CN107670118A - A kind of manufacture method of 3D printing artificial bone - Google Patents

A kind of manufacture method of 3D printing artificial bone Download PDF

Info

Publication number
CN107670118A
CN107670118A CN201711147920.6A CN201711147920A CN107670118A CN 107670118 A CN107670118 A CN 107670118A CN 201711147920 A CN201711147920 A CN 201711147920A CN 107670118 A CN107670118 A CN 107670118A
Authority
CN
China
Prior art keywords
sensitive drug
suspension
bone
decorating film
drug
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201711147920.6A
Other languages
Chinese (zh)
Inventor
李征宇
曾庆丰
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mai Hai New Material Technology (guan) Co Ltd
Original Assignee
Mai Hai New Material Technology (guan) Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mai Hai New Material Technology (guan) Co Ltd filed Critical Mai Hai New Material Technology (guan) Co Ltd
Priority to CN201711147920.6A priority Critical patent/CN107670118A/en
Publication of CN107670118A publication Critical patent/CN107670118A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • A61L27/54Biologically active materials, e.g. therapeutic substances
    • 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
    • A61L27/02Inorganic materials
    • A61L27/04Metals or alloys
    • 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
    • A61L27/02Inorganic materials
    • A61L27/12Phosphorus-containing materials, e.g. apatite
    • 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
    • A61L27/14Macromolecular materials
    • A61L27/18Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • 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
    • A61L27/14Macromolecular materials
    • A61L27/20Polysaccharides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B33ADDITIVE MANUFACTURING TECHNOLOGY
    • B33YADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
    • B33Y10/00Processes of additive manufacturing
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Dermatology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Transplantation (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Molecular Biology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Materials For Medical Uses (AREA)

Abstract

A kind of manufacture method for 3D printing artificial bone that the embodiment of the present application provides, is related to field of medical technology, and 3D figures are obtained by obtaining three dimensional CT;Obtain the 3D models of closure bone window;Obtain the first sensitive drug, the second sensitive drug;Chitosan is dissolved into solvent with distilled water;First sensitive drug is dissolved in the solvent, the first suspension is made;Hydroxyapatite etc. is included in again is configured to the first decorating film;Second sensitive drug is dissolved in the solvent, the second suspension is made;Then after adding first decorating film, add hydroxyapatite etc. and be configured to the first creamy material for raw material;It is added into biological 3D printer and is printed, forms the first artificial bone.Solve simultaneously because there is no bone window closed system, so that medicine flows out, it is impossible to medicine is stayed in the technical problem at the position that needs play a role, reaching makes 3D printing artificial bone is coincide with bone window structure, be advantageous to drug blockage, while the later stage can increase the technique effect of bone amount.

