New Jersey Institute of Technology

Hoechst Celanese Corporation

Celanese Gmbh

Celanese Acetate Limited

Warsaw Orthopedic, Inc.

Michael L Jaffe

Anthony East

Willis Hammond

Xianhong Feng

M Ishaq Haider

Herbert L Davis

Paul N Chen, Sr

John A Flint

Treena Lynne Arinzeh

Edward J Powers

William J MacKnight

Frank E Karasz

Zohar Ophir

Joseph J DiBiase

John Edward Cornetta

Morton M Glick

Herman L LaNieve, Iii

David J Williams

Louis Leung

Lawrence A Shimp

Ronald N DeMartino

Rohitkumar H Vora

Subhash Makhija

Alex S Forschirm

Edward C Chenevey

George Collins

Michael M Besso

Charles M Schiff

Amir Hossein Rajabi

Luiz H Catalani

Yi Zhang

Norbert Weber

Sherry Hsiu-Ying Wang

Shobana Shanmugasundaram

Treena Arinzeh

The present invention provides novel methods for poling piezoelectric materials, e.g., collagen, which are carried out in the absence of liquid media and at a relatively low temperature. The present invention also provides electroactive scaffolds comprising poled collagen for promoting cell growth and differentiation.

System and method for a piezoelectric collagen scaffold

An AB monomer, useful for the production of condensation polymers, wherein the AB monomer has the structure: A-X-C-Y-B; wherein A is reactive carbonyl derivative of carboxylic acids; Y is a bisanhydrohexitol unit derived from the group consisting of isosorbide, isoidide and isomannide; X is selected from the group consisting of: aromatic rings, including 1,4-phenylene, 1,3-phenylene, 2,6-naphthalene 2,7-naphthalene, and substituted derivatives thereof; heterocycles including, 2,5-furan, 2,5-thiophene, substituted 2,5-furan and substituted 2,5-thiophene; and saturated or unsaturated aliphatic chains; B is OH; and C is selected from the group consisting of ether oxygen, a sulfide, and an amine, wherein the amine is NH or NR wherein R is C1 to C6, attaching X to Y.

Polyester ethers derived from asymmetrical monomers based upon bisanhydrohexitols

An AB monomer, useful for the production of condensation polymers, wherein the AB monomer has the structure: A&#x2014;X&#x2014;C&#x2014;Y&#x2014;B; wherein A is a carboxylic acid or ester or reactive carbonyl derivative, Y is a bisanhydrohexitol unit derived from isosorbide, isoidide or isomannide; X is selected from the group consisting of aromatic rings, substituted or unsubstituted heterocycles, and saturated or unsaturated aliphatic chains; and B is OH and C is an ester carbonyl link with the carbon attached to X and the oxygen attached to Y, and wherein the AB monomer is at least about 98% pure endo-substituted bisanhydrohexitol derivative or an at least about 98% pure exo-substituted bisanhydrohexitol derivative.

Polyesters from assymetrical monomers based upon bisanhydrohexitols

Due to the size and complexity of tissues such as the spinal cord and articular cartilage, specialized constructs incorporating cells as well as smart materials may be a promising strategy for achieving functional recovery. Aspects of the present invention describe the use of an electroactive, or piezoelectric, material that will act as a scaffold for stem cell induced tissue repair. Embodiments of the inventive material can also act alone as an electroactive scaffold for repairing tissues. The piezoelectric material of the present invention acts as a highly sensitive mechanoelectrical transducer that will generate charges in response to minute vibrational forces.

Electrospun electroactive polymers for regenerative medicine applications

Isosorbide-derived epoxies and methods of making same are disclosed. Isosorbide and its isomers are attached to glycidyl ether to make crosslinkable epoxy resin monomers. Adding the hydrophobic functional group into the backbone of isosorbide epoxy or adjusting the amount and type of crosslinker is operable to modify the mechanical properties and water uptake ratio (from &#x3c;1 wt % to &#x3e;50 wt %) of the isosorbide-derived epoxies for different uses. High water uptake epoxies with controllable biodegradation rate are suitable for drug delivery systems or extracellular matrices for biomedical applications, while low water uptake epoxies with strong mechanical properties may be used for can coatings, bone cements and other industrial additives and adhesives.

