Field of the Invention

The invention relates to surgical implants, methods for making such implants, and methods for using such implants to fill holes in bone tissue.

Background of the Invention

Craniotomy is a procedure during which a surgeon makes a bone flap and removes the flap temporarily to access the brain during surgery. The bone flap is formed by first drilling a plurality, usually two to four, of spaced-apart bore holes though the skull of the patient and then cutting through the bone between the bore holes using a saw. At the end of the procedure, the bone flap is replaced and reattached to the skull. However, the bore holes seldom heal and provide no protection to the underlying brain. Such bore holes that cannot heal can be filled using autograph, allograph or synthetic scaffold materials. Scaffold strategies involve providing metal meshes or porous ceramic materials. Current strategies using metal mesh do not induce tissue healing. Currently used ceramics are utilized only to provide osteoconductive support but will not provide fixation of the bone flap to adjacent cranial bone. Most commonly, the bore holes are left untreated.

Summary of the Invention

The present invention is directed to implants, methods of making implants and methods of implanting an implant in a bore hole. The implants and methods overcome various disadvantages of prior art strategies and methods relating to cranial bore holes.

In one embodiment, the invention is directed to an implant for filling a bore hole in a bone characterised in that it comprises a single ceramic implant body of width D and thickness H, and a plurality of substantially laterally extending anchoring arms. In another embodiment, the invention is directed to methods of forming an implant according to the invention, for filling a bore hole in a bone, characterised in that the method comprises the steps of moulding a cement composition around at least one substantially laterally extending anchoring arm and subsequently allowing said cement composition to cure. In yet another embodiment, the invention is directed to methods of implanting an implant according to the invention in a bore hole between a bone flap and surrounding bone, the method comprising the steps of in a bore hole between a bone flap and surrounding bone, the method comprising the steps of 1) placing the implant body in the bore hole, and

2) fixing one or more anchoring arms to the bone flap and another one or more anchoring arms to the surrounding bone.

The implants and methods of the invention are advantageous in providing both a filling function for filling a bore hole and a fixative function, for securement to adjacent bone, i.e., the skull. Additionally, the implant is easily attached to the adjacent bone structure during surgery. These and additional embodiments, aspects and advantages of the implants and methods of the present invention will be more fully apparent in view of the following Detailed Description. Brief Description of the Drawings

The Drawings will facilitate understanding of the Detailed Description, wherein

Fig. 1 shows schematically a skull with an bone flap and bore holes;

Fig. 2 shows schematically an enlarged portion of the skull shown in Fig. 1 with a bore hole plugged with an implant in accordance with one embodiment of the present invention; Figs. 3a)-3c) show schematically the implant of Fig. 2, in perspective, plan and side views, respectively;

Fig. 4 shows schematically an enlarged portion of the skull shown in Fig. 1 with a bore hole plugged with an implant in accordance with a second embodiment of the present invention; Fig. 5a)-5c) show schematically the implant of Fig. 4, in perspective, plan and side views respectively;

Fig. 6 shows schematically an enlarged portion of the skull shown in Fig. 1 with a bore hole plugged with an implant in accordance with a third embodiment of the present invention; Fig. 7a)-7c) show schematically the implant of Fig. 6, in perspective, plan and side views, respectively;

Figs. 8a) and 8b) show schematically a fourth embodiment of an implant in accordance with the present invention,

Figs. 9a) and 9b) show schematically in plan view and in section along line A-A of Fig. 9a), respectively, a mould used for making an implant in accordance with the present invention; Fig. 9c) shows in section another embodiment of a mould and a wire for making an implant in accordance with the present invention;

Fig. 10 shows schematically an enlarged portion of the skull shown in Fig. 1 with a bore hole plugged with an implant in accordance with a further embodiment of the present invention; Figs. l la)-l lc) show schematically the implant of Fig. 10, in perspective, plan and side views, respectively;

Fig. 12 shows schematically an enlarged portion of the skull shown in Fig. 1 with a bore hole plugged with an implant in accordance with a yet another embodiment of the present invention;

Figs. 13a) and 13b) show schematically in plan view and in section along line A-A in Fig. 13a), respectively, a further embodiment of a mould used for making an implant in accordance with the present invention;

Fig. 13c) shows in section yet a further embodiment of a mould and a plate for making an implant in accordance with the present invention; and

Figs. 14a) and 14b) show plan and side views, respectively, of an embodiment of a wire mesh as employed in Example 1.

The Drawings are non-limiting of the invention defined in the claims.

Detailed Description of the Invention

The present invention is directed to an implant (an implant is a kind of medical device made to replace and act as a missing biological structure), alternatively referred to as a surgical implant and/or a biomedical implant. The implant comprises a single ceramic implant body of width D and thickness H, formed, for example, of a biomaterial mosaic element, and a plurality of substantially laterally extending anchoring arms formed, for example, of wire or plates. The implant provides increased combined bone in-growth and better mechanical properties compared to prior art systems.

