CN111529135A - Acetabular cup and acetabular prosthesis system - Google Patents
Acetabular cup and acetabular prosthesis system Download PDFInfo
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- CN111529135A CN111529135A CN202010445961.9A CN202010445961A CN111529135A CN 111529135 A CN111529135 A CN 111529135A CN 202010445961 A CN202010445961 A CN 202010445961A CN 111529135 A CN111529135 A CN 111529135A
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- porous layer
- acetabular cup
- drug
- bone growth
- antibacterial
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Images
Classifications
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- A61F2/00—Filters 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
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- A61F2/00—Filters 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
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- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
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- A61F2/00—Filters 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
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- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
- A61F2/30771—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
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- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
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Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
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Abstract
The application provides an acetabular cup and an acetabular prosthesis system, and relates to the technical field of medical instruments. The acetabular cup includes a first base and a first porous layer. The first porous layer has a plurality of uniformly distributed and interconnected pores. The first porous layer is loaded with a bone growth promoting drug and an antibacterial and anti-inflammatory drug, wherein the bone growth promoting drug is filled in the inner layer of the first porous layer, and the antibacterial and anti-inflammatory drug is filled in the outer layer of the first porous layer. The slow release medicament loaded in the first porous layer can be continuously and continuously administered after the acetabular cup is implanted into a human body, the antibacterial and anti-inflammatory medicament filled in the outer layer of the first porous layer is slowly released to realize antibacterial and anti-inflammatory to prevent infection at the initial stage of implantation, and after the acetabular cup is preliminarily combined with bone tissues of the human body, the bone growth promoting medicament filled in the inner layer of the first porous layer is slowly released to promote bone growth for a long time, so that the fusion degree and the fusion efficiency of the human body and the implanted acetabular cup are improved.
Description
Technical Field
The application relates to the technical field of medical equipment, in particular to an acetabular cup and an acetabular prosthesis system.
Background
When tumors occur around the acetabulum, a surgical resection treatment is needed, so that the acetabulum part has large bone loss, the continuity of the pelvis is interrupted, and a part of soft tissues around the pelvis is lost, so that the lost pelvis needs to be reconstructed.
In recent years, more and more acetabular cup prostheses are implanted into the missing pelvis for pelvic repair, but the human body is repulsive to foreign implant prostheses, resulting in inefficient fusion. Also, infection is inevitably accompanied during transplantation.
Disclosure of Invention
An object of the embodiment of the application is to provide an acetabular cup and an acetabular prosthesis system, which can improve the technical problems of low implantation efficiency and high infection rate of acetabular cup prostheses.
In a first aspect, embodiments of the present application provide an acetabular cup that includes a first substrate and a first porous layer, wherein a portion or all of a surface of the first substrate is covered with the first porous layer.
The first porous layer has a plurality of pores uniformly distributed and interconnected.
The first porous layer is loaded with a bone growth promoting drug and an antibacterial and anti-inflammatory drug, wherein the bone growth promoting drug is filled in the inner layer of the first porous layer, and the antibacterial and anti-inflammatory drug is filled in the outer layer of the first porous layer.
In the implementation process, the acetabular cup provided by the application comprises a first porous layer arranged on the surface of a first substrate, the first porous layer can be loaded with a slow release drug, and the slow release drug loaded in the first porous layer can be continuously administered after the acetabular cup is implanted into a human body.
The antibacterial and anti-inflammatory drugs filled in the outer layer of the first porous layer are slowly released to realize antibacterial and anti-inflammatory effects and prevent infection at the initial stage of implantation, and after the acetabular cup is preliminarily combined with the bone tissue of a human body, the bone growth promoting drugs filled in the inner layer of the first porous layer are slowly released to promote bone growth in a longer time, so that the fusion degree and the fusion efficiency of the human body and the transplanted acetabular cup are improved.
In one possible embodiment, the surface of the first porous layer is coated with an antibacterial anti-inflammatory drug.
In one possible embodiment, the bone growth promoting agent comprises a bone morphogenic protein BMP, a fibroblast growth factor FGF, or a transforming growth factor TGF-beta.
In the above implementation process, a bone growth promoting agent such as bone morphogenetic protein BMP, fibroblast growth factor FGF, or transforming growth factor TGF-beta can be filled in the inner layer of the first porous layer, and after acetabular cup implantation, the agent can be slowly released and promotes bone growth over a long period of time.
