WO2013108963A1 - Dental block bone graft and method for manufacturing same - Google Patents

Dental block bone graft and method for manufacturing same Download PDF

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Publication number
WO2013108963A1
WO2013108963A1 PCT/KR2012/003450 KR2012003450W WO2013108963A1 WO 2013108963 A1 WO2013108963 A1 WO 2013108963A1 KR 2012003450 W KR2012003450 W KR 2012003450W WO 2013108963 A1 WO2013108963 A1 WO 2013108963A1
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Prior art keywords
bone
graft
tooth
cortical
bone graft
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PCT/KR2012/003450
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French (fr)
Korean (ko)
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조성용
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Cho Seong-Yong
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Publication of WO2013108963A1 publication Critical patent/WO2013108963A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/28Bones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/28Bones
    • A61F2/2803Bones for mandibular reconstruction
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61CDENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C8/00Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools
    • 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
    • A61L27/36Materials for grafts or prostheses or for coating grafts or prostheses containing ingredients of undetermined constitution or reaction products thereof, e.g. transplant tissue, natural bone, extracellular matrix
    • A61L27/38Materials for grafts or prostheses or for coating grafts or prostheses containing ingredients of undetermined constitution or reaction products thereof, e.g. transplant tissue, natural bone, extracellular matrix containing added animal cells
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61CDENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C8/00Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools
    • A61C8/0003Not used, see subgroups
    • A61C8/0004Consolidating natural teeth
    • A61C8/0006Periodontal tissue or bone regeneration
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/28Bones
    • A61F2002/2835Bone graft implants for filling a bony defect or an endoprosthesis cavity, e.g. by synthetic material or biological material
    • A61F2002/2839Bone plugs or bone graft dowels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30003Material related properties of the prosthesis or of a coating on the prosthesis
    • A61F2002/30004Material related properties of the prosthesis or of a coating on the prosthesis the prosthesis being made from materials having different values of a given property at different locations within the same prosthesis
    • A61F2002/30057Material related properties of the prosthesis or of a coating on the prosthesis the prosthesis being made from materials having different values of a given property at different locations within the same prosthesis made from both cortical and cancellous adjacent parts

Definitions

  • the present invention relates to a tooth block bone graft for repairing alveolar bone defects. More particularly, the present invention relates to a dental bone block graft material and a method of manufacturing the same, wherein the dental block bone graft material comprises cortical bones and sponges similar to human alveolar bone.
  • Bone grafting substitutes are the replacement of bone defects due to various dental diseases or trauma, disease degeneration, or other tissue loss, thereby filling the space within the bone tissue and forming new bone. Implants used to promote the disease.
  • the best alveolar bone graft substitute is a fresh autograft, which takes a portion of the patient's own bone and transplants it to another damaged area.
  • Dental bone grafts provide bone substrates and living cells involved in bone formation at the site of transplantation, resulting in better bone formation, less immune rejection, and less bone absorption, resulting in bone conduction and bone induction. Very good, there is an advantage in the formation of a solid new bone that can support the fixture (fixture) in implant treatment.
  • Implants used in the treatment of alveolar bone defects are divided into powdered powders and block shaped blocks.
  • Powder-type implants are used when the alveolar bone defects are small, and known techniques include Korean Patent Publication KR 10-2010-0040427, KR 10-2011-0092477 and KR 10-2010-0134306.
  • Block form is a method of applying when filling the space while maintaining a constant form of a large number of alveolar bone defects, the known techniques are typical of Korea Patent Registration KR 10-1062381, KR 10-0978562 and the like.
  • Human alveolar bone is composed of cortical bone and cancellous bone, and while complementary to each other, known block membrane grafts are manufactured only in the form of spongy bone or sponge during the deliming process.
  • the known block-type implants have a problem that when the new bone is formed, the skin surrounding the implant and the alveolar bone are partially absorbed by the biosynthesis and lose about 50% of the volume after the initial transplantation. have.
  • the tooth block bone graft material consists of cortical and spongy bones similar to the human alveolar bone, and the spongy bone area promotes union with the alveolar bone, thereby forming a solid new bone that can support a fixture in implant treatment, and cortical bone.
  • the site requires a dental block bone graft that can maintain its shape after time-lapse.
  • the present invention has been invented to solve the above problems, the known block membrane graft is mostly made only in the form of spongy bone or sponge, in order to improve the problem that the graft is lost during the new bone formation process, the tooth made of cortical bone and spongy bone similar to the human alveolar bone It relates to a block bone graft material and a method of manufacturing the same.
  • the cortical bone and the cancellous bone similar to the human alveolar bone promotes the union of the alveolar bone, thereby forming a solid new bone that can support the fixture in the implant treatment.
  • Cortical bone area is characterized by maintaining the initial shape without the loss of the volume of the implant during the formation of new bone after the procedure.
  • the tooth block bone graft material of the present invention is formed of cortical bone and sponge bone similar to human alveolar bone through a series of processes using enamel of teeth collected from autologous, xenogeneic and allogeneic type, and new bone is implanted after the procedure in the patient. It is characterized in that no volume loss of the implant occurs during formation.
  • the tooth block bone graft material manufacturing method of the present invention in the tooth block bone graft material, the first disinfecting step of removing the tooth, the teeth collected from the heterogeneous and homologous, the germs of the tooth, and remove tartar and soft tissues (a ); After step (a), the dentin of the tooth is completely removed, and a design step of designing an appropriate implant size using only enamel (b); After step (b), coating a portion of the tooth to form a cortical bone Step (c); After the step (c), the step of forming a spongy bone by drilling a plurality of holes (10) by a punching operation using a cloth mill in the other side coated; After the step (d), the first deliming step (e); After the step (e), removing the coating material attached to the step (c) (f); After the step (f), forming a screw hole (20) for fixing during alveolar bone graft (g); After step (g), secondary deliming step (h); After the step (h),
  • the tooth block bone graft manufacturing method of the present invention is characterized in that in the deliming step of the steps (e) and (h), using a solution of hydrochloric acid and citric acid.
  • the present invention maintains its shape without loss in the process of new bone formation.
  • implants need to be inserted as much as the alveolar bone defect, reducing pain and providing aesthetics.
  • the implant fixture can be prevented from being exposed to the outside to maintain aesthetics.
  • cortical and spongy bones similar to human alveolar bone, promoting alveolar bone and union, and induces the formation of new bone due to the tissue of the spongy bone to provide a solid support to the implant fixture.
  • autologous teeth can be a safe, economical procedure without immune rejection.
