Tel Aviv University

Technology Innovation Momentum Fund (israel) Limited Partnership

Other

Technion Research & Development Foundation Ltd

The Medical Research, Infrastructure and Health Services Fund of the Tel Aviv Medical Center

Chi2gel Ltd.

Mor Research Applications Ltd.

Ramot University Authority for Applied Research and Industrial

Technology Innovation Momentum Fund (isreal) Limited Partnership

Chit2gel Ltd.

Nevo, Zvi

Katzir, Abraham

Simhon, David

Zvi Nevo

Dror Robinson

Ehud Gazit

Ludmila Buzhansky

Lihi Adler-Abramovich

Shmuel Einav

Moran Aviv

Abraham Patchornik

Eyal Zussman

Abraham Katzir

Yael Dror

Shmuel Chervinsky

Noah Ben-Shalom

David Simhon

Shimon Rochkind

Avner Yayon

Mark M Levy

Uzi Gafter

Zoharia Evron

Talia Weinstein

Samuel Levin

Samuel Itay

A combined treatment for nerve injury is provided. Accordingly there is provided a composition comprising a hyaluronic acid, a laminin polypeptide, an antioxidant and an anti-gliotic agent. Also provided are matrices and hydrogels of the composition and methods of using same.

Combined treatment for nerve injuries

Hybrid hydrogels formed of a plurality of peptides that are capable of self-assembling into a hydrogel in an aqueous solution and a biocompatible polymer that is characterized by high swelling capability, high elasticity and low mechanical strength are disclosed, with exemplary hybrid hydrogels being formed of a plurality of aromatic dipeptides and hyaluronic acid. The hybrid hydrogels are characterized by controllable mechanical and biological properties which can be adjusted by controlling the concentration ratio of the peptides and the polymer, and which average the mechanical and biological properties of the peptides and the polymer. Processes of preparing the hydrogels and uses thereof in pharmaceutical, cosmetic or cosmeceutic applications such as tissue engineering and/or regeneration are further disclosed.

Malleable hydrogel hybrids made of self-assembled peptides and biocompatible polymers and uses thereof

A composition suitable for treating a variety of medical, aesthetic and cosmetic conditions in mucous membranes and occluded skin areas, comprising hyaluronic acid, N-acetylcysteine, an active agent and set to pH of less than 6, which is characterized by high in vivo stability, is disclosed, as well as uses thereof in temporally extended delivery of active agent to mucous membrane in bodily sites.

Malodor neutralizing composition

A chitosan composition which forms a hydrogel at near physiological pH and 37&#xb0; C., comprising at least one type of chitosan having a degree of acetylation in the range of from about 30% to about 60%, and at least one type of chitosan having a degree of deacetylation of at least about 70% is disclosed. Further disclosed is a chitosan composition which forms a hydrogel at near physiological pH and 37&#xb0; C., that includes at least one type of chitosan having a degree of deacetylation of at least about 70% and a molecular weight of from 10-4000 kDa, and at least one type of a chitosan having a molecular weight of from 200-20000 Da. Further disclosed are methods of preparation and uses of the chitosan compositions.

Injectable chitosan mixtures forming hydrogels

A method of treating a disease or condition in which up-regulating GAGs is therapeutically beneficial is disclosed, in particular osteoarthritis and skin diseases. The method comprises locally administering to a subject a therapeutically effective amount of an agent capable of down-regulating activity or expression of a component of the renin-angiotensin system.

Inhibition of the renin-angiotensin system for the treatment of renal, vascular and cartilage pathology

Provided are method of generating a fiber from a globular protein such as albumin. Also provided are albumin fibers and fabrics and methods of using same for bonding a damaged tissue or for ex vivo or in vivo formation of a tissue.

Albumin fibers and fabrics and methods of generating and using same

A novel laminin polypeptide comprising the amino acid sequence set forth by SEQ ID NO:3 is disclosed. Also disclosed are compositions-of-matter comprising a polysaccharide (e.g., hyaluronic acid) and the novel laminin polypeptide; or hyaluronic acid, a laminin polypeptide and an antioxidant (e.g., superoxide dismutase), as well as matrices and hydrogels comprising same which can be used for ex vivo or in vivo tissue formation and for treatment of pathologies characterized by diseased, damaged or loss of tissue.

