CN110559488A - calcium sulfate-containing polyetheretherketone particulate bone filling material and preparation method thereof - Google Patents

calcium sulfate-containing polyetheretherketone particulate bone filling material and preparation method thereof Download PDF

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CN110559488A
CN110559488A CN201911022125.3A CN201911022125A CN110559488A CN 110559488 A CN110559488 A CN 110559488A CN 201911022125 A CN201911022125 A CN 201911022125A CN 110559488 A CN110559488 A CN 110559488A
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caso
peek
particle size
particles
polyetheretherketone
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章培标
纪庆明
焦自学
王宗良
孙烁
王鹏
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Changchun Institute of Applied Chemistry of CAS
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Changchun Institute of Applied Chemistry of CAS
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/40Composite materials, i.e. containing one material dispersed in a matrix of the same or different material
    • A61L27/44Composite materials, i.e. containing one material dispersed in a matrix of the same or different material having a macromolecular matrix
    • A61L27/446Composite materials, i.e. containing one material dispersed in a matrix of the same or different material having a macromolecular matrix with other specific inorganic fillers other than those covered by A61L27/443 or A61L27/46
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • A61L27/56Porous materials, e.g. foams or sponges
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2430/00Materials or treatment for tissue regeneration
    • A61L2430/02Materials or treatment for tissue regeneration for reconstruction of bones; weight-bearing implants

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Abstract

The invention provides a calcium sulfate-containing polyetheretherketone particulate bone filling material and a preparation method thereof, wherein the method comprises the following steps: polyether ether ketone powder, concentrated sulfuric acid and CaSO4mixing and standing to obtain a mixed solution; the mixed solution is prepared into particles by adopting an air flow method and then is settled in ethanol-CaSO4in saturated solution, adding ethanol-CaSO4Soaking in saturated solution, and sieving; the obtained CaSO with the particle size of 500-600 mu m4-PEEK microparticles and CaSO4Carrying out hydrothermal treatment on the saturated liquid, and drying in vacuum to obtain the calcium sulfate-containing polyetheretherketone particulate bone filling material with the particle size of 400-500 mu m. The method adopts CaSO4The polyether ether ketone powder is blended to obtain a blended material which has high hydrophilicity, is beneficial to cell proliferation and adhesion, promotes cell differentiation and improves biomineralizationThe capability of enhancing the osteoinductive property and the biological activity of the material and promoting the full fusion with tissues. Can also be used as microcarrier for carrying growth factors.

Description

Calcium sulfate-containing polyetheretherketone particulate bone filling material and preparation method thereof
Technical Field
The invention belongs to the technical field of bone repair materials, and particularly relates to a calcium sulfate-containing polyetheretherketone particulate bone filling material and a preparation method thereof.
Background
In the orthopedic field, bone defects caused by various reasons such as severe trauma, bone tumors, osteomyelitis and the like are very common, especially large-area and irregular bone defects. What kind of material and way to perform the bone grafting operation is the hot spot of the current research. Currently, the bone repair materials commonly used in clinic include autologous bones, allogeneic bones, metal prostheses, polymer synthetic materials and the like. Although autogenous bone is an ideal bone defect repairing material, the bone taking process increases the trauma and pain of patients, the bone source is limited, the shaping is not easy, and the requirement of large-section bone transplantation is difficult to meet; allogeneic bone may transmit diseases and cause postoperative complications due to immunological rejection; the metal prosthesis is easy to loosen, break, and has poor histocompatibility and inflammatory reaction; the polymer synthetic material has the problems that the degradation rate is not matched with the osteogenesis rate, degradation byproducts change the surrounding microenvironment to influence bone repair and the like, and the clinical application is limited to different degrees.
