The present disclosure relates to an implant fixture for reducing periodontitis.
In general, when permanent teeth are damaged due to aging or other factors, artificial teeth are implanted into the jawbone. When permanent teeth are damaged due to various factors and the damaged permanent teeth are extracted, artificial teeth are implanted in their place.
Specifically, prosthetic implant components are attached to implant fixtures implanted in the jawbone, and artificial teeth are combined with the implant to complete the implantation of the artificial teeth. Typical implants used for implanting artificial teeth consist of a fixture, an abutment, and a screw. The fixture is inserted into the jawbone and coupled by threads, and, in a state in which the abutment to which the artificial teeth will be fixed is located above the fixture, the screw is connected to the abutment, and then, is coupled to the fixture, such that the abutment is coupled to the top of the fixture. Generally, the fixture has threads formed along the outer surface thereof, such that the fixture is coupled to the jawbone.
However, if the implant does not fully integrate with the alveolar bone, the connection of the implant fixture along the thread may become loose from the gums. If load is continuously applied in a state in which a portion of the implant fixture is disassembled, a gap may be formed, and the load transferred by the implant fixture is concentrated on a portion of the bone tissue, so the bone tissue is damaged and the implant fixture is detached from the bone tissue.
Additionally, conventional methods simply use the shape of the implant and the surface treatment technique for bone integration. However, the currently used implant systems have several disadvantages in that, after implantation of the implant, peri-implantitis is likely to occur, the rate of bone integration survival is often low due to the small surface area of the implant, and frequent fractures of the implant itself occur due to the application of occlusal force.
To overcome the limitations of traditional implants, the surface area of the implant fixture must be increased to increase the success rate of bone integration and survival rate. In particular, it is necessary to develop an implant system that can increase the survival rate by reducing the occurrence of peri-implantitis.
The background technology of the present invention is disclosed in Korean Patent No. 10-1122134.
Accordingly, the present invention has been made in view of the above-mentioned problems occurring in the related art, and it is an object of the present invention to provide an implant fixture for reducing periodontitis which can widen the surface area of the outer surface to increase fixing force to the bone tissue, and provide bone formation inducers to at least a portion of the outer surface to increase stability and the success rate of bone integration.
However, the technical problems that the embodiments of the present invention aim to solve are not limited to the aforementioned technical problems, and there may exist other technical problems to be solved.
To accomplish the above-mentioned objects, according to the present invention, there is provided an implant fixture for reducing periodontitis including: a body part which is implanted into bone tissue to form an artificial tooth root, wherein the outer surface of the body part has a predetermined roughness to enhance fixing force of the body part to the bone tissue, and at least a portion of the outer surface of the body part is provided with bone formation inducers.
Moreover, an upper portion of the body part has a machined surface with smoother surface characteristics compared to the outer surface of the body part to improve adhesion with soft tissue.
Furthermore, the body part includes: a first body part corresponding to a predetermined depth section downwards from the machined surface; and a second body part corresponding to the lower end of the fixture, which corresponds to a lower portion of the first body part.
Moreover, the first body part and the second body part have distinct outer surface characteristics.
Additionally, the bone formation inducer provided on the outer surface of the first body part is a first type inducer, and the bone formation inducer provided on the outer surface of the second body part is a second type inducer, different from the first type inducers.
In addition, the first type inducer includes poly lactic-co glycolic acid (PLGA).
Moreover, the second type inducer includes bone morphogenetic protein (BMP).
Furthermore, the implant fixture for reducing periodontitis according to an embodiment of the present invention may further include a cavity formed by recessing upwards from the lower end of the body part.
Additionally, after the implant fixture is implanted, at least a portion of the bone tissue can be drawn into the cavity.
In addition, the implant fixture for reducing periodontitis according to an embodiment of the present invention may include at least one through-hole formed to allow communication between the cavity and the outside of the body part.
Moreover, the bone formation inducers are provided on the inner surface of the cavity.
Furthermore, the bone formation inducers are provided at a plurality of different positions on the outer surface, each at a predetermined distance from each other.
Additionally, a plurality of dimple-shaped concave grooves are formed on the outer surface of the body part.
In addition, the bone formation inducers are provided corresponding to the plurality of grooves.