Polypeptides, matrices, hydrogels and methods of using same for tissue regeneration and repair

A chitosan composition which forms a hydrogel at near physiological pH and 37&#xb0; C., comprising at least one type of chitosan having a degree of acetylation in the range of from about 30% to about 60%, and at least one type of chitosan having a degree of deacetylation of at least about 70% is disclosed. Further disclosed is a chitosan composition which forms a hydrogel at near physiological pH and 37&#xb0; C., comprising at least one type of chitosan having a degree of deacetylation of at least about 70% and a molecular weight of from 10-4000 kDa, and at least one type of a chitosan having a molecular weight of from 200-20000 Da. Further disclosed are methods of preparation and uses of the chitosan compositions.

A scaffold for use as a growth supportive base for cells and tissue explants is formed of naturally occurring derived connective or skeletal tissue that has been treated for elimination of cellular and cytosolic components comprising DNA, RNA, peptides, lipids and proteoglycans. The treated tissue can be crosslinked and treated for producing a higher porosity such as by mechanical or chemical treatment. Alternatively, the treated tissue is ground to form flakes having a size below 1000&mgr;, and the flakes are attached to each other to provide a scaffold having a porosity of at least 85%. The scaffold may be composed of several single-flake layers arranged on top of the other. The scaffold can be impregnated with cells to form tissue such as epiphysial tissue, and may contain adhesive molecules or growth factors. A prosthesis for implanting can be formed using the scaffold. The scaffold may be composed of fused epiphyses.

Scaffold formed of tissue treated to eliminate cellular and cytosolic elements

A growth support scaffold for cells and tissue is formed of naturally derived connective or skeletal tissue which has been treated for elimination of cellular and cytosolic elements, and modified by cross-linking with hyaluronic acid, proteoglycans, glycosaminoglycans, chondroitin sulfates, heparan sulfates, heparins or dextran sulfates. The scaffold may contain cell adhesive molecules and growth factors, and can be formulated as a malleable prosthesis. A tissue maintenance system is provided containing a chamber having a constant atmosphere which may contain the scaffold impregnated with cells, a medium-containing reservoir, a pump which can be computer controlled for circulating the medium between the chamber and reservoir and may change direction of medium flow every 1 to 3 minutes, and a pressure generator, which can be the pump, for producing rhythmic pulses of pressure such as between 0.5 to 30 atm and frequency of 5-300 per minute.

Tissue maintenance system that applies rhythmic pulses of pressure

The present invention concerns fibroblast growth factor receptor 3 (FGFR3) as a novel marker for mesenchymal skeletal progenitor cells. By utilizing this novel marker it was possible both to identify and locate mesenchymal skeletal progenitor cells in a tissue, as well as to obtain a substantially pure culture of such cells. The pure culture of the mesenchymal skeletal progenitor cells may be used, optionally after various manipulations ex vivo, as an active ingredient in pharmaceutical compositions or implants for the purpose of bone and/or cartilage repair. FGFR3 may also be used as a marker for the identification and the localization of cartilage- and bone-derived tumors. Agents capable of binding to FGFR3 may also be used for targeting cytotoxic agents to cartilage- and bone-derived tumors.

FGFR3 as a marker for mesenchymal skeletal progenitor cells

There are provided compositions for repairing defects of cartilage and bones. These are provided in gel form either as such, or embedded in natural or artificial bones. The gel comprises certain types of cells. These may be committed embryonal chondocytes or any kind of mesenchyme originated cells which potentially can be converted to cartilage cells, generally by the influence of chondrogenic inducing factors, in combination with fibrinogen, antiprotease and thrombin. The cells ought to be of the species to which the composition is transplanted. It is advantageous to incorporate in the gel extracellular matrix (ECM) of chondrocytes or other hormones and/or growth factors such as SM (Somatomedin=IGF-I), FGF (fibroblast growth factor), CGF (cartilage growth factor), BDGF (bone derived growth factor) or a combination of any of these.

Growing community of inventors

Herzlia, Israel

Zvi Nevo