Polyetheretherketone (PEEK) is a synthetic wholly aromatic semi-crystalline polymer with many excellent properties: high strength, toughness and rigidity, good oxidation resistance and fatigue resistance, and certain biocompatibility, so the PEEK can be applied to a plurality of fields, such as: medical treatment, aerospace, automobile manufacturing, chemical manufacturing, precision instrument manufacturing and other high-tech fields. However, the polyetheretherketone material is a biologically inert material, and needs to be modified to improve the bioactivity thereof, so that the polyetheretherketone material has wider application.
disclosure of Invention
In view of the above, the present invention aims to provide a calcium sulfate-containing polyetheretherketone particulate bone filler and a method for preparing the same, wherein the bone filler prepared by the method has excellent hydrophilicity.
the invention provides a preparation method of a polyether-ether-ketone particulate bone filling material containing calcium sulfate, which comprises the following steps:
Polyether ether ketone powder, concentrated sulfuric acid and CaSO4Mixing and standing to obtain a mixed solution;
Making the mixed solution into particles by adopting an air flow method, and settling the particles in ethanol-CaSO4In saturated solution, and then in CaSO4Soaking in saturated solution, and sieving to obtain CaSO with particle size of 500-600 μm4-PEEK microparticles;
The CaSO with the particle size of 500-600 mu m4-PEEK microparticles and CaSO4Carrying out hydrothermal treatment on the saturated liquid, and drying in vacuum to obtain the calcium sulfate-containing polyetheretherketone particulate bone filling material with the particle size of 400-500 mu m.
Preferably, the polyether ether ketone powder, concentrated sulfuric acid and CaSO4The standing after mixing specifically comprises:
Adding polyether ether ketone powder into concentrated sulfuric acid, stirring, and adding CaSO4And (5) stirring the powder again, and standing to obtain a mixed solution.
Preferably, the flow velocity of the air flow for preparing the particles by the air flow method is 6-7L/min.
Preferably, said in CaSO4The soaking time in the saturated solution is 24h, and the soaking solution is changed every 8 h.
Preferably, the temperature of the hydrothermal treatment is 170-190 ℃; the time of the hydrothermal treatment is 7-9 h.
Preferably, CaSO is contained in the calcium sulfate-containing polyetheretherketone particulate bone filling material with the particle size of 400-500 mu m4The mass content of (A) is 10-60%.
The invention provides a polyether-ether-ketone particulate bone filling material containing calcium sulfate, which is prepared by the preparation method of the technical scheme.
The invention provides a polyether-ether-ketone particulate bone filling material containing calcium sulfate prepared by the preparation method in the technical scheme or an application of the polyether-ether-ketone particulate bone filling material containing calcium sulfate in a bone repair material in the technical scheme.
The invention provides a preparation method of a polyether-ether-ketone particulate bone filling material containing calcium sulfate, which comprises the following steps: mixing polyether ether ketone powder and concentrated sulfuric acidAnd CaSO4Mixing and standing to obtain a mixed solution; making the mixed solution into particles by adopting an air flow method, and settling the particles in ethanol-CaSO4In saturated solution, adding ethanol-CaSO4Soaking in saturated solution, and sieving to obtain CaSO with particle size of 500-600 μm4-PEEK microparticles; the CaSO with the particle size of 500-600 mu m4-PEEK microparticles and CaSO4Carrying out hydrothermal treatment on the saturated liquid, and drying in vacuum to obtain the calcium sulfate-containing polyetheretherketone particulate bone filling material with the particle size of 400-500 mu m. The method provided by the invention adopts CaSO4The polyether-ether-ketone powder is blended to obtain a blended material which has high hydrophilicity, is beneficial to cell proliferation and adhesion, promotes cell differentiation, improves the biomineralization capacity, enhances the bone inductivity and the bioactivity of the material, promotes the full fusion with tissues, has a honeycomb-like hole structure in the section display of the polyether-ether-ketone particulate bone filling material, is similar to cancellous bone, accelerates the healing process of large-area bone defect tissues and realizes the pre-organization process. Meanwhile, the particle can also be used as a microcarrier for carrying growth factors and the like.
