WO2019004506A1 - Artificial crown and manufacturing method therefor - Google Patents

Artificial crown and manufacturing method therefor Download PDF

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Publication number
WO2019004506A1
WO2019004506A1 PCT/KR2017/006972 KR2017006972W WO2019004506A1 WO 2019004506 A1 WO2019004506 A1 WO 2019004506A1 KR 2017006972 W KR2017006972 W KR 2017006972W WO 2019004506 A1 WO2019004506 A1 WO 2019004506A1
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Prior art keywords
crown
artificial
artificial crown
tooth
manufacturing
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PCT/KR2017/006972
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French (fr)
Korean (ko)
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한형렬
안용국
한인혜
한성웅
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(주)하이템
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Priority to PCT/KR2017/006972 priority Critical patent/WO2019004506A1/en
Publication of WO2019004506A1 publication Critical patent/WO2019004506A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61CDENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C13/00Dental prostheses; Making same
    • A61C13/08Artificial teeth; Making same
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61CDENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C13/00Dental prostheses; Making same
    • A61C13/08Artificial teeth; Making same
    • A61C13/09Composite teeth, e.g. front and back section; Multilayer teeth
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61CDENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C5/00Filling or capping teeth
    • A61C5/70Tooth crowns; Making thereof
    • A61C5/77Methods or devices for making crowns

Definitions

  • the present invention relates to an artificial crown and its manufacturing method, and more particularly, to an artificial crown having improved physical properties by introducing high-strength functional fibers into a crown made only of a conventional resin, And more particularly, to an artificial crown for facilitating the manufacture of a customized prosthesis and providing convenience to dentists and dental technicians, as well as patients.
  • the crown of the tooth refers to the head of the tooth, and the head of the molar is like a crown. It is roughly the upper third of the total teeth.
  • the crown of the front part is essential for esthetical role and accurate pronunciation, while the crown of the molar part functions to chew food, but it is difficult to function properly with only the head of the teeth, and it is possible to have a backed tooth root and healthy periodontal support.
  • An artificial crown is a dental restoration that wraps around the entire tooth. Use it to strengthen the teeth when the teeth are cracked, broken or weakened, when grooving at the root, or when there is not enough tooth structure to support the filler.
  • Artificial crown made of 100% ceramic is mainly used for anterior teeth (front teeth). Ceramic artificial crown is natural and translucent, so it is suitable for use on cosmetic front teeth. On the other hand, if strength is more important than beauty, tooth-colored dental crown is used, which is a mixture of ceramics and metal.
  • Gold teeth are used in the posterior teeth (molar teeth) or in the back teeth. The gold teeth are strong and resistant, and they are stronger than the ceramic teeth and are not broken.
  • Conventional artificial crown products are predominantly crown shaped, predominantly made of aluminum crown for posterior teeth (for molar teeth) and zirconia crown for anterior teeth (forearm teeth).
  • the existing products have a disadvantage in that it is necessary to erase the teeth in order to fit the crown, and it takes a long time to manufacture them to fit them, and it is impossible to wear them immediately. Therefore, the patient has inconvenience and time wasted due to hospital visit again.
  • the present invention has been completed in order to provide convenience to patients, dentists and dental technicians by developing an artificial crown which is easy to manufacture a customized prosthesis by introducing high-strength functional fibers and short-time thermal deformation.
  • one object of the present invention is to provide an artificial crown having improved physical properties by introducing high-strength functional fibers into a crown made only of a conventional resin.
  • Another object of the present invention is to provide an artificial crown manufactured by mixing a nanofiller, a thermoplastic resin and silica on a fiber, compressing and alighting the fiber, cooling through a molding process, and a method of manufacturing the artificial crown .
  • the present invention provides a method of manufacturing a semiconductor device, comprising: (1) mixing a material; (2) applying the mixed material on the fiber in the step (1); (3) pressing the fibers applied in the step (2) and cutting the fibers into a plate; (4) molding the plate, which has been removed in the step (3); (5) cooling the plate formed in the step (4).
  • FIG. 1 The manufacturing method according to the present invention is shown in FIG. 1, and a method of manufacturing an artificial crown according to the present invention will now be described in detail with reference to FIG. 1.
  • a nanofiller, a thermoplastic resin and silica are used as a material, and a nanofiller and a thermoplastic resin are mixed and then silica is mixed.
  • the matrix containing the thermoplastic resin is mostly filled with a ceramic cluster filler containing zirconia (Zirconia) and alumina (Alumina).
  • Zirconia zirconia
  • Alumina alumina
  • the nanofiller and the thermoplastic resin are mixed at a ratio of 90 wt%: 10 wt%.
  • the nanofiller and the thermoplastic resin are mixed at a ratio of 80 wt%: 20 wt%, more preferably at a ratio of 70 wt%: 30 wt%.
  • the thermoplastic resin may be at least one selected from the group consisting of polyglycolic acid (PGA), poly- ⁇ -caprolactone, polydioxanone, polylactic acid-glycolic acid copolymer (PLGA), polydioxane-caprolactone copolymer polyhydroxybutyric acid-co-hydroxy resin, polydioxanone-co- ⁇ -caprolactone, polylactic acid-caprolactone copolymer, polyhydroxybutyric acid-co-hydroxyvleric acid copolymer, Polyoxyethylene-polylactic acid copolymer, polyethylene oxide-polylactic acid copolymer, polyethylene oxide-polylactic glycolic acid copolymer, and polyethylene oxide-polycaprolactone copolymer are used in combination.
  • Yellow and red pigments may be mixed with the thermoplastic resin to control the color tone of the permanent-tooth pipe.
  • the pigments may be used at 0.0001 phr (parts per hundred rubber) to 0.1 phr. Preferably 0.001 to 0.1 phr, more preferably 0.02 to 0.08 phr.
  • the silica (SiO 2 ) is the most abundant component in the crust and is a chemical compound of silicon and oxygen.
  • Silica is a typical glass-forming mineral, and when the liquid is quenched, it readily changes to a glassy state and becomes quartz glass. Quartz glass is highly heat-resistant, has a very low coefficient of thermal expansion, is strong against thermal shock, and has excellent chemical resistance.
  • the hardness of the artificial crown of the present invention can be controlled by controlling the mixing ratio of silica having such characteristics.
  • the fibers may be one or two or more selected from the group consisting of glass fiber, carbon fiber, and aramid fiber.
  • Carbon fiber is a fiber made by heating and carbonizing organic fibers in an inert gas and has properties such as high strength, high tensile strength, light weight, conductivity, corrosion resistance, chemical resistance, fatigue resistance and biocompatibility. Core materials, medical CT equipment, robot parts, aviation, wind power equipment, and automobile parts.
  • Fiberglass is a fiber made by finely milling inorganic fiber obtained by melt-spinning a qualitative glass raw material at a high temperature of 1,600 °C ⁇ 1,800 °C for several hundreds of minutes depending on the application. It has properties such as heat resistance, heat insulation, chemical resistance and thermal stability (FRP) industrial raw materials, leisure products, general industrial products, etc., in combination with organic materials.
  • FRP chemical resistance and thermal stability
  • Aramid fiber is a polymer polyamide formed by bonding an amide bond and an aromatic ring such as a benzene ring.
  • the aramid fiber is excellent in tensile strength, toughness and heat resistance, and has high strength and high elastic modulus. In addition, it is used as plastic reinforcement material because it does not increase even if you apply any force. It is applied to military materials such as bulletproof jacket and helmet, golf club, tennis racket, etc. by taking advantage of these advantages.
  • the application is performed so that the mixed material is coated on the fiber so that the total thickness is 0.1 m to 0.5 m, preferably 0.2 m to 0.4 m, and more preferably 0.25 m to 0.35 m.
  • the plate may be pressed with the mixed material-applied fiber under pressure, and the plate may be cut to a size suitable for its use, for example, a width X length of 300 mm x 300 mm.
  • the artificial crown can be standardized in various sizes.
  • the above standard refers to tooth size, crown length, crown diameter of crown, crown diameter of cervical crown, crown of crown and crown diameter, size and size of each crown.
  • each permanent tooth constituting the maxilla and mandible is divided into a tooth shape, a tooth crown length, a root crown of a crown, a root crown of a cervical crown, a crown of a crown, Respectively.