  • Figure 1 is a preferred embodiment of the present invention method for producing tooth block bone graft
  • Figure 2 is a tooth block bone graft after the first disinfection step (a)
  • Figure 3 is a tooth block bone graft immediately after the design step (b) to remove the dentin, molded into a suitable shape with enamel
  • Figure 4 is a tooth block bone graft immediately after applying the coating to a portion in the coating step (c)
  • Figure 5 is a tooth block bone graft immediately after the drilling step (d) for the formation of spongy bone
  • Figure 6 is a tooth block bone graft comprising a screw hole for fixation at alveolar bone graft after removing the coating material
  • FIG. 7 is a cross-sectional view of the dental block bone graft material of the final product in the form of cortical bone and spongy bone after a series of deliming, degreasing cleaning and disinfection
  • the present invention is based on the rules as defined by the Law on Bioethics and Safety, and the allogeneic teeth of the present invention are limited to being donated among the teeth discarded and discarded during dental treatment.
  • Figure 1 is a preferred embodiment of the present invention method for producing tooth block bone graft
  • Figure 2 is a tooth block bone graft material after the first disinfection step (a)
  • Figure 3 removes the dentin, molded into a suitable shape with enamel
  • One is a tooth block bone graft immediately after the design step (b)
  • Figure 4 is a tooth block bone graft immediately after applying the coating to a portion in the coating step (c)
  • Figure 6 is a tooth block bone graft material including a screw hole for fixation when implantation of the alveolar bone after removing the coating material
  • Figure 7 is a cortical bone and sponge bone form through a series of deliming, degreasing, cleaning and disinfection A cross-sectional view of the tooth block bone graft product of the final product.
  • i and j, and i and l are confused in the serial numbers, so that they are specified by J and L, respectively.
  • the present invention relates to a dental block bone graft material for alveolar bone defects required for implantation. More particularly, the present invention relates to a tooth block bone graft material and a method of manufacturing the same, wherein the tooth block bone graft material comprises cortical bones and spongy bones similar to human alveolar bone.
  • the enamel of one tooth selected from autologous, heterogeneous, and allogeneic is formed into cortical bones and sponges similar to human alveolar bone through a series of processes, and the implant is applied to the patient. It is characterized in that the volume loss of the implant does not occur during the formation of new bone after the procedure.
  • the tooth block bone graft manufacturing method one tooth selected from the autologous, heterogeneous, allogeneic, and removing the germs of the tooth, the first disinfection step of removing tartar and soft tissue (a); After the step (a), the dentin of the tooth is completely removed, designing step of designing the implant size using only enamel (b); After step (b), coating a portion of the tooth to form a cortical bone (c); After the step (c), forming the spongy bone with a plurality of holes (10) by a punching operation using a cloth mill in the other side coated; After the step (d), the first deliming step (e); After the step (e), removing the coating material attached to the step (c) (f); After step (f), forming a screw hole for fixing during alveolar bone graft (g), after step (g), and second deliming step (h); After the step (h), the first washing step using sterile distilled water (i); After step (i), a degre
  • the method for producing a tooth block bone graft material characterized in that in the deliming step of step (e) and (g), using a solution mixed with hydrochloric acid and citric acid.
  • the first disinfection step (a) which removes germs of teeth collected from the patient and removes tartar and soft tissues, soaks the teeth in 10 to 35% hydrogen peroxide drug for 1 to 10 hours or more, and then vibrates 10 to 300 RPM.
  • step (b) completely removes the dentin of the tooth and cuts to an appropriate graft size using only enamel. It also removes tartar, soft tissue, and nerves from your teeth.
  • the step of coating a portion of the tooth to form a cortical bone (c), the site to form a cortical bone to distinguish between the cortical bone (Canicalous bone) and the cortical bone similar to the bones of the human body Coated with a coating material.
  • the coating material inhibits the drug action during the deliming operation, thereby preventing the enamel from becoming a sponge-like structure.
  • the coating should be of a material that is adhesive, stable in chemical structure, and does not affect the processing drug.
  • the dense holes 10 are formed in a predetermined pattern of squares of mm or less. Usually 30 to 80 holes 10 are formed per implant.
  • the hole is formed to facilitate and effectively perform cleaning or degreasing, dehydration, and deliming.
  • the hole 10 is stretched so that it can be easily molded to fit the alveolar bone as well as the implantation operation when implanted into the alveolar bone.
  • the first deliming step (e) uses a mixed solution containing 1 to 20% citric acid and 1 to 50% hydrochloric acid as a main raw material.
  • the mixed solution is suitably 20 to 40 times the volume of the designed implant.
  • the deliming operation is immersed for 2 to 20 hours until the remaining amount of calcium in the spongy bone area, which is not coated in the mixed solution, becomes 1 to 50%, and is stirred on a vibration machine of 10 to 300 RPM at the same time.
  • step (f) of removing the coating material the coating material attached to the step (c) by the physical operation to remove the coating site clean.
  • step (f) when the implant is implanted in the missing alveolar bone, forming a screw hole 20 for fixing the dental block bone graft (g).
  • the second deliming step (h) is performed in the same manner as the mixed solution of the first deliming step (e), when the calcium remaining amount of the site to form the cortical bone becomes 50 to 99% Until.
  • the cortical bone and the spongy bone has a tissue similar to the human alveolar bone.
  • the first washing step (i) using sterile distilled water is immersed in sterile distilled water 20 to 40 times the volume of the implant, put on a vibrating machine of 10 to 300 RPM and agitate for 10 minutes or more.
  • the degreasing step (J) after completely removing the sterile distilled water, immersed in 50 to 100% trichloromethane solution, put on a vibrating machine of 10 to 300RPM and stirred for 1 to 20 hours or more do.
  • the second washing and dehydration step (k) using sterile distilled water and ethyl alcohol after washing in the same manner as in (h) to remove the trichloromethane solution of the degreasing step, After sterile distilled water is completely removed, soaked in 100% ethyl alcohol, put on a vibration machine of 10 to 300 RPM and stirred for 1 to 20 hours or more.
  • the second disinfection using hydrogen peroxide (m) is immersed in 10 to 35% hydrogen peroxide for 1 to 10 hours or more, and then put on a vibration machine of 10 to 300 RPM to perform stirring for 1 to 10 hours or more. .
  • step (m) the fourth washing step (n) using sterile distilled water is washed in the same manner as in (h). Further cleaning may be further included until the processed tooth remains completely removed from the washed tooth.
  • step (n) After the step (n), lyophilization and sterilization step (o), put the implant in the lyophilizer, lyophilized for 1 to 20 hours or more, and then sterilized in a radiation or EO gas sterilizer.
  • the above procedure is performed by implanting into the alveolar bone defect of the patient.
  • the tooth block bone graft of the present invention is composed of cortical bone and spongy bone, characterized in that the volume loss of the graft does not occur during the formation of new bone after the procedure in the patient.
