The present invention relates to a calcium phosphate-synthetic resin-metal composite body having excellent workability and biocompatibility and usable as artificial dental roots, bone reinforcements, etc., and a method for producing such a composite body.
Calcium phosphate is utilized for biomaterials such as artificial dental roots, bone reinforcements and dental cements because of excellent biocompatibility. However, it is poor in toughness due to its nature as a ceramic and cannot be used for members requiring impact resistance. Thus, artificial dental roots and bone reinforcements are made of metallic materials, which are not harmful to the human body, such as titanium and stainless steel. However, because calcium phosphate compounds, particularly hydroxyapatite, are much better in terms of biocompatibility, their use has been desired.
Under such circumstances, attempt has been made to combine calcium phosphate compounds with glass materials, metallic materials and synthetic resins, and some of the resultant composite bodies have been already put into practical use. However, when they are combined with the glass materials, there are problems that the glass elutes from the resultant composite bodies into the human body as time goes on, and that the composite bodies lack toughness.
Though attempt has been made to blend a molten synthetic resin and calcium phosphate particles to provide their composite body, the calcium phosphate particles easily collapse during blending, and the molten synthetic resin easily covers the calcium phosphate particles in the course of molding the composite body. In addition, burring disadvantageously occurs during grinding.
Known is a combination of a calcium phosphate-synthetic resin composite body with a calcium phosphate block to have improved biocompatibility. Though this composite body is excellent in workability, biocompatibility and water resistance, it does not have excellent impact resistance because of the use of synthetic resin particles as reinforcements.
The composite material composed of a calcium phosphate compound and metallic materials is generally obtained by burying calcium phosphate compound particles in a metal frame, or by sintering a mixture of metal powder and calcium phosphate compound powder. In the former case, however, the calcium phosphate compound is likely to move from the metal frame in a living body. In the latter case, the calcium phosphate compound particles exposed on the surface of the composite, sintered body are easily detached.
This application is related to Japanese Application No. 2002-200085, filed Jul. 9, 2002, and U.S. application Ser. No. 10/615,013, filed Jul. 9, 2003, still pending which claims priority of this Japanese application, the disclosures of which are incorporated by reference herein in their entireties.
Therefore, an object of the present invention is to provide a calcium phosphate-synthetic resin-metal composite body having excellent workability, biocompatibility and water resistance as well as high impact resistance.
Another object of the present invention is to provide a method for producing such a calcium phosphate-synthetic resin-metal composite body.
As a result of an intensive study in view of the above objects, the inventors have discovered that a composite body would be provided with further improved workability, biocompatibility, water resistance and impact resistance, if a metal member having excellent mechanical strength exists in a step of heat-pressing calcium phosphate particles (or calcium phosphate particles and a calcium phosphate block), synthetic resin particles I, which are at least partially cross-linked in advance, and uncross-linked, synthetic resin particles II. The present invention has been completed based on this finding.
Thus, the calcium phosphate-synthetic resin-metal composite body of the present invention is produced by pressing a metal member, calcium phosphate particles (or calcium phosphate particles and a calcium phosphate block), synthetic resin particles I, which are at least partially cross-linked in advance, and uncross-linked, synthetic resin particles II while heating, the calcium phosphate particles (or the calcium phosphate particles and the calcium phosphate block) being exposed on at least part of the surface of the composite body.
In the calcium phosphate-synthetic resin-metal composite body of the present invention, the synthetic resin particles I are softened while retaining their shapes to some extent, whereas the uncross-linked, synthetic resin particles II having thermoplasticity are softened or melted during pressing while heating. When the composite body contains a porous calcium phosphate block, the softened or molten synthetic resin particles preferably enter into pores of the calcium phosphate block. The metal member and calcium phosphate particles (or calcium phosphate particles and a calcium phosphate block) are firmly fixed in the composite body by bonding the synthetic resin particles to the metal member and the calcium phosphate particles (or the calcium phosphate particles and the calcium phosphate block).
In the calcium phosphate-synthetic resin-metal composite body, it is preferable that the synthetic resin particles I, which are at least partially cross-linked in advance, and the uncross-linked, synthetic resin particles II are bonded to each other. By pressing while heating, the synthetic resin particles I are softened while retaining the shapes to some extent for bonding, and the synthetic resin particles II are softened or melted to enter voids between the particles to form a calcium phosphate-synthetic resin composite body. The synthetic resin particles II filling voids between the particles act as binders.