In one possible embodiment, the anti-bacterial and anti-inflammatory agent comprises a penicillin, a cefamycin, or an aspirin.
In the implementation process, antibacterial and anti-inflammatory medicines such as penicillin medicines, cefamycin medicines or aspirin medicines and the like can be filled in the outer layer of the first porous layer, and after the acetabular cup is transplanted, the medicines can be slowly released to realize antibacterial, anti-inflammatory and infection prevention.
In one possible embodiment, the porosity of the first porous layer is 86 to 90%, and the cross-sectional pore diameter of the pores is 200 to 1200 μm.
In the implementation process, the first porous layer with the porosity of 86-90% is similar to the host bone tissue, so that the bonding strength of the interface of the acetabular cup and the host bone tissue can be improved, and the acetabular cup and the host bone tissue can be deeply fused.
In a possible embodiment, the material of the first porous layer is titanium alloy or titanium simple substance, and the surface roughness of the first porous layer is 2 to 9 μm.
In the implementation process, the porous titanium is a good bionic material, has good biocompatibility and excellent biomechanics, and has the elastic modulus close to that of bone tissues.
In a second aspect, the present application provides an acetabular prosthesis system, which includes an augment component and the acetabular cup described above, wherein the acetabular cup has a first curved surface, the augment component has a second curved surface, and the augment component and the acetabular cup are connected in a matching manner through the first curved surface and the second curved surface.
In such implementations, the augment component is used to fill a cavity formed by the removed damaged or surgically removed acetabulum.
The acetabular cup prosthesis system and the host bone tissue are more matched in shape through the cooperation of the acetabular cup and the enlarging component. And the slow release medicament loaded by the first porous layer of the acetabular cup prosthesis system is continuously administered after the acetabular cup prosthesis system is implanted into a human body, so that infection of the acetabular cup prosthesis system after the acetabular cup prosthesis system is implanted is prevented, and the fusion degree and the fusion efficiency of the human body and the implanted acetabular cup prosthesis system are improved.
In one possible embodiment, the augment component includes a second substrate and a second porous layer, wherein part or all of the surface of the second substrate is covered with the second porous layer, and the second porous layer has a plurality of uniformly distributed interconnected pores.
In the implementation process, the enlarging element is also provided with a second porous layer, and the second porous layer is similar to the host bone tissue, so that the bonding strength of the interface of the enlarging element and the host bone tissue can be improved, and the enlarging element and the host bone tissue can realize deep fusion.
In one possible embodiment, the second porous layer is loaded with a bone growth promoting drug and an antibacterial anti-inflammatory drug, wherein the bone growth promoting drug is filled in an inner layer of the second porous layer and the antibacterial anti-inflammatory drug is filled in an outer layer of the second porous layer.
In the implementation process, the second porous layer can also be used as a carrier and is loaded with bone growth promoting drugs and antibacterial and anti-inflammatory drugs, the antibacterial and anti-inflammatory drugs filled in the outer layer of the second porous layer are slowly released at the initial implantation stage to realize antibacterial and anti-inflammatory effects and prevent infection, and after the augmentation component is initially combined with the bone tissue of the human body, the bone growth promoting drugs filled in the inner layer of the second porous layer are slowly released to promote bone growth for a long time, so that the fusion degree and the fusion efficiency of the human body and the implanted augmentation component are improved.
In one possible embodiment, the surface of the second porous layer is coated with an antibacterial anti-inflammatory drug.
Drawings
In order to more clearly illustrate the technical solutions of the embodiments of the present application, the drawings that are required to be used in the embodiments will be briefly described below, it should be understood that the following drawings only illustrate some embodiments of the present application and therefore should not be considered as limiting the scope, and for those skilled in the art, other related drawings can be obtained from the drawings without inventive effort.