  • the implant fixture can be prevented from being exposed to the outside, thereby maintaining aesthetics.
  • the tissue of the spongy bone induces the formation of new bone, providing a strong support for the implant fixture.
  • the present invention relates to a tooth block bone graft for repairing alveolar bone defects. More specifically, the dental block bone graft can be used in the field of dental bone block graft and its manufacturing method, characterized in that it consists of cortical bone and spongy bone similar to human alveolar bone.

Abstract

The present invention relates to a dental block bone graft which can be used in alveolar bone loss treatment. More particularly, the present invention relates to a dental block bone graft comprised of cortical bone and cancellous bone, which are similar to human alveolar bone, and to a method for manufacturing same. For the dental block bone graft of the present invention, one selected from dental enamel from the patient's own tissue, heterogeneous dental enamel, or homogenous dental enamel is formed into cortical and cancellous bone, which are similar to human alveolar bone, and after the graft is administered to the patient, the volume of the graft does not diminish while newly generated bone is formed. In contrast to the prior art, in which a greater amount of a graft is inserted due to the inevitable loss of block-type grafts, which causes pain and gum disfigurement for the patient, the present invention maintains the same shape without any loss even during the forming of newly generated bone. Therefore, it is sufficient to insert a graft only in the amount of alveolar bone which was lost so as to reduce pain for the patient and maintain aesthetics by preventing a fixture from being outwardly exposed. Also, the graft is formed of cortical bone and cancellous bone, which are similar in form to human alveolar bone, wherein that the cancellous bone portion accelerates fusion with the alveolar bone, thereby reducing the time taken to form newly generated solid bone which can support a fixture in implant treatment, and the cortical bone portion has the effect of preventing a loss in volume of the graft during the formation of newly generated bone.

Description

치아 블록골 이식재 및 그 제조방법Tooth block bone graft and its manufacturing method
본 발명은 치조골 결손을 회복하기 위한 치아 블록골 이식재에 관한 것이다. 더욱 상세하게는 치아 블록골 이식재가 인체 치조골과 유사한 피질골과 해면골로 이루어지는 것을 특징으로 하는 치아골 블록 이식재 및 그 제조방법에 관한 것이다.The present invention relates to a tooth block bone graft for repairing alveolar bone defects. More particularly, the present invention relates to a dental bone block graft material and a method of manufacturing the same, wherein the dental block bone graft material comprises cortical bones and sponges similar to human alveolar bone.
치조골 이식 대체재(Bone grafting substitute, BGS)란 여러 가지 치과질환 또는 외상, 질병에 의한 퇴화 또는 기타 조직의 손실로 인하여 뼈 조직의 결손부가 생긴 경우, 이를 대체하여 뼈 조직 내의 공간을 충진 시키고 신생골의 형성을 촉진시키기 위하여 사용하는 이식재를 말한다. Bone grafting substitutes (BGS) are the replacement of bone defects due to various dental diseases or trauma, disease degeneration, or other tissue loss, thereby filling the space within the bone tissue and forming new bone. Implants used to promote the disease.
가장 좋은 치조골 이식 대체재는 환자 자신의 뼈 일부분을 채취하여 손상된 다른 부위에 이식하는 자가골 이식(fresh autograft)이다. 치아골 이식은 뼈의 기질과 뼈 형성에 관련하는 살아있는 세포들이 이식 부위에 제공되므로 뼈의 생성이 다른 이식물에 비해 뛰어나고, 면역거부반응도 거의 없으며, 뼈 흡수가 거의 없어 골전도 및 골유도 능력이 매우 뛰어나, 임플란트 치료에서 픽스처(fixture)를 지지할 수 있는 견고한 신생골의 형성할 수 있는 장점이 있다. The best alveolar bone graft substitute is a fresh autograft, which takes a portion of the patient's own bone and transplants it to another damaged area. Dental bone grafts provide bone substrates and living cells involved in bone formation at the site of transplantation, resulting in better bone formation, less immune rejection, and less bone absorption, resulting in bone conduction and bone induction. Very good, there is an advantage in the formation of a solid new bone that can support the fixture (fixture) in implant treatment.
치조골 결손 치료에 사용되는 이식재는 가루형태의 파우더와 일정한 형태를 갖춘 블록 형태로 구분한다. 파우더 형태의 이식재는 치조골 결손부분이 적을 때 사용하는 것으로, 공지기술로는 대한민국 공개특허 KR 10-2010-0040427, KR 10-2011-0092477과 KR 10-2010-0134306 등이 있다. 블록 형태는 치조골 결손부분이 많아 일정한 형태를 유지하면서 공간을 충진할 경우에 적용하는 방법으로, 공지된 기술은 대한민국 등록특허 KR 10-1062381과, KR 10-0978562 등이 대표적이다. Implants used in the treatment of alveolar bone defects are divided into powdered powders and block shaped blocks. Powder-type implants are used when the alveolar bone defects are small, and known techniques include Korean Patent Publication KR 10-2010-0040427, KR 10-2011-0092477 and KR 10-2010-0134306. Block form is a method of applying when filling the space while maintaining a constant form of a large number of alveolar bone defects, the known techniques are typical of Korea Patent Registration KR 10-1062381, KR 10-0978562 and the like.
인체 치조골은 피질골(Cotical bone)과 해면골(Cancellous bone)로 이뤄져 있고, 상호 보완적으로 작용하는데 비해, 공지된 블록막 이식재는 탈회과정을 거치면서 해면골 또는 스폰지 형태로만 제조된다. Human alveolar bone is composed of cortical bone and cancellous bone, and while complementary to each other, known block membrane grafts are manufactured only in the form of spongy bone or sponge during the deliming process.
그로 인해, 공지된 블록형 이식재는 신생골로 형성시 이식재를 감싸고 있는 피부의 장력과, 치조골과 유합되면서 일부 생체흡수되어 6내지 12개월 경과 이후에는 최초 이식 대비 체적이 50%정도 소실되는 문제점을 가지고 있다. Therefore, the known block-type implants have a problem that when the new bone is formed, the skin surrounding the implant and the alveolar bone are partially absorbed by the biosynthesis and lose about 50% of the volume after the initial transplantation. have.
따라서, 치아 블록골 이식재에 있어서, 인체 치조골과 유사한 피질골과 해면골로 이루어져, 해면골 부위는 치조골과 유합을 촉진하여, 임플란트 치료에서 픽스처(fixture)를 지지할 수 있는 견고한 신생골의 형성이 가능하며, 피질골 부위는 시간경과 후에도 소실없이 그 형태를 유지할 수 있는 치아 블록골 이식재가 필요하다. Therefore, in the tooth block bone graft material, it consists of cortical and spongy bones similar to the human alveolar bone, and the spongy bone area promotes union with the alveolar bone, thereby forming a solid new bone that can support a fixture in implant treatment, and cortical bone. The site requires a dental block bone graft that can maintain its shape after time-lapse.