For the purpose of the present disclosure, a wire anchoring arm comprises one or a plurality of wires. In a specific embodiment, the wire or wires are arranged in a configuration in which one or more wires cross. In such arrangements, the crossing wires may be joined to each other, or may be unjoined. Within the context of the present description, a mesh comprises wire or wires arranged in a configuration in which at least two crossing wires are joined at one, some, or all of their intersections. A biomaterial is any matter, surface, or construct that interacts with biological systems. The implant combines a plurality of high strength, optionally flexible, wire or plate anchoring arms with at least one mosaic tile formed of a biomaterial. The invention can be employed as a replacement for the bone removed by drilling during, for example, craniotomy. The biomedical implant can be composed of resorbable biomaterials and/or stable biomaterials such as polymers, ceramics and metals. In one embodiment, the implant is osteo-conductive (i.e. can serve as a scaffold on which bone cells can attach, migrate, and grow and divide) or osteo-inductive (i.e. can serve to induce new bone formation), and has high mechanical strength. This is satisfied by an implant system that combines an anchoring system (for example one or more wires) with a solid biomaterial tile - the implant body. In a specific embodiment, the anchoring system is made of a biomaterial. This system has the beneficial effects of a mechanically strong anchoring system (e.g. a wire) and an osteo-conductive and/or osteo-inductive solid implant (e.g. made of a ceramic material). The implant system can be easily attached to a skull in the operation room. The anchoring system may be attached to adjacent cranial bone and a bone flap by screws. Alternatively, the anchoring system may use anchoring channels formed in the skull and or bone flap which are positioned to receive the wires. Combinations of screws and anchoring channels are also possible. The solid implant body, which preferably is moulded onto the anchoring arms, i.e., wire or plates, during manufacturing of the implant, is preferably composed of an osteo-conductive and/or osteo-inductive material that facilitates bone in-growth onto the implant system.

Within the present disclosure, a plurality of anchoring arms refers to two or more anchoring arms. The implants may therefore have two, three, four, five, six, or more anchoring arms. In a specific embodiment, the anchoring system comprises one or more wires that may be manipulated by the surgeon to match a groove in the skull. The implant body may also be flat or, preferably, it is dished to provide a better match to the curvature of a skull. In one embodiment of the present invention, a biomaterial body is moulded around the one or more wires or plates. In this way a structure comprising a wire-supported implant body is formed.

In another embodiment of the present invention, the wires extend out of the implant body and then re-enter the implant body, thereby forming a closed loop which can be anchored in channels formed with a matching shape and appropriate dimensions in the bone.

Non-limiting examples of suitable wire materials include polymers, shape memory alloys, Ti, Ti alloys (e.g. Ti6A14V, having a chemical composition of 6% aluminium, 4% vanadium, 0.25% (maximum) iron, 0.2% (maximum) oxygen, and the remainder titanium, and stainless steel. In the present specification, the word "wire" is intended to include filaments made of any such material. Non-limiting examples of plate material include titanium or polymer, including degradable polymer or non-degradable polymer. The biomaterial implant body is preferably mouldable from the chemically bonded ceramic class of materials or a biopolymer, non-limiting examples include Ca-salts, for example, calcium sulphate, calcium phosphate, calcium silicate, calcium carbonate or combinations thereof. The materials are preferably moulded onto the anchoring arms, i.e., wires or plates, using a non-aqueous water-miscible liquid or using a mixture of water and a non-aqueous water-miscible liquid, allowed to harden to form a mosaic implant in a water-containing bath, or other humid environment, and, subsequently, the mosaic implant is released from the mould. After packing and sterilization, the implant is ready to be used.

A typical mould and manufacturing process of an implant system in accordance with an embodiment of the present invention involves the following steps:

1. Manufacture of a positive model of implant.

2. Manufacture a mould for the scaffold. The mould is preferably produced of a polymer that is easy to de-mould after setting, for example sodium alginate or polyether. One preferred mould material is silicone rubber, due to its high biocompatibility and easy handling. The model is used to manufacture the mould by applying the mould material onto the positive model and let the mould material set. Examples of suitable mould materials include: Silagum, Silagum light (DMG Dental) and Silupran 2450 (Wacker silicones). The first two are dental impression materials and the later is used for temporary implants.

3. Placing anchoring arms, i.e., wire or plates, into the mould and filling the mould with a chemically bonded ceramic precursor powder mixed with a non-aqueous water- miscible liquid and optionally water.

4. Letting the filled mould harden in a moist or wet environment, preferably in

temperatures between room temperature and 120° C. According to one embodiment, the material is set and hardened under an external pressure, e.g. using a mechanical press or the like. This produces a final product with a higher mechanical strength compared to a final product hardened in the absence of an external pressure.

5. Demoulding the sample and optionally letting the sample further harden in a moist or wet environment preferably at elevated temperatures as described below. 6. Optional soaking of the sample to remove any excess non-aqueous water-miscible liquid.

7. Optional final polishing of the sample.

8. Packing and sterilisation using conventional sterilising methods and packaging

solutions.

The inventive implant provides both filling of a bone defect with osteoconductive /inductive material and, simultaneously, fixation of the bone flap with the anchoring system. In a specific embodiment of the invention, the ceramic tile forming the body of the implant may be simply put into the defect and fixed with screws inserted into openings or loops in anchoring arms. In a more specific embodiment, two anchoring arms are attached to the bone flap and two anchoring arms are attached to adjacent bone.

Fig. 1 shows schematically a side view of a skull 1 with three bore holes 3. The bore holes are joined by saw cuts 5 which together with the bore holes form a continuous cut line through the skull, thereby releasing a bone flap 7 from the rest of the skull. Bone flap 7 can be lifted to allow access to the underlying tissue. When the bone flap 7 is replaced it is desirable not only to anchor it into place but also to at least partly fill the bore holes 3.

Fig. 2 shows schematically an enlarged portion of the skull shown in Fig. 1 with a bore hole 3 plugged with an implant 11 in accordance with the present invention. Implant 11 comprises a round tile 13 and a plurality of anchoring arms 15 extending substantially laterally from the tile 13. Other implant tile body shapes are also conceivable, for example, oval, triangular, square, rectangular, pentagonal, hexagonal, etc, however a circular shape is preferred as it can most closely match a circular bore hole which is typically formed during formation of the bone flap. Each arm 15 is accommodated in its own groove 17 formed in the skull. The arms are each retained in their grooves by retaining means - shown by dashed lines, for example via plates 16 and screws 18 and/or clamps and/or sutures 20 or any other retaining means.