Description

A kind of manufacture method of 3D printing artificial bone
Technical field
The present invention relates to field of medical technology, more particularly to a kind of manufacture method of 3D printing artificial bone.
Background technology
Osteomyelitis is the infection and destruction of a kind of bone, and it is by aerobic or anaerobic bacteria, mycobacteria and fungus-caused.In bone After generally requiring penetrability bone injury site in the scorching treatment of marrow, it is filled by materials such as bone cements.
But present inventor has found above-mentioned technology extremely during inventive technique scheme in realizing the embodiment of the present application Following technical problem less be present:
In the prior art, in the clinical treatment of osteomyelitis, often there are the mode for window of boning and open seam, at present clinical practice Slow releasing pharmaceutical, shape is single, simple in construction, at the same without reference to windowing closed system, do not simply fail to meet various inhomogeneities The requirement of type bone surgery, simultaneously because not having bone window closed system so that medicine flows out, it is impossible to which staying in medicine needs to play The position of effect.
The content of the invention
The embodiment of the present application solves bone cement in the prior art by providing a kind of manufacture method of 3D printing artificial bone Slow releasing pharmaceutical can not be effectively carried, and the technical problem for different sufferer personalization drug combinations can not be reached, has and meets Various bone surgery demands and a variety of different pharmaceuticals are carried simultaneously, reach multi-medicament while discharge, the technology of drug combination effect Fruit.
In view of the above problems, it is proposed that the embodiment of the present application is to provide a kind of manufacture method of 3D printing artificial bone.
The embodiment of the present application provides a kind of manufacture method of 3D printing artificial bone, and methods described includes:Pass through three dimensional CT Obtain 3D figures;The 3D models of closure bone window are obtained by modeling technique according to the 3D figures;Obtain the first sensitive drug; The second sensitive drug is obtained, wherein the sensitiveness of first sensitive drug is less than second sensitive drug;Will weight The chitosan that amount percentage is 1-90% is dissolved into solvent with distilled water;The first sensitiveness medicine is dissolved in the solvent Thing, and the first suspension is made;The calcium containing compound that percentage by weight is 5%-50% will be included in first suspension to match somebody with somebody It is set to the first decorating film;Second sensitive drug is dissolved in the solvent, and the second suspension is made;Described second After first decorating film is added in suspension, it is that raw material is prepared to add the calcium containing compound that percentage by weight is 0.5%-30% Into the first creamy material;First creamy material is added in biological 3D printer and printed, forms the first artificial bone.
Preferably, methods described also includes:Obtain the 3rd sensitive drug;The 4th sensitive drug is obtained, wherein, it is described The sensitiveness of second sensitive drug is less than the 3rd sensitive drug, and the sensitiveness of the 3rd sensitive drug is less than institute State the 4th sensitive drug;The 3rd sensitive drug is dissolved in the solvent, and the 3rd suspension is made;By described The calcium containing compound that percentage by weight is 5%-50% is included in three suspensions and is configured to the second decorating film;It is molten in the solvent The 4th sensitive drug is solved, and the 4th suspension is made;After second decorating film being added in the 4th suspension, It is that raw material is configured to the second creamy material to add the calcium containing compound that percentage by weight is 0.5%-30%;By second paste Material is added in the biological 3D printer, and is printed based on first artificial bone, forms the second artificial bone.
Preferably, it is described that the calcium containing compound configuration that percentage by weight is 5%-50% will be included in first suspension Into after the first decorating film, methods described also includes:Obtain the 5th sensitive drug, wherein, the 5th sensitive drug it is quick Perception is higher than first sensitive drug;The 5th sensitive drug is dissolved in the solvent, and it is suspended to be made the 5th Liquid;After adding first decorating film in the 5th suspension, the calcic chemical combination that percentage by weight is 5%-50% is included in Thing is configured to the 3rd decorating film.
Preferably, methods described also includes:Obtain the 6th sensitive drug, wherein, the 6th sensitive drug it is quick Perception is higher than the 5th sensitive drug;The 6th sensitive drug is dissolved in the solvent, and it is suspended to be made the 6th Liquid;After adding the 3rd decorating film in the 6th suspension, the calcic chemical combination that percentage by weight is 5%-50% is included in Thing is configured to the 4th decorating film.
Preferably, methods described is additionally included in add the 4th decorating film in second suspension after, add weight The calcium containing compound that percentage is 0.5%-30% is that raw material is configured to the 3rd creamy material;3rd creamy material is added Printed in the biological 3D printer, form third party's work bone.
The one or more technical schemes provided in the embodiment of the present application, have at least the following technical effects or advantages:
1st, the manufacture method for a kind of 3D printing artificial bone that the embodiment of the present application provides, 3D figures are obtained by three dimensional CT; The 3D models of closure bone window are obtained by modeling technique according to the 3D figures;Obtain the first sensitive drug;It is quick to obtain second Sensitive drug, wherein the sensitiveness of first sensitive drug is less than second sensitive drug;It is by percentage by weight 1-90% chitosan is dissolved into solvent with distilled water;First sensitive drug is dissolved in the solvent, and is made One suspension;The calcium containing compound that percentage by weight is 5%-50% will be included in first suspension and is configured to the first solid fraction Thing;Second sensitive drug is dissolved in the solvent, and the second suspension is made;Added in second suspension After first decorating film, it is that raw material is configured to the first paste material to add the calcium containing compound that percentage by weight is 0.5%-30% Material;First creamy material is added in biological 3D printer and printed, forms the first artificial bone.People described herein In the ointment-containing body material of work bone, due to being made of chitosan and distilled water are raw material containing band medicine decorating film, solve In the prior art due to there is no bone window closed system, the requirement for meeting various types of bone surgeries is not simply failed to, while by In there is no bone window closed system so that medicine flows out, it is impossible to medicine is stayed in the technical problem at the position that needs play a role, reaches To making artificial bone be coincide with bone window structure according to 3D printing, be advantageous to drug blockage, medicine will not be flowed out, while the later stage can To increase the technique effect of bone amount.
2. the embodiment of the present application is by obtaining the 3rd sensitive drug;The 4th sensitive drug is obtained, wherein, described second The sensitiveness of sensitive drug is less than the 3rd sensitive drug, and the sensitiveness of the 3rd sensitive drug is less than described the Four sensitive drugs;The 3rd sensitive drug is dissolved in the solvent, and the 3rd suspension is made;Described 3rd is hanged The calcium containing compound that percentage by weight is 5%-50% is included in turbid and is configured to the second decorating film;Institute is dissolved in the solvent The 4th sensitive drug is stated, and the 4th suspension is made;After adding second decorating film in the 4th suspension, add The calcium containing compound that percentage by weight is 0.5%-30% is that raw material is configured to the second creamy material;By second creamy material Add in the biological 3D printer, and printed based on first artificial bone, form the second artificial bone.Reach according to trouble Person's state of an illness needs to select multi-medicament, carries the decorating film of different pharmaceutical respectively by multilayer artificial bone, further makes a variety of medicines Thing discharges simultaneously, drug combination, effectively improves the technique effect of drug effect.