In a normal condition, not only are the calcium phosphate particles firmly fixed by the synthetic resin particles I and II, but also the synthetic resin particles I and II are firmly bonded to each other. At the time of grinding and polishing, however, exfoliation occurs at interfaces between the calcium phosphate particles and the synthetic resin particles and at interfaces between the synthetic resin particles I and II. Therefore, the calcium phosphate-synthetic resin-metal composite body of the present invention has excellent workability.
A calcium phosphate-synthetic resin composite layer preferably covers the entire surface of the metal member. Particularly excellent in biocompatibility is the calcium phosphate-synthetic resin-metal composite body comprising a composite layer covering the entire surface of the metal member such that the metal member is not exposed.
The metal member is preferably made of a metal or an alloy selected from the group consisting of pure titanium, titanium alloys and stainless steel. At least part of the metal member preferably has a thickness of 0.5 mm or more. An example of preferable shapes of the metal member is a screw shape. In this case, a composite layer composed of calcium phosphate particles and synthetic resin particles I and II is preferably formed on a trunk of a screw.
The metal member is preferably in the form of a mesh. In this case, each side of the metal mesh is preferably covered with the calcium phosphate-synthetic resin composite layer. When the metal member is in the form of a mesh, the calcium phosphate-synthetic resin composite layer easily adheres to the metal member.
A further example of preferable shapes of the metal member is a hollow shape. In this case, the entire surface of the metal member is preferably covered with a hollow calcium phosphate-synthetic resin composite layer. When the hollow composite body is implanted in a living body, a bone material may be charged into the composite body. It is preferable that the metal member has a window, and that the calcium phosphate-synthetic resin-metal composite body has an opening in alignment with the window.
The calcium phosphate particles are preferably porous in terms of biocompatibility. The average particle size of the calcium phosphate particles is preferably 0.001 to 10 mm, and the calcium/phosphorus molar ratio is preferably 1.4 to 2.0. The calcium phosphate particles are preferably sintered in advance.
Both of the synthetic resin particles I and II are preferably made of a water-insoluble acrylic or polystyrene resin, particularly polymethyl methacrylate. The content of the uncross-linked, synthetic resin particles II is preferably 0.2 to 50% by mass based on the total amount of the synthetic resin particles I and II.
The mass ratio of the calcium phosphate particles to the synthetic resin particles in the calcium phosphate-synthetic resin-metal composite body is preferably 1/9 to 8/2.
When the calcium phosphate-synthetic resin-metal composite body comprises a calcium phosphate block, the calcium phosphate block is preferably porous in terms of biocompatibility. A calcium/phosphorus molar ratio in the calcium phosphate block is preferably 1.4 to 2.0. Also, preferably used from a practical standpoint is the sintered calcium phosphate block having a thickness of at least 1 mm.
The method for producing the calcium phosphate-synthetic resin-metal composite body of the present invention comprises the steps of (a) introducing a metal member, the calcium phosphate particles (or calcium phosphate particles and a calcium phosphate block), and synthetic resin particles I and II into a cavity of a molding die, such that the synthetic resin particles surround the calcium phosphate particles, and such that the calcium phosphate particles and/or the calcium phosphate block are present on at least part of a surface of the composite body; and (b) pressing them in a cavity of a molding die while heating, so that the synthetic resin particles are bonded to the metal member and the calcium phosphate particles (or calcium phosphate particles and a calcium phosphate block).
The calcium phosphate particles (and/or the calcium phosphate block) are preferably sintered. Its sintering temperature is preferably 500° C. to 1,300° C.
The step of pressing while heating is preferably carried out in vacuum or in an atmosphere containing no oxygen.
The method for producing the calcium phosphate-synthetic resin-metal composite body according to a preferable embodiment of the present invention comprises using a hollow metal member; pressing a mixture of the calcium phosphate particles and the synthetic resin particles I and II surrounding the metal member while heating to provide a composite body comprising the metal member embedded in a calcium phosphate-synthetic resin composite body; and grinding part of the calcium phosphate-synthetic resin composite body in the metal member-embedded composite body to provide a hollow calcium phosphate-synthetic resin-metal composite body.
In a preferable example of the above-described method, a hollow metal member having a window is used, and the calcium phosphate-synthetic resin composite body is partially cut by machining at a position aligned with the window to form a hollow calcium phosphate-synthetic resin-metal composite body having a window.