FIG. 1 is a schematic structural view of an acetabular cup according to an embodiment of the application;
FIG. 2 is a cross-sectional view of an acetabular cup of an embodiment of the application;
FIG. 3 is a schematic view of a first fill structure for the sustained release of a drug in a first porous layer according to embodiments of the present application;
FIG. 4 is a schematic view of a second fill configuration for the sustained release of a drug in a first porous layer according to embodiments of the present application;
FIG. 5 is a schematic view of a third fill configuration for the sustained release of a drug in the first porous layer according to embodiments of the present application;
FIG. 6 is a schematic view of a fourth fill configuration for the extended release of a drug in the first porous layer according to embodiments of the present application;
FIG. 7 is a schematic view of a fifth fill configuration for the sustained release of a drug in the first porous layer according to embodiments of the present application;
FIG. 8 is a schematic unconnected structural view of an acetabular prosthesis system according to an embodiment of the present application;
FIG. 9 is a schematic view of the acetabular prosthesis system of an embodiment of the application after attachment;
FIG. 10 is a cross-sectional view of an augment component of an embodiment of the present application.
Icon: 10-an acetabular prosthesis system; 100-acetabular cup; 101-a first curved surface; 102-connecting hole; 110-a first substrate; 120-a first porous layer; 130-antibacterial and anti-inflammatory drugs; 140-bone growth promoting agents; 200-an enlarging member; 201-a second curved surface; 210-a second substrate; 220-a second porous layer; 300-screw.
Detailed Description
In order to make the objects, technical solutions and advantages of the embodiments of the present application clearer, the technical solutions in the embodiments of the present application will be clearly and completely described below with reference to the drawings in the embodiments of the present application, and it is obvious that the described embodiments are some embodiments of the present application, but not all embodiments. The components of the embodiments of the present application, generally described and illustrated in the figures herein, can be arranged and designed in a wide variety of different configurations.
Thus, the following detailed description of the embodiments of the present application, presented in the accompanying drawings, is not intended to limit the scope of the claimed application, but is merely representative of selected embodiments of the application. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present application.
It should be noted that: like reference numbers and letters refer to like items in the following figures, and thus, once an item is defined in one figure, it need not be further defined and explained in subsequent figures.
In the description of the present application, it should be noted that the terms "inside", "outside", and the like indicate orientations or positional relationships based on the orientations or positional relationships shown in the drawings or orientations or positional relationships that the products of the application usually place when using, and are only used for convenience in describing the present application and simplifying the description, but do not indicate or imply that the devices or elements that are referred to must have a specific orientation, be constructed in a specific orientation, and operate, and thus, should not be construed as limiting the present application. Furthermore, the terms "first," "second," and the like are used merely to distinguish one description from another, and are not to be construed as indicating or implying relative importance.
In the description of the present application, it is also to be noted that, unless otherwise explicitly specified or limited, the terms "disposed" and "connected" are to be interpreted broadly, e.g., as being either fixedly connected, detachably connected, or integrally connected; either mechanically or electrically. The specific meaning of the above terms in the present application can be understood in a specific case by those of ordinary skill in the art.
Referring to fig. 1-2, an acetabular cup 100 according to an embodiment of the present disclosure includes a first substrate 110 and a first porous layer 120, wherein a portion or all of a surface of the first substrate 110 is covered with the first porous layer 120.
In the embodiment shown in fig. 1-2, the first porous layer 120 completely surrounds the first substrate 110, i.e., the entire surface of the first substrate 110 is covered with the first porous layer 120. In other embodiments of the present application, the first porous layer 120 may be coated only on the surface of the acetabular cup 100 bonded to the host bone tissue, and the first porous layer 120 may not be coated on the edge portion of the first substrate 110.
The first porous layer 120 has a plurality of irregularly shaped pores uniformly distributed in the interior and on the surface. Irregularly shaped pores distributed within and on the surface of the first porous layer 120 communicate with each other to form a biomimetic transport channel.
The porosity of the first porous layer 120 is 86-90%, the cross-sectional aperture of the pores is 200-1200 μm, and the depth of the pores is more than 1500 μm.
In the embodiment shown in FIGS. 1-2, the porosity of the first porous layer 120 is 88%, the cross-sectional pore diameter of the pores is 200-1200 μm, and the depth of the pores is more than 1500 μm. In other embodiments, the porosity of the first porous layer 120 may be 86%, 87%, 89% or 90%, the cross-sectional pore diameter of the pores of the first porous layer 120 may be 300-800 μm, 500-1000 μm, 700-900 μm, 400-700 μm or 700-1000 μm, and the depth of the pores may be > 1600 μm, > 1650 μm or > 1850 μm.