3. the embodiment of the present application by obtain the 5th sensitive drug, wherein, the sensitiveness of the 5th sensitive drug Higher than first sensitive drug;The 5th sensitive drug is dissolved in the solvent, and the 5th suspension is made; After adding first decorating film in 5th suspension, it is included in the calcium containing compound that percentage by weight is 5%-50% and configures Into the 3rd decorating film;The 6th sensitive drug is obtained, wherein, the sensitiveness of the 6th sensitive drug is quick higher than the described 5th Sensitive drug;The 6th sensitive drug is dissolved in the solvent, and the 6th suspension is made;In the 6th suspension After middle addition the 3rd decorating film, it is included in the calcium containing compound that percentage by weight is 5%-50% and is configured to the 4th decorating film; After the 4th decorating film is added in second suspension, the calcium containing compound that percentage by weight is 0.5%-30% is added The 3rd creamy material is configured to for raw material;3rd creamy material is added in the biological 3D printer and printed, shape Into third party's work bone.Reach is needed to select multi-medicament according to conditions of patients, and consolidating for a variety of different pharmaceuticals is carried by artificial bone Shape thing, further make multi-medicament while discharge, drug combination, effectively improve the technique effect of drug effect.
4. the embodiment of the present application by by the copolymer containing lactic acid acetic acid that percentage by weight is 0.1%-20% with 1, 4- dioxane is dissolved into solvent;First sensitive drug is dissolved in the solvent, and the first suspension is made;By institute State be included in the first suspension percentage by weight be 5%-50% calcium containing compound be configured to the first decorating film;In the solvent Middle dissolving second sensitive drug, and the second suspension is made;First solid fraction is added in second suspension After thing, it is that raw material is configured to the first creamy material to add the calcium containing compound that percentage by weight is 0.5%-30%;By described One creamy material is added in biological 3D printer and printed, and forms the first artificial bone.Due to said ratio material in vivo not Easily decompose, a variety of different pharmaceuticals is discharged successively, further make multi-medicament while discharge, drug combination, effectively improve The technique effect of drug effect.
Described above is only the general introduction of technical solution of the present invention, in order to better understand the technological means of the present invention, And can be practiced according to the content of specification, and in order to allow above and other objects of the present invention, feature and advantage can Become apparent, below especially exemplified by the embodiment of the present invention.
Brief description of the drawings
, below will be to embodiment or description of the prior art in order to illustrate more clearly of the technical scheme in the embodiment of the present application In the required accompanying drawing used be briefly described, it should be apparent that, drawings in the following description are some realities of the application Example is applied, for those of ordinary skill in the art, without having to pay creative labor, can also be attached according to these Figure obtains other accompanying drawings.
Fig. 1 is a kind of schematic flow sheet of the manufacture method for 3D printing artificial bone that the embodiment of the present application provides;
Fig. 2 is the schematic flow sheet of the manufacture method for another 3D printing artificial bone that the embodiment of the present application provides;
Fig. 3 is the schematic flow sheet of the manufacture method for another 3D printing artificial bone that the embodiment of the present application provides.
Embodiment
A kind of manufacture method methods described for 3D printing artificial bone that the embodiment of the present application provides includes:Obtained by three dimensional CT Obtain 3D figures;The 3D models of closure bone window are obtained by modeling technique according to the 3D figures;Obtain the first sensitive drug;Obtain The second sensitive drug is obtained, wherein the sensitiveness of first sensitive drug is less than second sensitive drug;By weight Percentage is that 1-90% chitosan is dissolved into solvent with distilled water;First sensitive drug is dissolved in the solvent, And the first suspension is made;The calcium containing compound that percentage by weight is 5%-50% will be included in first suspension to be configured to First decorating film;Second sensitive drug is dissolved in the solvent, and the second suspension is made;It is suspended described second After first decorating film is added in liquid, it is that raw material is configured to the to add the calcium containing compound that percentage by weight is 0.5%-30% One creamy material;First creamy material is added in biological 3D printer and printed, forms the first artificial bone.Solve In the prior art due to there is no bone window closed system, the requirement for meeting various types of bone surgeries is not simply failed to, while by In there is no bone window closed system so that medicine flows out, it is impossible to medicine is stayed in the technical problem at the position that needs play a role, reaches To making artificial bone be coincide with bone window structure according to 3D printing, be advantageous to drug blockage, medicine will not be flowed out, while the later stage can To increase the technique effect of bone amount.
The exemplary embodiment of the disclosure is more fully described below with reference to accompanying drawings.Although the disclosure is shown in accompanying drawing Exemplary embodiment, it being understood, however, that may be realized in various forms the disclosure without should be by embodiments set forth here Limited.On the contrary, these embodiments are provided to facilitate a more thoroughly understanding of the present invention, and can be by the scope of the present disclosure Completely it is communicated to those skilled in the art.
In order to become apparent from a kind of manufacture method for 3D printing artificial bone that open the embodiment of the present application is provided, it is described below Some terms.
1st, 3D printer, also known as three-dimensional printer (3DP), it is the one of a kind of increases material manufacturing technology, i.e. RP technique Kind machine, it is a kind of based on mathematical model file, can be glued with special wax material, powdery metal, plastics or ceramics etc. Condensation material, the object of three-dimensional is manufactured by printing jointing material from level to level.For the application, using biological 3D Printer, comparatively speaking, it is particular in that its material used is biomaterial, such as described in the embodiment of the present application The first creamy material etc..
2nd, the copolymer of lactic acid acetic acid includes Poly(D,L-lactide-co-glycolide, PLGA, PLA, PLG etc., and different proportion Mixture.Poly(D,L-lactide-co-glycolide (poly (lactic-co-glycolic acid), PLGA) is by two kinds of lists Body --- lactic acid and hydroxyacetic acid are polymerized at random, are a kind of degradable functional polymer organic compounds, have good Biocompatibility, the performance of nontoxic, good encystation and film forming, be widely used in pharmacy, medical engineering material and modern times Chemical industry field.In the U.S., PLGA is formally included into American Pharmacopeia by FDA certifications as pharmaceutic adjuvant.
3rd, calcium containing compound includes hydroxyapatite, tricalcium phosphate, the mixture of calcirm-fluoride and different proportion.Hydroxy-apatite Stone, also known as hydroxyapatite, alkali calcium phosphate, it is apatite calcium (Ca5(PO4)3(OH) mineralizing naturally).But often write Into (Ca10(PO4)6(OH)2) form with it is prominent it be dimeric:Hydroxyl and apatite.OH-group can be fluorinated thing, Chloride and carbanion replace, and generate fluorine-based apatite or chloro apatite, calcium ion therein can be by various metals Ion is replaced by the way that ion-exchange reactions occurs, and forms the M apatite (metal of M representative substitution calcium ions of corresponding metal ion Ion).Hydroxyapatite (HA) is the host inorganic constituent of vertebrate skeletal and tooth, hydroxyl phosphorus in the enamel of people The content of lime stone about 96Wt.% (92Vol.%), 69Wt.% is also accounted in bone.Hydroxyapatite has excellent biology Compatibility and bioactivity, and can have as a kind of bone or the inducible factor of tooth in oral hygiene to tooth Preferable remineralization, desensitization and whitening function.Experiment proves HA particles and enamel good biocompatibility, and compatibility is high, its Mineralized liquid can be effectively formed remineralization deposition, prevent calcium ion from being lost in, solve the problems, such as enamel decalcification, fundamentally pre- preventing decayed tooth Tooth disease.Toothpaste containing HA materials has strong suction-operated to sialoprotein, glucan, can reduce the bacterial plaque in patient oral cavity, Promote gingivitis healing, have preferable preventive and therapeutic effect to dental caries, periodontosis