Figs. 3a)-3c) show schematically the implant 11 of Fig. 2, in perspective, plan and side views, respectively. Implant 11 has a circular body 13 of diameter D and height H. In one embodiment, D is greater than H. In specific embodiments, D is from 8 to 20 mm, or from 9 to 15 mm, or from 10 to 14 mm. Additionally, in specific embodiments, height H is from 1 to 10 mm, or from 2 to 8 mm, or from 3 to 6 mm. Any of these combinations of D and H are suitable. Protruding substantially laterally, for example, radially, from body 13 are the anchoring wires 15. Each wire protrudes a distance P from body 13 and has a diameter T. In specific embodiments, the length of distance P is from 2 to 15 mm, or from 3 to 10 mm, or from 4 to 8 mm. The diameter T of each wire is suitably less than 3 mm, more specifically less than 2 mm, or 1 mm or less. In this example of the first embodiment of the invention, there are four anchoring wires 15 made from two lengths of wire which cross inside the tile as shown by dotted lines in Figs. 3a) and 3b). Instead of having crossing wires, it is conceivable to have two bent wires which do not cross, as shown by dashed lines in Fig. 3b) or to use four wires (not shown), with each wire forming an anchoring wire. Alternatively, the anchoring wires may be replaced by flat plates with a height, for example, of from 0.2 to 2 mm, a width, for example, of from 2 to 6 mm, and a length, for example, of from 5 to 15 mm. Each plate is provided with a through hole which allows an attachment screw to be inserted through the plate and screwed into the underlying bone. Examples of plate material are titanium or degradable polymer. Plates can be moulded into the ceramic tile and extended outside the tile laterally on a plurality of sides.

Figs. 4 and 5a)-5c) show schematically a second embodiment of the present invention in which each anchoring wire 415 extending from the body 413 of the implant 411 is provided with a substantially circular anchoring tile 419 at its distal end. Each anchoring tile has a diameter d and a height h. In specific embodiments, d is from 2 to 10 mm, or from 3 to 8 mm, or from 4 to 6 mm. In specific embodiments, height h is from 0.5 to 6 mm, or from 1 to 5 mm, or from 1.5 to 4 mm. The anchoring tile is intended to be positioned in an anchoring chamber 421 formed at the end of each of the anchoring grooves 417. In one embodiment, d is less than D and h is less than H in order to minimise the amount of material which has to be removed to form anchoring chambers. The arms and/or anchoring tiles are each retained in their grooves by retaining means - not shown - for example via plates and screws and/or clamps and/or sutures or any other fixing means, wire actually overlaps both the primary tile- retaining channel and the distal tile -retaining channel. The implant illustrated in this embodiment may be manufactured by a method as described above, with the option of allowing the anchoring arms, i.e., wires, extend to an anchoring tile mould cavity for formation of the anchoring tiles on the distal ends of the wires. The anchoring tiles may be formed simultaneously with the body or in a separate moulding step. In further embodiments, the anchoring tiles are preformed and subsequently attached to the anchoring arm wires. Figs. 6 and 7a)-5c) show schematically a third embodiment of the present invention in which the anchoring wire 615 of the implant 611 forms one or more closed loops 623 protruding from the body 613 of the implant. As can be seen in Fig. 7b), a single anchoring wire is formed into a figure of eight shape with its ends almost meeting at the centre of the figure of eight shape. The body 613 of the implant is formed over these ends. The closed loops extend a distance E from the body 613. In specific embodiments, E is from 5 to 15 mm, or from 6 to 12 mm, or from 8 to 10 mm. The anchoring loops are intended to be positioned in suitably formed anchoring grooves 617 which extend from a bore hole 603 and then return to the same bore hole. The arms are each retained in their grooves by retaining means - shown by dashed lines, for example via plates 616 and screws 618 and/or clamps and/or sutures 620 or any other fixing means.

Figs. 8a) and 8b) show schematically a fourth embodiment of the present invention in which the single anchoring wire 815 of the implant 811, in addition to being bent into a flattened figure of eight shape to form two closed loops 823, is provided with at least one (in this example two) substantially circular anchoring tiles 819 at intermediate portions of the loops. Each anchoring tile has a diameter d and a height h. In specific embodiments, d is from 2 to 10 mm, or from 3 to 8 mm, or from 4 to 6 mm. In specific embodiments, height h is from 0.5 to 6 mm, or from 1 to 5 mm, or from 1.5 to 4 mm. Each anchoring tile is intended to be positioned in an anchoring chamber formed at an appropriately located position in an anchoring groove (not shown). Alternatively, each anchoring tile may be provided with an opening to accept a screw which can be used instead of an anchoring groove or in addition to an anchoring groove to attach the anchoring tile to the underlying skull. The arms and/or anchoring tiles may also each be retained in their grooves by retaining means - not shown - for example via plates and screws and/or clamps and/or sutures or any other fixing means.

It is conceivable to form the loops from a plurality of wires with the ends of each wire embedded in the implant body 813 and the anchoring tiles 819, however the use of a single wire is preferred as it is easier to handle.

It is of course possible to attach any anchoring means in accordance with the present invention directly to the bone flap and bone without forming anchoring channels - this may be achieved by fixing the anchoring wires or plates by suitably placed screws which clamp the anchoring wires or plates or tile between the underside of the screw and the underlying bone or bone flap, or by using sutures or any other fixing means.