Drawings
FIG. 1 shows CaSO with a diameter of 500-600 μm prepared in example 1 of the present invention4-scanning electron microscopy test patterns before and after hydrothermal treatment of PEEK particles;
FIG. 2 shows CaSO with a particle size of 400-500 μm prepared in example 3 of the present invention4The shapes and the section diagrams of the PEEK particles and the PEEK particles prepared by the comparative example;
FIG. 3 shows CaSO with a particle size of 400-500 μm prepared in examples 1-5 of the present invention4the infrared spectrogram of PEEK particles with topological appearance prepared by the PEEK particles and the comparative example;
FIG. 4 shows CaSO prepared in examples 1 to 5 of the present invention4PEEK micro-particles and PEEK with topological morphology prepared by a comparative example have a water contact angle test chart;
FIG. 5 shows CaSO with a particle size of 400-500 μm prepared in example 4 of the present invention4PEEK particles mineralization 4-week topography and elemental analysis (EDX) spectra of topological topography prepared by/PEEK particles and comparative example;
FIG. 6 shows Ca of 400 to 500 μm particle size prepared in examples 1 to 4 of the present inventionSO4CCK cell proliferation test results for PEEK microparticles, smooth PEEK prepared in comparative example, and topological PEEK;
FIG. 7 shows CaSO with a particle size of 400-500 μm prepared in example 4 of the present invention4Morphology of cell adhesion for 7 days for PEEK microparticles/PEEK microparticles and PEEK microparticles with topology prepared in comparative example.
Detailed Description
The invention provides a preparation method of a polyether-ether-ketone particulate bone filling material containing calcium sulfate, which comprises the following steps:
Polyether ether ketone powder, concentrated sulfuric acid and CaSO4Mixing and standing to obtain a mixed solution;
Making the mixed solution into particles by adopting an air flow method, and settling the particles in ethanol-CaSO4In saturated solution, adding ethanol-CaSO4Soaking in saturated solution, and sieving to obtain CaSO with particle size of 500-600 μm4-PEEK microparticles;
The CaSO with the particle size of 500-600 mu m4-PEEK microparticles and CaSO4Carrying out hydrothermal treatment on the saturated liquid, and drying in vacuum to obtain the calcium sulfate-containing polyetheretherketone particulate bone filling material with the particle size of 400-500 mu m.
The method provided by the invention adopts CaSO4the polyether ether ketone powder is blended to obtain a blended material which has higher hydrophilicity, is beneficial to cell proliferation and adhesion, promotes cell differentiation, improves the biomineralization capability, enhances the osteoinductive property and the biological activity of the material, promotes the full fusion with tissues, and contains CaSO4The section of the PEEK particles shows that the interior of the section has a honeycomb-like hole structure, which is similar to cancellous bone, so that the healing process of large-area bone defect tissues is accelerated, and the pre-organization process is realized. Meanwhile, the particle can also be used as a microcarrier for carrying growth factors and the like.
The invention is used for polyether ether ketone powder and CaSO4And the source of concentrated sulfuric acid is not particularly limited, and commercially available products thereof may be used.
According to the invention, PEEK powder is preferably added into concentrated sulfuric acid; the mass concentration of the concentrated sulfuric acid is preferably 95-98%. In the invention, the volume ratio of the mass of the PEEK powder to concentrated sulfuric acid is preferably (1.7-1.9) g, (28-33) mL, more preferably (1.75-1.85) g, (29-32) mL; in a specific embodiment, the volume ratio of the PEEK powder to concentrated sulfuric acid is 1.8g:30 mL.