4th, chitosan (chitosan) is also known as chitosan, is by de- second by the chitin that nature is widely present Acyl acts on what is obtained, and chemical name is Chitosan (1-4) -2- amino-B-D glucose.From 1859, Frenchman Rouget After obtaining chitosan first, the biological functionality and compatibility of this natural polymer, blood compatibility, security, microorganism The premium properties such as degradability by all trades and professions extensive concern, medicine, food, chemical industry, cosmetics, water process, METAL EXTRACTION and The application study of the numerous areas such as recovery, biochemical and biomedical engineering achieves major progress.For patient, chitosan drop blood Fat, the existing research report of hypoglycemic effect.Meanwhile chitosan is included in state food additive as thickener, fruit glaze agent Use standard GB-2760.
Embodiment one
Fig. 1 is a kind of schematic flow sheet of the manufacture method for 3D printing artificial bone that the embodiment of the present application provides.Such as Fig. 1 institutes Show, methods described includes:
Step 101:3D figures are obtained by three dimensional CT;
Specifically, by doing three dimensional CT to patient affected part, the 3D solid figures in affected part, above-mentioned 3D solid figures energy are obtained Enough shapes for really seeing affected part bone.For example, a patient suffers from bone tumour, after surgery excision bone tumour, affected part Bone can leave breach, and the breach is different according to the size shape of bone tumour and determines, it may be said that every is suffered from excision bone tumour Breach afterwards is all different, so, by three dimensional CT, can obtain and the shape of subjects bones' breach, size identical Figure.
Step 102:The 3D models of closure bone window are obtained by modeling technique according to the 3D figures;
Specifically, according to the 3D figures, using computer software by modeling technique, construct and the patient bone The 3D models for the closure bone window that bone breach matches, the closure bone window 3D models are the mould for filling up subjects bones' breach Type.It is high with subjects bones' breach goodness of fit by the artificial bone 3D models that 3D modeling constructs, solve in current clinical practice Slow releasing pharmaceutical used, shape is single, simple in construction, can not meet the deficiency of various types of bone surgery requirements.Such as Bone window is too narrow, and plug is not entered;Or bone window is too big, it is difficult to closes, after suturing on the contrary so that the problem of medicine used flows out. After 3D printing, drug composite system can be made to be matched with bone window structure, beneficial to filling, and bone can be pressed in closure Window removes bone, i.e. the scarce size of bone, rationally designs closure 3D printing artificial bone, plays the closing for being advantageous to medicine, will not The effect for flowing out medicine.
Step 103:Obtain the first sensitive drug;
Specifically, sensitive drug refers in osteomyelitis therapeutic process, and carrying out long-term sustained release for destination object controls Medicine needed for treating.Wherein, the first sensitive drug, the second sensitiveness medicine can be divided into according to the height of drug susceptibility Thing, the 3rd sensitive drug, the 4th sensitive drug etc., wherein, can be with according to the sensitiveness high and low level for destination object It is defined as:The sensitiveness of first sensitive drug is less than second sensitive drug, and the sensitiveness of the second sensitive drug is low In the 3rd sensitive drug, the sensitiveness of the 3rd sensitive drug is less than the 4th sensitive drug, the like.
Further, the setting for sensitiveness high and low level can be obtained by the way of proportioning, such as by experimental data More conventional combination is obtained, for example A classes sensitive drug and B classes sensitive drug proportioning are relatively adapted to first kind destination object, C classes Sensitive drug and D classes sensitive drug are relatively adapted to the second class destination object, and such as penicillin, gentamicin, streptomysin can With the demand according to patient to medicine, it is combined, as example, the sensitiveness height that can design different ratio mode is different The combination of medicine.
Step 104:The second sensitive drug is obtained, wherein, the sensitiveness of first sensitive drug is less than described the Two sensitive drugs;
Specifically, the application defines different sensitive drugs, i.e. the first sensitive drug, the second sensitiveness medicine Thing, the 3rd sensitive drug, the 4th sensitive drug etc..Why different sensitive drug is defined, it is therefore intended that by difference Sensitive drug be placed in the different aspects of different artificial bones, and pass through first outside and then inside isolation;Similarly, some people Contain the microballoon with medicine in work bone, the microballoon can be arranged to sandwich construction according to the state of an illness, different sensitive drugs is put Different sensitive drugs are constantly released to target in the different aspects of different microballoons, and by first outside and then inside isolation Object, and then realize the technique effect of long-term sustained release treatment.Pin is reached according to the result of above-mentioned sensitive experiment meanwhile, it is capable to realize To the technique effect of property treatment.
Step 105:The chitosan that percentage by weight is 1-90% is dissolved into solvent with distilled water;
Step 106:First sensitive drug is dissolved in the solvent, and the first suspension is made;
Specifically, it is in step 130 and step 140, percentage by weight is molten for 1-90% chitosan distilled water Solution adds first sensitive drug into solvent, is configured to the first suspension.Because chitosan is a kind of degradable Functional polymer organic compound, there is the biological functionality of natural polymer and compatibility, blood compatibility, security, micro- The premium properties such as biological degradability.So the embodiment of the present application is used to house the first sensitivity from above-mentioned chitosan as carrier Property medicine, the effect for enabling entrained multi-medicament to reach while discharging.Further, above-mentioned first sensitive drug can To be powdered, then realize and the first suspension is formed in above-mentioned solvent.
Step 107:The calcium containing compound that percentage by weight is 5%-50% will be included in first suspension to be configured to First decorating film;
Specifically, hydroxyapatite, tricalcium phosphate, calcirm-fluoride and calcium containing compound are vertebrate skeletal and tooth Host inorganic part, it may have excellent biocompatibility and bioactivity, meanwhile, its mineralized liquid can be effectively formed again Mineralising deposits, therefore uses percentage by weight the first suspension can be configured into the first solid fraction for 5%-50% calcium containing compound Thing;Wherein, calcium containing compound can be hydroxyapatite, tricalcium phosphate, the mixture of calcirm-fluoride and different proportion, wherein, It is preferred reality that the hydroxyapatite that percentage by weight is 10%-15% is included in first suspension and is configured to the first decorating film Apply example.Above-mentioned first decorating film is the microballoon described in those skilled in the art, and the shape of the decorating film is not particularly limited, It can be added in the ointment material of printing artificial bone, and then increase slow release effect.
Step 108:Second sensitive drug is dissolved in the solvent, and the second suspension is made;
Step 109:After first decorating film is added in second suspension, addition percentage by weight is 0.5%- 30% calcium containing compound is that raw material is configured to the first creamy material;
Specifically, in step 160 and step 170, second sensitive drug is dissolved in the solvent, and make Into the second suspension, second sensitive drug can be powdered, then realize and described second is formed in above-mentioned solvent Suspension, then first decorating film is dispersed randomly in second suspension, adding percentage by weight is 0.5%-30% calcium containing compound is that raw material is configured to the first creamy material.