An implant in accordance with the above embodiments of the present invention can be implanted in a patient by a method comprising the steps of:

i) optionally forming one or more anchoring grooves in the bone and/or bone flap surrounding a bore hole, and, if the implant comprises one or more anchoring tiles or, forming one or more anchoring chambers in the bone and/or bone flap,

ii) if necessary bending the anchoring wires to match the orientations of the one or more anchoring grooves and any anchoring chambers if anchoring grooves or anchoring chambers are present,

iii) placing the implant body in the bore hole,

iv) optionally placing the one or more anchoring wires in the one or more anchoring grooves if present and/or, if present the one or more anchoring tiles in the one or more anchoring chambers,

iv) fixing any anchoring wires or plates which are not anchored in anchoring grooves or anchoring chambers, preferably by anchoring means such as a screw or suture or the like, to the surrounding bone and to the bone flap. Thus implants can be fixed to the bone flap and skull by anchoring means fitted and retained in anchoring grooves or channels, or by screws passing though anchoring loops or holes or by plates and screws and the like and by combinations of these methods.

One embodiment of a method of manufacturing a mosaic implant in accordance with the present invention employs a mould 901 of thickness M. As shown in plan view in Fig. 9a) and in Fig. 9b), as a section along line A-A of Fig. 9a), the mould comprises at least one cavity 903 of depth H and width D. Each cavity has the shape of an implant body. The depth D of the cavities and the thickness of the resulting tile is less than the depth M of the mould. Each cavity 903 has a closed bottom end 905 which is closed by the floor 907 of the mould 901 and is open at the opposite open end 909 to allow filling of the cavity 903. Floor 907 does not have to be permanently attached to the mould but may, for example, be a surface which the mould is in contact with during manufacturing of the implant and which can be removed after moulding to facilitate release of the implant from the mould. In one embodiment, each cavity, and thus each tile subsequently formed, in is in the shape of a circle. However, it is conceivable that the cavity and the subsequently formed implant body may have another shape such as a triangle, a square, a rectangle, a pentagon, a hexagon, etc. In this embodiment of a mould, the wall 911 of each cavity 903 is pierced by at least one narrow, wire -retaining channel 913 of width T and depth which the same as T (which is used when the top surface of the anchoring wire is to be flush with the top surface of the implant body) or greater than T (which is used when the top surface of the anchoring wire is intended to be below the top surface of the implant body). It is also possible that the depth of the wire-retaining channels is less than T in which case the upper surface of the anchoring wire will be above the top surface of the implant body. Wire -retaining channels 913 are intended to receive, and to retain during the casting process, the wires used to form the implant anchoring arrangement. In this embodiment of the invention, each cavity is only crossed by one wire in the first direction and one wire in the substantially perpendicular direction. Other arrangements such as two wires crossing at 120° or any other non-perpendicular angle are also conceivable. In another embodiment of a mould 901 ', shown in Fig. 9c), the wire -retaining channels are omitted and instead the wire 916 may be bent so that the portions 918 of the wire outside the cavity lies on the upper surface of the mould and extends radially away from the cavity, an intermediate portion 920 projects down into the mould cavity, and the remaining portion of the wire 922 extends parallel to the top surface of the mould. The intermediate and remaining portions of the wire are subsequently covered by the cement. An implant made in this way will be able to be fitted with its top surface flush with the top surface of the bone flap and/or skull, with only the exposed portions of the wire(s) protruding above the surface of the bone flap and/or skull. While the cavities have been shown with vertical walls 911, it is of course possible to have walls sloping such that the width across any section of the bottom closed end of each cavity is smaller than the width of the corresponding section of the open end of the cavity in order to form release slopes which aid releasing of the moulded product from the mould.

An implant in accordance with the present invention can be made by placing wires in the wire-retaining channels, filling the mould with cement, allowing the cement to cure, and then removing the thus formed implant from the mould.

Other moulding methods may be used to form a mosaic implant in accordance with the present invention. For example, one or more anchoring wires can be placed on the exposed surface of a first mould half comprising one or more cavities of depth less than D separated by walls. The first mould half is provided with an excess amount of cement composition which not only fills the cavities and covers the wire(s) but also extends away from the exposed surface of the first mould half. A second mould half, which preferably has cavities of depth less than D but which together with the depth of the cavities of the first mould half are equal to D, is provided. The cavities are arranged as a mirror-image of the first mould half, and the second mould half is subsequently put on top of the wire and compressed toward the bottom mould to allow moulding of implant bodies around the wires. The excess amount of cement composition should be sufficient to fill the cavities in the second mould half and should be positioned to be able to fill the second mould half. Excess cement is removed after the mould halves have been united and preferably before hardening of the cement. Hardening of the cement may be achieved by adding moisture via holes, each hole being connected to each moulding cavity within the mould. Such holes preferably are dimensioned so that they are also suitable for allowing excess cement to leave the mould.

Figs. 10 and 1 la)-l lc) show schematically a further embodiment of the present invention in which each anchoring wire 1015 extending from the body 1013 of the implant 1011 is provided with a substantially circular anchoring loop 1019 at its distal end. Each anchoring loop has a diameter dl and a height hi. In specific embodiments, dl is from 2 to 10 mm, or from 3 to 8 mm, or from 4 to 6 mm. In specific embodiments, height hi is the same as the thickness of the anchoring wire and is from 0.1 to 2 mm, or from 0.25 to 1.25 mm, or from 0.3 to 0.8 mm. The anchoring loop is intended to be positioned directly on the bone or bone flap and to be retained by a screw 1018 or the like passing though the loop 1019 and into the underlying bone. Anchoring loops may be closed as shown by loops with reference number 1019 or open as shown by loops with reference number 1019'.