The first porous layer 120 has a trabecular bone-like structure, the porous structure of which can be used to load a slow release drug, increasing the load capacity of the acetabular cup 100. Meanwhile, the elastic modulus of the first porous layer 120 is close to that of bone tissue by adjusting the pore structure of the first porous layer 120, including the porosity, the section aperture of the pores and the depth of the pores, so that the biocompatibility is good, the bonding strength of the interface of the acetabular cup 100 and the host bone tissue can be improved, and the deep fusion of the acetabular cup 100 and the host bone tissue can be realized.
The first substrate 110 is made of metal.
In the embodiment shown in FIGS. 1-2, the first substrate 110 is made of a titanium alloy. In other embodiments of the present application, the first substrate 110 may also be made of other metal materials, such as elemental silver, iron alloy, elemental titanium, and the like.
The first porous layer 120 is made of a titanium simple substance or a titanium alloy, and the surface roughness of the first porous layer 120 is 2-9 μm.
In the embodiment shown in FIGS. 1-2, the first porous layer 120 is formed by printing titanium powder by 3D printing technique and has a surface roughness of 3-6 μm. In other embodiments of the present disclosure, the first porous layer 120 may be prepared by a technique capable of preparing a porous structure, and the surface roughness may be 2 to 6 μm, 3 to 7 μm, 4 to 8 μm, 5 to 9 μm, 2 to 8 μm, or 3 to 9 μm.
It should be noted that, the infiltration response of the porous titanium surface layer structure in the embodiment of the present application is favorable for the functional synthesis of the bone-like tissue of the components in blood.
Referring to fig. 3 to 7, the first porous layer 120 is loaded with the bone growth promoting drug 140 and the anti-bacterial and anti-inflammatory drug 130, wherein the bone growth promoting drug 140 is filled in an inner layer of the first porous layer 120, and the anti-bacterial and anti-inflammatory drug 130 is filled in an outer layer of the first porous layer 120.
It should be noted that in the embodiment of the present application, the inner layer and the outer layer of the first porous layer 120 are opposite, the drug filled in the outer layer of the first porous layer 120 can be released relatively quickly after the implantation of the prosthesis, and the drug filled in the inner layer of the first porous layer 120 can be released for a longer period of time after the implantation of the prosthesis.
Therefore, the antibacterial and anti-inflammatory drug 130 filled in the outer layer of the first porous layer 120 can be released within 3-4 weeks after the acetabular cup 100 is transplanted, i.e., the antibacterial and anti-inflammatory drug 130 can be continuously administered in the inflammation elimination period after the acetabular cup 100 is transplanted to achieve antibacterial and anti-inflammatory effects and prevent infection, so that the acetabular cup 100 can be stably used in the excessive inflammation elimination period after the acetabular cup is transplanted. The bone growth promoting drug 140 filled in the inner layer of the first porous layer 120 can be released half a year after the acetabular cup 100 is implanted, i.e., the bone growth promoting drug 140 can be continuously administered in the overall recovery period after the acetabular cup 100 is implanted to promote bone growth, so that the fusion degree and the fusion efficiency of the human body and the implanted acetabular cup 100 are improved.
The amounts of the antibacterial anti-inflammatory drug 130 and the bone growth promoting drug 140 in the first porous layer 120 in the embodiment of the present application are adapted according to the slow release period thereof and the filling rate of the growth of human bone tissue. For example, the amount of the antibiotic anti-inflammatory drug 130 filled in first porous layer 120 may ensure a sustained release period of at least 3 to 4 weeks, and the amount of the bone growth promoting drug 140 filled in first porous layer 120 may ensure a sustained release period of at least half a year.
The anti-bacterial anti-inflammatory drug 130 and the bone growth promoting drug 140 in the first porous layer 120 can be filled as follows:
in the embodiment shown in fig. 3, the thicknesses of the antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 filled in the first porous layer 120 may be equal, and the antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 do not overlap each other to fill the pores of the entire first porous layer 120.
In the embodiment shown in fig. 4, the thicknesses of the antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 filled in the first porous layer 120 are not equal, wherein the thickness of the bone growth promoting drug 140 filled is greater than the thickness of the antibacterial and anti-inflammatory drug 130 filled, and the antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 do not overlap each other to fill the pores of the entire first porous layer 120.
