deferoxamine as the active substance, phospholipids, Glycerol and SPAN80 were used as auxiliary materials to prepare deferoxamine lipid nanoparticles with a particle size of about 336nm and a PDI of 0.21; the obtained nanoparticle solution was frozen at -80°C and then freeze-dried for 24 hours;
[0053] Preparation of electrospinning solution: Weigh 1g of silk fibroin; add it to 6ml of trifluoroethanol and dichloromethane mixed solvent, stir evenly on a magnetic stirrer to obtain a polymer solution; take 4.2ml of the solution and add lysophosphatidic acid nano 40 mg of particles, add 15 mg of zinc oxide nanoparticles, magnetically stir until evenly distributed; at the same time take 1.8ml of the solution, add 4 mg of deferoxamin...
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