The mixed PEEK powder and concentrated sulfuric acid are heated in a water bath manner; the temperature of the water bath heating is preferably 25 ℃. The PEEK powder and concentrated sulfuric acid are mechanically stirred until the PEEK powder is completely dissolved, and then CaSO is added4(ii) a Adding CaSO4Then mechanically stirring again until CaSO4After being dispersed evenly, the mixture is kept stand to obtain mixed liquid. The mechanical stirring time is preferably 55-65 min, and more preferably 60 min; the time for the mechanical stirring again is preferably 55-65 min, and more preferably 60 min. The CaSO4The mass fraction in the mixed solution is preferably 5-65%, and more preferably 10-60%; in a specific embodiment, CaSO4The mass fraction in the mixed solution is 10%, 20%, 30%, 40%, 50% or 60%.
after the mixed solution is obtained, the mixed solution is prepared into particles by adopting an air flow method and then is settled in ethanol-CaSO4In saturated solution, adding ethanol-CaSO4Soaking in saturated solution, and sieving to obtain particulate bone filler containing calcium sulfate and polyetheretherketone with particle size of 500-600 μm (CaSO with particle size of 500-600 μm)4PEEK microparticles. The invention preferably puts the mixed solution into the syringe; the volume of the syringe is 50 mL; the diameter of the Teflon needle head of the syringe is 25-27G; in particular embodiments, the Teflon needle has a diameter of 25G, 26G or 27G. The invention adopts ethanol-CaSO4Taking saturated liquid as sedimentation liquid; ethanol-CaSO4The volume of the saturated solution is 1000 mL; the ethanol-CaSO4The saturated liquid is CaSO4Saturating in ethanol to obtain saturated solution; the mass concentration of the ethanol is preferably 28-32%, and more preferably 30%.
The invention preferably carries out sedimentation under ice bath condition; during sedimentation, the height of the needle from the liquid level of the sedimentation liquid is preferably 13-15 cm, more preferably 13.5-14.5 cm, and most preferably 14 cm. The air flow velocity of the particles prepared by the air flow method is preferably 6-7L/min; the gas used in the gas flow method is preferably nitrogen.
Settling in ethanol-CaSO4Microparticles obtained in a saturated liquidThen CaSO4Soaking in saturated solution. The CaSO4The saturated liquid is water saturated liquid of calcium sulfate. In CaSO4The soaking time in the saturated solution is preferably 24h, and the soaking solution is changed every 8 h. Soaking, sieving, and sieving to obtain CaSO with particle size of 500-600 μm4-PEEK microparticles.
Obtaining CaSO with the particle size of 500-600 mu m4After PEEK particles are adopted, the CaSO with the particle size of 500-600 mu m is added4-PEEK microparticles and CaSO4Carrying out hydrothermal treatment on the saturated liquid, and drying in vacuum to obtain the calcium sulfate-containing polyetheretherketone particulate bone filling material with the particle size of 400-500 mu m.
CaSO with the particle size of 500-600 mu m is preferably selected4Placing PEEK particles in a reaction kettle to neutralize CaSO4Mixing saturated solutions; the volume of the reaction kettle is 50 mL; added CaSO4The volume of the saturated solution was 30 mL. In order to make the CaSO with the particle size of 500-600 mu m4The PEEK particles are reduced in volume and subjected to a hydrothermal treatment. The temperature of the hydrothermal treatment is preferably 170-190 ℃, and more preferably 175-185 ℃; the time of the hydrothermal treatment is preferably 7-9 h, and more preferably 7.5-8.5 h; in the specific embodiment, the temperature of the hydrothermal treatment is 180 ℃ and the time is 8 h.
In the invention, CaSO is contained in the calcium sulfate-containing polyetheretherketone particulate bone filling material with the particle size of 400-500 mu m4The mass content of (A) is preferably 10 to 60%.
The invention provides a polyether-ether-ketone particulate bone filling material containing calcium sulfate, which is prepared by the preparation method of the technical scheme.
The section of the polyether-ether-ketone particulate bone filling material containing calcium sulfate provided by the invention shows that the interior of the section has a honeycomb-like hole structure, is similar to cancellous bone, promotes the sufficient fusion with tissues, accelerates the bone healing process and realizes the pre-organization process. The special size of the particles enables the particles to have special functions such as bone filling function which are not possessed by other materials, and even the particles can be implanted into the body in a minimally invasive mode such as injection and the like, so that the surgical injury and the surgical time are reduced; meanwhile, the particle can also be used as a microcarrier for carrying growth factors and the like.