In the embodiment shown in fig. 5, the thicknesses of the antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 filled in the first porous layer 120 are not equal, wherein the thickness of the antibacterial and anti-inflammatory drug 130 is greater than the thickness of the bone growth promoting drug 140 filled, and the antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 do not overlap each other to fill the pores of the entire first porous layer 120.
In the embodiment shown in fig. 6, the thickness of the antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 filled in the first porous layer 120 may be equal, and the antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 are overlapped with each other in the middle to fill the pores of the entire first porous layer 120.
In the embodiment shown in fig. 7, the thickness of the antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 filled in the first porous layer 120 may be equal, and the antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 do not overlap each other and do not fill the pores of the entire first porous layer 120.
In other embodiments of the present application, the thicknesses of the antibacterial and anti-inflammatory agent 130 and the bone growth promoting agent 140 filled in the first porous layer 120 may not be equal, and the antibacterial and anti-inflammatory agent 130 and the bone growth promoting agent 140 are overlapped with each other in the middle to fill the pores of the entire first porous layer 120. Or the thicknesses of the antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 filled in the first porous layer 120 may not be equal, and the antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 do not overlap each other and do not fill the entire pores of the first porous layer 120.
The present application does not limit the types of the antibacterial and anti-inflammatory agent 130 and the bone growth promoting agent 140, as long as they exert antibacterial and anti-inflammatory effects and promote bone growth, and they are harmless to the human body.
In the embodiment of the present application, the anti-bacterial and anti-inflammatory drugs 130 include penicillins, cephalosporins, tetracyclines, chloromycetins, macrolides, lincomycin, fluoroquinolones, nitroimidazoles, polypeptides and quaternary ammonium salts of the anti-bacterial and anti-inflammatory drugs 130, and aspirin, p-indomethacin, naproxen, diclofenac, ibuprofen, nimesulide, celecoxib of the anti-bacterial and anti-inflammatory drugs 130; bone growth promoting agent 140 includes one or more of bone morphogenetic protein BMP, fibroblast growth factor FGF, transforming growth factor TGF-beta and insulin-like growth factor IGF.
The antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 are filled in the pores of the first porous layer 120 by embedding or coating.
When the coating method is used, a part of the anti-bacterial and anti-inflammatory drug 130 may be finally coated on the surface of the first porous layer 120, the coated anti-bacterial and anti-inflammatory drug 130 is partially sunk into the pores inside the first porous layer 120 due to gravity, and the other anti-bacterial and anti-inflammatory drug 130 is distributed on the surface of the first porous layer 120.
The antibacterial and anti-inflammatory drug 130 coated on the surface of the first porous layer 120 can directly act, quickly act, and play a good role in resisting bacteria and diminishing inflammation for the just-transplanted acetabular cup 100.
Referring to fig. 8-9, the present application provides an acetabular prosthesis system 10 including an augment component 200 for filling a cavity formed by a removed damaged or surgically removed acetabulum and the acetabular cup 100 described above, wherein the acetabular cup 100 has a first curved surface 101, the augment component 200 has a second curved surface 201, and the augment component 200 and the acetabular cup 100 are connected by the first curved surface 101 and the second curved surface 201.
In the embodiment shown in fig. 8-9, the acetabular prosthesis system 10 further comprises a screw 300, the acetabular cup 100 and the augment component 200 are provided with a through connecting hole 102 which are matched with each other, and the screw 300 is sequentially connected with the connecting hole 102 of the acetabular cup 100 and the connecting hole 102 of the augment component 200 and finally fixed on the bone tissue of the human body, so that the acetabular cup 100 and the augment component 200 are stably connected.
The enlarging member 200 includes a second substrate 210 and a second porous layer 220, and a part of or the entire surface of the second substrate 210 is covered with the second porous layer 220.
In the embodiment shown in fig. 8-10, the second porous layer 220 completely surrounds the second substrate 210, i.e., the entire surface of the second substrate 210 is covered with the second porous layer 220. In other embodiments of the present application, the surface of the augment component 200 that is bonded to the host bone tissue may be covered with the second porous layer 220 only, and the edge portion of the second substrate 210 may not be covered with the second porous layer 220.
The second porous layer 220 has a similar structure to the first porous layer 120, and also has a plurality of irregularly shaped pores uniformly distributed in the interior and on the surface. Irregularly shaped pores distributed in and on the surface of the second porous layer 220 are communicated with each other to form a biomimetic transport channel.