The method for producing a screw-shaped, calcium phosphate-synthetic resin-metal composite body according to another preferable embodiment of the present invention comprises using screw-shaped metal member; placing the metal member in a cavity of a molding die with a cap put on its thread; charging a mixture of the calcium phosphate particles and the synthetic resin particles I and II into the molding die cavity; pressing them while heating to form a calcium phosphate-synthetic resin composite body around the metal member; removing the cap from the thread of the screw; and threading the calcium phosphate-synthetic resin composite body around a trunk of the screw-shaped metal member.
Preferably used in the above method is a molding die comprising a stationary die member having a cavity extending in its entire length in a vertical direction; a lower punch having a cavity having a shape for receiving the capped, screw-shaped metal member and entering into the cavity of the stationary die member from its lower end; a protection die having a cavity extending in its entire length in a vertical direction and a cavity having a shape for receiving the capped, screw-shaped metal member, which abuts the lower punch; and a vertically movable upper punch having a cavity having the same shape as that of the cavity of the lower punch at a position aligned with the cavity of the lower punch, which enters into the vertical cavity of the protection die from above to abut the lower punch.
In a preferred embodiment, the capped, screw-shaped metal member is placed in the cavity of the lower punch; the lower punch is positioned in the cavity of the stationary die member; the protection die is caused to move downward so that the cavity of the protection die abuts the cavity of the lower punch; a mixture of the calcium phosphate particles and the synthetic resin particles I and II is charged into the combined cavities of the lower punch and the protection die; the upper punch is caused to move downward to press the mixture while heating, thereby forming the calcium phosphate-synthetic resin composite body around the trunk of the metal member.
a) is a top view showing one example of the calcium phosphate-synthetic resin-metal composite body of the present invention;
b) is a side view showing the example shown in
a) is a top view showing another example of the calcium phosphate-synthetic resin-metal composite body of the present invention;
b) is a vertical, cross-sectional view taken along the line A—A in
a) is a top view showing a further example of the calcium phosphate-synthetic resin-metal composite body of the present invention;
b) is a vertical, cross-sectional view taken along the line B—B in
a) is a top view showing a still further example of the calcium phosphate-synthetic resin-metal composite body of the present invention;
b) is a vertical, cross-sectional view taken along the line C—C in
a) is a top view showing a still further example of the calcium phosphate-synthetic resin-metal composite body of the present invention;
b) is a vertical, cross-sectional view taken along the line D—D in
a) is a top view showing a still further example of the calcium phosphate-synthetic resin-metal composite body of the present invention;
b) is a vertical, cross-sectional view taken along the line E—E in
a) is a top view showing a still further example of the calcium phosphate-synthetic resin-metal composite body of the present invention;
b) is a vertical, cross-sectional view taken along the line F—F in
a) is a top view showing a still further example of the calcium phosphate-synthetic resin-metal composite body of the present invention;
b) is a vertical, cross-sectional view taken along the line G—G in
a) is a top view showing a still further example of the calcium phosphate-synthetic resin-metal composite body of the present invention;
b) is a vertical, cross-sectional view taken along the line H—H in
a) is a perspective view showing a still further example of the calcium phosphate-synthetic resin-metal composite body of the present invention;
b) is an enlarged cross-sectional view showing part of the example shown in
a) is a perspective view showing a still further example of the calcium phosphate-synthetic resin-metal composite body of the present invention;
b) is an enlarged cross-sectional view showing part of the example shown in
a) is a side view showing the calcium phosphate-synthetic resin-metal composite body shown in
b) is a cross-sectional view taken along the line J—J in
c) is a cross-sectional view taken along the line K—K in
a) is a side view showing a still further example of the calcium phosphate-synthetic resin-metal composite body of the present invention;
b) is a cross-sectional view showing the example shown in
a) is a cross-sectional view showing the step of producing a plate-shaped calcium phosphate-synthetic resin-metal composite body, in which a cylindrical metal member and a mixture are charged into a cavity of the molding die of the vacuum pressing/heating apparatus;
b) is a cross-sectional view showing the step of producing a plate-shaped calcium phosphate-synthetic resin-metal composite body, in which the metal member and the mixture charged into the molding die cavity are heated while pressing;
a) is a cross-sectional view showing the step of producing a metal member-embedded composite body, in which a cylindrical metal member and a mixture are charged into a cavity of the molding die of the vacuum pressing/heating apparatus;
b) is a cross-sectional view showing the step of producing a metal member-embedded composite body, in which the metal member and the mixture charged into the molding die cavity are heated while pressing;
a) is a side view showing the cylindrical metal member-embedded composite body shown in
b) is a cross-sectional view taken along the line L—L in
c) is a cross-sectional view taken along the line M—M in
a) is a top view showing a protection die used in the vacuum pressing/heating apparatus shown in
b) is a cross-sectional view taken along the line O—O in
c) is a cross-sectional view taken along the line P—P in
d) is a cross-sectional view taken along the line Q—Q in
e) is a cross-sectional view taken along the line R—R in
a) is a vertical cross-sectional view showing a state in which the mixture is heated while pressing with the capped screw fixed in the molding die;
b) is a cross-sectional view taken along the line S—S in
[1] Calcium Phosphate-synthetic Resin-metal Composite Body
The calcium phosphate-synthetic resin-metal composite body comprises calcium phosphate particles (or calcium phosphate particles and a calcium phosphate block), synthetic resin particles I, which are at least partially cross-linked in advance, and uncross-linked, synthetic resin particles II.
