Abstract: The present invention concerns a bioactive implant material having a cartilage-inducing and/or bone-inducing activity composed of two components A and B, of which A is a bone-inducing and/or cartilage-inducing protein or protein mixture and preferably one or several proteins from the TGF-? superfamily, preferably MP52 or a DNA sequence coding therefor and B is a carrier matrix composed of calcium phosphate ceramics with an interconnecting microporosity which already alone has bone-inducing properties. The invention additionally concerns the production of these compounds and their use for the treatment of diseases which affect cartilage and/or bones as well as to treat damage to cartilage and/or bone tissue.

Abstract: The invention relates to a resorbable bone replacement and bone formation material (augmentation material) based on porous ?-tricalcium phosphate (?-TCP).

Abstract: The invention relates to a resorbable bone replacement and bone formation material (augmentation material) based on porous ?-tricalcium phosphate (?-TCP).

Abstract: The present invention concerns a bioactive implant material having a cartilage-inducing and/or bone-inducing activity composed of two components A and B, of which A is a bone-inducing and/or cartilage-inducing protein or protein mixture and preferably one or several proteins from the TGF-? superfamily, preferably MP52 or a DNA sequence coding therefor and B is a carrier matrix composed of calcium phosphate ceramics with an interconnecting microporosity which already alone has bone-inducing properties. The invention additionally concerns the production of these compounds and their use for the treatment of diseases which affect cartilage and/or bones as well as to treat damage to cartilage and/or bone tissue.

Abstract: The invention relates to a resorbable bone replacement and bone formation material (augmentation material) based on porous ?-tricalcium phosphate (?-TCP).

Abstract: The invention relates to a resorbable bone replacement and bone formation material (augmentation material) based on porous &bgr;-tricalcium phosphate (&bgr;-TCP).

Abstract: A solidified drug supply for generating inhalable drug particles with the aid of a metering device includes a removal unit, with the drug supply being brittle and textureless. The density and the mechanical strength of the drug supply is abraded everywhere in such a way that the structure of the material removed from one side of the drug supply by the metering device is uniform across the entire usage region in the direction of the removal.

Abstract: A device for mechanically generating inhalable active substance particles from a consolidated medication supply and for conveying the active substance particles into the respiratory tract, wherein, in order to generate the active substance particles, there is a drivable face mill against which the front of a medication supply in the form of a ring-shaped body can be pressed, whereby the ring-shaped body forms the beginning of an inhalation tube ending in a mouthpiece and in that the housing surrounding the ring-shaped body and the face mill is provided with air inlet openings in the blade area of the face mill and said air inlet openings, together with the depressions located between the blades and the inhalation tube, form an air channel leading to the mouthpiece.

Abstract: A gas generator for air bags is provided which includes a first outer shell and a second outer shell, each having a circular part and an outer wall formed along the outer periphery of the circular part. A gas generating device is installed in the hollow portion formed within the outer shells. Openings for communicating the hollow portion with an air bag are provided. A plurality of concentric wall members axially extending from the circular part of the first outer shell and a plurality of concentric wall members axially extending from the circular part of the second outer shell, located at positions corresponding to the outer wall members of the first outer shell define circumferential chambers within the gas generator. Gaps are formed between terminal end surfaces of opposing outer wall members whereby gases produced by the gas generating device on receiving impacts flow through the generator and are introduced into the air bag to protect a passenger from impacts.

Abstract: The present invention provides a gas generator for air bags that includes a first shell having a circular part and an outer wall. The outer wall formed is of a porous material which allows gas to pass freely therethrough. A second shell is attached to the first shell to form a housing into which is installed a gas generating device. The gas generating device includes a canister filled with a gas generant. A plurality of first and second blade members fasten the first and second shells together. The blade members are at least equal in height to the total height of the housing, the first blade members being shaped to fit the outer circumferential surface of the canister and placed in contact with the outer circumferential surface of the canister and arranged along the circumference of the canister at periodic intervals to form a ring.

Abstract: The present invention provides a gas generator for air bags that includes a first shell having a circular part and an outer wall. The outer wall is formed of a porous material which allows gas to pass freely therethrough. A second shell is attached to the first shell to form a housing into which is installed a gas generating device. A plurality of first and second blade members fasten the first and second shells together. The blade members are placed in contact with the circumferential surface of the canister and arranged along the circumference of the canister at periodic intervals to form a ring. The second blade members have a width at least equal to the circumferential interval between the first blade members and are spaced radially from the first blade members and shifted in the circumferential direction from the first blade members to positions facing the intervals between the first blade members.