The porosity of the second porous layer 220 is 86-90%, the cross-sectional aperture of the hole is 200-1200 μm, and the depth of the hole is more than 1500 μm.
In the embodiment shown in FIG. 10, the porosity of the second porous layer 220 is 88%, the cross-sectional pore diameter of the pores is 200-1200 μm, and the depth of the pores is > 1500 μm. In other embodiments of the present disclosure, the porosity of the second porous layer 220 may be 86%, 87%, 89% or 90%, the cross-sectional pore diameter of the pores of the second porous layer 220 may be 400-800 μm, 500-9000 μm, 200-900 μm, 200-700 μm or 300-1000 μm, and the depth of the pores may be more than 1700 μm, more than 1750 μm or more than 1900 μm.
The second porous layer 220 has a trabecular bone-like structure, which is similar to the host bone tissue, and can improve the bonding strength of the augment component 200 to the host bone tissue interface, enabling the augment component 200 to achieve deep fusion with the host bone tissue. And the porous structure of the second porous layer 220 can be used to support the slow release drug, increasing the loading capacity of the augment component 200.
The second substrate 210 is made of metal.
In the embodiment shown in fig. 10, the second substrate 210 is made of a titanium alloy. In other embodiments of the present application, the second substrate 210 may also be made of other metal materials, such as elemental silver, iron alloy, elemental titanium, and the like.
The second porous layer 220 is made of a titanium simple substance or a titanium alloy, and the surface roughness of the second porous layer 220 is 2-9 μm.
In the embodiment shown in FIGS. 8 to 10, the second porous layer 220 is formed by printing titanium powder by 3D printing technology, and has a surface roughness of 3 to 6 μm. In other embodiments of the present disclosure, the second porous layer 220 may be prepared by a technique capable of preparing a porous structure, and the surface roughness thereof may be 2 to 5 μm, 3 to 5 μm, 4 to 7 μm, 4 to 9 μm, 3 to 8 μm, or 5 to 9 μm.
Similarly, the second porous layer 220 may also be loaded with the bone growth promoting drug 140 and the anti-bacterial and anti-inflammatory drug 130, wherein the bone growth promoting drug 140 is filled in the inner layer of the second porous layer 220, and the anti-bacterial and anti-inflammatory drug 130 is filled in the outer layer of the second porous layer 220.
The amounts of the antibacterial anti-inflammatory drug 130 and the bone growth promoting drug 140 in the second porous layer 220 in the embodiment of the present application are adapted according to the slow release period thereof and the filling rate of the growth of human bone tissue. The antibacterial and anti-inflammatory drug 130 filled in the outer layer of the second porous layer 220 can be released within 3-4 weeks after the acetabular prosthesis system 10 is transplanted, i.e., the antibacterial and anti-inflammatory drug 130 can be continuously administered in the inflammation elimination period after the acetabular prosthesis system 10 is transplanted to realize antibacterial and anti-inflammatory to prevent infection, so that the acetabular prosthesis system 10 can be stably in the excessive inflammation elimination period after the acetabular prosthesis system 10 is transplanted. The bone growth promoting drug 140 filled in the inner layer of the second porous layer 220 can be released half a year after the implantation of the acetabular prosthesis system 10, that is, the bone growth promoting drug 140 can be continuously administered in the overall recovery period after the implantation of the acetabular prosthesis system 10 to promote the bone growth, so that the fusion degree and the fusion efficiency of the human body and the implanted acetabular prosthesis system 10 are improved.
The filling structure of the antibiotic anti-inflammatory drug 130 and the bone growth promoting drug 140 in the second porous layer 220 is similar to that of the first porous layer 120.
The antibacterial and anti-inflammatory drug 130 and the bone growth promoting drug 140 are filled in the pores of the second porous layer 220 by embedding or coating.
When the coating method is adopted, a part of the antibacterial and anti-inflammatory drug 130 may be finally coated on the surface of the second porous layer 220, the coated antibacterial and anti-inflammatory drug 130 is partially sunk into the pores inside the second porous layer 220 due to gravity, and the other antibacterial and anti-inflammatory drug 130 is distributed on the surface of the second porous layer 220.
The antibacterial and anti-inflammatory drug 130 filled on the surface of the second porous layer 220 can directly act, quickly act, and play a good role in resisting bacteria and diminishing inflammation for the just-transplanted acetabular prosthesis system 10.
