Porous PCL-TCP (polycaprolactone-tricalcium phosphate) artificial bone scaffold with drug sustained release function and preparation method of porous PCL-TCP artificial bone scaffold

An artificial bone and drug technology, applied in the fields of medical formula, drug delivery, medical science, etc., can solve the problems of reducing osteoblast activity and bone reconstruction function, cortical bone microporous bone strength, and bone defect difficult to heal, etc., to achieve Good mechanical support and degradable properties, promoting early osseointegration and osseointegration, and good osseointegration ability

Active Publication Date: 2019-09-27
FOURTH MILITARY MEDICAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0004] The main reason why diabetes makes it difficult to heal bone defects is that the disorder of blood sugar produces blood sugar oxidation products that destroy the microvascular and mu

Method used

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  • Porous PCL-TCP (polycaprolactone-tricalcium phosphate) artificial bone scaffold with drug sustained release function and preparation method of porous PCL-TCP artificial bone scaffold
  • Porous PCL-TCP (polycaprolactone-tricalcium phosphate) artificial bone scaffold with drug sustained release function and preparation method of porous PCL-TCP artificial bone scaffold
  • Porous PCL-TCP (polycaprolactone-tricalcium phosphate) artificial bone scaffold with drug sustained release function and preparation method of porous PCL-TCP artificial bone scaffold

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Embodiment Construction

[0025] The present invention will be described in further detail below in conjunction with the accompanying drawings.

[0026] 1) Preparation of chitosan microspheres loaded with bone formation-promoting drugs by emulsification cross-linking method

[0027] First, take 100mg ~ 1500mg chitosan and dissolve it in 8 ~ 75ml dilute acetic acid solution with a volume concentration of 1 ~ 5%, and ultrasonically disperse the chitosan to completely dissolve the chitosan solution; secondly, according to 1:1 ~ 8: Add bone-promoting drugs (parathyroid hormone, fluoride, growth hormone or statins) to a zinc acetate solution with a volume concentration of 1% to 10%, incubate at 4°C for 24 to 48 hours, freeze Dry collection of Zn-drug powder;

[0028] Then, stir the chitosan solution and the Zn-drug powder evenly according to the volume-to-mass ratio of 5:1-30:1, and slowly add 50ml-300ml of Span 80 liquid paraffin solution with a volume concentration of 1%-5%. , stir evenly, and then drop...

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Abstract

The invention provides a preparation method of a porous PCL-TCP (polycaprolactone-tricalcium phosphate) artificial bone scaffold with a drug sustained release function. The PCL-TCP artificial bone scaffold prepared with the method has biological activity and regular pore diameter, the porosity is higher than or equal to 60%, the pore diameter is in a range of 300-500 mu m, the compressive strength is higher than or equal to 20 MPa, the compression modulus is 0.5-1 GPa, the degradation time of the PCL-TCP artificial bone scaffold is gradually prolonged from the edge layer to the middle layer, the degradation time of the middle layer of the scaffold is 1-3 years, the degradation time of the edge layer is 2-6 months, besides, composite printing with chitosan microspheres/collagen wires is performed, chitosan microspheres wrap a drug for promoting bone formation, and the sustained release function of the drug is played. The prepared PCL-TCP artificial bone scaffold has elasticity modulus and mechanical strength which are close to those of natural bone tissue, a porous structure and the chitosan microspheres in the porous structure can realize sustained release of the drug for promoting bone formation, new bone tissue is induced to grow, the problem about bone-material interface bonding is solved, a good osseointegration effect is realized, the PCL-TCP artificial bone scaffold has better mechanical compatibility and osseointegration capacity than a metal material, and the ideal material and preparation method are provided for overcoming poor bone healing of a patient with bone defects.

Description

technical field [0001] The invention belongs to the field of bone fusion internal fixation for large segmental bone defects, and in particular relates to a porous PCL-TCP artificial bone support with drug slow release function and a preparation method thereof. Background technique [0002] At present, the methods used clinically to treat bone defects include autologous bone graft, allogeneic bone graft and artificial bone scaffold graft. Autologous bone grafts cause damage to the patient's donor site; the source of allogeneic bone grafts is limited, with potential risks of disease transmission and immune rejection; degradable artificial bone scaffolds overcome the defects of autologous bone and allogeneic bone, but currently commonly used tricalcium phosphate (tricalcium phosphate) Phosphate, TCP), polycaprolactone (polycaprolactone, PCL), poly L-lactic acid (poly (L-lactic acid), PLLA) and poly lactic acid-glycolic acid (poly (lactic acid-hydroxyacetic acid), PLGA) and othe...

Claims

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Application Information

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IPC IPC(8): A61L27/56A61L27/50A61L27/58A61L27/18A61L27/12A61L27/54A61L27/20A61L27/24
CPCA61L27/12A61L27/18A61L27/20A61L27/24A61L27/50A61L27/54A61L27/56A61L27/58A61L2300/252A61L2300/412A61L2300/604A61L2300/622A61L2430/02C08L67/04C08L5/08
Inventor 郭征王宁伍苏华
Owner FOURTH MILITARY MEDICAL UNIVERSITY
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