본 발명은 상기의 문제점을 해결하고자 발명한 것으로, 공지된 블록막 이식재는 대부분 해면골 또는 스폰지 형태로만 만들어져, 신생골 형성과정 동안 이식재가 소실되는 문제점을 개선하고자, 인체 치조골과 유사한 피질골과 해면골로 이루어진 치아 블록골 이식재 및 그 제조방법에 관한 것이다.The present invention has been invented to solve the above problems, the known block membrane graft is mostly made only in the form of spongy bone or sponge, in order to improve the problem that the graft is lost during the new bone formation process, the tooth made of cortical bone and spongy bone similar to the human alveolar bone It relates to a block bone graft material and a method of manufacturing the same.
그로 인해 본 발명의 치아 블록골 이식재에 있어서, 인체 치조골과 유사한 피질골과 해면골로 이루어져, 해면골 부위는 치조골과 유합을 촉진하여, 임플란트 치료에서 픽스처(fixture)를 지지할 수 있는 견고한 신생골의 형성이 가능하며, 피질골 부위는 시술이후 신생골이 형성되는 동안 이식재의 체적 소실이 발생하지 않고 최초 형태를 유지하는 것이 특징이다.Therefore, in the dental block bone graft material of the present invention, the cortical bone and the cancellous bone similar to the human alveolar bone, the spongy bone area promotes the union of the alveolar bone, thereby forming a solid new bone that can support the fixture in the implant treatment. Cortical bone area is characterized by maintaining the initial shape without the loss of the volume of the implant during the formation of new bone after the procedure.
본 발명의 치아 블록골 이식재는 자가, 이종 및 동종에게서 채취한 치아의 법랑질을 이용하여, 상기 법랑질을 일련의 공정을 거쳐 인체 치조골과 유사한 피질골과 해면골로 형성되어, 이식재를 환자에 시술이후 신생골이 형성되는 동안 이식재의 체적 소실이 발생하지 않는 것을 특징으로 한다.The tooth block bone graft material of the present invention is formed of cortical bone and sponge bone similar to human alveolar bone through a series of processes using enamel of teeth collected from autologous, xenogeneic and allogeneic type, and new bone is implanted after the procedure in the patient. It is characterized in that no volume loss of the implant occurs during formation.
또한 본 발명의 치아 블록골 이식재 제조방법은, 치아 블록골 이식재에 있어서, 자가, 이종 및 동종에게서 채취한 치아, 상기 치아의 병균을 제거하고, 치석과 연조직 등을 제거하는 1차 소독 단계(a); 상기 (a)단계 이후, 치아의 상아질은 완전히 제거하고, 법랑질만 이용하여 적당한 이식재 크기로 디자인하는 디자인 단계(b);상기 (b)단계 이후, 피질골을 형성하기 위하여, 치아의 일부분을 코팅하는 단계(c); 상기 (c)단계 이후, 상기 코팅된 타측부에 천공장치를 이용하여 천공작업으로 다수의 구멍(10)을 천공하여 해면골을 형성하는 단계(d); 상기 (d)단계 이후, 1차 탈회 단계(e); 상기 (e)단계 이후, 상기(c)단계에 부착된 코팅재를 제거하는 단계(f); 상기 (f)단계 이후, 치조골 이식시 고정하기 위한 스크류 홀(20)을 형성하는 단계(g); 상기 (g)단계이후, 2차 탈회 단계(h); 상기 (h)단계 이후, 멸균 증류수를 이용한 1차 세척 단계(i); 상기 (i)단계 이후, 탈지 단계(J); 상기 (J) 단계 이후, 멸균증류수와 에틸알콜을 이용한 2차 세척 및 탈수 단계(k); 상기 (k)단계 이후, 멸균증류수를 이용한 3차 세척 단계((L); 상기 (L)단계 이후, 과산화수소를 이용한 2차 소독(m); 상기 (m)단계 이후, 멸균증류수를 이용한 4차 세척 단계(n); 상기 (n)단계 이후, 동결건조 및 멸균소독 단계(o)를 포함하고, 상기 (n)단계에서의 추가 세척하는 단계를 더 포함하여 최종 제품이 인체 치조골과 유사한 피질골과 해면골로 이루어지는 것을 특징으로 한다.In addition, the tooth block bone graft material manufacturing method of the present invention, in the tooth block bone graft material, the first disinfecting step of removing the tooth, the teeth collected from the heterogeneous and homologous, the germs of the tooth, and remove tartar and soft tissues (a ); After step (a), the dentin of the tooth is completely removed, and a design step of designing an appropriate implant size using only enamel (b); After step (b), coating a portion of the tooth to form a cortical bone Step (c); After the step (c), the step of forming a spongy bone by drilling a plurality of holes (10) by a punching operation using a cloth mill in the other side coated; After the step (d), the first deliming step (e); After the step (e), removing the coating material attached to the step (c) (f); After the step (f), forming a screw hole (20) for fixing during alveolar bone graft (g); After step (g), secondary deliming step (h); After the step (h), the first washing step using sterile distilled water (i); After step (i), a degreasing step (J); After the step (J), the second washing and dehydration step using sterile distilled water and ethyl alcohol (k); After the step (k), the third washing step using sterile distilled water ((L); after the (L) step, the second disinfection using hydrogen peroxide (m); after the step (m), after the fourth step using sterile distilled water (N) washing step (n), after the step (n), lyophilization and sterilization step (o), further comprising the step of further washing in the step (n) the final product is cortical bone similar to the human alveolar bone It is characterized by consisting of spongy bone.
마지막으로 본 발명의 치아 블록골 이식재 제조방법은 상기 (e)단계와 (h) 단계의 탈회단계에 있어서, 염산과 구연산을 혼합한 용액을 사용하는 것을 특징으로 한다.Finally, the tooth block bone graft manufacturing method of the present invention is characterized in that in the deliming step of the steps (e) and (h), using a solution of hydrochloric acid and citric acid.
종래기술은 이식재 체적 소실되는 것을 고려하여 더 많은 이식재를 삽입하여 환자에게 고통과 불균형의 잇몸을 제공하는 반면, 본 발명은 신생골 형성과정에도 소실 없이 그 형태를 유지한다. 그로 인해 치조골 결손부위만큼만 이식재를 삽입하면 되어 환자의 고통을 줄여주고 심미성을 제공한다. 임플란트 시술의 경우에는 임플란트 픽스쳐가 외부로 노출되는 것을 막아주어 심미성을 유지할 수 있다.While the prior art provides for pain and imbalanced gums to the patient by inserting more implants in consideration of the loss of implant volume, the present invention maintains its shape without loss in the process of new bone formation. As a result, implants need to be inserted as much as the alveolar bone defect, reducing pain and providing aesthetics. In the case of an implant procedure, the implant fixture can be prevented from being exposed to the outside to maintain aesthetics.