In summary, in the acetabular cup and acetabular prosthesis system provided by the embodiments of the present disclosure, the acetabular cup 100 includes the first substrate 110 and the first porous layer 120 disposed on the surface of the first substrate 110, the first porous layer 120 can be loaded with a slow-release drug, and the slow-release drug loaded in the first porous layer 120 can be continuously administered after the acetabular cup 100 is implanted into a human body. The acetabular prosthesis system 10 includes the acetabular cup 100 and the augment component 200 described above, the augment component 200 includes a second substrate 210 and a second porous layer 220 disposed on a surface of the second substrate 210, the second porous layer 220 is also capable of being loaded with a slow-release drug, and the slow-release drug loaded in the second porous layer 220 is capable of continuing to be administered continuously after the augment component 200 is implanted in a human. And, the amounts of the antibacterial anti-inflammatory drug 130 and the bone growth promoting drug 140 in the first and second porous layers 120 and 220 are adapted according to the slow release period thereof and the filling rate of the growth of human bone tissue. The amount of the antibacterial and anti-inflammatory drug 130 filled in the first porous layer 120 and the second porous layer 220 can ensure a sustained release period of at least 3-4 weeks, and the amount of the bone growth promoting drug 140 filled in the first porous layer 120 and the second porous layer 220 can ensure a sustained release period of at least half a year.
The above description is only a preferred embodiment of the present application and is not intended to limit the present application, and various modifications and changes may be made by those skilled in the art. Any modification, equivalent replacement, improvement and the like made within the spirit and principle of the present application shall be included in the protection scope of the present application.
Claims (10)
1. An acetabular cup comprising a first substrate and a first porous layer, wherein part or all of the surface of the first substrate is covered with the first porous layer;
the first porous layer is provided with a plurality of uniformly distributed and mutually communicated holes;
the first porous layer is loaded with a bone growth promoting drug and an antibacterial and anti-inflammatory drug, wherein the bone growth promoting drug is filled in the holes of the inner layer of the first porous layer, and the antibacterial and anti-inflammatory drug is filled in the holes of the outer layer of the first porous layer.
2. The acetabular cup of claim 1, wherein a surface of the first porous layer is coated with the anti-bacterial, anti-inflammatory drug.
3. The acetabular cup of claim 1, wherein the bone growth promoting drug comprises Bone Morphogenic Protein (BMP), Fibroblast Growth Factor (FGF) or transforming growth factor (TGF-BETA).
4. The acetabular cup of claim 1, wherein the anti-bacterial and anti-inflammatory agent comprises a penicillin, a cefamycin, or an aspirin.
5. The acetabular cup of claim 1 wherein the porosity of the first porous layer is 86-90% and the cross-sectional pore size of the pores is 200-1200 μm.
6. The acetabular cup of claim 1, wherein the first porous layer is made of a titanium alloy or a titanium simple substance, and the surface roughness of the first porous layer is 2-9 μm.
7. An acetabular prosthesis system comprising an acetabular cup according to any of claims 1 to 6 and an augment component, the acetabular cup having a first curved surface, the augment component having a second curved surface, the augment component and acetabular cup being cooperatively connected by the first curved surface and the second curved surface.
8. The acetabular prosthesis system of claim 7, wherein the augment component includes a second substrate and a second porous layer, a portion or all of a surface of the second substrate being covered with the second porous layer, the second porous layer having a plurality of evenly distributed and interconnected pores.
9. The acetabular prosthesis system of claim 8, wherein the second porous layer is loaded with the bone growth promoting drug and the anti-bacterial and anti-inflammatory drug, wherein the bone growth promoting drug is filled in an inner layer of the second porous layer and the anti-bacterial and anti-inflammatory drug is filled in an outer layer of the second porous layer.