The above-mentioned technical solutions are merely illustrative, and should not be interpreted as limiting the present invention. In addition to the illustrative embodiments mentioned above, additional embodiments may exist in the drawings and detailed description of the present invention.
According to the present invention, the implant fixture for reducing periodontitis can widen the surface area of the outer surface to increase fixing force to the bone tissue, and provide the bone formation inducers to at least a portion of the outer surface to increase stability and the success rate of bone integration.
According to the present invention, the implant fixture for reducing periodontitis includes the cavity recessed upwards from the lower portion of the body such that a portion of the bone tissue is drawn inwards after the implant is placed, thereby preventing fracture of the implant and significantly improving the fixation of the implant.
However, the effects obtainable from the present invention are not limited to those mentioned above, and other effects may exist.
Hereinafter, the embodiments of the present disclosure will be described in detail with reference to accompanying drawings so that the embodiments may be easily implemented by those skilled in the art. However, the present disclosure may be implemented in various ways without being limited to the embodiments. In addition, in the drawings, well-known elements or components may be omitted to avoid unnecessarily obscuring the presented embodiments, and like reference numerals denote like elements throughout the specification.
In the entire specification of the present disclosure, when a part is “connected” to another part, this includes not only being “directly connected” but also being “electrically connected” or “indirectly connected” through another element.
In the entire specification of the present disclosure, when any member is located “on,” “above,” “at the top of,” “below,” “beneath,” or “at the bottom of” another member, this includes a case in which still another member is prevent between both members as well as a case in which one member is in contact with another member.
In the entire specification of the present disclosure, when any portion “includes” any component, this does not exclude other components but means that any other component can be further included, unless stated otherwise.
The present invention relates to an implant fixture for reducing periodontitis.
Referring to
Moreover, the outer surface of the body part 100 may be provided with a predetermined roughness to enhance fixing force of the body part 100 to the bone tissue.
Furthermore, an upper portion of the body part 100 may have a machined surface 130 with smoother surface characteristics compared to the outer surface of the body part 100 to improve adhesion with soft tissue.
In other words, the implant fixture 10 disclosed in the present invention is configured such that the machined surface 130 with a smooth surface is formed on the top of the implant fixture to prevent damage to the gum tissue where the implant is placed and to improve adhesion with the soft tissue area. In this instance, the body part 100 below the machined surface 130 may have a rougher surface than the machined surface 130 to enhance the fixing force to the bone tissue in the area where the implant is placed.
Meanwhile, in the description of the embodiments of the present invention, the body part 100 can be divided into a first body part 110 and a second body part 120 based on a predetermined depth section in the vertical direction.
Specifically, the first body part 110 can correspond to a preset depth section downwards from the bottom surface of the machined surface 130, and the second body part 120 can correspond to the lower end of the implant fixture 10 that lies beneath the first body part 110.
In this regard, the outer surface characteristics of the first body part 110 and the second body part 120 may be distinct from each other. Specifically, according to an embodiment of the present invention, the first body part 110, which is a relatively upper area, can be provided in a pin-type, and the second body part 120, which is a relatively lower area, can be provided in a screw-type with threads formed on the outer surface thereof.
In this regard, the shape of the upper first body part 110, which is positioned corresponding to the boundary between the soft tissue and the bone tissue of the site where the implant fixture 10 is implanted, can be provided in a pin-type including a plurality of wing members. The wing members may be made of a material with higher strength compared to the material of the second body part 120, located relatively below, thereby reducing the risk of fracture of the implant fixture 10.
In other words, according to an embodiment of the present invention, the strength of the first body part 110 may be set higher than that of the second body part 120, thereby reducing the risk of fracture of the implant fixture 10.
Additionally, according to an embodiment of the present invention, at least a portion of the outer surface of the body part 100 may be provided with bone formation inducers.
Specifically, the bone formation inducers provided on the outer surface of the first body part 110 may be a first type inducers. Distinctly, the bone formation inducers provided on the outer surface of the second body part 120 may be a second type inducers, different from the first type inducers of the first body part 110.
According to an embodiment of the present invention, the first type inducer may include poly lactic-co glycolic acid (PLGA). Additionally, according to an embodiment of the present invention, the second type inducer may include bone morphogenetic protein (BMP).