또한, 인체 치조골과 유사한 피질골과 해면골로 이루어져, 치조골과 유합을 촉진하며, 해면골의 조직으로 인해 신생골의 형성을 쉽게 유도하여 임플란트 픽스쳐에 견고한 지지대를 제공한다.In addition, it consists of cortical and spongy bones similar to human alveolar bone, promoting alveolar bone and union, and induces the formation of new bone due to the tissue of the spongy bone to provide a solid support to the implant fixture.
이외에도 일반적은 자가골 이식재의 효과와 같이 자가 치아를 이용하므로 뼈이식 재료의 양을 늘릴 수 있고, 임프란트 시술의 안정성을 향상시킬 수 있다.In addition, since the use of autologous teeth in general, such as the effect of autologous bone graft can increase the amount of bone graft material, it is possible to improve the stability of the implant procedure.
또한, 자신의 치아를 사용함으로 이종(동물) 이식재의 전염성 질환의 전이를 예방하고, 자가 치아는 면역 거부 반응 없는 안전하고, 경제적인 시술을 할 수 있다.In addition, the use of their own teeth to prevent the transmission of infectious diseases of xenograft (animal) implants, autologous teeth can be a safe, economical procedure without immune rejection.
도 1은 본 발명 치아 블록골 이식재 제조방법의 바람직한 일실시예 Figure 1 is a preferred embodiment of the present invention method for producing tooth block bone graft
도 2는 1차 소독단계이후(a)의 치아 블록골 이식재Figure 2 is a tooth block bone graft after the first disinfection step (a)
도 3은 상아질을 제거하고, 법랑질로 적당한 형상으로 성형한 디자인 단계(b) 직후의 치아 블록골 이식재Figure 3 is a tooth block bone graft immediately after the design step (b) to remove the dentin, molded into a suitable shape with enamel
도 4는 코팅단계(c)에서 코팅재를 일부분에 도포한 직후의 치아 블록골 이식재Figure 4 is a tooth block bone graft immediately after applying the coating to a portion in the coating step (c)
도 5는 해면골 형성을 위해 천공단계(d) 직후의 치아 블록골 이식재 Figure 5 is a tooth block bone graft immediately after the drilling step (d) for the formation of spongy bone
도 6은 코팅재를 제거한 후 치조골 이식시 고정을 위한 스크류 홀을 포함하는 치아 블록골 이식재 Figure 6 is a tooth block bone graft comprising a screw hole for fixation at alveolar bone graft after removing the coating material
도 7은 일련의 탈회, 탈지 세척 및 소독단계를 거쳐 피질골과 해면골 형태의 최종제품의 치아 블록골 이식재 단면도7 is a cross-sectional view of the dental block bone graft material of the final product in the form of cortical bone and spongy bone after a series of deliming, degreasing cleaning and disinfection
본 발명의 권리범위는 본 실시예에 국한되지 않으며, 당업자 수준에서 용이하게 변경가능하며, 본 발명의 기술적 사상과 동일한, 여하한 발명이라도 본 발명의 권리범위 내에 속한다.The scope of the present invention is not limited to this embodiment, and can be easily changed at the level of those skilled in the art, and any invention that is the same as the technical idea of the present invention falls within the scope of the present invention.
본 발명은 생명윤리 및 안전에 관한 법률이 규정하는 바의 규칙에 의거하며, 본 발명의 동종치아는 치과진료 중 발치하여 버려지는 치아들 중에서 기증되는 것으로 국한된다. The present invention is based on the rules as defined by the Law on Bioethics and Safety, and the allogeneic teeth of the present invention are limited to being donated among the teeth discarded and discarded during dental treatment.
도 1은 본 발명 치아 블록골 이식재 제조방법의 바람직한 일실시예이며, 도 2는 1차 소독단계이후(a)의 치아 블록골 이식재이며, 도 3은 상아질을 제거하고, 법랑질로 적당한 형상으로 성형한 디자인 단계(b) 직후의 치아 블록골 이식재이며, 도 4는 코팅단계(c)에서 코팅재를 일부분에 도포한 직후의 치아 블록골 이식재이며, 도 5는 해면골 형성을 위해 천공단계(d) 직후의 치아 블록골 이식재이며, 도 6은 코팅재를 제거한 후 치조골 이식시 고정을 위한 스크류 홀을 포함하는 치아 블록골 이식재이며, 도 7은 일련의 탈회, 탈지, 세척 및 소독단계를 거쳐 피질골과 해면골 형태의 최종 제품의 치아 블록골 이식재 제품의 단면도이다. Figure 1 is a preferred embodiment of the present invention method for producing tooth block bone graft, Figure 2 is a tooth block bone graft material after the first disinfection step (a), Figure 3 removes the dentin, molded into a suitable shape with enamel One is a tooth block bone graft immediately after the design step (b), Figure 4 is a tooth block bone graft immediately after applying the coating to a portion in the coating step (c), Figure 5 is immediately after the drilling step (d) for the formation of spongy bone 6 is a tooth block bone graft material, Figure 6 is a tooth block bone graft material including a screw hole for fixation when implantation of the alveolar bone after removing the coating material, Figure 7 is a cortical bone and sponge bone form through a series of deliming, degreasing, cleaning and disinfection A cross-sectional view of the tooth block bone graft product of the final product.
도 1에서 일련번호 중에서 i와 j 및 i와 l이 혼돈여지가 있어서 각각 J와 L로 구분하여 명기한다. In FIG. 1, i and j, and i and l are confused in the serial numbers, so that they are specified by J and L, respectively.
본 발명은 치조골이 결손되어 임플란트 시술에 필요한 치아 블록골 이식재에 관한 것이다. 더욱 상세하게는 치아 블록골 이식재가 인체 치조골과 유사한 피질골과 해면골로 이루어지는 것을 특징으로 하는 치아 블록골 이식재 및 그 제조방법에 관한 것이다.The present invention relates to a dental block bone graft material for alveolar bone defects required for implantation. More particularly, the present invention relates to a tooth block bone graft material and a method of manufacturing the same, wherein the tooth block bone graft material comprises cortical bones and spongy bones similar to human alveolar bone.