Abstract: A method for the synthesis of an oxide high-temperature superconductor of defined composition by sintering of the starting oxides, wherein sintering is effected in a chemically and phyically closed system by generating a preset oxygen partial pressure through the use of peroxide additives, and the oxidic starting mixture is chemically shielded against the container material and stabilized thermodynamically.

Abstract: Metallic implants with a coating of hydroxyl apatite are described. Hot isostatic pressing permits pore-free compaction of the hydroxyl apatite layer and results in firm bonding of the layer on the metallic core. The surface of the layer is partially dehydrated by means of ion bombardment, and a bioactive layer for osteogenesis is produced.

Abstract: A circular knitting needle includes two rigid tips interconnected by an intermediate flexible portion. Each of the tips is formed with a projection inserted into an elongated recess formed in each end of the intermediate portion. Each projection is provided with a lug having an outer cylindrical surface and each recess of the intermediate portion has three longitudinal contact surfaces which are in engagement with the outer cylindrical surface of the respective lug.

Abstract: An implantable drug depot for the treatment of diseases of the bone or bone marrow. The depot consisting of a matrix in which at least one active ingredient is incorporated and contains at least one adjuvant agent to control the kinetics of the drug release. The matrix material consists of resorbable sintered calcium phosphate composed of CaO and P.sub.2 O.sub.5 in a ratio between 5:1 and 2:1.

Abstract: An implantable bone replacement material (body) based on completely or partially resorbable particles incorporated in a matrix material. The particles are composed of bioactive sintered calcium phosphate ceramic material having a CaO:P.sub.2 O.sub.5 composition ratio between 3:1 and 4:1. The replacement material (body) consists of a metal containing calcium phosphate ceramic material in the form of a monolayer of particles in the peripheral areas of the material (body) which serve as interfaces to the body tissue. The metal is compatible with body tissue. The ceramic particles have a size range between about 500 .mu.m and a few millimeters. The calcium phosphate particles are located so that they lie exposed on the upper surface of the material (body). Other embodiments and processes are also disclosed.

Abstract: An implantable prosthesis anchorage which contains a non-porous outer coating in the regions which is positioned in contact with bone. The non-porous outer coating consists of (i) at least one bioactive resorbable ceramic material which is a calcium phosphate and (ii) at least one polymer which is mechanically and chemically stable in the body. The ceramic material is in particulate form having particle diameters between 0.5 and 1 mm. The ceramic material particles is incorporated in the polymer in such a way that resorption of the ceramic material leads to a polymer structure with continuous pores filled with living bone tissue. Bioactivating bonding residues of the ceramic material are left on the inner surfaces of the filled pores which were created by the resorption of the ceramic material.

Abstract: Bone replacement or prosthesis anchoring material on the basis of sintered calcium phosphates which consists of a mixture of calcium phosphates with low or high-molecular-weight organic substances. More specifically, the anchoring material consists of a mixture of calcium phosphates composed of CaO and P.sub.2 O.sub.5 in a quantitative ratio of 2:1 to 4:1 with biodegradable polymers in a ratio of 10:1 to 1:1 of phosphate to polymer and is implantable as a solid body. A method for the production of the material wherein calcium phosphate with a porosity of 15 to 30 volume percent is used and its pores are filled by impregnation with polymer material.

Abstract: An artificial tooth with an implantable root adapted to permanently grow together with the jawbone and, also under high mechanical loads as is the case for natural teeth, will not allow for the production of a rejection or repelling reaction between the natural bone and the implant. The tooth root is essentially constituted of a biostable polymer matrix which is compatible with human tissue, in which there is introduced reabsorbable bioreactive calcium phospate in a finely dispersed form, which is encompassed by a thin porous layer of non-reabsorbable calcium phospate, and into which there is inserted a core as a connecting member for the mounting of a dental superstructure in the form of a tooth crown, a fastening element for dental bridges or the like.

Abstract: A process for producing ceramic, ceramic-metal or metal catalyst supports or catalysts with open, interconnecting pores. The process forming a dense agglomeration of spherical, cylindrical or similar bodies of generally uniform size. These bodies are connected together at their mutual contact points, thereby producing a framework corresponding generally to the macropores and pore interconnections of the finished material in terms of size and arrangement. The framework is then filled with a suspension containing as solid components the catalyst support material and/or the catalyst material. The suspension can also contain a binding agent. The framework is subsequently dissolved away after at least the partial hardening of the cast mass without destroying the structure produced during hardening.