  • Tables 1 to 3 The results are shown in Tables 1 to 3 below. More specifically, the following Table 1 is a "large” standard, Table 2 is a “medium” standard, and Table 3 is a "small” standard.
  • the tooth size, the length of the crown, the diameter of the crown of the crown, the diameter of the crown of the cervical crown, the diameter of the crown, and the diameter of the crown were set to a single size.
  • the following Tables 1 to 3 are the permanent tooth size standards, and Table 4 is an example of the tooth size basic standard or the present invention.
  • the permanent teeth can be manufactured to the standardized artificial crown according to the present invention in the standards shown in Tables 1 to 3 above, and the artificial crown according to the present invention can be manufactured according to the standard shown in Table 4 .
  • the molding in the step (4) is to form the crown for the purpose of the present invention so as to have various sizes and shapes of the above-mentioned standardized sizes.
  • the molding can be carried out by a conventional method, and one specific example can be formed by a compression molding method.
  • Compression molding is a method of putting a plastic material into a mold, heating it, and applying pressure to the desired shape.
  • the plate put in step (3) is placed in a die mold having the above standard, heated with heat at 100 to 200 DEG C, and then mixed with a material layer in which the fiber portion of the plate is mixed by applying pressure To form a shell.
  • a softening and holding process may be added in the molding step.
  • the softening is a process for increasing the workability of a plate formed in a shell shape, and the formed shell-shaped plate is heated to 100 to 150 ° C to increase the workability.
  • the pressure is applied to compensate for the shrinkage of the plate in the mold when the molded plate is cooled, so that the shape of the product can be maintained as desired and the defective portion of the molded product can be prevented through the pressure holding process.
  • the crown-shaped crown can be manufactured by cooling it by a conventional method for 30 to 40 seconds.
  • the artificial crown manufactured according to the present invention can be used as an injection tube (for a child) or a permanent tooth tube (for an adult).
  • the tooth is called a child's tooth, and the tooth is replaced with a permanent tooth.
  • the artificial crown for an artificial tooth has a characteristic of being deformed within 100 ° C. It can be put into boiling water for 20 to 50 seconds, and if it has a slight ductility, it can be directly used by pressing it into the oral cavity. It is preferably used in boiling water for 25 to 40 seconds, more preferably 30 to 35 seconds.
  • the permanent teeth have a large shape, rich in minerals, high in hardness, and small in size ( ⁇ ⁇ cavity) compared with the teeth, because they function during their lifetime.
  • the artificial crown for permanent tooth can be deformed at over 100 °C and it can be used by pressing directly on the gypsum model with the deteriorator.
  • the artificial crown of the present invention may be a single crown, but it may be a connecting crown for artificial tangles in which two or more are connected together.
  • the connecting crown can be manufactured by the same method as that of the remaining artificial crown except that the blending ratio of the nanofiller and the thermoplastic resin is blended with nanofiller ( ⁇ 80 wt%) and thermoplastic resin ( ⁇ 20 wt%).
  • the primer is applied inside the manufactured artificial crown, and light curing is performed for 5 to 30 seconds.
  • light curing is performed for 7 to 15 seconds, and more preferably light curing is performed for 9 to 12 seconds.
  • the composite resin is filled in the artificial crown, and light curing is performed again for 10 to 30 seconds.
  • composite resin is a mixed material composed of organic polymer and inorganic filler. Due to the development of polymer engineering, composite resins are widely used in various fields ranging from automobiles, aircrafts, household appliances, and medical equipments that require high strength in daily life, and they are attracting attention as dental restorative materials. Dental restorative materials have traditionally been used with materials such as gold, alloys, or amalgam because high strength is required to restore the chewing function. These metallic materials have the disadvantage of being non-esthetic because they do not have the color of teeth. Also, since the metallic material is not bonded to the teeth, many deletions of the teeth must be preceded in order to prevent the restoration from falling off. In contrast, the adhesive restoration including the composite resin has the advantage of minimizing tooth deletion and enhancing the structure of the vulnerable tooth by the defect, so that the tooth can be preserved without unnecessary tooth erasure.
  • the artificial crown manufactured according to the above manufacturing method can be used to easily manufacture a customized prosthesis that enables the restoration of the lost tooth function and the aesthetic shape.
  • the artificial crown of the present invention can be easily used for manufacturing a customized prosthesis for restoration of a lost tooth function and an aesthetic shape, thereby providing convenience to dentists and dental technicians, as well as patients.
  • FIG. 1 is a flow chart of a manufacturing process of an artificial crown of the present invention.
  • Fig. 2 shows a sample preparation process for evaluating the properties of an artificial crown of the present invention.
  • FIG. 3 shows a sample preparation process for evaluating the water absorption and solubility of the artificial crown of the present invention.
  • an inorganic composite resin is prepared by mixing nanofiller ( ⁇ 70 wt%), thermoplastic resin ( ⁇ 30 wt%) and silica so as to have a total thickness of 0.3 m on the high- Respectively.
  • yellow and red pigments were mixed with a thermoplastic resin to show the color tone of the artificial crown.
  • the high-strength functional fiber coated with the inorganic composite resin was pressed to produce a plate having a size of 300 mm x 300 mm.
  • the prepared plate was placed in a metal mold, heated at about 150 ° C. for 15 seconds, and then shaped into a shell. Then, it was softened by heating to about 120 DEG C, and a pressure holding process was performed. After cooling for 30 to 40 seconds, a crown-shaped crown was prepared.
  • the connecting crown was prepared in the same manner as the other artificial crown manufacturing methods except that the blending ratio of the nanofiller and the thermoplastic resin was blended with nanofiller ( ⁇ 80 wt%) and thermoplastic resin ( ⁇ 20 wt%).
  • the artificial crown can be manufactured as an inlet tube (for a child) or a permanent tooth tube (for an adult).
  • the inlet pipe has a characteristic of being deformed within 100 °C and it is put into boiling water for more than 30 seconds and if it has a slight ductility, it is directly pressed to the oral cavity and molded.
  • the permanent-tooth tube is a crown with increased hardness by varying the content of silica and has a characteristic of being deformed at a temperature of 100 ° C or higher. It is lightly heated by a deteriorator and directly press-molded into a plaster model.
  • the prepared artificial crown was coated with a primer in a crown-shaped artificial crown, subjected to light curing for about 10 seconds, filled with a composite resin, and then subjected to light curing for about 20 seconds It is covered on the teeth to be treated and finally used by polishing.
  • the specimens of the artificial crown prepared in the above Example 1 were classified into bubbles and defects according to the Guideline of the Food and Drug Administration's Safety Directive and Related Standard and Food Safety Management Notice No. 2014-115, : ISO 22112), surface finish (related standards: ISO 22112, ISO 10477), color consistency (ISO 7491), color stability, water absorption, water solubility and biosafety.
  • the specimens for the color stability test were 37 ⁇ 1 for 23 ⁇ 1 hours.
  • the sample preparation process is shown in Fig.
  • the water absorption and water solubility test specimens were immersed in water at 37 ⁇ 1 ° C for 7 days ⁇ 2 hours and then wetted specimens were weighed and the wet specimens were heated at 37 ⁇ 1 ° C Dried in an oven at 23 ⁇ 1 ° C for 60 ⁇ 10 hours and then used.
  • the sample preparation process is shown in Fig.
  • Cytotoxicity test was carried out using the sample solution to evaluate the biological safety of the sample.
  • the artificial crown manufactured according to the manufacturing method of the present invention meets the Common Criteria for Biological Safety of Medical Devices, Guideline of the Food and Drug Administration, and Related Standard and Food Safety Management Notice No. 2014-115, It is confirmed that it can be useful for the dental equipments industry for making prosthetic prosthesis.
  • the present invention relates to an artificial crown capable of improving physical properties in the production of an artificial crown and capable of easily fabricating a customized prosthesis, and a method of manufacturing the same.

Abstract

The present invention provides an artificial crown and a manufacturing method therefor, and according to the manufacturing method of the present invention, an artificial crown having a crown shape can be prepared by mixing a nanofiller, a thermoplastic resin and silica, and then applying the mixture onto fibers so as to prepare a plate, placing the prepared plate into a mold, applying heat thereto so as to perform molding, and then cooling the same. In addition, the artificial crown of the present invention can be thermally deformed in a short time and can be easily used for the production of a customized denture capable of restoring lost dental functions and an aesthetic appearance, thereby enabling convenience to be provided to patients and also to dentists and dental technicians.