본 발명에서의 치아 블록골 이식재에 있어서, 자가, 이종, 동종중에서 선택된 하나의 치아의 법랑질을 이용하여, 상기 법랑질을 일련의 공정을 거쳐 인체 치조골과 유사한 피질골과 해면골로 형성되어, 이식재를 환자에 시술이후 신생골이 형성되는 동안 이식재의 체적 소실이 발생하지 않는 것을 특징으로 한다.In the tooth block bone graft material of the present invention, by using the enamel of one tooth selected from autologous, heterogeneous, and allogeneic, the enamel is formed into cortical bones and sponges similar to human alveolar bone through a series of processes, and the implant is applied to the patient. It is characterized in that the volume loss of the implant does not occur during the formation of new bone after the procedure.
또한, 치아 블록골 이식재 제조방법은, 자가, 이종, 동종중에서 선택된 하나의 치아와, 상기 치아의 병균을 제거하고, 치석과 연조직을 제거하는 1차 소독 단계(a); 상기 (a)단계 이후, 치아의 상아질은 완전히 제거하고, 법랑질만 이용하여 이식재 크기로 디자인하는 디자인 단계(b); 상기 (b)단계 이후, 피질골을 형성하기 위하여, 치아의 일부분을 코팅하는 단계(c); 상기 (c)단계 이후, 상기 코팅된 타측부에 천공장치를 이용하여 천공작업으로 다수의 구멍(10)으로 해면골을 형성하는 단계(d); 상기 (d)단계 이후, 1차 탈회 단계(e); 상기 (e)단계 이후, 상기(c)단계에 부착된 코팅재를 제거하는 단계(f); 상기 (f)단계 이후, 치조골 이식시 고정하기 위한 스크류 홀을 형성하는 단계(g), 상기 (g)단계 이후, 2차 탈회 단계(h); 상기 (h)단계 이후, 멸균 증류수를 이용한 1차 세척 단계(i); 상기 (i)단계 이후, 탈지 단계(J); 상기 (J) 단계 이후, 멸균증류수와 에틸알콜을 이용한 2차 세척 및 탈수 단계(k); 상기 (k)단계 이후, 멸균증류수를 이용한 3차 세척 단계((L); 상기 (L)단계 이후, 과산화수소를 이용한 2차 소독(m); 상기 (m)단계 이후, 멸균증류수를 이용한 4차 세척 단계(n); 상기 (n)단계 이후, 동결건조 및 멸균소독 단계(o)를 포함하고, 상기 (n)단계에서의 추가 세척하는 단계를 더 포함하여 최종 제품이 인체 치조골과 유사한 피질골과 해면골로 이루어지는 것을 특징으로 한다. In addition, the tooth block bone graft manufacturing method, one tooth selected from the autologous, heterogeneous, allogeneic, and removing the germs of the tooth, the first disinfection step of removing tartar and soft tissue (a); After the step (a), the dentin of the tooth is completely removed, designing step of designing the implant size using only enamel (b); After step (b), coating a portion of the tooth to form a cortical bone (c); After the step (c), forming the spongy bone with a plurality of holes (10) by a punching operation using a cloth mill in the other side coated; After the step (d), the first deliming step (e); After the step (e), removing the coating material attached to the step (c) (f); After step (f), forming a screw hole for fixing during alveolar bone graft (g), after step (g), and second deliming step (h); After the step (h), the first washing step using sterile distilled water (i); After step (i), a degreasing step (J); After the step (J), the second washing and dehydration step using sterile distilled water and ethyl alcohol (k); After the step (k), the third washing step using sterile distilled water ((L); after the (L) step, the second disinfection using hydrogen peroxide (m); after the step (m), after the fourth step using sterile distilled water (N) washing step (n), after the step (n), lyophilization and sterilization step (o), further comprising the step of further washing in the step (n) the final product is cortical bone similar to the human alveolar bone It is characterized by consisting of spongy bone.
또한, 치아 블록골 이식재 제조방법은, 상기 (e)단계와 (g) 단계의 탈회단계에 있어서, 염산과 구연산을 혼합한 용액을 사용하는 것을 특징으로 한다. In addition, the method for producing a tooth block bone graft material, characterized in that in the deliming step of step (e) and (g), using a solution mixed with hydrochloric acid and citric acid.
상기 치아 블록골 이식재 제조방법을 구체적으로 설명하면 하기와 같다. The tooth block bone graft manufacturing method will be described in detail below.
환자에게서 채취한 치아의 병균을 제거하고, 치석과 연조직 등을 제거하는 1차 소독 단계(a)는 치아를 10 내지 35%의 과산화수소 약물에 1 내지 10시간 이상 담군 후, 10 내지 300 RPM의 진동 기계에 올려 1 내지 20 시간 이상 교반작업을 통해 치아 외부의 병균을 제거하는 1차 소독과, 치아에 부착되어 있는 치석, 연조직 등을 1차적으로 제거한다.The first disinfection step (a), which removes germs of teeth collected from the patient and removes tartar and soft tissues, soaks the teeth in 10 to 35% hydrogen peroxide drug for 1 to 10 hours or more, and then vibrates 10 to 300 RPM. First disinfection to remove germs from the outside of the tooth by stirring on the machine for 1 to 20 hours or more, and calculus, soft tissue, etc. attached to the tooth is primarily removed.
상기 (a)단계 이후, 디자인 단계(b)는 치아의 상아질은 완전히 제거하고, 법랑질만 이용하여 적당한 이식재 크기로 절단한다. 또한 치아에 붙어 있는 치석, 연조직, 치아 신경 등을 깨끗하게 제거한다.After step (a), design step (b) completely removes the dentin of the tooth and cuts to an appropriate graft size using only enamel. It also removes tartar, soft tissue, and nerves from your teeth.
상기 (b)단계 이후, 피질골을 형성하기 위하여 치아의 일부분을 코팅하는 단계(c)는, 인체의 뼈와 유사한 피질골(Cotical bone)과 해면골(Cancellous bone)을 구분하기 위해 피질골을 형성하고자 하는 부위를 코팅재로 코팅을 한다. 코팅재는 탈회작업기간동안 약물작용을 억제하여, 법랑질이 해면골과 같은 구조가 되는 것을 방지한다. 코팅재는 접착성을 갖으며, 화학적 구조가 안정된 재료이며, 가공 약물에 영향을 미치지 않는 재료이여야 한다. After the step (b), the step of coating a portion of the tooth to form a cortical bone (c), the site to form a cortical bone to distinguish between the cortical bone (Canicalous bone) and the cortical bone similar to the bones of the human body Coated with a coating material. The coating material inhibits the drug action during the deliming operation, thereby preventing the enamel from becoming a sponge-like structure. The coating should be of a material that is adhesive, stable in chemical structure, and does not affect the processing drug.