Fig. 12 shows schematically yet another embodiment of the present invention similar to that of Figs. 10 and 1 la) to 1 lc) in which the anchoring wires have been replaced by anchoring plates 1215 which extend from the body 1213 of the implant 1211. The plates have a height HI, which, in a specific embodiment, is from 0.2 to 2 mm, and a width Wl, which, in a specific embodiment, is from 2 to 6 mm, and a length LI, which, in a specific embodiment, is preferably from 5 to 15 mm. Each plate is provided with a through hole which allows an attachment screw to be inserted through the plate and screwed into the underlying bone. Each plate is provided with an anchoring opening 1219 at its distal end, the opening being intended to receive a screw, suture or the like for fastening in underlying bone.

Preferably the implant should have at least two anchoring arms in the form of anchoring wires and/or anchoring plates, one anchoring means being intended to be attached to the bone flap and the other for attachment to the surrounding bone. Increased stability of the implant is achieved by having three or more anchoring arms.

Figs. 13a) and 13b) illustrate schematically respectively a plan view and a section along line B-B of Fig. 13a) of a mould for use in manufacturing a mosaic implant in accordance with the embodiment of the invention shown in Fig. 12. A mould 1301 of thickness M is used which, as shown in Figs. 13a) and 13b), comprises at least one cavity 1303 of depth H and width D. Each cavity has the shape of an implant body. The depth H of the cavities and the thickness of the resulting tile is less than the depth M of the mould. Each cavity 1303 has a closed bottom end 1305 which is closed by the floor 1307 of the mould 1301 and is open at the opposite open end 1309 to allow filling of the cavity 1303. Floor 1307 does not have to be permanently attached to the mould but may, for example, be a surface which the mould is in contact with during manufacturing of the implant and which can be removed after moulding to facilitate release of the implant from the mould. In one embodiment, each cavity, and thus each tile subsequently formed, is in the shape of a circle. However, it is conceivable that the cavity and the subsequently formed implant body may have another shape such as a triangle, a square, a rectangle, a pentagon, a hexagon, etc. The wall 1311 of each cavity 1303 is pierced by at least one narrow, plate -retaining channel 1313 of width T and depth H2, which is more than, the same as, or less than the thickness of the plate HI depending on whether the upper surface of the plate is be above, level with, or below the upper surface of the implant body. These plate- retaining channels 1313 are intended to receive and to retain during the casting process the anchoring plates used to form the implant anchoring arrangement. In another embodiment of a mould 130 , shown in section in Fig. 13c), the plate -retaining channels are omitted and instead the plates 1316 may be bent so that the portion 1318 of the plate outside the cavity is on the upper surface of the mould and extends radially away from the cavity, an intermediate portion 1320 projects down into the mould cavity, and the remaining portion of the plate 1322 extends parallel to the top surface of the mould. The intermediate and remaining portions of the plate are subsequently covered by the cement while the portion of the plate outside the cavity is available for attachment to an underlying surface. An implant made in this way will be able to be fitted with its top surface flush with the top surface of the bone flap and/or skull, with only the exposed portion of the plate(s) protruding above the surface of the bone flap and/or skull. An implant in accordance with embodiments of the present invention may be implanted in a patient by a method comprising the steps of:

1) placing the implant body in the bore hole, and

2) fixing the anchoring arms, for example, wires or plates, preferably by screws and/or sutures or the like, to the surrounding bone and to the bone flap.

An implant in accordance with the present invention may be implanted in a patient by a further method comprising the steps of:

1) attaching the implant by at least one screw to the bone flap before the bone flap is positioned in the cut-out in the skull in order to avoid putting pressure on the underlying brain while said screw is being attached to the bone flap,

2) placing the implant body in the bore hole, and

3) fixing the anchoring wires or plates, preferably by screws and/or sutures or the like, to the surrounding bone and to the bone flap. In all embodiments of the present invention, depending on the composition of the cement, the hardening of the cement can be performed at reduced, or normal or elevated temperature, and in humid or wet environment. The mould may be made of any dimensionally- stable material which does not react negatively with the cement or mesh/wires. If the mould material is water-permeable, it may assist in hardening of the cement.

Various biomaterial cement moulding systems may be used to form the implant tile body. In specific embodiments, one of the following three options regarding the cement moulding is employed:

1. Use of (a) a Ca-salt precursor powder composition, and (b) non-aqueous water- miscible liquid. In this case the setting needs to be in a wet environment in order to initiate the hardening.

2. Use of (a) a Ca-salt precursor powder composition, and (b) a mixture of water and a non-aqueous water-miscible liquid. Setting will initiate automatically but for final hardening a wet environment is needed. 3. Use of (a) a Ca-salt precursor powder composition, and (b) water-based liquid.

Hardening is initiated upon mixing. It is not necessary to perform hardening in a wet environment but hardening could be in a wet environment.

Methods 1 and 2 are preferred because they give a longer working time before the material hardens. This makes it easier to handle the cement and to clean up excess cement after forming the tiles. However too much water in the mixture of method 2 can prevent hardening of the cement and the amount of water in the water/non-aqueous water-miscible liquid mixture should not be more than 50% by weight. The Ca-salt precursor composition may comprise one or more Ca-salts selected from the group consisting of anhydrous dicalcium phosphate, dicalcium phosphate dihydrate, octacalcium phosphate, a-tricalcium phosphate, β- tricalcium phosphate, amorphous calcium phosphate, calcium-deficient hydroxyapatite, non- stoichiometric hydroxyapatite, tetracalcium phosphate and monocalcium phosphate monohydrate (MCPM), anhydrous monocalcium phosphate, phosphoric acid, pyrophosphoric acid, calcium sulphate (alfa or beta, preferably alfa) or calcium silicate (tricalciumsilicate, dicalciumsilicate or monocalcium silicate), calcium carbonate (aragonite, vaterite, calcite or amorphous) or combinations thereof.