10. The acetabular prosthesis system of claim 9, wherein a surface of the second porous layer is coated with the anti-bacterial, anti-inflammatory drug.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112998912A (en) * | 2021-03-12 | 2021-06-22 | 浙江大学医学院附属第一医院 | 3D printing acetabular cup prosthesis for artificial hip joint replacement surgery |
CN116898639A (en) * | 2023-09-12 | 2023-10-20 | 北京爱康宜诚医疗器材有限公司 | Acetabular prosthesis |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030050705A1 (en) * | 2001-09-11 | 2003-03-13 | Benoist Girard Sas | Acetabular cup |
US20050273176A1 (en) * | 2001-05-01 | 2005-12-08 | Amedica Corporation | Hip prosthesis with monoblock ceramic acetabular cup |
US20060089722A1 (en) * | 2002-04-29 | 2006-04-27 | Montevecchi Franco M | Bone prosthesis with multilayer interface |
US20060116774A1 (en) * | 2004-10-12 | 2006-06-01 | Benoist Girard Sas | Prosthetic acetabular cup and method of manufacture |
DE102005028523A1 (en) * | 2005-05-19 | 2006-11-23 | Plus Orthopedics Ag | Socket for a hip joint endo prosthesis incorporates an insert which is located between the outer and inner shells, and has an inner glide surface corresponding to the outer glide surface of the inner shell |
EP2323587A1 (en) * | 2008-08-13 | 2011-05-25 | Smed-Ta/Td, Llc | Drug delivery implants |
CN104740692A (en) * | 2013-12-31 | 2015-07-01 | 上海微创骨科医疗科技有限公司 | Intraosseous fixation implant and preparation method thereof |
CN107280813A (en) * | 2017-07-18 | 2017-10-24 | 优适医疗科技(苏州)有限公司 | Acetabular component prosthese |
CN206934218U (en) * | 2017-01-23 | 2018-01-30 | 北京华康天怡生物科技有限公司 | A kind of metal outer cup and acetabular bone system |
US20180207320A1 (en) * | 2015-07-22 | 2018-07-26 | Biomet Deutschland Gmbh | Implant with an bioactive coating and method for providing the same |
CN213076094U (en) * | 2020-05-22 | 2021-04-30 | 北京科仪邦恩医疗器械科技有限公司 | Acetabular cup and acetabular prosthesis system |
-
2020
- 2020-05-22 CN CN202010445961.9A patent/CN111529135A/en active Pending
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050273176A1 (en) * | 2001-05-01 | 2005-12-08 | Amedica Corporation | Hip prosthesis with monoblock ceramic acetabular cup |
US20030050705A1 (en) * | 2001-09-11 | 2003-03-13 | Benoist Girard Sas | Acetabular cup |
US20060089722A1 (en) * | 2002-04-29 | 2006-04-27 | Montevecchi Franco M | Bone prosthesis with multilayer interface |
US20060116774A1 (en) * | 2004-10-12 | 2006-06-01 | Benoist Girard Sas | Prosthetic acetabular cup and method of manufacture |
DE102005028523A1 (en) * | 2005-05-19 | 2006-11-23 | Plus Orthopedics Ag | Socket for a hip joint endo prosthesis incorporates an insert which is located between the outer and inner shells, and has an inner glide surface corresponding to the outer glide surface of the inner shell |
EP2323587A1 (en) * | 2008-08-13 | 2011-05-25 | Smed-Ta/Td, Llc | Drug delivery implants |
CN104740692A (en) * | 2013-12-31 | 2015-07-01 | 上海微创骨科医疗科技有限公司 | Intraosseous fixation implant and preparation method thereof |
US20180207320A1 (en) * | 2015-07-22 | 2018-07-26 | Biomet Deutschland Gmbh | Implant with an bioactive coating and method for providing the same |
CN206934218U (en) * | 2017-01-23 | 2018-01-30 | 北京华康天怡生物科技有限公司 | A kind of metal outer cup and acetabular bone system |
CN107280813A (en) * | 2017-07-18 | 2017-10-24 | 优适医疗科技(苏州)有限公司 | Acetabular component prosthese |
CN213076094U (en) * | 2020-05-22 | 2021-04-30 | 北京科仪邦恩医疗器械科技有限公司 | Acetabular cup and acetabular prosthesis system |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112998912A (en) * | 2021-03-12 | 2021-06-22 | 浙江大学医学院附属第一医院 | 3D printing acetabular cup prosthesis for artificial hip joint replacement surgery |
CN116898639A (en) * | 2023-09-12 | 2023-10-20 | 北京爱康宜诚医疗器材有限公司 | Acetabular prosthesis |
CN116898639B (en) * | 2023-09-12 | 2024-01-23 | 北京爱康宜诚医疗器材有限公司 | Acetabular prosthesis |
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