상기 (c)단계 이후, 상기 코팅된 타측부에 천공장치를 이용하여 천공작업으로 다수의 구멍(10)으로 해면골을 형성하는 단계(d)는 레이져, 드릴등의 천공장치를 이용하여 0.5 내지0.8mm 이하의 사각형의 일정 패턴으로 치밀한 구멍(10)을 형성한다. 보통 이식재 1개당 30 내지 80개의 구멍(10)을 형성한다. 상기 구멍은 세척 내지는 탈지, 탈수, 탈회과정을 용이하고 효과적으로 수행하기 위해서 형성하는 것이다. 또한, 상기 과정을 거치면서, 상기 구멍(10)은 신축성이 생겨 치조골에 이식 시술을 할 때 이식 작업뿐만 아니라 치조골에 맞게 쉽게 성형할 수 있게 한다. After the step (c), the step (d) of forming the spongy bone with a plurality of holes 10 by a drilling operation using the fabric mill in the other side of the coating using a mill mill such as a laser, drill The dense holes 10 are formed in a predetermined pattern of squares of mm or less. Usually 30 to 80 holes 10 are formed per implant. The hole is formed to facilitate and effectively perform cleaning or degreasing, dehydration, and deliming. In addition, while going through the above process, the hole 10 is stretched so that it can be easily molded to fit the alveolar bone as well as the implantation operation when implanted into the alveolar bone.
상기 (d)단계 이후, 1차 탈회 단계(e)는 1 내지 20%의 구연산과 1 내지 50%의 염산을 주원료로 하는 혼합용액을 사용한다. 상기 혼합용액은 디자인 된 이식재 부피의 20 내지 40배가 적당하다. 탈회 작업은 상기 혼합용액에 코팅을 하지 않은 해면골 부위의 칼슘 잔존량이 1 내지 50%가 될 때까지 2 내지 20 시간을 담구고, 동시에 10 내지 300 RPM의 진동 기계에 올려 교반을 시행한다.After the step (d), the first deliming step (e) uses a mixed solution containing 1 to 20% citric acid and 1 to 50% hydrochloric acid as a main raw material. The mixed solution is suitably 20 to 40 times the volume of the designed implant. The deliming operation is immersed for 2 to 20 hours until the remaining amount of calcium in the spongy bone area, which is not coated in the mixed solution, becomes 1 to 50%, and is stirred on a vibration machine of 10 to 300 RPM at the same time.
상기 (e)단계 이후, 코팅재를 제거하는 단계(f)는, 상기(c)단계에 부착된 코팅재를 물리적 작업으로 코팅 부위를 깨끗이 제거한다.After the step (e), step (f) of removing the coating material, the coating material attached to the step (c) by the physical operation to remove the coating site clean.
상기 (f)단계 이후, 결손된 치조골에 이식재를 시술할 경우, 상기 치아 블록골 이식재를 고정하기 위한 스크류 홀(20)을 형성하는 단계(g)를 포함한다. After the step (f), when the implant is implanted in the missing alveolar bone, forming a screw hole 20 for fixing the dental block bone graft (g).
상기 (g)단계 이후, 2차 탈회 단계(h)는, 상기 1차 탈회 단계(e)와 동일한 혼합용액과 동일한 방법으로, 피질골을 형성하고자 하는 부위의 칼슘 잔존량이 50 내지 99%가 될 때까지 실시한다. After the step (g), the second deliming step (h) is performed in the same manner as the mixed solution of the first deliming step (e), when the calcium remaining amount of the site to form the cortical bone becomes 50 to 99% Until.
상기 과정을 거쳐, 피질골과 해면골을 하지는 인체 치조골과 유사한 조직을 가지게 된다. Through the above process, the cortical bone and the spongy bone has a tissue similar to the human alveolar bone.
상기 (h)단계 이후, 멸균 증류수를 이용한 1차 세척 단계(i)는 이식재 부피의 20 내지 40배의 멸균 증류수에 담구고, 10 내지 300 RPM의 진동 기계에 올려 10분 이상 교반을 실시한다. After the step (h), the first washing step (i) using sterile distilled water is immersed in sterile distilled water 20 to 40 times the volume of the implant, put on a vibrating machine of 10 to 300 RPM and agitate for 10 minutes or more.
상기 (i)단계 이후, 탈지 단계(J)는, 상기 멸균 증류수를 완전히 제거 후, 50 내지 100% 트리클로로메탄 용액에 담군 후, 10 내지 300RPM의 진동 기계에 올려 1 내지 20시간 이상 교반을 실시한다. After the step (i), the degreasing step (J), after completely removing the sterile distilled water, immersed in 50 to 100% trichloromethane solution, put on a vibrating machine of 10 to 300RPM and stirred for 1 to 20 hours or more do.
상기 (J) 단계 이후, 멸균증류수와 에틸알콜을 이용한 2차 세척 및 탈수 단계(k)는, 상기 탈지단계의 트리클로로메탄 용액을 제거하기 위하여, 상기(h)와 동일한 방법으로 세척한 후, 멸균 증류수를 완전히 제거 후 100% 에틸알콜에 담군 후 10 내지 300RPM의 진동 기계에 올려 1 내지 20 시간 이상 교반을 실시한다. After the step (J), the second washing and dehydration step (k) using sterile distilled water and ethyl alcohol, after washing in the same manner as in (h) to remove the trichloromethane solution of the degreasing step, After sterile distilled water is completely removed, soaked in 100% ethyl alcohol, put on a vibration machine of 10 to 300 RPM and stirred for 1 to 20 hours or more.
상기 (k)단계 이후, 멸균증류수를 이용한 3차 세척 단계((L)는, 상기(h)와 동일한 방법으로 세척한다. After the step (k), the third washing step using sterile distilled water ((L), is washed in the same manner as in (h).
상기 (L)단계 이후, 과산화수소를 이용한 2차 소독(m)는, 10 내지 35%의 과산화수소에 1 내지 10시간 이상 담군 후, 10 내지 300RPM의 진동 기계에 올려 1 내지 10시간 이상 교반을 실시한다. After the step (L), the second disinfection using hydrogen peroxide (m) is immersed in 10 to 35% hydrogen peroxide for 1 to 10 hours or more, and then put on a vibration machine of 10 to 300 RPM to perform stirring for 1 to 10 hours or more. .
상기 (m)단계 이후, 멸균증류수를 이용한 4차 세척 단계(n)는, 상기(h)와 동일한 방법으로 세척한다. 상기 세척된 치아에 잔존 가공약물을 완전히 제거할 때까지 추가 세척작업이 더 포함할 수도 있다. After step (m), the fourth washing step (n) using sterile distilled water is washed in the same manner as in (h). Further cleaning may be further included until the processed tooth remains completely removed from the washed tooth.