(1) Metal Member
The metal member is not limited as long as it has sufficient strength to function as reinforcement in the composite body and it is not harmful to the human body, and may be made of generally used materials. The metal member is preferably at least one metal or alloy selected from the group consisting of pure titanium, titanium alloys and stainless steel.
The metal member is preferably in a shape of column, cylinder, screw, mesh or plate. The outer diameter of the columnar metal member is preferably the same as or about 1 to 5 mm smaller than that of the calcium phosphate-synthetic resin-metal composite body. Though not particularly limited as long as the metal member is shorter than the calcium phosphate-synthetic resin-metal composite body, the height of the metal member is preferably about 0.5 mm to 100 mm. When the screw-shaped metal member is used, the outer diameter of the trunk of the screw is preferably 1 to 10 mm. When a cylindrical metal member is used, the thickness of the metal member is preferably 0.5 mm to 20 mm. When the thickness of the metal member is less than 0.5 mm, the metal member is not strong enough to function as reinforcement in the composite body. On the other hand, when the thickness of the metal member exceeds 20 mm, the composite body has low workability and biocompatibility.
The metal mesh is preferably constituted by wires having a diameter of 3 mm or less. The number of mesh openings is not particularly limited; the mesh openings may be small or large. To have improved adhesion to synthetic resins, the surface of the metal member may be subjected to an anchoring treatment, etc. before heat-pressing.
In the case of a plate-shaped metal member, it preferably has a thickness of about 0.5 to 5 mm. The metal member is preferably provided with a plurality of through-holes perpendicular to its plane. In a case where the plate-shape metal member is completely covered with the calcium phosphate-synthetic resin composite body, the calcium phosphate-synthetic resin composite layers on both sides of the metal member can be connected with each other via the through-holes. The through-holes are arranged preferably at an equal interval. A percentage of the through-holes to the metal member in area is preferably 5 to 90%. When the total area of the through-holes is less than 5%, the contact area of the calcium phosphate-synthetic resin composite layers is too small, resulting in easy peeling from the metal member. On the other hand, when it exceeds 90%, the metal member does not have enough strength as reinforcement.
The metal member preferably (a) is hollow, (b) has an upper end and a lower end, at least one of which is open, and (c) has one or more windows. It is thus in a shape of a cylinder having a circular, oval or rectangular cross section.
Though not particularly restrictive, the number of the windows in the metal member is practically 5 or less, preferably 4 or less in each surface in the case of the cylindrical calcium phosphate-synthetic resin-metal composite body having a rectangular cross section. The total area of the windows 221 is preferably 80% or less of the area of each sidewall. When the total area of the windows 221 is more than 80%, the metal member does not have enough strength as reinforcement for the composite body.
(2) Calcium Phosphate Particles
The calcium/phosphorus molar ratio in the calcium phosphate particles is preferably 1.4 to 2.0. Specific examples of the calcium phosphate particles include apatites such as hydroxyapatite and fluoroapatite, calcium phosphates such as tricalcium phosphate and tetracalcium phosphate, and mixtures thereof.
The calcium phosphate particles may be porous or non-porous particles, but porous ones are more preferable. In the case of porous calcium phosphate particles, their porosity is preferably 20 to 70%. Though the pores of the porous particles may be of various sizes, they preferably have diameters of 10 to 2000 μm.
It is preferable that the calcium phosphate particles have adjusted particle sizes so that their average particle diameter is 0.001 to 10 mm. The more preferable average particle diameter of the calcium phosphate particles is 0.01 to 6 mm. When the average particle diameter of the calcium phosphate particles is more than 10 mm, the calcium phosphate particles are easily detached from the calcium phosphate-synthetic resin-metal composite body during use. On the other hand, when it is less than 0.001 mm, they are easily agglomerated with poor dispersibility and suffer from a high cost. The average particle diameter may be measured by known methods.