Description

인공치관 및 그 제조 방법Artificial crown and its manufacturing method
본 발명은 인공치관 및 그 제조 방법에 관한 것으로, 더욱 상세하게는 기존의 레진으로만 제조된 치관에 고강도 기능성 섬유를 도입하여 물성이 개선된 인공치관을 제조하고, 이를 이용하여 단시간 열변형에 의한 맞춤형 보철 제작을 용이하게하여 환자는 물론 치과의사, 치과기공사들에게 편의성을 제공하는 인공치관 및 그 제조방법에 관한 것이다.The present invention relates to an artificial crown and its manufacturing method, and more particularly, to an artificial crown having improved physical properties by introducing high-strength functional fibers into a crown made only of a conventional resin, And more particularly, to an artificial crown for facilitating the manufacture of a customized prosthesis and providing convenience to dentists and dental technicians, as well as patients.
일반적으로 치아는 충치나 잇몸 질환, 발치 등에 의해 손상되면 음식물의 섭취를 위한 파쇄가 어렵게 되거나, 서서히 얼굴의 형태를 비대칭적으로 변형시켜 타인의 시선에 대해 위축감을 가질 수 있으므로 손상되거나 발치된 부위는 건강한 생활을 영위하기 위하여 신속한 치료와 인공 치아로의 시술이 필수적이다.Generally, when a tooth is damaged by tooth decay, gum disease, or tooth extraction, it is difficult to break up for ingestion of food, or the shape of the face may be asymmetrically deformed, Rapid treatment and treatment with artificial teeth are essential for a healthy life.
치관은 치아의 머리 부분을 지칭하며, 어금니의 머리 부위가 마치 왕관 모양을 닮았다고 하여 붙여진 이름이다. 전체 치아 중 대략 상부 1/3에 해당한다. 앞니 부분의 치관은 심미적인 역할과 정확한 발음에 필수적이며, 어금니 부분의 치관은 음식물을 씹는 기능을 하지만, 치아머리만으로는 제대로 기능을 하기 어렵고 하부의 치아뿌리와 건강한 치주조직의 뒷받침이 있어야 가능하다. The crown of the tooth refers to the head of the tooth, and the head of the molar is like a crown. It is roughly the upper third of the total teeth. The crown of the front part is essential for esthetical role and accurate pronunciation, while the crown of the molar part functions to chew food, but it is difficult to function properly with only the head of the teeth, and it is possible to have a backed tooth root and healthy periodontal support.
인공치관(artificial crown)은 치아 전체를 감싸는 치과적 복구 방법이다. 치아가 금이 가고 깨지거나 약해졌을 때, 뿌리 부분에 홈을 만드는 처리를 했을 때 치아를 강하게 하기 위해 사용하며, 혹은 충전재를 지지할만한 충분한 치아 구조가 없을 때 인공치관을 사용한다. 100% 세라믹으로 만들어진 인공치관은 주로 전치부(앞니)에 사용한다. 세라믹 인공치관은 자연스럽고 반투명하므로 미용상 앞니에 사용하기에 적합하다. 한편, 미용보다는 강도가 중요한 경우, 치아 색으로 염색된 치관을 사용하는데, 이는 도자기 성분과 금속 성분을 혼합하여 사용한다. 구치부(어금니)나 뒤쪽에 위치하는 치아에는 금니를 사용하는데, 금니는 강하고 내성이 있으며, 도자기 치관보다 더 튼튼하여 잘 부서지지 않는 장점이 있다. An artificial crown is a dental restoration that wraps around the entire tooth. Use it to strengthen the teeth when the teeth are cracked, broken or weakened, when grooving at the root, or when there is not enough tooth structure to support the filler. Artificial crown made of 100% ceramic is mainly used for anterior teeth (front teeth). Ceramic artificial crown is natural and translucent, so it is suitable for use on cosmetic front teeth. On the other hand, if strength is more important than beauty, tooth-colored dental crown is used, which is a mixture of ceramics and metal. Gold teeth are used in the posterior teeth (molar teeth) or in the back teeth. The gold teeth are strong and resistant, and they are stronger than the ceramic teeth and are not broken.
기존의 인공치관 제품은 치관의 형태가 미리 형성된 것으로 구치부(어금니용)에 알루미늄 치관, 전치부(앞니용)에 지르코니아 치관을 사용한 소아용 유치관 제품이 주를 이루고 있다. 또한, 기존의 제품은 치관에 맞게끔 치아를 삭제하여야 하고, 그에 꼭 맞게 제작하기 위해서는 제작 시간이 오래 걸려 즉시 착용이 불가능하다는 단점이 있다. 따라서 환자의 병원 재방문으로 인한 번거로움과 시간적인 낭비가 발생하였다.Conventional artificial crown products are predominantly crown shaped, predominantly made of aluminum crown for posterior teeth (for molar teeth) and zirconia crown for anterior teeth (forearm teeth). In addition, the existing products have a disadvantage in that it is necessary to erase the teeth in order to fit the crown, and it takes a long time to manufacture them to fit them, and it is impossible to wear them immediately. Therefore, the patient has inconvenience and time wasted due to hospital visit again.
이에 본 발명에서는 고강도 기능성 섬유가 도입되어 단시간 열변형에 의한 맞춤형 보철 제작이 용이한 인공치관을 개발함으로써 환자는 물론 치과의사, 치과기공사들에게 편의성을 제공하고자 본 발명을 완성하게 되었다.Accordingly, the present invention has been completed in order to provide convenience to patients, dentists and dental technicians by developing an artificial crown which is easy to manufacture a customized prosthesis by introducing high-strength functional fibers and short-time thermal deformation.
따라서, 본 발명의 하나의 목적은 기존의 레진으로만 제조된 치관에 고강도 기능성 섬유를 도입하여 물성이 개선된 인공치관을 제공하기 위한 것이다. Accordingly, one object of the present invention is to provide an artificial crown having improved physical properties by introducing high-strength functional fibers into a crown made only of a conventional resin.
본 발명의 다른 하나의 목적은 나노필러, 열가소성 레진 및 실리카를 혼합하여 섬유 위에 도포하고, 이를 압착 및 제단한 후, 성형 과정을 거쳐 냉각시켜 제조한 인공치관 및 그 제조하는 방법을 제공하기 위한 것이다. Another object of the present invention is to provide an artificial crown manufactured by mixing a nanofiller, a thermoplastic resin and silica on a fiber, compressing and alighting the fiber, cooling through a molding process, and a method of manufacturing the artificial crown .
하나의 양태로서, 본 발명은 (1) 재료를 혼합하는 단계; (2) 상기 (1)단계에서 혼합된 재료를 섬유 위에 도포하는 단계; (3) 상기 (2)단계에서 도포된 섬유를 압착하여 플레이트로 제단하는 단계; (4) 상기 (3)단계에서 제단된 플레이트를 성형하는 단계; (5) 상기 (4)단계에서 성형된 플레이트를 냉각하는 단계;를 포함하는 인공치관의 제조방법을 제공한다. In one aspect, the present invention provides a method of manufacturing a semiconductor device, comprising: (1) mixing a material; (2) applying the mixed material on the fiber in the step (1); (3) pressing the fibers applied in the step (2) and cutting the fibers into a plate; (4) molding the plate, which has been removed in the step (3); (5) cooling the plate formed in the step (4).
본 발명에 따른 상기 제조방법을 도 1에 나타내었으며, 이하에서는 본 발명에 따른 인공치관의 제조방법을 도 1을 참고로 각 단계별로 상세히 설명한다.The manufacturing method according to the present invention is shown in FIG. 1, and a method of manufacturing an artificial crown according to the present invention will now be described in detail with reference to FIG. 1.