Further, because hydroxyapatite, tricalcium phosphate, calcirm-fluoride and calcium containing compound have excellent bio-compatible Property and bioactivity, meanwhile, its mineralized liquid can be effectively formed remineralization deposition, that is to say, that in the volume addition on State hydroxyapatite, tricalcium phosphate, the ratio of calcirm-fluoride and calcium containing compound is bigger, and obtained material hardness is bigger, easy decomposition Degree is lower.So the hydroxyapatite of the first creamy material by making preparation, tricalcium phosphate, calcirm-fluoride and calcic chemical combination Thing content is less than the hydroxyapatite of first decorating film, tricalcium phosphate, calcirm-fluoride and calcium containing compound content, so as to reach After first decomposing first creamy material, then first decorating film is decomposed, and then realize that the material of hypersensitivity first discharges, it is low Discharged after the material of sensitiveness, be finally reached secondary sustained release, and then increase slow release effect.
Further, and because first decorating film be 1-90% by percentage by weight chitosan and distilled water be What raw material was made, chitosan is illustrated with reference to step 130, it is known that first decorating film can be by itself institute The medicine of carrying discharges simultaneously, reaches the effect of drug combination.
Step 110:First creamy material is added in biological 3D printer and printed, forms the first artificial bone.
Specifically, the first creamy material for meeting biological 3D printer input requirements is added in biological 3D printer Row 3D printing, because 3D printing technique already belongs to basic technology, therefore the embodiment of the present application is no longer specifically described 3D printer Print procedure and method.It should be noted that the structure of above-mentioned 3D printer printing should be with the bone phase shortage needed for destination object Match somebody with somebody, that is to say, that by the personalization features of 3D printing technique, can be lacked as destination object with the bone of destination object, be beaten with 3D Print technology is means, prints the 3D printing artificial bone matched with bone phase shortage.Above-mentioned 3D printing technique solves clinical at present answer The slow releasing pharmaceutical used in, shape is single, simple in construction, can not meet the deficiency of various types of bone surgery requirements.Than As said, bone window is too narrow, and plug is not entered;Or bone window is too big, it is difficult to closes, after suturing on the contrary so that the medicine outflow used Problem.After 3D printing, drug composite system can be made to be matched with bone window structure, beneficial to filling, and can in closure By bone window or removal bone, the i.e. scarce size of bone, to rationally design closure 3D printing artificial bone, play the envelope for being advantageous to medicine Close, the effect that will not flow out medicine.
Embodiment two
In order to realize the use of more kinds of sensitive drugs, reach further lifting slow release effect, the embodiment of the present application is also A kind of manufacture method of 3D printing artificial bone is provided, as shown in Fig. 2 methods described includes:
Step 210:Obtain the 3rd sensitive drug;
Step 220:The 4th sensitive drug is obtained, wherein, the sensitiveness of second sensitive drug is less than described the Three sensitive drugs, the sensitiveness of the 3rd sensitive drug are less than the 4th sensitive drug;
Specifically, step 210 and step 220 can refer to the explanation of step 110 and step 120, and described second is quick The sensitiveness of sensitive drug is less than the 3rd sensitive drug, and the sensitiveness of the 3rd sensitive drug is less than the described 4th Sensitive drug.
Step 230:The 3rd sensitive drug is dissolved in the solvent, and the 3rd suspension is made;
Step 240:The calcium containing compound that percentage by weight is 5%-50% will be included in 3rd suspension to be configured to Second decorating film;
Specifically, the calcium containing compound that percentage by weight is 5%-50% is included in the 3rd suspension, is prepared Into second decorating film, second decorating film and the medicine-containing microsphere that first decorating film is in creamy material are different What point was the second decorating film carrying is the second sensitive drug, and what first decorating film carried is the first sensitiveness medicine Thing.The two is scattered in the creamy material of different layers respectively, reaches the effect of two level sustained release.
Step 250:The 4th sensitive drug is dissolved in the solvent, and the 4th suspension is made;
Step 260:After adding second decorating film in the 4th suspension, addition percentage by weight is 0.5%- 30% calcium containing compound is that raw material is configured to the second creamy material;
Specifically, second creamy material and first creamy material are for biological 3D printing artificial bone Raw material, difference is that internal contained drug is different, for printing the different layers of the artificial bone.Contain in second creamy material There is the 4th powdered sensitive drug, and carry the microballoon of the 3rd sensitive drug, i.e., it is described due to the alkyl phosphorus of microballoon Lime stone content is lower than the hydroxyl-apatite content of the creamy material, can be formed and first decompose release creamy material, then decomposes microballoon, And then ladder is realized, there is step, science, controllable medicament slow release therapeutic effect
Step 270:Second creamy material is added in the biological 3D printer, and using first artificial bone as Basis printing, forms the second artificial bone.
Specifically, second creamy material is printed on the basis of first creamy material, also It is to say, the second creamy material is covered on the content of the first creamy material formation, can be by people according to different situations Work bone is designed to 2 layers, and 3 layers, the embodiment of the present application is not intended to be limited in any to the number of plies of the artificial bone.In specific slow release effect On, it can be formed and first be sustained the second creamy material, then discharge the second decorating film in the second creamy material, then be sustained the first paste Material, the effect of the first decorating film in the first creamy material is finally discharged, and due in different creamy materials and decorating film Contained drug sensitiveness is different, and outer layer sensitiveness is high, and internal layer sensitiveness is relatively low, and then realizes that the material of hypersensitivity first discharges, Discharged after the material of hyposensitivity, and then lift the technique effect of slow release effect.
Embodiment three:
In order to realize the use of more middle sensitive drugs, reach further lifting slow release effect, the embodiment of the present application is also A kind of manufacture method of 3D printing artificial bone is provided, as shown in figure 3, methods described includes:
Step 310:The 5th sensitive drug is obtained, wherein, the sensitiveness of the 5th sensitive drug is higher than described the One sensitive drug;
Step 320:The 5th sensitive drug is dissolved in the solvent, and the 5th suspension is made;
Step 330:After adding first decorating film in the 5th suspension, it is 5%- to be included in percentage by weight 50% calcium containing compound is configured to the 3rd decorating film.
Step 340:The 6th sensitive drug is obtained, wherein, the sensitiveness of the 6th sensitive drug is higher than described the Five sensitive drugs;
Step 350:The 6th sensitive drug is dissolved in the solvent, and the 6th suspension is made;
Step 360:After adding the 3rd decorating film in the 6th suspension, it is 5%- to be included in percentage by weight 50% calcium containing compound is configured to the 4th decorating film.
Step 370:After the 4th decorating film is added in second suspension, addition percentage by weight is 0.5%- 30% calcium containing compound is that raw material is configured to the 3rd creamy material;
Step 380:3rd creamy material is added in the biological 3D printer and printed, forms third party's work Bone.