The calcium phosphate particles are preferably sintered before pressing while heating. The sintering temperature is preferably 500 to 1300° C. and more preferably 700 to 1200° C. When the sintering temperature is below 500° C., the calcium phosphate particles are easily collapsed. Particularly in the case of the porous calcium phosphate particles, they are deformed and lose their porosity due to the crushing of pores by the application of pressure. When the sintering temperature is above 1300° C., the calcium phosphate compound is undesirably decomposed or deteriorated.
A sintering time, in which the above sintering temperature is kept, is preferably 1 to 10 hours. When the sintering time is less than 1 hour, the calcium phosphate particles would not exhibit a sufficient reinforcing effect even if sintered. On the other hand, even when the sintering time is more than 10 hours, no further effect is obtained, only resulting in increase in cost. The more preferable sintering time is 2 to 5 hours. Though not particularly limited, a sintering atmosphere is preferably air to prevent the decomposition of the calcium phosphate particles.
(3) Synthetic Resin Particles
The synthetic resin particles comprise synthetic resin particles I, which are at least partially cross-linked in advance, and uncross-linked, synthetic resin particles II. The synthetic resin particles I, which are at least partially cross-linked in advance, and the uncross-linked, synthetic resin particles II are not limited as long as they are not harmful to the human body, and materials known in the art can be used therefor. The synthetic resin particles I and II preferably comprise a water-insoluble acrylic or polystyrene resin and the like, particularly polymethyl methacrylate. The same or different materials may be used for the synthetic resin particles I and II.
Each of the synthetic resin particles I and II has an average particle diameter of preferably 0.05 to 500 μm, more preferably 0.1 to 100 μm. Also, the average particle diameters of the synthetic resin particles are preferably smaller than that of the calcium phosphate particles.
The content of the synthetic resin particles II is preferably 0.2 to 50% by mass based on the total amount of the synthetic resin particles I and II. When the content of the synthetic resin particles II is less than 0.2%, the composite body is not sufficiently stable in water. On the other hand, when their content is more than 50% by mass, not only are the synthetic resin particles II likely to intrude into the porous calcium phosphate particles at the step of pressing while heating, but also the resultant composite body has low workability.
(4) Calcium Phosphate Block
The calcium phosphate-synthetic resin-metal composite body of the present invention may or may not contain a calcium phosphate block. When containing the calcium phosphate block, its composition is preferably the same as that of the calcium phosphate particles.
The calcium phosphate block may be porous or non-porous, though a porous one is more preferable. In the case of a porous calcium phosphate block, its porosity is preferably 5 to 90%. Though the pores of the calcium phosphate block may be of various sizes, they preferably have diameters of 20 to 2000 μm.
Though not particularly limited, the calcium phosphate block may be in a shape of a rectangular column or a circular column. Though not particularly limited as long as the calcium phosphate block is thinner than that of the calcium phosphate-synthetic resin-metal composite body, the thickness of the calcium phosphate block is preferably 1 mm or more from a practical standpoint.
(5) Structure of Calcium Phosphate-synthetic Resin-metal Composite Body
In the calcium phosphate-synthetic resin-metal composite body of the present invention, the calcium phosphate particles (or the calcium phosphate particles and the calcium phosphate block) are exposed on at least part of surface thereof.
a) is a top view showing a calcium phosphate-synthetic resin-metal composite body, and
In each of
The calcium phosphate-synthetic resin-metal composite body shown in
The calcium phosphate-synthetic resin-metal composite body shown in
The calcium phosphate-synthetic resin-metal composite body shown in
The calcium phosphate-synthetic resin-metal composite body shown in
The calcium phosphate-synthetic resin-metal composite body shown in
The calcium phosphate-synthetic resin-metal composite body shown in
The calcium phosphate-synthetic resin-metal composite body shown in
The calcium phosphate-synthetic resin-metal composite body shown in
a) is a side view showing the calcium phosphate-synthetic resin-metal composite body of
a) shows a side of a screw-shaped composite body, and
[2] Production of Calcium Phosphate-synthetic Resin-metal Composite Body
The present invention utilizes a pressing/heating method to produce the calcium phosphate-synthetic resin-metal composite body. The calcium phosphate-synthetic resin-metal composite body may or may not contain a calcium phosphate block. Explanation will be made below mainly on the production of a composite body containing a calcium phosphate block. The composite body containing no calcium phosphate block can also be obtained by a similar pressing/heating method.