상기 (1)단계에서 재료는 나노필러, 열가소성 레진 및 실리카를 사용하며, 나노필러와 열가소성 레진을 혼합한 다음 실리카를 혼합하여 사용한다. 통상적으로 열가소성 레진이 함유된 기질(matrix)은 대부분이 지르코니아(Zirconia)와 알루미나(Alumina)가 함유된 세라믹 클러스터 필러로 채워져 있다. 여기에 나노필러로 기질(matrix)의 틈새 공간을 채우면 레진의 마모와 파절에 대한 저항성을 향상시킬 수 있으므로 나노필러와 열가소성 레진을 90 wt% : 10 wt% 비율로 혼합하여 사용한다. 바람직하게는 나노필러와 열가소성 레진을 80 wt% : 20 wt% 비율로 혼합하여 사용하며, 보다 바람직하게는 70 wt% : 30 wt% 비율로 혼합하여 사용한다. In the step (1), a nanofiller, a thermoplastic resin and silica are used as a material, and a nanofiller and a thermoplastic resin are mixed and then silica is mixed. Typically, the matrix containing the thermoplastic resin is mostly filled with a ceramic cluster filler containing zirconia (Zirconia) and alumina (Alumina). In this case, filling the interstitial spaces of the matrix with the nanopiller can improve the resistance to abrasion and fracture of the resin. Therefore, the nanofiller and the thermoplastic resin are mixed at a ratio of 90 wt%: 10 wt%. Preferably, the nanofiller and the thermoplastic resin are mixed at a ratio of 80 wt%: 20 wt%, more preferably at a ratio of 70 wt%: 30 wt%.
상기 열가소성 레진은 폴리글로콜산(PGA), 폴리카프로락톤(Poly-ε-caprolactone), 폴리다이옥산온(polydioxanone), 폴리락틴산-글리콜산 공중합체(PLGA), 폴리다이옥산-카프로락톤 공중합체(polydioxanone-co-ε-caprolactone), 폴리락틴산-카프로락톤 공중합체(PLA co-ε-caprolactone), 폴리하이드록시부티릭산-하이드록시빌러릭산 공중합체(polyhydroxybutyric acid-co-hydroxyvleric acid), 폴리포스포에스터(polyphosphoester), 폴리에틸렌옥사이드-폴리락틴산 공중합체, 폴리에틸렌옥사이드-폴리락틱글리콜산 공중합체 및 폴리에틸렌옥사이드-폴리카프로락톤 공중합체 중에서 선택된 1종 또는 2종 이상을 혼합하여 사용한다. The thermoplastic resin may be at least one selected from the group consisting of polyglycolic acid (PGA), poly-ε-caprolactone, polydioxanone, polylactic acid-glycolic acid copolymer (PLGA), polydioxane-caprolactone copolymer polyhydroxybutyric acid-co-hydroxy resin, polydioxanone-co-ε-caprolactone, polylactic acid-caprolactone copolymer, polyhydroxybutyric acid-co-hydroxyvleric acid copolymer, Polyoxyethylene-polylactic acid copolymer, polyethylene oxide-polylactic acid copolymer, polyethylene oxide-polylactic glycolic acid copolymer, and polyethylene oxide-polycaprolactone copolymer are used in combination.
상기 열가소성 레진에 Yellow와 Red 안료를 혼합하여 영구치관의 색조를 조절할 수 있으며, 안료는 0.0001 phr(parts per hundred rubber) 내지 0.1 phr을 사용할 수 있다. 바람직하게는 0.001 phr 내지 0.1 phr을 사용하며, 보다 바람직하게는 0.02 phr 내지 0.08 phr을 사용한다. Yellow and red pigments may be mixed with the thermoplastic resin to control the color tone of the permanent-tooth pipe. The pigments may be used at 0.0001 phr (parts per hundred rubber) to 0.1 phr. Preferably 0.001 to 0.1 phr, more preferably 0.02 to 0.08 phr.
상기 실리카(SiO2)는 지각 중에 가장 많이 존재하는 성분으로, 규소와 산소의 화학적 결합체이다. 실리카는 대표적인 유리 형성 광물이고, 액체를 급냉하면 쉽사리 유리상태로 변화하여, 석영 유리가 된다. 석영 유리는 고내열(高耐熱)이어서 열팽창률이 대단히 작고, 열충격에 강할 뿐만 아니라 내약품성이 우수하다. 이러한 특성을 가지는 실리카의 혼합비를 조절하여 본 발명의 인공치관의 경도를 조절할 수 있다. The silica (SiO 2 ) is the most abundant component in the crust and is a chemical compound of silicon and oxygen. Silica is a typical glass-forming mineral, and when the liquid is quenched, it readily changes to a glassy state and becomes quartz glass. Quartz glass is highly heat-resistant, has a very low coefficient of thermal expansion, is strong against thermal shock, and has excellent chemical resistance. The hardness of the artificial crown of the present invention can be controlled by controlling the mixing ratio of silica having such characteristics.
상기 (2)단계에서 섬유는 유리 섬유(glass fiber), 탄소 섬유(carbon fiber), 아라미드 섬유(aramid fiber)로 이루어진 기능성 섬유소재 군에서 선택된 1종 또는 2종 이상을 혼합하여 사용한다. In the step (2), the fibers may be one or two or more selected from the group consisting of glass fiber, carbon fiber, and aramid fiber.
탄소 섬유는 유기 섬유를 비활성 기체 속에서 가열 및 탄화하여 만든 섬유로 고강도, 고인장강도, 경량, 전도성, 내식, 내약품성, 내피로성, 생체적합성 등의 특성을 가지며, 국방 기술의 전략적 무기체계의 핵심소재, 의료용 CT장비, 로봇용 부품, 항공, 풍력 발전 기기, 자동차 부품 등에 적용되고 있다. Carbon fiber is a fiber made by heating and carbonizing organic fibers in an inert gas and has properties such as high strength, high tensile strength, light weight, conductivity, corrosion resistance, chemical resistance, fatigue resistance and biocompatibility. Core materials, medical CT equipment, robot parts, aviation, wind power equipment, and automobile parts.
유리 섬유는 정성된 유리 원료를 1,600 ℃ ~ 1,800 ℃의 고온으로 용융 방사하여 얻어지는 미세한 무기질 섬유를 사용 용도에 따라 수백분씩 접속 처리하여 만든 섬유로 내열성, 단열성, 내약품성, 열안전성 등의 특성을 가지며, 유기재료와 복합하여 섬유강화플라스틱(FRP) 공업용 원부자재, 레져용, 일반 산업용 등에 적용되고 있다.Fiberglass is a fiber made by finely milling inorganic fiber obtained by melt-spinning a qualitative glass raw material at a high temperature of 1,600 ℃ ~ 1,800 ℃ for several hundreds of minutes depending on the application. It has properties such as heat resistance, heat insulation, chemical resistance and thermal stability (FRP) industrial raw materials, leisure products, general industrial products, etc., in combination with organic materials.
아라미드 섬유는 아마이드 결합과 벤젠고리와 같은 방향족 고리를 결합시켜 형성시킨 고분자 폴리아마이드로 인장강도, 강인성, 내열성이 뛰어나며, 고강력, 고탄성률 등의 특성을 가진다. 또한, 아무리 힘을 가해도 늘어나지 않아 플라스틱 보강재(補强材)로 쓰이며, 이러한 장점을 이용하여 방탄 재킷, 헬멧 등의 군수물자와 골프채, 테니스 라켓 등에 적용되고 있다. Aramid fiber is a polymer polyamide formed by bonding an amide bond and an aromatic ring such as a benzene ring. The aramid fiber is excellent in tensile strength, toughness and heat resistance, and has high strength and high elastic modulus. In addition, it is used as plastic reinforcement material because it does not increase even if you apply any force. It is applied to military materials such as bulletproof jacket and helmet, golf club, tennis racket, etc. by taking advantage of these advantages.
상기 도포는 총 두께가 0.1 m ~ 0.5 m가 되도록 섬유 위에 혼합된 재료가 코팅되도록 도포하며, 바람직하게는 0.2 m ~ 0.4 m, 보다 바람직하게는 0.25 m ~ 0.35 m가 되도록 도포한다. The application is performed so that the mixed material is coated on the fiber so that the total thickness is 0.1 m to 0.5 m, preferably 0.2 m to 0.4 m, and more preferably 0.25 m to 0.35 m.