For the embodiment of the present application, the 5th sensitive drug and the 6th sensitive drug are obtained, wherein, described the The sensitiveness of five sensitive drugs is higher than first sensitive drug, and the sensitiveness of the 6th sensitive drug is higher than described 5th sensitive drug.After 5th sensitive drug is made into the 5th suspension, first decorating film is added In 5th suspension, addition percentage by weight is 5%-50% calcium containing compound, it is become more sticky state, It is put into the sieve of fixed dimension, sifts out the microballoon of identical size, freezing, air-dry, the 3rd decorating film is formed, then by institute State the 3rd decorating film to be put into the suspension containing the 6th sensitive drug, addition percentage by weight contains calcification for 5%-50%'s Compound, it is become more sticky state, be put into the sieve of fixed dimension, sift out the microballoon of identical size, freezing, wind It is dry, finally obtain the 4th decorating film with three-decker.The sieve aperture size can have a variety of different size sizes, tool Body size selects according to clinical demand, and the embodiment of the present application imposes any restrictions not to this.
Further, the 4th decorating film is added in second suspension, obtained the 3rd creamy material Comprising the 4th decorating film and creamy material, the 4th decorating film is the medicine-containing microsphere with three-decker, is divided per Rotating fields Not Han You different sensitive drugs, its sensitiveness is successively weakened by outer layer to internal layer, along with above-mentioned material is not easily decomposed, is made micro- Ball can reach the effect for successively decomposing release medicine in itself, and the 4th decorating film is scattered in containing different sensitive drugs Creamy material in, further enhance prolonged drug sustained release and substep medication technique effect.
Further, the 3rd creamy material is added in the biological 3D printer and shape is printed according to patient demand The sizeable artificial bone of shape, because above-mentioned artificial bone can contain a variety of different pharmaceuticals, can reach it is lasting, long-term, Substep medication, increase slow release effect, avoid the pain of patient's Repeated Operation.
The one or more technical schemes provided in the embodiment of the present application, have at least the following technical effects or advantages:
1st, the manufacture method for a kind of 3D printing artificial bone that the embodiment of the present application provides, 3D figures are obtained by three dimensional CT; The 3D models of closure bone window are obtained by modeling technique according to the 3D figures;Obtain the first sensitive drug;It is quick to obtain second Sensitive drug, wherein the sensitiveness of first sensitive drug is less than second sensitive drug;It is by percentage by weight 1-90% chitosan is dissolved into solvent with distilled water;First sensitive drug is dissolved in the solvent, and is made One suspension;The calcium containing compound that percentage by weight is 5%-50% will be included in first suspension and is configured to the first solid fraction Thing;Second sensitive drug is dissolved in the solvent, and the second suspension is made;Added in second suspension After first decorating film, it is that raw material is configured to the first paste material to add the calcium containing compound that percentage by weight is 0.5%-30% Material;First creamy material is added in biological 3D printer and printed, forms the first artificial bone.People described herein In the ointment-containing body material of work bone, due to being made of chitosan and distilled water are raw material containing band medicine decorating film, solve In the prior art due to there is no bone window closed system, the requirement for meeting various types of bone surgeries is not simply failed to, while by In there is no bone window closed system so that medicine flows out, it is impossible to medicine is stayed in the technical problem at the position that needs play a role, reaches To making artificial bone be coincide with bone window structure according to 3D printing, be advantageous to drug blockage, medicine will not be flowed out, while the later stage can To increase the technique effect of bone amount.
2. the embodiment of the present application is by obtaining the 3rd sensitive drug;The 4th sensitive drug is obtained, wherein, described second The sensitiveness of sensitive drug is less than the 3rd sensitive drug, and the sensitiveness of the 3rd sensitive drug is less than described the Four sensitive drugs;The 3rd sensitive drug is dissolved in the solvent, and the 3rd suspension is made;Described 3rd is hanged The calcium containing compound that percentage by weight is 5%-50% is included in turbid and is configured to the second decorating film;Institute is dissolved in the solvent The 4th sensitive drug is stated, and the 4th suspension is made;After adding second decorating film in the 4th suspension, add The calcium containing compound that percentage by weight is 0.5%-30% is that raw material is configured to the second creamy material;By second creamy material Add in the biological 3D printer, and printed based on first artificial bone, form the second artificial bone.Reach according to trouble Person's state of an illness needs to select multi-medicament, carries the decorating film of different pharmaceutical respectively by multilayer artificial bone, further makes a variety of medicines Thing discharges simultaneously, drug combination, effectively improves the technique effect of drug effect.
3. the embodiment of the present application by obtain the 5th sensitive drug, wherein, the sensitiveness of the 5th sensitive drug Higher than first sensitive drug;The 5th sensitive drug is dissolved in the solvent, and the 5th suspension is made; After adding first decorating film in 5th suspension, it is included in the calcium containing compound that percentage by weight is 5%-50% and configures Into the 3rd decorating film;The 6th sensitive drug is obtained, wherein, the sensitiveness of the 6th sensitive drug is quick higher than the described 5th Sensitive drug;The 6th sensitive drug is dissolved in the solvent, and the 6th suspension is made;In the 6th suspension After middle addition the 3rd decorating film, it is included in the calcium containing compound that percentage by weight is 5%-50% and is configured to the 4th decorating film; After the 4th decorating film is added in second suspension, the calcium containing compound that percentage by weight is 0.5%-30% is added The 3rd creamy material is configured to for raw material;3rd creamy material is added in the biological 3D printer and printed, shape Into third party's work bone.Reach is needed to select multi-medicament according to conditions of patients, and consolidating for a variety of different pharmaceuticals is carried by artificial bone Shape thing, further make multi-medicament while discharge, drug combination, effectively improve the technique effect of drug effect.
4. the embodiment of the present application by by the copolymer containing lactic acid acetic acid that percentage by weight is 0.1%-20% with 1, 4- dioxane is dissolved into solvent;First sensitive drug is dissolved in the solvent, and the first suspension is made;By institute State be included in the first suspension percentage by weight be 5%-50% calcium containing compound be configured to the first decorating film;In the solvent Middle dissolving second sensitive drug, and the second suspension is made;First solid fraction is added in second suspension After thing, it is that raw material is configured to the first creamy material to add the calcium containing compound that percentage by weight is 0.5%-30%;By described One creamy material is added in biological 3D printer and printed, and forms the first artificial bone.Due to said ratio material in vivo not Easily decompose, a variety of different pharmaceuticals is discharged successively, further make multi-medicament while discharge, drug combination, effectively improve The technique effect of drug effect.
Although preferred embodiments of the present invention have been described, but those skilled in the art once know basic creation Property concept, then can make other change and modification to these embodiments.So appended claims be intended to be construed to include it is excellent Select embodiment and fall into having altered and changing for the scope of the invention.
Obviously, those skilled in the art can carry out the essence of various changes and modification without departing from the present invention to the present invention God and scope.So, if these modifications and variations of the present invention belong to the scope of the claims in the present invention and its equivalent technologies Within, then the present invention is also intended to comprising including these changes and modification.
It should be noted last that above embodiment is merely illustrative of the technical solution of the present invention and unrestricted, Although the present invention is described in detail with reference to example, it will be understood by those within the art that, can be to the present invention Technical scheme modify or equivalent substitution, without departing from the spirit and scope of technical solution of the present invention, it all should cover Among scope of the presently claimed invention.