The invention provides a polyether-ether-ketone particulate bone filling material containing calcium sulfate prepared by the preparation method in the technical scheme or an application of the polyether-ether-ketone particulate bone filling material containing calcium sulfate in a bone repair material in the technical scheme.
In order to further illustrate the present invention, the particulate bone filler material of polyetheretherketone containing calcium sulphate, a process for its preparation and its use according to the present invention are described in detail below with reference to the examples, which should not be construed as limiting the scope of the present invention.
Comparative example: preparation of PEEK microparticles
Weighing 1.8G of PEEK powder, adding the PEEK powder into 30mL of concentrated sulfuric acid, placing the concentrated sulfuric acid into a water bath kettle at 25 ℃, mechanically stirring for one hour, standing after the PEEK powder is completely dissolved, adding the liquid into a 50mL needle cylinder, wherein the diameters of Teflon needle heads are respectively 27G, preparing 1000mL of 30% ethanol solution as a sedimentation liquid, carrying out ice bath, and preparing PEEK particles by adopting an air flow method, wherein the height of the needle head from the liquid level of the sedimentation liquid is 14cm, and the air flow velocity is 6-7L/min. And (3) after obtaining the PEEK particles, soaking the PEEK particles for 24h in water once, changing the soaking solution for 1 time every 8h, and filtering the PEEK particles by using a screen to obtain the PEEK particles with the diameter of 500-600 microns and smooth surfaces. And transferring the PEEK microspheres with smooth surfaces into a 50mL reaction kettle, adding 30mL deionized water, heating at 180 ℃ for 8h, cooling to room temperature, and then carrying out vacuum drying to obtain the PEEK microspheres with special topological surfaces.
Example 1
weighing 1.8g of PEEK powder, adding the PEEK powder into 30mL of concentrated sulfuric acid, placing the mixture in a water bath kettle at 25 ℃, mechanically stirring the mixture for one hour, and adding CaSO with different masses after the PEEK powder is completely dissolved4,CaSO4The mass of (A) is PEEK powder and CaSO410% of the total mass; mechanically stirring again for one hour until CaSO4Dispersing uniformly, standing, adding the above mixed liquid into a 50mL syringe with Teflon needle diameters of 27G, 26G and 25G respectively, and preparing 1000mL of 30% ethanol/CaSO4Taking saturated liquid as sedimentation liquid, performing ice bath, making the height of a needle head at the distance of 14cm from the liquid level of the sedimentation liquid, and preparing CaSO by adopting an air flow method4PEEK particles with an airflow rate of 6-7L/min. Obtaining CaSO4After PEEK microgranules,CaSO4Soaking in saturated solution for 24h, changing the soaking solution for 1 time every 8h, and filtering with a screen to obtain CaSO with the diameter of 500-600 μm4-PEEK microparticles.
CaSO with the diameter of 500-600 mu m4Transferring the PEEK particles into a 50mL reaction kettle, and adding 30mL CaSO4Carrying out hydrothermal treatment on the saturated solution at 180 ℃ for 8h, cooling to room temperature, and then carrying out vacuum drying to obtain CaSO with the particle size of 400-500 mu m4PEEK microparticles.
FIG. 1 shows CaSO with a diameter of 500-600 μm prepared in example 1 of the present invention4Scanning electron microscope test images before and after PEEK particle hydrothermal treatment; wherein a is CaSO4Scanning electron microscope image of PEEK particles before hydrothermal treatment, b is CaSO4Scanning electron microscope images of PEEK particles after hydrothermal treatment. As can be seen from fig. 1: a is CaSO before hydrothermal treatment4PEEK particles are larger and have a diameter of 500-600 μm; b is CaSO after hydrothermal treatment4The PEEK particles are larger and have a diameter of 400 to 500 μm.
example 2
In contrast to example 1, CaSO4The mass of (A) is PEEK powder and CaSO420 percent of the total mass.