상기 (3)단계에서 플레이트는 상기 혼합된 재료가 도포된 섬유를 압력을 가해 압착하고, 이를 사용하기에 적합한 크기, 예를 들어 가로 X 세로가 300 mm X 300 mm로 제단할 수 있다. In the step (3), the plate may be pressed with the mixed material-applied fiber under pressure, and the plate may be cut to a size suitable for its use, for example, a width X length of 300 mm x 300 mm.
본 발명에 있어서 상기 인공치관은 다양한 사이즈로 규격화되어 제조될 수 있다.In the present invention, the artificial crown can be standardized in various sizes.
상기 규격은 치아의 외형, 치관의 길이, 치관의 근·원심경, 치경부의 근·원심경 및 치관의 순설과 협설경을 크기별로 분류하고 이를 일정화 및 계량화시킨 것을 말한다.The above standard refers to tooth size, crown length, crown diameter of crown, crown diameter of cervical crown, crown of crown and crown diameter, size and size of each crown.
상기 규격에 대한 하나의 구체적 예로서, 상악 및 하악을 구성하는 각 영구치를 치아의 외형, 치관의 길이, 치관의 근·원심경, 치경부의 근·원심경 및 치관의 순설과 협설경을 크기별로 대, 중 및 소로 구별하였으며, 이를 하기 표 1 내지 3에 나타내었다. 보다 구체적으로, 하기 표 1은 "대" 규격이며, 표 2는 "중" 규격이며, 표 3은 "소" 규격이다. 유치에서는 치아의 외형, 치관의 길이, 치관의 근·원심경, 치경부의 근·원심경 및 치관의 순설과 협설경을 단일 크기로 하였고, 표 4는 유치 규격이다. 하기 표 1 내지 3은 영구치 규격이고, 표 4는 유치기본 규격이나, 본 발명을 이루는 상기 규격에 대한 하나의 예로서, 상기 규격이 이로 반드시 제한되는 것은 아니다. As a specific example of the above standard, each permanent tooth constituting the maxilla and mandible is divided into a tooth shape, a tooth crown length, a root crown of a crown, a root crown of a cervical crown, a crown of a crown, Respectively. The results are shown in Tables 1 to 3 below. More specifically, the following Table 1 is a "large" standard, Table 2 is a "medium" standard, and Table 3 is a "small" standard. The tooth size, the length of the crown, the diameter of the crown of the crown, the diameter of the crown of the cervical crown, the diameter of the crown, and the diameter of the crown were set to a single size. The following Tables 1 to 3 are the permanent tooth size standards, and Table 4 is an example of the tooth size basic standard or the present invention.
영구치 치아(단위=mm)Permanent tooth (unit = mm) 치관의 길이Length of crown 치관의 근원심경Root of crown 치경부의 근원심경Root of cervical spine 치관의 순설, 협설경Crown of the crown,
상악Maxilla 중절치Central incisor 11.511.5 9.59.5 8.08.0 8.08.0
측절치Lateral incisal 10.010.0 7.57.5 6.06.0 7.07.0
견치Canine 11.011.0 8.58.5 6.56.5 9.09.0
제 1소구치First premolar 9.59.5 8.08.0 6.06.0 10.010.0
제 2소구치Second premolar 9.59.5 8.08.0 6.06.0 10.010.0
제 1대구치First molar 8.58.5 11.011.0 9.09.0 12.012.0
제 2대구치Second molar 8.08.0 10.010.0 8.08.0 12.012.0
하악Mandatory 중절치Central incisor 10.010.0 6.06.0 4.54.5 7.07.0
측절치Lateral incisal 10.510.5 6.56.5 5.05.0 7.57.5
견치Canine 12.012.0 8.08.0 6.56.5 8.58.5
제 1소구치First premolar 9.59.5 8.08.0 6.06.0 8.58.5
제 2소구치Second premolar 9.09.0 8.08.0 6.06.0 9.09.0
제 1대구치First molar 8.58.5 12.012.0 10.010.0 11.511.5
제 2대구치Second molar 8.08.0 11.511.5 9.09.0 11.011.0
영구치 치아(단위=mm)Permanent tooth (unit = mm) 치관의 길이Length of crown 치관의 근원심경Root of crown 치경부의 근원심경Root of cervical spine 치관의 순설, 협설경Crown of the crown,
상악Maxilla 중절치Central incisor 10.510.5 8.58.5 7.07.0 7.07.0
측절치Lateral incisal 9.09.0 6.56.5 5.05.0 6.06.0
견치Canine 10.010.0 7.57.5 5.55.5 8.08.0
제 1소구치First premolar 8.58.5 7.07.0 5.05.0 9.09.0
제 2소구치Second premolar 8.58.5 7.07.0 5.05.0 9.09.0
제 1대구치First molar 7.57.5 10.010.0 8.08.0 11.011.0
제 2대구치Second molar 7.07.0 9.09.0 7.07.0 11.011.0
하악Mandatory 중절치Central incisor 9.09.0 5.05.0 3.53.5 6.06.0
측절치Lateral incisal 9.59.5 5.55.5 4.04.0 6.56.5
견치Canine 11.011.0 7.07.0 5.55.5 7.57.5
제 1소구치First premolar 8.58.5 7.07.0 5.05.0 7.57.5
제 2소구치Second premolar 8.08.0 7.07.0 5.05.0 8.08.0
제 1대구치First molar 7.57.5 11.011.0 9.09.0 10.510.5
제 2대구치Second molar 7.07.0 10.510.5 8.08.0 10.010.0
영구치 치아(단위=mm)Permanent tooth (unit = mm) 치관의 길이Length of crown 치관의 근원심경Root of crown 치경부의 근원심경Root of cervical spine 치관의 순설, 협설경Crown of the crown,
상악Maxilla 중절치Central incisor 9.59.5 7.57.5 6.06.0 6.06.0
측절치Lateral incisal 8.08.0 5.55.5 4.04.0 5.05.0
견치Canine 9.09.0 6.56.5 4.54.5 7.07.0
제 1소구치First premolar 7.57.5 6.06.0 4.04.0 8.08.0
제 2소구치Second premolar 7.57.5 6.06.0 4.04.0 8.08.0
제 1대구치First molar 6.56.5 9.09.0 7.07.0 10.010.0
제 2대구치Second molar 6.06.0 8.08.0 6.06.0 10.010.0
하악Mandatory 중절치Central incisor 8.08.0 4.04.0 2.52.5 5.05.0
측절치Lateral incisal 8.58.5 4.54.5 3.03.0 5.55.5
견치Canine 10.010.0 6.06.0 4.54.5 6.56.5
제 1소구치First premolar 7.57.5 6.06.0 4.04.0 6.56.5
제 2소구치Second premolar 7.07.0 6.06.0 4.04.0 7.07.0
제 1대구치First molar 6.56.5 10.010.0 8.08.0 9.59.5
제 2대구치Second molar 6.06.0 9.59.5 7.07.0 9.09.0
유치 치아(단위=mm)Tooth tooth (unit = mm) 치관의 길이Length of crown 치관의 근원심경Root of crown 치경부의 근원심경Root of cervical spine 치관의 순설, 협설경Crown of the crown,
상악Maxilla 중절치Central incisor 6.06.0 6.56.5 4.54.5 5.05.0
측절치Lateral incisal 5.65.6 5.15.1 3.73.7 4.84.8
견치Canine 6.56.5 7.07.0 5.15.1 7.07.0
제 1구치First Goal 5.15.1 7.37.3 5.25.2 8.58.5
제 2구치Second posterior 5.75.7 8.28.2 6.46.4 10.010.0
하악Mandatory 중절치Central incisor 5.05.0 4.24.2 3.03.0 4.04.0
측절치Lateral incisal 5.25.2 4.14.1 3.03.0 4.04.0
견치Canine 6.56.5 5.05.0 3.73.7 4.84.8
제 1구치First Goal 6.06.0 7.77.7 6.56.5 7.07.0
제 2구치Second posterior 5.55.5 9.99.9 7.27.2 8.78.7
상기한 바와 같이, 영구치는 상기 표 1 내지 3에서 나타낸 규격으로 본 발명에 따른 규격화된 인공치관을 제조할 수 있으며, 유치는 상기 표 4에서 나타낸 규격으로 본 발명에 따른 규격화된 인공치관을 제조할 수 있다.As described above, the permanent teeth can be manufactured to the standardized artificial crown according to the present invention in the standards shown in Tables 1 to 3 above, and the artificial crown according to the present invention can be manufactured according to the standard shown in Table 4 .