(a) Production of Calcium Phosphate Block
The calcium phosphate block may be produced by common methods, but it is preferably produced by the methods described in JP 2-167868 A and JP 8-48583 A, foaming methods, and methods of adding thermally decomposable beads. The disclosures of JP 2-167868 A and JP 8-48583 A are incorporated by reference herein in their entireties. The method for producing a calcium phosphate-synthetic resin composite body, which is described in JP 2-167868 A, is a method (I) where a slurry or a fluid gel containing calcium phosphate compound powder and a polymer material is foamed and then thickened or gelated, and the resultant foamed body is sintered if necessary. The method for producing a calcium phosphate-synthetic resin composite body, which is described in JP 8-48583 A, is a method (II) where polysaccharide particles and ceramic particles are mixed and compressed to form a green compact, which is sintered.
(b) Production of Calcium Phosphate-synthetic Resin-metal Composite Body
(I) Pressing/Heating Apparatus
Preferable pressing/heating methods for producing the calcium phosphate-synthetic resin-metal composite body include a method where a metal member, a mixture comprising the calcium phosphate particles and the synthetic resin particles I and II, and a calcium phosphate block are charged between a pair of dies connected to a heat source, which are heated while applying pressure. The pressing/heating is preferably carried out in vacuum, or in an atmosphere of an inert gas such as N2, He and Ar.
Each ram 5a and 5b is driven by a press-driving mechanism 9 to press the mixture 3 while heating each punch 4a and 4b, with electric power received from a power supply 8 connected via a terminal (not shown). A control means 10 is connected to the press-driving mechanism 9, the power supply 8, the vacuum pump 7 and the thermocouple to control a heating temperature in the stationary die member 2 and a degree of vacuum in the vacuum chamber 6.
As is shown in
(II) Charging
The metal member, a mixture comprising the calcium phosphate particles and the synthetic resin particles I and II, and the calcium phosphate block are charged into the cavity 2a of the stationary die member 2 such that the calcium phosphate particles and a calcium phosphate block are exposed on at least part of the surface of the resultant composite body, and that the synthetic resin particles I and II surround the calcium phosphate particles.
The mass ratio of the calcium phosphate particles to the synthetic resin particles is preferably 1/9 to 8/2. When the mass ratio of the calcium phosphate particles is more than 8/2, the calcium phosphate particles are not completely surrounded by the synthetic resin particles, resulting in easy detachment of the calcium phosphate particles. On the other hand, when the mass ratio of the calcium phosphate particles is less than 1/9, the ratio of calcium phosphate in the composite body is too low, resulting in low biocompatibility.
For instance, when the calcium phosphate-synthetic resin-metal composite body shown in
(III) Pressing/Heating Treatment
In the case of the calcium phosphate-synthetic resin-metal composite body shown in
When the press-driving mechanism 9 is operated by the control means 10, at least one of the rams 5a and 5b moves in a direction to approach one another, so that the punches 4a and 4b secured thereto press the mixture 3. The pressing power of the punches 4a and 4b is preferably 0.5 to 50 MPa, and more preferably 1.0 to 20 MPa. When the pressing power is less than 0.5 MPa, sufficient adhesion is not achieved between the synthetic resin particles and the metal member, the synthetic resin particles and the calcium phosphate particles, and the synthetic resin particles and the calcium phosphate block, resulting in easy detachment of the metal member, the calcium phosphate particles and the calcium phosphate block from the resultant composite body. Even if it were more than 50 MPa, however, correspondingly improved shape retention would not be obtained, rather resulting in problems such as the collapse of the calcium phosphate particles and the calcium phosphate block.
The punches 4a and 4b are heated by the power supply 8 to heat the mixture 3 under pressure. The mixture 3 is preferably heated according to a predetermined temperature elevation program. In that case, the temperature of the mixture 3 is detected by a thermocouple (not shown) disposed in the stationary die member 2, and an output of the thermocouple is sent to the control means 10. The control means 10 produces a signal for temperature elevation according to the temperature elevation program on the basis of input temperature data, and sends it to the power supply 8. The power supply 8 supplies appropriate current to the rams 5a and 5b according to a command from the control means 10.
The heating temperature is preferably 130° C. to 300° C., and more preferably 150° C. to 250° C. When the heating temperature is lower than 130° C., sufficient adhesion is not achieved between the synthetic resin particles and the metal member, the synthetic resin particles and the calcium phosphate particles, and the synthetic resin particles and the calcium phosphate block, resulting in easy detachment of the metal member, the calcium phosphate particles and the calcium phosphate block from the composite body. The heating temperature higher than 300° C. is not preferable, because the synthetic resin particles cannot retain their shapes, sometimes resulting in integration by melting.