Example 3
In contrast to example 1, CaSO4The mass of (A) is PEEK powder and CaSO430 percent of the total mass.
Example 4
In contrast to example 1, CaSO4The mass of (A) is PEEK powder and CaSO440 percent of the total mass.
FIG. 2 shows CaSO with a particle size of 400-500 μm prepared in example 3 of the present invention4The shape and the section of PEEK particles and PEEK particles prepared by the comparative example are shown, wherein (a-1) and (a-2) are CaSO with the particle size of 400-500 mu m4Shape picture of PEEK particle, (a-3) and (a-4) are CaSO with particle size of 400-500 μm4Sectional pictures of PEEK particles; (b-1) and (b-2) are morphology diagrams of PEEK microparticles prepared in comparative examples, and (b-3) and (b-4) are cross-sectional diagrams of PEEK microparticles prepared in comparative examples. As can be seen from fig. 2: CaSO4Long rod-like calcium sulfate exists on the surface and the section of the PEEK microsphere.
FIG. 3 is a drawing showingCaSO with particle size of 400-500 μm prepared in embodiments 1-5 of the invention4infrared spectrograms of PEEK particles and PEEK particles with topological appearance prepared by comparative example, wherein a curve 1 is the infrared spectrogram of the PEEK particles with topological appearance prepared by the comparative example, and a curve 2 is CaSO prepared by example 14infrared spectrum of/PEEK particles, curve 3 CaSO prepared in example 24Infrared spectrum of/PEEK particles, curve 4 CaSO prepared in example 34Infrared spectrum of/PEEK particles, curve 5 CaSO prepared in example 44Infrared spectrum of/PEEK particles, curve 6 CaSO prepared in example 54Infrared spectrum of/PEEK particles. As can be seen in fig. 3: at 1115cm-1And 1255cm-1A characteristic sulfate peak occurs.
FIG. 4 shows CaSO prepared in examples 1 to 5 of the present invention4Water contact Angle test patterns for PEEK microparticles and PEEK prepared in comparative example, wherein (a) is a water contact Angle test pattern for PEEK with topology prepared in comparative example, and (b) is CaSO prepared in example 14Water contact angle test pattern for PEEK microparticles (c) CaSO prepared in example 24Water contact angle test pattern for PEEK microparticles (d) CaSO prepared in example 34Water contact angle test pattern for PEEK microparticles, (e) CaSO prepared in example 44Water contact angle test pattern of PEEK particle; as can be seen from FIG. 4, with CaSO4In CaSO4Increasing concentrations in the PEEK particles, the hydrophilicity gradually increased. Contact angle: PEEK particles with topological morphology 95.80 degrees +/-1.49 degrees and 10 percent CaSO4PEEK microparticles 76.56 ° + -2.21 °, 20% CaSO4PEEK microparticles 70.34 ° + -1.44 °, 30% CaSO4PEEK microparticles 66.44 ° + -2.58 °, 40% CaSO4PEEK microparticles 62.98 ° ± 1.36 °.
FIG. 5 shows CaSO with a particle size of 400-500 μm prepared in example 4 of the present invention4PEEK particles mineralization 4-week topography and elemental analysis (EDX) spectra of topological topography prepared by/PEEK particles and comparative example; wherein (a-1), (a-2) and (a-3) are CaSO with the particle size of 400-500 μm prepared in example 44Morphology and elemental analysis (EDX) spectra of PEEK microparticles (b-1), (b-2) and (b-3) prepared for comparative example with the extensionMorphology and elemental analysis (EDX) spectra of PEEK microparticles in flutter morphology. As can be seen from fig. 5: CaSO4Blending PEEK particles facilitates biomineralization.
FIG. 6 shows CaSO with particle size of 400-500 μm prepared in embodiments 1-4 of the present invention4CCK cell proliferation test results for/PEEK microparticles, lubricious PEEK microparticles, and topologic PEEK microparticles.