Claims (5)

  1. A kind of 1. method of 3D printing artificial bone, it is characterised in that methods described includes:
    3D figures are obtained by three dimensional CT;
    The 3D models of closure bone window are obtained by modeling technique according to the 3D figures;
    Obtain the first sensitive drug;
    The second sensitive drug is obtained, wherein the sensitiveness of first sensitive drug is less than second sensitive drug;
    The chitosan that percentage by weight is 1-90% is dissolved into solvent with distilled water;
    First sensitive drug is dissolved in the solvent, and the first suspension is made;
    The calcium containing compound that percentage by weight is 5%-50% will be included in first suspension and is configured to the first decorating film;
    Second sensitive drug is dissolved in the solvent, and the second suspension is made;
    After first decorating film is added in second suspension, add percentage by weight and contain calcification for 0.5%-30% Compound is that raw material is configured to the first creamy material;
    First creamy material is added in biological 3D printer and printed, forms the first artificial bone.
  2. 2. the method as described in claim 1, it is characterised in that described that first creamy material is added into biological 3D printer In printed after, methods described also includes:
    Obtain the 3rd sensitive drug;
    The 4th sensitive drug is obtained, wherein, the sensitiveness of second sensitive drug is less than the 3rd sensitive drug, The sensitiveness of 3rd sensitive drug is less than the 4th sensitive drug;
    The 3rd sensitive drug is dissolved in the solvent, and the 3rd suspension is made;
    The calcium containing compound that percentage by weight is 5%-50% will be included in 3rd suspension and is configured to the second decorating film;
    The 4th sensitive drug is dissolved in the solvent, and the 4th suspension is made;
    After adding second decorating film in the 4th suspension, add percentage by weight and contain calcification for 0.5%-30% Compound is that raw material is configured to the second creamy material;
    Second creamy material is added in the biological 3D printer, and printed based on first artificial bone, shape Into the second artificial bone.
  3. 3. the method as described in claim 1, it is characterised in that described to be included in percentage by weight in first suspension and be After 5%-50% calcium containing compound is configured to the first decorating film, methods described also includes:
    The 5th sensitive drug is obtained, wherein, the sensitiveness of the 5th sensitive drug is higher than first sensitive drug;
    The 5th sensitive drug is dissolved in the solvent, and the 5th suspension is made;
    After adding first decorating film in the 5th suspension, the calcic chemical combination that percentage by weight is 5%-50% is included in Thing is configured to the 3rd decorating film.
  4. 4. method as claimed in claim 3, it is characterised in that methods described also includes:
    The 6th sensitive drug is obtained, wherein, the sensitiveness of the 6th sensitive drug is higher than the 5th sensitive drug;
    The 6th sensitive drug is dissolved in the solvent, and the 6th suspension is made;
    After adding the 3rd decorating film in the 6th suspension, the calcic chemical combination that percentage by weight is 5%-50% is included in Thing is configured to the 4th decorating film.
  5. 5. method as claimed in claim 4, it is characterised in that methods described also includes
    After the 4th decorating film is added in second suspension, add percentage by weight and contain calcification for 0.5%-30% Compound is that raw material is configured to the 3rd creamy material;
    3rd creamy material is added in the biological 3D printer and printed, forms third party's work bone.
CN201711147920.6A 2017-11-17 2017-11-17 A kind of manufacture method of 3D printing artificial bone Pending CN107670118A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201711147920.6A CN107670118A (en) 2017-11-17 2017-11-17 A kind of manufacture method of 3D printing artificial bone