상기 (4)단계에서 성형은 본 발명의 목적으로 하는 치관을 상기의 규격화된 다양한 크기와 모양을 가질 수 있도록 형태를 만드는 것이다. 성형은 통상의 방법으로 이루어질 수 있는데, 하나의 구체적인 예로서 압축 성형의 방법으로 형태를 만들 수 있다. 압축 성형은 플라스틱 재료를 형틀에 넣고 가열한 다음 압력을 가해 원하는 모양으로 만드는 방법이다. 본 발명의 하나의 구체적 예로서 상기 (3)단계에서 제단된 플레이트를 상기 규격을 가지는 금형틀에 넣고, 100 ~ 200 ℃의 열로 가열한 다음 압력을 가해 플레이트의 섬유 부분이 혼합된 재료층과 섞이게 하여 shell 형태로 성형한다. 바람직하게는 120 ~ 180 ℃의 열을 가해 성형하며, 보다 바람직하게는 140 ~ 160 ℃의 열을 가해 성형한다. 한편, 상기 성형 단계에서 연화 및 보압 공정을 추가할 수 있다. 연화는 shell 형태로 성형된 플레이트의 가공성을 증가시키기 위해 처리하는 과정으로서 상기 성형된 shell 형태의 플레이트를 100 ~ 150 ℃로 가열하여 가공성을 증가시킨다. 바람직하게는 110 ~ 140 ℃로 가열하며, 보다 바람직하게는 115 ~ 130 ℃로 가열한다. 보압은 상기 성형된 플레이트를 냉각할 때, 금형틀 내의 플레이트의 수축을 보상하기 위해서 압력을 가하는 것으로 보압 과정을 통해 제품의 형상을 원하는 대로 유지하고 성형품의 불량을 방지할 수 있다.The molding in the step (4) is to form the crown for the purpose of the present invention so as to have various sizes and shapes of the above-mentioned standardized sizes. The molding can be carried out by a conventional method, and one specific example can be formed by a compression molding method. Compression molding is a method of putting a plastic material into a mold, heating it, and applying pressure to the desired shape. As a specific example of the present invention, the plate put in step (3) is placed in a die mold having the above standard, heated with heat at 100 to 200 DEG C, and then mixed with a material layer in which the fiber portion of the plate is mixed by applying pressure To form a shell. Preferably 120 to 180 캜, and more preferably 140 to 160 캜. On the other hand, a softening and holding process may be added in the molding step. The softening is a process for increasing the workability of a plate formed in a shell shape, and the formed shell-shaped plate is heated to 100 to 150 ° C to increase the workability. Preferably 110 to 140 占 폚, and more preferably 115 to 130 占 폚. The pressure is applied to compensate for the shrinkage of the plate in the mold when the molded plate is cooled, so that the shape of the product can be maintained as desired and the defective portion of the molded product can be prevented through the pressure holding process.
상기 (5)단계에서 30 ~ 40초 동안 통상의 방법에 의해 냉각하여 크라운 형태의 인공치관을 제조할 수 있다. In the step (5), the crown-shaped crown can be manufactured by cooling it by a conventional method for 30 to 40 seconds.
본 발명에 따라 상기 제조된 인공치관은 유치관(소아용) 또는 영구치관(성인용)으로 사용될 수 있다. 어린아이의 치아를 유치라고 하며, 유치는 다시 영구치로 대체된다. 유치관용 인공치관은 100 ℃ 이내에서 변형되는 특성을 가지며 끓는 물속에 20 ~ 50초 동안 넣어 약간의 연성이 생기면 구강에 직접 압접하여 성형하여 사용할 수 있다. 바람직하게는 끓는 물속에 25 ~ 40초 동안 넣어 사용하며, 보다 바람직하게는 30 ~ 35초 동안 넣어 사용한다. 반면, 영구치는 유치가 빠진 뒤에 나는 일생 동안 기능을 영위하는 이로 유치에 비해 형이 크고 무기질이 풍부하며 경도가 높고, 치수강(齒髓腔)이 좁다. 영구치관용 인공치관은 100 ℃ 이상에서 변형되는 특성을 가지며 열화기로 달구어 석고 모형에 직접 압접하여 성형하여 사용할 수 있다. The artificial crown manufactured according to the present invention can be used as an injection tube (for a child) or a permanent tooth tube (for an adult). The tooth is called a child's tooth, and the tooth is replaced with a permanent tooth. The artificial crown for an artificial tooth has a characteristic of being deformed within 100 ° C. It can be put into boiling water for 20 to 50 seconds, and if it has a slight ductility, it can be directly used by pressing it into the oral cavity. It is preferably used in boiling water for 25 to 40 seconds, more preferably 30 to 35 seconds. On the other hand, the permanent teeth have a large shape, rich in minerals, high in hardness, and small in size (齒 髓 cavity) compared with the teeth, because they function during their lifetime. The artificial crown for permanent tooth can be deformed at over 100 ℃ and it can be used by pressing directly on the gypsum model with the deteriorator.
또한, 본 발명의 인공치관은 단일로 이루어질 수 있으나, 2이상이 서로 연접하여 이루어진 인공치관용 연결치관 일 수 있다. 연결치관은 상기 나노필러와 열가소성 레진의 배합비를 나노필러(~80 wt%), 열가소성 레진(~20 wt%)으로 배합하는 것을 제외한 나머지 인공치관 제조방법과 동일한 방법으로 제조할 수 있다.In addition, the artificial crown of the present invention may be a single crown, but it may be a connecting crown for artificial tangles in which two or more are connected together. The connecting crown can be manufactured by the same method as that of the remaining artificial crown except that the blending ratio of the nanofiller and the thermoplastic resin is blended with nanofiller (~ 80 wt%) and thermoplastic resin (~ 20 wt%).
본 발명의 하나의 구체적인 사용 방법으로 상기 제조된 인공치관 내부에 프라이머를 도포하고, 5 ~ 30초 동안 라이트 큐닝을 실시한다. 바람직하게는 7 ~ 15초 동안 라이트 큐닝하며, 보다 바람직하게는 9 ~ 12초 동안 라이트 큐닝한다. 그 다음, 인공치관 내부에 복합(composite) 레진을 충진시키고, 다시 10 ~ 30초 동안 라이트 큐닝을 실시한다. 바람직하게는 15 ~ 25초 동안 라이트 큐닝하며, 보다 바람직하게는 17 ~ 22초 동안 라이트 큐닝한다. 그 다음, 치료될 치아위에 씌우고 최종적으로 연마 과정을 수행하여 사용한다.In one specific use method of the present invention, the primer is applied inside the manufactured artificial crown, and light curing is performed for 5 to 30 seconds. Preferably, light curing is performed for 7 to 15 seconds, and more preferably light curing is performed for 9 to 12 seconds. Next, the composite resin is filled in the artificial crown, and light curing is performed again for 10 to 30 seconds. Preferably 15 to 25 seconds, and more preferably 17 to 22 seconds. It is then placed on the tooth to be treated and finally used for polishing.
한편, 복합(composite) 레진은 유기질 고분자와 무기질 충진재로 구성된 혼합물질이다. 고분자 공학의 발전으로 인하여 복합레진은 일상에서 고강도를 필요로 하는 자동차, 항공기, 가전제품 및 의료용 기자재에 이르기까지 다양한 분야에 보편적으로 사용되며, 치과용 수복 재료로 각광 받고 있다. 치과용 수복재는 씹는 기능을 회복하기 위하여 높은 강도가 요구되므로 전통적으로 금이나 합금 또는 아말감과 같은 재료가 사용되어 왔다. 이들 금속성 재료는 치아의 색을 갖지 못하기 때문에 비심미적이라는 단점이 있다. 또한, 금속성 재료는 치아와 결합하지 않기 때문에, 수복물의 탈락을 방지하기 위하여 치아의 많은 삭제가 선행되어야 한다. 이에 비하여 복합레진을 포함한 접착성 수복은 치아의 삭제가 최소로 이루어지며 결손에 의해 취약한 치아의 구조를 강화시키는 역할을 하여, 불필요한 치아 삭제 없이 보존적으로 치아를 유지할 수 있는 장점이 있다.On the other hand, composite resin is a mixed material composed of organic polymer and inorganic filler. Due to the development of polymer engineering, composite resins are widely used in various fields ranging from automobiles, aircrafts, household appliances, and medical equipments that require high strength in daily life, and they are attracting attention as dental restorative materials. Dental restorative materials have traditionally been used with materials such as gold, alloys, or amalgam because high strength is required to restore the chewing function. These metallic materials have the disadvantage of being non-esthetic because they do not have the color of teeth. Also, since the metallic material is not bonded to the teeth, many deletions of the teeth must be preceded in order to prevent the restoration from falling off. In contrast, the adhesive restoration including the composite resin has the advantage of minimizing tooth deletion and enhancing the structure of the vulnerable tooth by the defect, so that the tooth can be preserved without unnecessary tooth erasure.