CCK results after 7 days of cell culture showed that the OD value of the smooth PEEK particles prepared in the comparative example was 0.64 + -0.07, that of the PEEK particles with topological morphology was 0.73 + -0.09, and that 10% CaSO4The OD value of PEEK particles is 0.96 +/-0.06 and 20 percent of CaSO4PEEK particle OD value is 1.09 +/-0.04, 30% CaSO4PEEK particle OD value is 1.15 +/-0.07, 40% CaSO4The OD value of the PEEK particles is 1.27 +/-0.06.
FIG. 7 shows CaSO with a particle size of 400-500 μm prepared in example 4 of the present invention4A morphology of PEEK particles prepared by comparison example and PEEK particles prepared by comparison example, wherein, (a) is CaSO with particle size of 400-500 μm4A PEEK microparticle cell adhesion 7-day topography, and (b) a PEEK microparticle cell adhesion 7-day topography prepared by a comparative example. As can be seen from fig. 6 and 7: PEEK microparticle blending CaSO4And is favorable for cell proliferation and adhesion. PEEK microparticle blending CaSO4Thereafter, the number of adhered cells increased significantly, especially 40% CaSO4the/PEEK particles are almost completely covered with adherent cells.
example 5
In contrast to example 1, CaSO4The mass of (A) is PEEK powder and CaSO450 percent of the total mass.
Example 6
In contrast to example 1, CaSO4The mass of (A) is PEEK powder and CaSO460 percent of the total mass.
From the above embodiments, the present invention provides a preparation method of a particulate bone filling material containing calcium sulfate and polyetheretherketone, comprising the following steps: polyether ether ketone powder, concentrated sulfuric acid and CaSO4Mixing and standing to obtain a mixed solution; making the mixed solution into particles by adopting an air flow method, and settling the particles in ethanol-CaSO4In the saturated liquid, the mixture is added with a solvent,Then ethanol-CaSO4Soaking in saturated solution, and sieving to obtain CaSO with particle size of 500-600 μm4-PEEK microparticles; the CaSO with the particle size of 500-600 mu m4PEEK microparticles and CaSO4Carrying out hydrothermal treatment on the saturated liquid, and drying in vacuum to obtain the calcium sulfate-containing polyetheretherketone particulate bone filling material with the particle size of 400-500 mu m. The method provided by the invention adopts CaSO4The polyether ether ketone powder is blended to obtain a blended material which has higher hydrophilicity, is beneficial to cell proliferation and adhesion, promotes cell differentiation, improves the biomineralization capability, enhances the osteoinductive property and the biological activity of the material, promotes the full fusion with tissues, and contains CaSO4The section of the PEEK particles shows that the interior of the section has a honeycomb-like hole structure, which is similar to cancellous bone, so that the healing process of large-area bone defect tissues is accelerated, and the pre-organization process is realized. Meanwhile, the particle can also be used as a microcarrier for carrying growth factors and the like.
The foregoing is only a preferred embodiment of the present invention, and it should be noted that, for those skilled in the art, various modifications and decorations can be made without departing from the principle of the present invention, and these modifications and decorations should also be regarded as the protection scope of the present invention.

Claims (8)

1. A preparation method of a calcium sulfate-containing polyetheretherketone particulate bone filling material comprises the following steps:
Polyether ether ketone powder, concentrated sulfuric acid and CaSO4Mixing and standing to obtain a mixed solution;
Making the mixed solution into particles by adopting an air flow method, and settling the particles in ethanol-CaSO4In saturated solution, and then in CaSO4Soaking in saturated solution, and sieving to obtain CaSO with particle size of 500-600 μm4-PEEK microparticles;
The CaSO with the particle size of 500-600 mu m4-PEEK microparticles and CaSO4Carrying out hydrothermal treatment on the saturated liquid, and drying in vacuum to obtain the calcium sulfate-containing polyetheretherketone particulate bone filling material with the particle size of 400-500 mu m.
