Patent classifications
A61L27/386
BIOACTIVE SCAFFOLD FOR INDUCTING TENDON REGENERATION, PREPARATION METHOD THEREFOR AND USE THEREOF
Provided is a method of preparing a bioactive scaffold for inducing tendon regeneration, the method includes decellularizing a fresh tendon tissue and to obtain a decellularized tendon sheet scaffold or slice scaffold, and adding ECM materials to the decellularized tendon sheet scaffold or slice scaffold.
Biopolymer compositions, scaffolds and devices
Compositions and blends of biopolymers and copolymers are described, along with their use to prepare biocompatible scaffolds and surgically implantable devices for use in supporting and facilitating the repair of soft tissue injuries.
Tissue use for repair of injury
The present disclosure describes methods of treating an injury in a subject using placental tissue streamers, engineered tissue placental tissue hybrids, suture placental tissue hybrids, placental tissue patch hybrids, and tissue hybrids, and the use of these compositions to repair, treat, or support an injury or degenerative process in a subject.
Implant materials for TMJ repair, methods of making the implant materials for TMJ repair, and method of using implant materials for TMJ repair
In accordance with the purpose(s) of the present disclosure, as embodied and broadly described herein, embodiments of the present disclosure, in one aspect, relate to TMJ implantation materials and implants (e.g., temporomandibular joint (TMJ) disc), methods of making TMJ implantation materials and implants, methods of forming a TMJ implantation material or an implant, and the like.
Engineered tendon graft for rotator cuff repair
The present disclosure relates to tissue engineering, and more particularly to a method for treating or repairing rotator cuff or other tendon tears or damage using scaffold-free, 3-dimensional engineered tendon constructs.
Tissue Use for Repair of Injury
The present disclosure describes methods of treating an injury in a subject using placental tissue streamers, engineered tissue placental tissue hybrids, suture placental tissue hybrids, placental tissue patch hybrids, and tissue hybrids, and the use of these compositions to repair, treat, or support an injury or degenerative process in a subject.
Stem cell composition
The present invention relates to a composition comprising stem cells, a cell culture medium and a polyacrylamide hydrogel (PAAG), wherein the PAAG contains less than 0.02% W.sub.monomer/W.sub.total PAAG] of a N-hydroxyethyl acrylamide (HEA) side chain. The invention also relates to the process of making the composition. In particular, the present invention relates to the composition, wherein the composition is administered by injection and wherein it is used in medicine, in particular for use in prevention and/or treatment of e.g. tendon injury in a mammal, arthritis in a mammal or arthropathy in a mammal. Tendon injury, arthritis or arthropathy may occur in a human, a racing animal or a companion animal.
Methods and compositions for treating tendon degeneration
Injectable compositions and methods for treating an injured tendon in an animal or human are disclosed herein. The injectable compositions include an effective amount of a carbohydrate to increase osteotendinous hydration and lubrication.
TISSUE USE FOR REPAIR OF INJURY
The present disclosure describes methods of treating an injury in a subject using placental tissue streamers, engineered tissue placental tissue hybrids, suture placental tissue hybrids, placental tissue patch hybrids, and tissue hybrids, and the use of these compositions to repair, treat, or support an injury or degenerative process in a subject.
METHODS FOR ATTACHING TENDONS AND/OR LIGAMENTS TO BONE AND/OR CARTILAGE
A method for repairing at least one of a tendon and a ligament in a joint region of a patient is provided. The method comprises inserting a tube, a needle, or a combination thereof into the joint region and proximal to the at least one of a tendon and a ligament. An implantable membrane is inserted into the tube, onto the needle, or a combination thereof, in the joint region. The implantable membrane comprises a biological material that promotes cell growth. The tube, the needle, or both is removed from the joint region while leaving the implantable member in the joint region and the implantable membrane contacted with the at least one of the tendon and the ligament. The method comprises securing the implantable membrane in the joint region.