상기 제조방법에 따라 제조된 인공치관을 이용하여 상실된 치아 기능과 심미적인 형태의 복원을 가능하게 하는 맞춤형 보철 제작을 용이하게 할 수 있다. The artificial crown manufactured according to the above manufacturing method can be used to easily manufacture a customized prosthesis that enables the restoration of the lost tooth function and the aesthetic shape.
본 발명에 따르면, 기존의 레진으로만 제조된 치관에 고강도 기능성 섬유를 도입하여 물성이 개선된 인공치관을 제조하는 방법을 제공할 수 있다. According to the present invention, it is possible to provide a method of manufacturing an artificial crown having improved physical properties by introducing high-strength functional fibers into a crown made only of a conventional resin.
따라서, 본 발명의 인공치관은 상실된 치아 기능 및 심미적인 형태의 복원을 위한 맞춤형 보철 제작에 용이하게 사용할 수 있어 환자는 물론 치과의사, 치과기공사들에게 편의성을 제공할 수 있다. Therefore, the artificial crown of the present invention can be easily used for manufacturing a customized prosthesis for restoration of a lost tooth function and an aesthetic shape, thereby providing convenience to dentists and dental technicians, as well as patients.
도 1은 본 발명의 인공치관의 제조 과정 흐름도이다.1 is a flow chart of a manufacturing process of an artificial crown of the present invention.
도 2는 본 발명의 인공치관 특성 평가를 위한 시편준비 과정을 나타낸다.Fig. 2 shows a sample preparation process for evaluating the properties of an artificial crown of the present invention.
도 3은 본 발명의 인공치관 물 흡수도 및 용해도 평가를 위한 시편준비 과정을 나타낸다.FIG. 3 shows a sample preparation process for evaluating the water absorption and solubility of the artificial crown of the present invention.
이하에서는 첨부된 도면을 참조하여, 본 발명의 실시예에 따른 인공치관 제조방법에 대하여 상세히 설명한다. 이들 실시예 등은 오로지 본 발명을 보다 구체적으로 설명하기 위한 것으로, 본 발명의 요지에 따라 본 발명의 범위가 이들 실시예 등에 의해 제한되지 않는다는 것은 당업계에서 통상의 지식을 가진 자에 있어서 자명할 것이다.Hereinafter, a method for manufacturing an artificial crown according to an embodiment of the present invention will be described in detail with reference to the accompanying drawings. It will be apparent to those skilled in the art that the scope of the present invention is not limited by these examples and the like according to the gist of the present invention. will be.
실시예 1: 인공치관의 제조방법Example 1: Manufacturing method of artificial crown
본 발명의 인공치관을 개발하기 위해 나노필러(~70 wt%), 열가소성 레진(~30 wt%), 실리카를 혼합하여 무기복합화 레진을 제조한 후, 고강도 기능성 섬유 위에 총 두께가 0.3 m가 되도록 도포하였다. 또한, 인공치관의 색조를 나타내기 위해 열가소성 레진에 Yellow 및 Red 안료를 혼합하여 사용하였다. 그 다음, 상기 무기복합화 레진이 도포된 고강도 기능성 섬유를 압착하여 가로세로 300 mm X 300 mm의 플레이트를 제작하였다. 제작된 플레이트를 금형틀에 넣고 약 150 ℃의 열을 15초 동안 가한 후, shell 형태로 성형하였다. 그 다음, 약 120 ℃로 가열하여 연화시키고 보압 과정을 수행하였다. 이후, 30 ~ 40초 동안 냉각한 뒤 크라운 형태의 인공치관을 제조하였다. In order to develop the artificial crown of the present invention, an inorganic composite resin is prepared by mixing nanofiller (~ 70 wt%), thermoplastic resin (~ 30 wt%) and silica so as to have a total thickness of 0.3 m on the high- Respectively. In addition, yellow and red pigments were mixed with a thermoplastic resin to show the color tone of the artificial crown. Then, the high-strength functional fiber coated with the inorganic composite resin was pressed to produce a plate having a size of 300 mm x 300 mm. The prepared plate was placed in a metal mold, heated at about 150 ° C. for 15 seconds, and then shaped into a shell. Then, it was softened by heating to about 120 DEG C, and a pressure holding process was performed. After cooling for 30 to 40 seconds, a crown-shaped crown was prepared.
한편, 상기 나노필러와 열가소성 레진의 배합비를 나노필러(~80 wt%), 열가소성 레진(~20 wt%)으로 배합하는 것을 제외한 나머지 인공치관 제조방법과 동일한 방법으로 연결치관을 제조하였다. The connecting crown was prepared in the same manner as the other artificial crown manufacturing methods except that the blending ratio of the nanofiller and the thermoplastic resin was blended with nanofiller (~ 80 wt%) and thermoplastic resin (~ 20 wt%).
또한, 상기 인공치관은 유치관(소아용) 또는 영구치관(성인용)으로 제조할 수 있다. 유치관은 100 ℃ 이내에서 변형되는 특성을 가지며 끓는 물속에 30초 이상 넣어 약간의 연성이 생기면 구강에 직접 압접하여 성형하여 사용한다. 영구치관은 실리카의 함량을 변화시켜 경도를 높인 치관으로 100 ℃ 이상에서 변형되는 특성을 가지며 열화기로 가볍게 달구어 석고 모형에 직접 압접하여 성형하여 사용한다.In addition, the artificial crown can be manufactured as an inlet tube (for a child) or a permanent tooth tube (for an adult). The inlet pipe has a characteristic of being deformed within 100 ℃ and it is put into boiling water for more than 30 seconds and if it has a slight ductility, it is directly pressed to the oral cavity and molded. The permanent-tooth tube is a crown with increased hardness by varying the content of silica and has a characteristic of being deformed at a temperature of 100 ° C or higher. It is lightly heated by a deteriorator and directly press-molded into a plaster model.
상기 제조된 인공치관은 크라운 형태의 인공치관 내부에 프라이머를 도포하고, 약 10초 동안 라이트 큐닝을 실시한 후, 내부에 복합(composite) 레진을 충진시킨 다음, 다시 약 20초 동안 라이트 큐닝을 실시하여 치료될 치아위에 씌워 최종적으로 연마 과정을 수행하여 사용한다.The prepared artificial crown was coated with a primer in a crown-shaped artificial crown, subjected to light curing for about 10 seconds, filled with a composite resin, and then subjected to light curing for about 20 seconds It is covered on the teeth to be treated and finally used by polishing.
실시예 2: 제조된 인공치관의 물리·화학적 및 생물학적 안전성 평가Example 2: Evaluation of physico-chemical and biological safety of manufactured artificial crown
상기 실시예 1에서 제작된 인공치관의 시편을 식품의약품안전처 가이드라인과 관련규격 및 식품의약품안전처 고시 제 2014-115호 의료기기의 생물학적 안전에 관한 공통기준 규격에 따라 기포와 결함(관련규격: ISO 22112), 표면마무리(관련규격: ISO 22112, ISO 10477), 색일치성(관련규격: ISO 7491), 색안정성, 물 흡수도, 물 용해도 및 생물학적 안전성 시험을 실시하였다. The specimens of the artificial crown prepared in the above Example 1 were classified into bubbles and defects according to the Guideline of the Food and Drug Administration's Safety Directive and Related Standard and Food Safety Management Notice No. 2014-115, : ISO 22112), surface finish (related standards: ISO 22112, ISO 10477), color consistency (ISO 7491), color stability, water absorption, water solubility and biosafety.