In a specific embodiment of the invention, a non-aqueous water-miscible liquid may be used in preparing a cement paste for delivery to the mould. Possible liquids include glycerol and related liquids, compounds and derivates (substances derived from non-aqueous water- miscible substances), substitutes (substances where part of the chemical structure has been substituted with another chemical structure), and the like. The purpose of the non-aqueous water-miscible liquid is to give a longer working time during the moulding of the mosaic, as compared with the use of water only, because if the material starts to set too early then it is impossible to accurately achieve the mosaic shape.

Certain alcohols may also be suitable for use as such a liquid. In a specific embodiment, the liquid is selected from glycerol, propylene glycol, poly(propylene glycol), poly(ethylene glycol) and combinations thereof. The composition may also include agents that facilitate a fast diffusion of water into the paste in situ, for example, non-ionic surfactants like polysorbates. The amount of surfactant is suitably from 0.01 to 5 wt% of the powder composition, or, more specifically, from 0.1 to 1 wt%. In an alternate embodiment of the present invention, the precursor powder composition is chosen to obtain a setting time above about 30 minutes and the liquid can then be water-based or water-containing. In this case, the liquid can be pure water. In some formulations, salts may be dissolved into the liquid to obtain a fast or slower setting, e.g. citric acid, H ₃ C ₆ H5O ₇ , disodium pyrophosphate, Na ₂ H ₂ P207, sulphuric acid, H ₂ SO ₄ , phosphoric acid, H ₃ PO ₄ , or the like. The hardening can then be performed in a dry environment.

The compositions may also include porogens to give a macroporous end product to facilitate fast resorption and tissue in-growth. The pores give a good foundation for bone cells to grow in. The porogen may include sugars and other fast-resorbing agents. The amount of porogen is suitably from 5 and 30 wt% of the powder composition.

The compositions may also include a non-toxic gelling agent to enhance cohesiveness and washout resistance. The gelling agent may include collagen, gum, gelatin, alginate, cellulose, polyacrylic acid (e.g. PAA, PAMA), neutral polyacrylic acid (e.g. Na-PAA, Na-PAMA acid), hydroxypropylmethyl cellulose (HPMC), hydroxymethyl cellulose (HMC) and

carboxymethyl cellulose (CMC), and combinations thereof. In specific embodiments, the amount of gelling agent may be from 0.1 wt% to 10 wt% of the powder composition, more specifically from 0.1 wt% to 2 wt%.

In all cement compositions selected above, the precursor powder to liquid ratio should preferably be within the range of 1 and 10 as this gives optimal results. In specific embodiments, the ratio is from 3 to 5. The mean grain size of the precursor powder is preferably below 100 micrometers, and more preferably below 30 micrometers as measured in the volumetric grain size mode. Smaller grain sizes give higher mechanical strength than larger grain sizes. However, in an embodiment of the invention containing porous granules, the granule size may be larger but preferably is still below about 500 micrometers. Normally, granules do not participate in the setting reaction of the paste. They are added as ballast to the material and the presence of pores gives a better biological response to the material.

Preferably, at least some of the pores in a granule should be large enough for cells to enter into the granule, normally above at least 10 microns. Inevitably there will also be smaller pores in the granules but they are of less importance for the cell integration. In another embodiment of a method of manufacturing an implant in accordance with the present invention, in the moulding step a non-aqueous, hydraulic cement composition which comprises a non-aqueous mixture of (a) a Brushite- or Monetite -forming calcium phosphate powder composition, and (b) non-aqueous water-miscible liquid, is moulded onto the wire mesh and allowed to harden in a wet to moist environment.

In another embodiment of a method of manufacturing an implant in accordance with the present invention in the moulding step a non-aqueous, hydraulic cement composition which comprises a non-aqueous mixture of (a) a non-hydrated powder composition comprising porous β-tricalcium phosphate (β-TCP) granules and at least one additional calcium phosphate powder, and (b) non-aqueous water-miscible liquid, is moulded onto the wire mesh and allowed to harden in a wet to moist environment. In more specific embodiments, the non-aqueous, hydraulic cement composition comprises a non-hydrated powder composition comprising porous β-tricalcium phosphate (β-TCP) powder and/or granules and at least one additional calcium phosphate powder comprising monocalcium phosphate monohydrate (MCPM) or anhydrous monocalcium phosphate (MCPA).

In further specific embodiments, the non-aqueous, hydraulic cement composition is a Monetite-forming composition. Non-limiting examples of such compositions comprise a non-hydrated powder composition comprising porous β-tricalcium phosphate (β-TCP) powder and/or granules and at least one additional calcium phosphate powder comprising monocalcium phosphate monohydrate (MCPM) or anhydrous monocalcium phosphate (MCPA) in a molar ratio of B-TCP:MCPA or B-TCP:MCPM of 40:60 to 75:25, or more specifically, 50:50 - 70:30. One specific example of a suitable Monetite-forming composition includes a 1 :1 molar ratio of β-tricalcium phosphate (for example, with grain size in the range from 0.1 to 100 micrometers) and monocalcium phosphate monohydrate (MCPM), or a 1 :1 molar ratio of β-tricalcium phosphate (for example, with grain size in the range from 0.1 to 100 micrometers) and anhydrous monocalcium phosphate (MCPA). The grain size of MCMP or MCPA may have a larger spread than the β-tricalcium phosphate, and preferably it is in the range from 1 to 800 micrometers. In a specific embodiment, the powder to liquid ratio is in the range of from 3 to 5, and, in a more specific embodiment, the ratio is from 3.5 to 4.5. An example of a wet environment is a water bath. An example of a moist environment is a chamber where the relative humidity is 100%. Optionally, hardening of the cement material can be performed at reduced, or normal or elevated temperature, combined with a humid, i.e. a relative humidity over 50%, environment or wet environment.