The heating time (time period in which the heating temperature is kept) is preferably 1 to 30 minutes. When the heating time is shorter than one minute, sufficient adhesion is not achieved between the synthetic resin particles and the metal member, the synthetic resin particles and the calcium phosphate particles, and the synthetic resin particles and the calcium phosphate block. The heating time longer than 30 minutes is not preferable, because it would not provide improved adhesion. A more preferable heating time is 3 to 10 minutes.
After the pressing/heating treatment, the calcium phosphate-synthetic resin-metal composite body is cooled to room temperature, and removed from the stationary die member. When the calcium phosphate particles are not exposed sufficiently on the surface of the composite body, the surface may be ground.
The production of the cylindrical calcium phosphate-synthetic resin-metal composite body shown in
As shown in
As shown in
a) is a side view showing a cylindrical metal member-embedded composite body 400,
Because of the special shape of the composite body shown in
The lower punch 4b has a semicylindrical cavity 14b for receiving the metal screw 200 on a top surface. The semicylindrical cavity 14b is open at one end and closed at the other end in a longitudinal direction. The semicylindrical cavity 14b is positioned such that it is exposed to the cavity 2a of the stationary die member 2. The upper punch 4a has a semicylindrical cavity 14a having the same shape as that of the semicylindrical cavity 14b of the lower punch 4b at a position in alignment with the semicylindrical cavity 14b. Both semicylindrical cavities 14a and 14b have a shape substantially complementary to the cap 210 and the head 203 of the metal screw 200, respectively.
a) to 26(e) shows the protection die 12;
Described below is an example of the production of the screw-shaped composite body shown in
In this state, the mixture 3 of the calcium phosphate particles and the synthetic resin particles I and II is charged into the cavity 14b of the lower punch 4b and the cavity 12a of the protection die 12. As shown in
After the completion of molding, as shown in
As shown in
The present invention will be explained in more detail by the following Examples without intention to limit the present invention thereto.
10 g of calcium phosphate powder having an average particle diameter of 30 μm was added to 20 g of an aqueous solution containing 1% by mass of methylcellulose, and blended at a predetermined speed for a predetermined period of time. The resultant foamed slurry was molded in a molding die frame, dried at 80° C. for 72 hours and then sintered in an air furnace at 1200° C. for 4 hours. Machining was carried out to provide a calcium phosphate block 300 having a calcium/phosphorus molar ratio of 1.67, an outer shape of 20 mm in diameter and 4 mm in thickness and a porosity of 45%.
10.0 g of porous calcium phosphate particles 100 having particle diameters of 0.2 to 0.6 mm and a calcium/phosphorus molar ratio of 1.67, which was sintered in an air furnace at 1200° C., 4.0 g of cross-linked acrylic powder I having an average particle diameter of 3.0 μm (Chemisnow MX-300 available from Soken Chemical & Engineering Co., Ltd.), and 1.0 g of uncross-linked acrylic powder II having an average particle diameter of 1.5 μm (Chemisnow MP-1400 available from Soken Chemical & Engineering Co., Ltd.) were mixed.
To obtain the calcium phosphate-synthetic resin-metal composite body having the structure shown in
The resultant calcium phosphate-synthetic resin-metal composite body was machined by a lathe to obtain a composite body with a diameter of 20 mm and a thickness of 15.7 mm. The observation of a surface of the calcium phosphate-synthetic resin composite layer 3a of this composite body by a scanning electron microscope revealed that the calcium phosphate was exposed on the surface without being covered with the acrylic resin.
To obtain the calcium phosphate-synthetic resin-metal composite body having the structure shown in
The above cylindrical, porous calcium phosphate block 300, a stainless steel column 200 (10 mm in diameter×15 mm in thickness), and 3.40 g of a mixture of porous calcium phosphate particles and the synthetic resin particles I and II, which was obtained in the same manner as in Example 1, were charged into the cavity 2a of the stationary die member 2 (20 mm in internal diameter×50 mm in height) of the pressing/heating apparatus shown in
The resultant calcium phosphate-synthetic resin-metal composite body was machined by a lathe to obtain a composite body with a diameter of 20 mm and a thickness of 15 mm. The observation of a surface of the calcium phosphate-synthetic resin composite layer 3a of this composite body by a scanning electron microscope revealed that the calcium phosphate was exposed on the surface without being covered with the acrylic resin.
