An implantable prosthesis includes a silicone shell having an apex, a base, a radius located between the apex and the base, and a dome extending between the apex and the radius. The silicone shell has an outer surface and an inner surface that surrounds an interior volume of the silicone shell. A silicone gel material is disposed within the interior volume of the silicone shell. A gelling enhancer layer containing a gelling enhancer covers the inner surface of the silicone shell. After the silicone gel material has been thermally cured, the silicone gel material that is located within a zone that is in the vicinity of the gelling enhancer layer has a higher level of cohesiveness than the silicone gel material that is located outside the zone. The gelling enhancer contains crosslinker and/or platinum catalyst, such as a Karstedt catalyst.

A medical device having a tubular membrane with openings adapted to receive the ends of an injured nerve and a lumen to allow the regeneration of the nerve, such that the tubular membrane includes fibers of polyhydroxyalkanoate (PHA) containing 3-hydroxybutyrate monomer units. The fibers have an average diameter from 500 nm to 2000 nm. Preferably, the PHA is a poly-3-hydroxybutyrate homopolymer and the tubular membrane further includes silver nanowires (Ag). The medical device has the advantages of not causing inflammation of the surrounding tissues surrounding the injured nerve, thus demonstrating a high biocompatibility, and at the same time exhibiting high ability to induce the regeneration of the injured nerve, providing a valid support for the maturation of the newly formed nerve fibers.

A method for producing an implant blank (100), in particular a dental implant blank from a starting body, said implant blank (100) comprising at least one first area, which is a surface area (102), and a second area, which is a core area (101), wherein the surface area (102) has at least one bioactive surface material (502) and extends from at least one first surface (103) in the direction of the core area (101), and the core area (101) has at least one carrier material that can be subjected to mechanical load. The starting body has a porosity for controlling a targeted distribution of the bioactive surface material (502) within the starting body and is loaded with a solution (500) of the bioactive surface material (502) in a first step, which is a loading step. In a second step, which is a distribution control step, the distribution of the bioactive surface material (502) within the starting body is controlled such that the solution (500) has a higher concentration within the surface area (102) than within the core area (101), the control being effected by regulating one or more environmental parameters in a closed environment (200), in particular by regulating the humidity and/or the pressure and/or the temperature.

The present disclosure is concerned with magneto-patterned cell-laden hydrogel materials and methods of making and using those materials. The disclosed materials are useful for, among other things, repair of tissue defects, e.g., tissue at a tissue interface such as a bone-cartilage interface.

An orthopedic implant having a metal surface and a hydroxyapatite layer comprising gallium ions therein disposed on at least part of the metal surface is described. The hydroxyapatite layer has an average crystallite size of less than about 75 nm in at least one direction and dissolves for more than 2 hours in vitro. The hydroxyapatite layer is substantially free of carbonate. The coating, which is formed on a sodium titanate surface, has increased shear strength and tensile strength. The coating is formed by a solution deposited hydroxyapatite process under inert conditions. The pH of the solution varies by less than 0.1 pH unit/hour during coating formation.

The present disclosure relates to manganese dioxide nanoparticles and their use in treatment of oxidative stress and conditions related to or characterized by oxidative stress, including osteoarthritis.

An implant, preferably for treating and/or reconstructing, in particular lining and/or sealing and/or relining and/or at least partially filling an acetabular defect, having at least one flat structure which contains a material that is at least partially decomposable or resorbable in vivo. The invention further relates to a surgical kit and the use of an unfinished flat structure for producing an implant.

Disclosed herein is an article comprising a metal alloy; where the metal alloy comprises a base metal, a second element and a third element; where the base metal is magnesium, calcium, strontium, zinc, or a combination thereof; where the second element is chemically different from the third element; and where the second element and the third element are scandium, yttrium, gadolium, cerium, neodymium, dysporium, or a combination thereof; and a protective layer disposed upon the metal alloy and is reactively bonded to the metal alloy; where the protective layer comprises a base non-metallic derivative, a second non-metallic derivative and a third non-metallic derivative of metals present in the metal alloy; and where the base non-metallic derivative, the second non-metallic derivative and the third non-metallic derivative are all chemically different from one another.

The invention relates to compositions including magnesium-lithium alloys containing various alloying elements suitable for medical implant devices. The devices may be constructed of the compositions or have applied thereto a coating formed therefrom. Within the structure of the magnesium-lithium alloy, there is a co-existence of alpha and beta phases. The invention also relates to methods of preparing the magnesium-lithium alloys and articles, such as medical implant devices, for use in medical applications, such as but not limited to, orthopedic, dental, craniofacial and cardiovascular surgery.

A solid suspension for use in bone regeneration and/or the repair of bone defects, comprising a source of at least one group II metal cation and a source of zinc cations, wherein the source of zinc cations comprises zinc oxide and wherein where there is only one group II metal cation this is strontium. A bone graft comprising a solid suspension, a method of preparation of a solid suspension and a use of a solid suspension in bone regeneration and/or in the repair of bone defects.