기포와 결함(관련규격: ISO 22112), 표면마무리(관련규격: ISO 22112, ISO 10477), 색일치성(관련규격: ISO 7491), 색안정성 시험을 위한 시편은 23±1시간 동안 37±1 ℃의 오븐에서 건조한 후, 23±2 ℃ 건조기에서 60±10시간 동안 건조한 후 사용하였다. 시편 준비과정은 도 2에 나타내었다.The specimens for the color stability test were 37 ± 1 for 23 ± 1 hours. The specimens for the color stability test were as follows: bubble and defect (related standard: ISO 22112), surface finish (ISO 22112, ISO 10477) Lt; RTI ID = 0.0 > C < / RTI > for 60 +/- 10 hours. The sample preparation process is shown in Fig.
한편, 물 흡수도 및 물 용해도 시험의 시편은 37±1 ℃ 물에 7일±2시간 동안 시편을 침적한 후 습윤시편의 무게를 측정한 다음, 습윤시편을 23±1시간 동안 37±1 ℃의 오븐에서 건조한 후, 23±1 ℃ 건조기에서 60±10시간 동안 건조한 후 사용하였다. 시편 준비과정은 도 3에 나타내었다. On the other hand, the water absorption and water solubility test specimens were immersed in water at 37 ± 1 ° C for 7 days ± 2 hours and then wetted specimens were weighed and the wet specimens were heated at 37 ± 1 ° C Dried in an oven at 23 ± 1 ° C for 60 ± 10 hours and then used. The sample preparation process is shown in Fig.
또한, 시편의 생물학적 안전성을 평가하기 위해서 시편 용출액을 이용하여 세포독성 시험, 구강점막 자극시험 및 감작성 시험을 수행하였다.Cytotoxicity test, oral mucosal irritation test and sensitization test were carried out using the sample solution to evaluate the biological safety of the sample.
시험 결과, 본 발명의 제조방법에 따라 제작된 인공치관은 식품의약품안전처 가이드라인과 관련규격 및 식품의약품안전처 고시 제 2014-115호 의료기기의 생물학적 안전에 관한 공통기준 규격에 부합하였으며, 치과용 보철 제작을 위한 치과기자재 산업에 유용하게 사용될 수 있음을 확인하였다.As a result of the test, the artificial crown manufactured according to the manufacturing method of the present invention meets the Common Criteria for Biological Safety of Medical Devices, Guideline of the Food and Drug Administration, and Related Standard and Food Safety Management Notice No. 2014-115, It is confirmed that it can be useful for the dental equipments industry for making prosthetic prosthesis.
본 발명은 인공치관의 제조시 물성을 개선시키고, 이에 맞춤형 보철을 용이하게 제작 가능한 인공치관 및 그 제조 방법에 관한 것으로서 산업상 이용가능성이 있다.TECHNICAL FIELD The present invention relates to an artificial crown capable of improving physical properties in the production of an artificial crown and capable of easily fabricating a customized prosthesis, and a method of manufacturing the same.

Claims (6)

  1. (1) 나노필러, 열가소성 레진 및 실리카를 혼합하는 단계;(1) mixing nanofiller, thermoplastic resin and silica;
    (2) 상기 (1)단계에서 혼합된 재료를 섬유 위에 도포하는 단계;(2) applying the mixed material on the fiber in the step (1);
    (3) 상기 (2)단계에서 도포된 섬유를 압착하여 플레이트로 제단하는 단계;(3) pressing the fibers applied in the step (2) and cutting the fibers into a plate;
    (4) 상기 (3)단계에서 제단된 플레이트를 성형하는 단계;(4) molding the plate, which has been removed in the step (3);
    (5) 상기 (4)단계에서 성형된 플레이트를 냉각하는 단계;를 포함하는 인공치관의 제조방법. (5) cooling the plate formed in the step (4).
  2. 제1항에 있어서, 상기 열가소성 레진은 폴리글로콜산(PGA), 폴리카프로락톤(Poly-ε-caprolactone), 폴리다이옥산온(polydioxanone), 폴리락틴산-글리콜산 공중합체(PLGA), 폴리다이옥산-카프로락톤 공중합체(polydioxanone-co-ε-caprolactone), 폴리락틴산-카프로락톤 공중합체(PLA co-ε-caprolactone), 폴리하이드록시부티릭산-하이드록시빌러릭산 공중합체(polyhydroxybutyric acid-co-hydroxyvleric acid), 폴리포스포에스터(polyphosphoester), 폴리에틸렌옥사이드-폴리락틴산 공중합체, 폴리에틸렌옥사이드-폴리락틱글리콜산 공중합체 및 폴리에틸렌옥사이드-폴리카프로락톤 공중합체로 이루어진 군에서 선택된 1종 또는 2종 이상을 혼합하여 사용하는 것을 특징으로 하는 인공치관의 제조방법. The thermoplastic resin composition according to claim 1, wherein the thermoplastic resin is selected from the group consisting of polyglycolic acid (PGA), poly-ε-caprolactone, polydioxanone, polylactic acid-glycolic acid copolymer (PLGA) Caprolactone copolymer, polyhydroxybutyric acid-co-caprolactone copolymer, polyhydroxybutyric acid-co-caprolactone copolymer, polyhydroxybutyric acid- at least one member selected from the group consisting of polyvinyl alcohol, polyvinyl alcohol, hydroxyvleric acid, polyphosphoester, polyethylene oxide-polylactic acid copolymer, polyethylene oxide-polylactic glycolic acid copolymer and polyethylene oxide-polycaprolactone copolymer Are mixed with each other and used.
  3. 제1항에 있어서, 섬유는 유리 섬유(glass fiber), 탄소 섬유(carbon fiber) 및 아라미드 섬유(aramid fiber)로 이루어진 군에서 선택된 1종 또는 2종 이상을 혼합하여 사용하는 것을 특징으로 하는 인공치관의 제조방법. The artificial crown according to claim 1, wherein the fibers are one or more selected from the group consisting of glass fibers, carbon fibers, and aramid fibers. ≪ / RTI >
  4. 제1항에 있어서, 상기 (4)단계의 성형은 100 ~ 200 ℃의 열을 가하여 이루어지는 것을 특징으로 하는 인공치관의 제조방법.The method according to claim 1, wherein the step (4) is performed by applying heat at 100 to 200 ° C.
  5. 제1항에 있어서, 상기 (4)성형 단계는 연화 및/또는 보압하는 공정이 추가로 포함되는 것을 특징으로 하는 인공치관의 제조방법.The method according to claim 1, wherein the forming step (4) further includes softening and / or pressing.
  6. 제1항 내지 제5항 중 어느 한 항의 제조방법에 의하여 제작된 인공치관.An artificial crown manufactured by the manufacturing method according to any one of claims 1 to 5.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112226055A (en) * 2020-09-28 2021-01-15 青岛科技大学 Denture and preparation method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040241614A1 (en) * 1998-04-13 2004-12-02 Goldberg A. Jon Prefabricated components for dental appliances
KR20090024816A (en) * 2006-06-30 2009-03-09 스틱 테크 오와이 Fiber-reinforced composites and method for the manufacture thereof
KR20160000364A (en) * 2014-06-24 2016-01-04 대림대학교산학협력단 Production method of photo-polymerizable resin composition for glass fiber prosthesis, and production method of glass fiber prosthesis using the composition
US20160128812A1 (en) * 2013-09-24 2016-05-12 Gc Corporation Method for manufacturing dental resin block

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040241614A1 (en) * 1998-04-13 2004-12-02 Goldberg A. Jon Prefabricated components for dental appliances
KR20090024816A (en) * 2006-06-30 2009-03-09 스틱 테크 오와이 Fiber-reinforced composites and method for the manufacture thereof
US20160128812A1 (en) * 2013-09-24 2016-05-12 Gc Corporation Method for manufacturing dental resin block
KR20160000364A (en) * 2014-06-24 2016-01-04 대림대학교산학협력단 Production method of photo-polymerizable resin composition for glass fiber prosthesis, and production method of glass fiber prosthesis using the composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112226055A (en) * 2020-09-28 2021-01-15 青岛科技大学 Denture and preparation method thereof

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