In an alternate embodiment, the precursor powder composition is basic (apatitic) and comprises (a) a basic calcium phosphate component comprising porous β-TCP granules and tetra calcium phosphate (TTCP) and/or amorphous calcium phosphate, and (b) an acidic phosphate, non-limiting examples of which include monocalcium phosphate monohydrate (MCPM), anhydrous monocalcium phosphate, phosphoric acid, pyrophosphoric acid or combinations thereof. The components of the apatitic precursor powder compositions are chosen such that (i) the pH of the cement paste during setting is higher then 6; and (ii) the end-product of the setting reaction comprises amorphous calcium phosphate hydrate, hydroxyapatite, ion-substituted hydroxyapatite, or combinations thereof.

Once the cement has hardened the cement and wire construction can be removed from the mould, any remaining unwanted cement, for example cement that has fastened onto the wires, is removed and the implant packaged and sterilized. Optionally the cement and wire construction of the implant system of the present invention could be exposed to pressure during hardening, for example by pressing an inverse mould against the cement, in order to obtain a stronger end product.

The implant system can be attached to the host tissue via sutures and/or plates and screws and/or clamps or any other fixing means.

The implant system can be used in tissue replacements (bone and soft tissue replacement) and in veterinary medicine. For soft tissue replacement, the implant structure is preferably composed of polymeric materials, preferably resorbable polymers. For hard tissue replacement, the implant system is preferable composed of metal wires and ceramic solids, preferably of metal wires and resorbable ceramics. In the event that the patient is still growing, it is appropriate to use resorbable materials for the wires and/or the mosaic plates. Suitable resorbable polymers are polydioxanone, poly L-lactic acid, and polyglycolic acid. The implant system may also optionally be combined with an injectable biomaterial or drug delivery vehicle that guides the tissue in-growth into the gaps between the bone and the implant. Non-limiting embodiments of the present implants and methods are provided in the following Examples.

Example 1

An implant was fabricated by filling calcium phosphate cement into a mould, with diameter 11 mm and depth 3 mm. The sidewalls of the mould were inclined 6°. A grade 4 titanium mesh as shown in Figs. 14a) and 14b) was placed in the mould after being bent so that the whole circle was placed at 1.5 mm height and the anchoring arms rested on the top part of the mould. The cement precursor powder consisted of an equimolar ratio of monocalcium phosphate monohydrate and beta tri calcium phosphate. Glycerol was added to the powder in a powder to liquid ratio of 4 g/mL. After mixing the cement was injected into the mould and the mould was immersed in 37°C water for 4 hours. Thereafter, the hardened implant was removed from the mould and placed in 20°C water for 24 hours with exchange of water after 4 hours. The implant was subsequently sterilized using autoclave (121°, 20 min). X-ray diffraction was used to analyse the phase composition of the cement after hardening and sterilization. Results showed that the cement consisted of 97% Monetite and 3 % unreacted beta-tricalcium phosphate.

The implant was placed into a 12 mm hole in a 3 mm thick solid rigid polyurethane foam sheet (Sawbones) representing burr holes in a cranium using standard titanium surgical screws. The implant fit well into the hole and did not break during fastening. In position, the implant could support a 455 g weight without breaking.

Example 2

An implant was fabricated by filling calcium phosphate cement into a mould, with diameter 13 mm and depth 5 mm. The sidewalls of the mould were inclined 12°. A grade 4 titanium mesh was placed in the mould. The cement precursor powder consisted of an equimolar ratio of monocalcium phosphate monohydrate and beta tri calcium phosphate. Glycerol was added to the powder in a powder to liquid ratio of 3.5 g/mL. After mixing the cement was injected into the mould and the mould was immersed in 60°C water for 2 hours. Thereafter, the hardened implant was removed from the mould and placed in water for 24 hours with exchange of water after 4 hours. The implant was subsequently dried at 180°C for 1 hour. X-ray diffraction was used to analyse the phase composition of the cement after hardening. Results showed that the cement consisted of 98% Monetite and 2 % unreacted beta-tricalcium phosphate.

The implant was placed into a 14 mm hole in a 3 mm thick solid rigid polyurethane foam sheet (Sawbones) representing burr holes in a cranium using standard titanium surgical screws. The implant fit well into the hole and did not break during fastening. In position, the implant could support a 455 g weight without breaking.

Example 3

An implant was fabricated by filling calcium phosphate cement into a mould, with diameter 11 mm and depth 3 mm. The sidewalls of the mould were inclined 6°. A grade 2 titanium mesh was placed in the mould. The cement precursor powder consisted of an equimolar ratio of monocalcium phosphate monohydrate and beta tri calcium phosphate with an addition of 2 % w/w calcium pyrophosphate. Water was added to the powder in a powder to liquid ratio of 3.2 g/mL. After mixing, the cement was injected into the mould and the mould was immersed in 37°C water for 4 hours. After removal from the mould, the implant was sterilized using an autoclave (121°C for 20 min).

X-ray diffraction was used to analyse the phase composition of the cement after hardening. Results showed that the cement consisted of 96% Monetite and 4 % unreacted beta-tricalcium phosphate.

The implant was placed into a 12 mm hole in a 3 mm thick solid rigid polyurethane foam sheet (Sawbones) representing burr holes in a cranium using standard titanium surgical screws. The implant fit well into the hole and did not break during fastening. In position, the implant could support a 455 g weight without breaking.