2. the method according to claim 1, wherein the reaction mixture is heated to a temperature in the reaction mixtureThe polyether ether ketone powder, concentrated sulfuric acid and CaSO4The standing after mixing specifically comprises:
Adding polyether ether ketone powder into concentrated sulfuric acid, stirring, and adding CaSO4And (5) stirring the powder again, and standing to obtain a mixed solution.
3. The method according to claim 1, wherein the flow rate of the gas stream for producing the fine particles by the gas stream method is 6 to 7L/min.
4. The method of claim 1, wherein the reaction is performed in CaSO4the soaking time in the saturated solution is 24h, and the soaking solution is changed every 8 h.
5. The preparation method according to claim 1, wherein the temperature of the hydrothermal treatment is 170-190 ℃; the time of the hydrothermal treatment is 7-9 h.
6. The method according to claim 1, wherein CaSO is contained in the particulate bone filler of polyetheretherketone containing calcium sulfate having a particle size of 400 to 500 μm4The mass content of (A) is 10-60%.
7. Particulate calcium sulphate-containing polyetheretherketone bone filler material obtainable by a process according to any one of claims 1 to 6.
8. Particulate bone filler material of polyetheretherketone containing calcium sulphate obtained by a process according to any one of claims 1 to 6 or a particulate bone filler material of polyetheretherketone containing calcium sulphate according to claim 7 for use in bone repair materials.
CN201911022125.3A 2019-10-25 2019-10-25 calcium sulfate-containing polyetheretherketone particulate bone filling material and preparation method thereof Pending CN110559488A (en)

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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101899193A (en) * 2010-07-09 2010-12-01 华东理工大学 Polyether-ether-ketone composite material containing fluorine phosphorus lime, preparation method and usage thereof
CN103483768A (en) * 2013-09-16 2014-01-01 华东理工大学 Bioglass / polyether-ether-ketone composite materials, method for preparing same, application thereof, bone repair body and bone repair body preparation method
CN104725771A (en) * 2013-12-24 2015-06-24 上海交通大学医学院附属第九人民医院 Nano calcium silicate-polyetheretherketone (PEEK) composite material and preparation method thereof
CN104974467A (en) * 2015-07-23 2015-10-14 深圳市科聚新材料有限公司 Nano-hydroxyapatite/polyether-ether-ketone composite material and bone repair body as well as preparation method and application thereof
CN109432494A (en) * 2018-11-20 2019-03-08 中国科学院长春应用化学研究所 A kind of surface has the PEEK microballoon and its preparation method and application of special topology
US10517998B2 (en) * 2013-11-26 2019-12-31 Abyrx, Inc. Settable surgical implants and their packaging

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101899193A (en) * 2010-07-09 2010-12-01 华东理工大学 Polyether-ether-ketone composite material containing fluorine phosphorus lime, preparation method and usage thereof
CN103483768A (en) * 2013-09-16 2014-01-01 华东理工大学 Bioglass / polyether-ether-ketone composite materials, method for preparing same, application thereof, bone repair body and bone repair body preparation method
US10517998B2 (en) * 2013-11-26 2019-12-31 Abyrx, Inc. Settable surgical implants and their packaging
CN104725771A (en) * 2013-12-24 2015-06-24 上海交通大学医学院附属第九人民医院 Nano calcium silicate-polyetheretherketone (PEEK) composite material and preparation method thereof
CN104974467A (en) * 2015-07-23 2015-10-14 深圳市科聚新材料有限公司 Nano-hydroxyapatite/polyether-ether-ketone composite material and bone repair body as well as preparation method and application thereof
CN109432494A (en) * 2018-11-20 2019-03-08 中国科学院长春应用化学研究所 A kind of surface has the PEEK microballoon and its preparation method and application of special topology

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
ERIK A. B. HUGHES: "Characterisation of a novel poly (ether ether ketone)/calcium sulphate composite for bone augmentation", 《HUGHES AND GROVER BIOMATERIALS RESEARCH》 *
王迎军: "《新型材料科学与技术 无机材料卷(下册)》", 31 October 2016, 华南理工大学出版社 *

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