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201711147920.6A CN107670118A (en) 2017-11-17 2017-11-17 A kind of manufacture method of 3D printing artificial bone

Publications (1)

Publication Number Publication Date
CN107670118A true CN107670118A (en) 2018-02-09

Family

ID=61149980

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201711147920.6A Pending CN107670118A (en) 2017-11-17 2017-11-17 A kind of manufacture method of 3D printing artificial bone

Country Status (1)

Country Link
CN (1) CN107670118A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109133907A (en) * 2018-08-16 2019-01-04 迈海新型材料科技(固安)有限公司 A kind of artificial bone and preparation method thereof comprising hydroxyapatite crystal whisker and biphase calcium phosphor

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101862230A (en) * 2009-04-17 2010-10-20 华中科技大学同济医学院附属协和医院 Controlled-release multilayer drug-loaded artificial bone and preparation method thereof
WO2011123180A1 (en) * 2010-04-03 2011-10-06 Praful Doshi Medical devices including medicaments and methods of making and using same
CN104689373A (en) * 2015-02-05 2015-06-10 广州医科大学附属口腔医院 Bioactive bone repair material containing williams elder twig as well as preparation method and application thereof
CN105031718A (en) * 2015-08-27 2015-11-11 华南理工大学 Bone repair porous compound scaffold based on 3D (three-dimensional)-Bioplotter printing technology and preparation method thereof
CN105536049A (en) * 2016-01-18 2016-05-04 西北工业大学 Preparation method of fixed-point qualitative medicament-encapsulated artificial bone bracket
CN105749337A (en) * 2016-03-29 2016-07-13 西北工业大学 Preparation method for artificial bone scaffold capable of loading drugs according to layers and quantity

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101862230A (en) * 2009-04-17 2010-10-20 华中科技大学同济医学院附属协和医院 Controlled-release multilayer drug-loaded artificial bone and preparation method thereof
WO2011123180A1 (en) * 2010-04-03 2011-10-06 Praful Doshi Medical devices including medicaments and methods of making and using same
CN104689373A (en) * 2015-02-05 2015-06-10 广州医科大学附属口腔医院 Bioactive bone repair material containing williams elder twig as well as preparation method and application thereof
CN105031718A (en) * 2015-08-27 2015-11-11 华南理工大学 Bone repair porous compound scaffold based on 3D (three-dimensional)-Bioplotter printing technology and preparation method thereof
CN105536049A (en) * 2016-01-18 2016-05-04 西北工业大学 Preparation method of fixed-point qualitative medicament-encapsulated artificial bone bracket
CN105749337A (en) * 2016-03-29 2016-07-13 西北工业大学 Preparation method for artificial bone scaffold capable of loading drugs according to layers and quantity

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109133907A (en) * 2018-08-16 2019-01-04 迈海新型材料科技(固安)有限公司 A kind of artificial bone and preparation method thereof comprising hydroxyapatite crystal whisker and biphase calcium phosphor

Similar Documents

Publication Publication Date Title
Zakaria et al. Nanophase hydroxyapatite as a biomaterial in advanced hard tissue engineering: a review
Rezaie et al. Biomaterials and their applications
CN104274866B (en) Sustained-release drug carrier composition
Sobczak-Kupiec et al. Effect of calcination parameters on behavior of bone hydroxyapatite in artificial saliva and its biosafety
Liu et al. Advances in the use of calcium silicate-based materials in bone tissue engineering
Kroczek et al. Characterisation of selected materials in medical applications
CN102114271A (en) Multi-medicament loaded calcium phosphate cement powder
CN100540073C (en) The composite biological material that is used for bone implant
Choi Biomaterials and bioceramics—part 1: traditional, natural, and nano
Damiri et al. Nano-hydroxyapatite (nHAp) scaffolds for bone regeneration: Preparation, characterization and biological applications
Wu et al. Core–shell structured porous calcium phosphate bioceramic spheres for enhanced bone regeneration
Bow et al. Evaluation of a polyurethane platform for delivery of nanohydroxyapatite and decellularized bone particles in a porous three-dimensional scaffold
Alavi et al. Biocomposite-based strategies for dental bone regeneration
CN107670118A (en) A kind of manufacture method of 3D printing artificial bone
CN107823702A (en) A kind of manufacture method of 3D printing artificial bone
Lee et al. An alternative treatment option for a bony defect from large odontoma using recycled demineralization at chairside
Ibrahim et al. Overview of Some Production Routes for Hydroxyapatite and Its Applications
Venkatesan et al. Silver-calcium titanate–titania decorated Ti6Al4V powders: An antimicrobial and biocompatible filler in composite scaffold for bone tissue engineering application
CN107875445A (en) A kind of manufacture method of 3D printing artificial bone
Andronescu et al. Nano-hydroxyapatite: novel approaches in biomedical applications
CN107823703A (en) A kind of method of 3D printing artificial bone manufacture injection-type preparation
Choi et al. Advances in calcium phosphate nanocoatings and nanocomposites
CN107929813A (en) A kind of manufacture method of 3D printing artificial bone
CN1326792C (en) Calcium phoshate bone cement powder containing traditional Chinese medicine and its preparation method
CN107875450A (en) A kind of method of 3D printing artificial bone manufacture drying type preparation

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20180209