Example 4 An implant was fabricated by filling calcium phosphate cement into a mould, with diameter 11 mm and depth 3 mm. The sidewalls of the mould were inclined 6°. A grade 4 titanium mesh was placed in the mould. The cement precursor powder consisted of alpha-calcium sulphate hemi hydrate mixed with water in a powder to liquid ratio of 3.3 g/mL. After mixing, the cement was injected into the mould and left to harden in air for 4 hours.

X-ray diffraction was used to analyse the phase composition of the cement after hardening. Results showed that the cement consisted of 100% calcium sulphate dihydrate. The implant was placed into a 12 mm hole in a 3 mm thick solid rigid polyurethane foam sheet (Sawbones) representing burr holes in a cranium using standard titanium surgical screws. The implant fit well into the hole and did not break during fastening. In position, the implant could support a 455 g weight without breaking. Example 5

An implant was fabricated by filling calcium phosphate cement into a mould, with diameter 11 mm and depth 3 mm. The sidewalls of the mould were inclined 6°. A grade 4 titanium mesh was placed in the mould. The cement precursor powder consisted of an equimolar ratio of monocalcium phosphate monohydrate and beta tri calcium phosphate. Glycerol was added to the powder in a powder to liquid ratio of 4 g/mL. After mixing, the cement was injected into the mould and the mould was immersed in 37°C water for 4 hours. Thereafter the hardened implant was removed from the mould and placed in 20°C water for 24 hours with exchange of water after 4 hours. The implant was subsequently dried at 60°C for 3 hours. X-ray diffraction was used to analyse the phase composition of the cement after hardening.

Results showed that the cement consisted of 97% Monetite and 3 % unreacted beta-tricalcium phosphate.

The implant was placed into a 12 mm hole in a 3 mm thick solid rigid polyurethane foam sheet (Sawbones) representing burr holes in a cranium using standard titanium surgical screws. The implant fit well into the hole and did not break during fastening. In position, the implant could support a 455 g weight without breaking.

Example 6 An implant was fabricated by filling calcium phosphate cement into a mould, with diameter 11 mm and depth 3 mm. The sidewalls of the mould were inclined 6°. A grade 4 titanium mesh was placed in the mould. The cement precursor powder consisted of a mixture of monocalcium phosphate monohydrate and beta tri calcium phosphate in weight ratio 52/48. Glycerol with 10% water content was added to the powder in a powder to liquid ratio of 3.5 g/mL. After mixing the cement was injected into the mould and the mould was immersed in 37°C water for 24 hours. There after the hardened implant was removed from the mould and placed in water for 24 hours. The implant was subsequently sterilized using autoclave (121°C, 20 min).

X-ray diffraction was used to analyse the phase composition of the cement after hardening and sterilization. Results showed that the cement consisted of 100% Monetite.

The implant was placed into a 12 mm hole in a 3 mm thick solid rigid polyurethane foam sheet (Sawbones) representing burr holes in a cranium using standard titanium surgical screws. The implant fit well into the hole and did not break during fastening. In position, the implant could support a 455 g weight without breaking.

Example 7

An implant was fabricated by filling calcium phosphate cement into a mould, with diameter 11 mm and depth 3 mm. The sidewalls of the mould were inclined 6°. A grade 4 titanium mesh was placed in the mould. The cement precursor powder consisted of a mixture of monocalcium phosphate monohydrate and beta tri calcium phosphate in molar ratio 40/60 (MCPM/beta TCP). Water was added to the powder in a powder to liquid ratio of 3.5 g/mL. After mixing the cement was injected into the mould and left to harden at room temperature. The implant was subsequently sterilized using autoclave (121°C, 20 min).

X-ray diffraction was used to analyse the phase composition of the cement after hardening and sterilization. Results showed that the cement consisted predominately of Monetite after sterilisation with traces of Brushite.

The implant was placed into a 12 mm hole in a 3 mm thick solid rigid polyurethane foam sheet (Sawbones) representing burr holes in a cranium using standard titanium surgical screws. The implant fit well into the hole and did not break during fastening. In position, the implant could support a 455 g weight without breaking.

Example 8

An implant was fabricated by filling calcium phosphate cement into a mould, with diameter 11 mm and depth 3 mm. The sidewalls of the mould were inclined 6°. A grade 4 titanium mesh was placed in the mould. The cement precursor powder consisted of alpha-tricalcium phosphate and the liquid phase consisted of an aqueous solution of 2.5 wt % of Na ₂ HPC>4. A powder to liquid ratio of 2.5 g/mL was employed. After mixing, the cement was injected into the mould and the cement set for 24 hours before removal from the mould. The implant was subsequently sterilized using autoclave (121°C, 20 min).

X-ray diffraction was used to analyse the phase composition of the cement after hardening and sterilization. Results showed that the cement consisted of 95% calcium-deficient hydroxyapatite and 5 % alpha-TCP.

The implant was placed into a 12 mm hole in a 3 mm thick solid rigid polyurethane foam sheet (Sawbones) representing burr holes in a cranium using standard titanium surgical screws. The implant fit well into the hole and did not break during fastening. In position, the implant could support a 455 g weight without breaking.

While the invention has been illustrated with examples in which an implant in accordance with the present invention is used to fill a bore hole between a bone flap and a surrounding bone, such implants are of course suitable for filling any type of hole when the size and shape of the implant is adapted to the size of the hole to be filled.

The invention is not limited to the embodiments shown, which can be varied freely within the framework of the following claims. In particular, the features of the various embodiments and examples described may be freely combined with each other in order to reach additional embodiments, which are all considered part of the scope of the present application.