상기 (n)단계 이후, 동결건조 및 멸균소독 단계(o)는, 동결건조기에 이식재를 넣고, 1 내지 20시간 이상 동결 건조시킨 후, 방사선이나 EO가스 소독기에 넣어 멸균한다.After the step (n), lyophilization and sterilization step (o), put the implant in the lyophilizer, lyophilized for 1 to 20 hours or more, and then sterilized in a radiation or EO gas sterilizer.
상기 과정을 거쳐 환자의 치조골 결손 부위에 이식하면 된다. The above procedure is performed by implanting into the alveolar bone defect of the patient.
본 발명의 치아 블록골 이식재는 피질골과 해면골로 이루어져 있어, 이식재를 환자에 시술이후 신생골이 형성되는 동안 이식재의 체적 소실이 발생하지 않는 것을 특징으로 한다. 그로 인해 임플란트 시술의 경우에는 임플란트 픽스쳐가 외부로 노출되는 것을 막아주어 심미성을 유지할 수 있다. 또한 해면골의 조직으로 인해 신생골의 형성을 쉽게 유도하여 임플란트 픽스쳐에 견고한 지지대를 제공한다. The tooth block bone graft of the present invention is composed of cortical bone and spongy bone, characterized in that the volume loss of the graft does not occur during the formation of new bone after the procedure in the patient. As a result, in the case of implantation, the implant fixture can be prevented from being exposed to the outside, thereby maintaining aesthetics. In addition, the tissue of the spongy bone induces the formation of new bone, providing a strong support for the implant fixture.
본 발명은 치조골 결손을 회복하기 위한 치아 블록골 이식재에 관한 것이다. 더욱 상세하게는 치아 블록골 이식재가 인체 치조골과 유사한 피질골과 해면골로 이루어지는 것을 특징으로 하는 치아골 블록 이식재 및 그 제조방법 분야에 이용가능하다.The present invention relates to a tooth block bone graft for repairing alveolar bone defects. More specifically, the dental block bone graft can be used in the field of dental bone block graft and its manufacturing method, characterized in that it consists of cortical bone and spongy bone similar to human alveolar bone.

Claims (3)

  1. 치아 블록골 이식재에 있어서, Tooth block bone graft,
    자가, 이종, 동종중에서 선택된 하나의 치아와, 상기 치아의 병균을 제거하고, 치석과 연조직을 제거하는 1차 소독 단계(a);(A) a first disinfection step of removing one tooth from among autologous, xenogeneic, and allogeneic types, and removing germs of the tooth and removing tartar and soft tissue;
    상기 (a)단계 이후, 치아의 상아질은 완전히 제거하고, 법랑질만 이용하여 이식재 크기로 디자인하는 디자인 단계(b);After the step (a), the dentin of the tooth is completely removed, designing step of designing the implant size using only enamel (b);
    상기 (b)단계 이후, 피질골을 형성하기 위하여, 치아의 일부분을 코팅하는 단계(c);After step (b), coating a portion of the tooth to form a cortical bone (c);
    상기 (c)단계 이후, 상기 코팅된 타측부에 천공장치를 이용하여 천공작업으로 다수의 구멍(10)을 천공하여 해면골을 형성하는 단계(d);After the step (c), the step of forming a spongy bone by drilling a plurality of holes (10) by a punching operation using a cloth mill in the other side coated;
    상기 (d)단계 이후, 1차 탈회 단계(e);After the step (d), the first deliming step (e);
    상기 (e)단계 이후, 상기(c)단계에 부착된 코팅재를 제거하는 단계(f);After the step (e), removing the coating material attached to the step (c) (f);
    상기 (f)단계 이후, 치조골 이식시 고정하기 위한 스크류 홀(20)을 형성하는 단계(g);After the step (f), forming a screw hole (20) for fixing during alveolar bone graft (g);
    상기 (g)단계 이후, 2차 탈회 단계(h);After step (g), a second deliming step (h);
    상기 (h)단계 이후, 멸균 증류수를 이용한 1차 세척 단계(i);After the step (h), the first washing step using sterile distilled water (i);
    상기 (i)단계 이후, 탈지 단계(J);After step (i), a degreasing step (J);
    상기 (J) 단계 이후, 멸균증류수와 에틸알콜을 이용한 2차 세척 및 탈수 단계(k);After the step (J), the second washing and dehydration step using sterile distilled water and ethyl alcohol (k);
    상기 (k)단계 이후, 멸균증류수를 이용한 3차 세척 단계((L);After the step (k), the third washing step using sterile distilled water ((L);
    상기 (L)단계 이후, 과산화수소를 이용한 2차 소독(m);After the step (L), secondary disinfection using hydrogen peroxide (m);
    상기 (m)단계 이후, 멸균증류수를 이용한 4차 세척 단계(n);After the step (m), the fourth washing step using sterile distilled water (n);
    상기 (n)단계 이후, 동결건조 및 멸균소독 단계(o)를 포함하고,After the step (n), and lyophilization and sterilization step (o),
    상기 (n)단계에서의 추가 세척하는 단계를 더 포함하여 최종제품이 인체 치조골과 유사한 피질골과 해면골로 이루어지는 것을 특징으로 치아 블록골 이식재 제조방법.The method of manufacturing a tooth block bone graft material, characterized in that further comprising the step of (n) further comprising the end product is cortical bone and sponge bone similar to human alveolar bone.
  2. 제 1항에 있어서,The method of claim 1,
    상기 (e)단계와 (h) 단계의 탈회단계에 있어서, 염산과 구연산을 혼합한 용액을 사용하는 것을 특징으로 하는 치아 블록골 이식재 제조방법.In the deliming step of step (e) and (h), a method for producing a dental block bone graft material, characterized in that using a mixture of hydrochloric acid and citric acid.
  3. 치아 블록골 이식재에 있어서,Tooth block bone graft,
    자가, 이종, 동종 중에서 선택된 하나의 채취한 치아의 법랑질을 이용하여, 상기 법랑질을 일련의 공정을 거쳐 인체 치조골과 유사한 피질골과 해면골로 형성되어, 이식재를 환자에 시술이후 신생골이 형성되는 동안 이식재의 체적 소실이 발생하지 않는 것을 특징으로 하는 치아 블록골 이식재.Using the enamel of the collected tooth selected from autologous, xenogeneous, or allogeneic, the enamel is formed into cortical and sponge bones similar to human alveolar bone through a series of processes, and the new implant is formed while the new bone is formed after the procedure. A tooth block bone graft, characterized in that no volume loss occurs.
PCT/KR2012/003450 2012-01-17 2012-05-03 Dental block bone graft and method for manufacturing same WO2013108963A1 (en)

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CN110732040A (en) * 2018-07-19 2020-01-31 上海交通大学医学院附属第九人民医院 bone repair material, method and use
CN113476183A (en) * 2021-05-21 2021-10-08 四川大学 Method for digitally designing and manufacturing personalized bone block

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