To obtain the calcium phosphate-synthetic resin-metal composite body having the structure shown in
The calcium phosphate-synthetic resin composite layer 3a adhering to the top surface of the cylindrical stainless steel member 200 was removed by machining to obtain the composite body. The observation by scanning electron microscope revealed that the calcium phosphate was exposed on the surface without being covered with the acrylic resin.
To produce a bone-connecting screw used as a biomaterial, as shown in
As shown in
After the cap 210 was detached from the molded product as shown in
(1) Preparation of Mixture
10 g of the porous calcium phosphate particles 100 having an average particle diameter of 0.2 to 0.6 mm and a calcium/phosphorus molar ratio of 1.67 was sintered in an air furnace at 1,200° C., 4 g of cross-linked acrylic powder I having an average particle diameter of 3 μm (Chemisnow MX-300 available from Soken Chemical & Engineering Co., Ltd.), and 1 g of uncross-linked acrylic powder II having an average particle diameter of 1.5 μm (Chemisnow MP-1400 available from Soken Chemical & Engineering Co., Ltd.) were mixed.
(2) Charging into Molding Die
As shown in
(3) Pressing/Heating Treatment
The content in the cavity 2a was kept at a temperature of 200° C. for 5 minutes while pressing from above and below at a pressure of 10 MPa, and then cooled to room temperature, and the pressure was released. In the resultant cylindrical metal member-embedded composite body 400, the metal member 200 was filled with the calcium phosphate-synthetic resin composite body without gap. The calcium phosphate-synthetic resin composite body of the cylindrical metal member-embedded composite body 400 was machined to the calcium phosphate-synthetic resin composite layer 3a having a thickness of about 1 mm by a milling machine with a machining center, thereby providing the calcium phosphate-synthetic resin-metal composite body (22.0 mm×12.0 mm×17 mm in height, 4.0 mm in thickness) having windows (3.0 mm×6.0 mm) as shown in
(1) Preparation of Mixture
6 g of the porous calcium phosphate particles 100 having an average particle diameter of 0.1 to 0.3 mm and a calcium/phosphorus molar ratio of 1.50, which was sintered in an air furnace at 700° C., 6 g of cross-linked acrylic powder I having an average particle diameter of 3 μm (Chemisnow MX-300 available from Soken Chemical & Engineering Co., Ltd.), and 0.5 g of uncross-linked acrylic powder II having an average particle diameter of 1.5 μm (Chemisnow MP-1400 available from Soken Chemical & Engineering Co., Ltd.) were mixed.
(2) Charging into Molding Die
After the mixture 3 prepared in the step (1) was charged into the cavity 2a (30 mm×40 mm×30 mm in height) of the stationary die member 2 of the pressing/heating apparatus to a height of approximately 6 mm, a titanium net (wire diameter: 1.0 mm, 8 meshes, 25.0 mm×35.0 mm) was placed thereon, and the rest of the mixture 3 was added thereon.
(3) Pressing/Heating Treatment
The content in the cavity 2a was kept at a temperature of 200° C. for 5 minutes while pressing at a pressure of 10 MPa from above and below. It was then cooled, and the pressure was released at room temperature. The resultant calcium phosphate-synthetic resin composite body was worked by a milling machine to a calcium phosphate-synthetic resin composite layer 3a of about 1 mm in thickness, thereby obtaining a calcium phosphate-synthetic resin-metal composite body shown in
A calcium phosphate-synthetic resin composite body was produced in the same manner as in Example 6 except for using no titanium net. The three-point bending strength of the resultant composite body was 25.5 MPa.
As described above, the calcium phosphate-synthetic resin-metal composite body of the present invention has high biocompatibility and mechanical strength, because the calcium phosphate particles and/or the calcium phosphate block having excellent biocompatibility are exposed on at least part of the surface of the composite body, and because it comprises a metal member having excellent mechanical strength. The calcium phosphate-synthetic resin-metal composite body of the present invention having such a structure is excellent in workability, biocompatibility, water resistance and impact resistance, and suitable for artificial dental roots, bone reinforcements, etc. The present disclosure relates to subject matter contained in Japanese Patent Application Nos. 2002-211690 (filed on Jul. 19, 2002) and 2003-176747 (filed on Jun. 20, 2003) which are expressly incorporated herein by reference in its entirety.
Number | Date | Country | Kind |
---|---|---|---|
2002-211690 | Jul 2002 | JP | national |
2003-176747 | Jun 2003 | JP | national |
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20040071954 A1 | Apr 2004 | US |