Although, out of conventionally developed implant fixture structures, some of implant fixture structures applying bone integration inducing substances like bone morphogenetic protein (BMP) on the entire outer surface have been disclosed. However, in the type where the bone formation (bone integration) inducing substances are applied to the entire outer surface of the fixture, despite requiring a relatively long period of time for stable bone integration after the implantation of the implant fixture, as most of the bone formation inducing substances applied to the entire outer surface of the fixture are absorbed into the bone tissue at the initial stage right after the implantation of the implant, so such conventional implant fixture structures often fail to achieve the effect of promoting bone integration by the bone formation inducing substances.
In contrast, the implant fixture 10 disclosed in the present invention provides the bone formation inducers on the outer surface of the body part 100. In this instance, the bone formation inducers are arranged locally at intervals in some areas of the outer surface, so that the bone formation inducers are provided (released) gradually to the bone tissue over a relatively long period of time, thereby enabling effective bone integration over an extended duration.
Referring to
According to an embodiment of the present invention, in case of the second body part 120 provided in a screw type, according to a protrusion area protruding toward the outside with the threads and a recessed area recessed inwards between the threads, the arrangement and spacing between areas to which each of the bone formation inducers is provided can be applied differently, so that an appropriately sustained release of the bone formation inducer towards the bone tissue can be achieved.
More specifically, referring to
In addition, referring to
According to an embodiment of the present invention, a plurality of dimple-shaped concave grooves (not shown) are formed on the outer surface of the body part 100, and the bone formation inducers may be provided corresponding to the plurality of grooves.
Hereinafter, referring to
Referring to
According to the first embodiment of the present invention, the cavity 220 can be formed as a space surrounded by the lower interior of the body part 100, i.e., at the lower end of the body part 100.
Accordingly, once the body part 100 is implanted into the bone tissue, at least a portion of the bone tissue enters and settles inside the cavity 220, and then, is hardened, such that the body part 100 is more strongly fixed, thereby enhancing the fixing force and durability of the implant fixture 10.
Additionally, according to an embodiment of the present invention, the inner surface of the cavity 220 may be provided with bone formation inducers, similar to the outer surface of the body part 100. Furthermore, according to an embodiment of the present invention, the bone formation inducers provided on the inner surface of the cavity 220 can be provided to the bone tissue that is at least partially drawn into the cavity 220 after a predetermined period of time following the implantation of the implant fixture 10, thereby continuously promoting the improvement of the fixing force of the implant by inducing bone integration through the bone formation inducers over a long period.
In addition, according to an embodiment of the present invention, considering that it takes a predetermined period of time for at least some of the bone tissue to be drawn into the cavity 220, the bone formation inducers provided on the inner surface of the cavity 220 may be provided at a relatively higher area ratio compared to those provided on the outer surface of the body part 100 that bonds with the bone tissue right after the implantation of the implant fixture 10.
For example, the size (such as diameter) of the dimple-shaped concave grooves (not shown) formed on the inner surface of the cavity 220 to provide the bone formation inducers can be set larger than those of the plurality of grooves (not shown) formed on the outer surface of the body part 100, or the spacing distance between multiple positions where the bone formation inducers are provided may be smaller than the outer surface of the body part 100.
Referring to
Referring to
According to this third embodiment, in case of the implant fixture 10 with the through-hole 230, the bone formation inducers provided on the inner surface of the cavity 220 pass through the through-hole 230 after the implantation of the implant fixture 10, and are provided to the bone tissue located outside the outer surface of the body part 100, thereby continuously promoting the enhancement of the fixing force of the implant by inducing bone integration through the bone formation inducers over a long period.
Referring to
The above description is only exemplary, and it will be understood by those skilled in the art that the invention may be embodied in other concrete forms without changing the technological scope and essential features. Therefore, the above-described embodiments should be considered only as examples in all aspects and not for purposes of limitation. For example, each component described as a single type may be realized in a distributed manner, and similarly, components that are described as being distributed may be realized in a coupled manner.
The scope of the present invention is defined by the appended claims, and encompasses all modifications or alterations derived from meanings, the scope and equivalents of the appended claims.
Number | Date | Country | Kind |
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10-2021-0087373 | Jul 2021 | KR | national |
Filing Document | Filing Date | Country | Kind |
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PCT/KR2022/008749 | 6/21/2022 | WO |