Isosorbide-derived epoxy resins and methods of making same

A process for producing copolymers of a polymer and asymmetrically substituted compounds of bisanhydrohexitols, including the bisanhydrohexitol isosorbide. In a specific example, the AB monomer isosorbide 2-(4-carbomethoxybenzoate) is synthesized and copolymerized with polyester to form a copolyester. The asymmetrically substituted compounds provide a way of incorporating bisanydrohexitols that may be derived from natural sources into polymers.

Polyesters from asymetrical monomers based upon bisanhydrohexitols

A process for producing a copolyester through the production of an AB monomer of isoidide - Isodide 2-(4-carbomethoxyphenyl) ether. In certain aspects, the AB monomer is produced by performing the steps of: protecting the 2-position of isosorbide with a protecting group; functionalizing the 5-position of isosorbide with a suitable leaving group to form a reactive ester; nucleophilicly displacing the leaving group in a reaction with an alkali metal alkoxide or phenoxide to give an isoidide ether through a stereochemical inversion of the 5-position; and removing the protective moiety to create the AB monomer. In certain embodiments, the copolyester is produced by melting the AB monomer and a polyester, optionally with a catalyst.

Polyester ethers derived from asymmetrical monomers based upon bisanydrohexitols

A composition includes bone and collagen, wherein the collagen has been acid treated, and cross-linked via dehydrothermal treatment or by a cross-linking agent (e.g., a citric acid derivative) under a compressive force of at least approximately 40 MPa.

Bone/collagen composites and uses thereof

Disclosed is a method for preparing polyoxazolidones wherein an ether of a bisanhydrohexitol is reacted with a diisocyanate under conditions which form polyoxazolidones. Preferred bisanhydrohexitols include isoidide, isomannide and isosorbide. The polyoxazolidones are highly crosslinked, rigid, and have high solvent resistance.

Polyoxazolidones derived from bisanhydrohexitols

Novel thermoset epoxy polymers using the bisglycidyl ethers of anhydrosugars, such as isosorbide, isomannide, and isoidide, are disclosed. The bisglycidyl ethers are useful as substitutes for bisphenol A in the manufacture of thermoset epoxy ethers. The anhydrosugars are derived from renewable sources and the bisglycidyl ethers are not xenoestrogenic and the thermoset curing agents are likewise derived form renewable resources.

Thermoset epoxy polymers from renewable resources

The present invention discloses and claims a novel process for the formation of high denier as-spun and heat-treated multilobal filaments of a thermotropic liquid crystalline polymer. Preferred embodiments include process for the formation of as-spun and heat treated octalobal monofilaments of a few wholly aromatic polyesters and polyesteramides. The process involves (a) heating of a thermotropic liquid crystalline polymer to above its melting transition temperature; (b) passing said molten polymer through an extrusion chamber equipped with an extrusion capillary having a multilobal cross-section to form a multilobal filament; and (c) winding the filament at a suitable draw-down. The filaments so formed are of at least 50 denier per filament (dpf) and feature essentially uniform molecular orientation across their cross-section. In a final optional step, the filaments are heat treated in stages to form filaments exhibiting excellent tensile properties. Both as-spun and heat-treated filaments feature remarkably good tensile properties comparable to those of round filaments. Most importantly, the multilobal filaments of this invention feature much superior adhesion properties than the conventional round filaments.

Process for making high denier multilobal filaments of thermotropic liquid crystalline polymers and compositions thereof

The present invention discloses and claims a novel process for the heat treatment of high denier filaments of a thermotropic liquid crystalline polymer. Preferred embodiments include process for the formation of heat treated filaments of a few wholly aromatic polyesters and polyesteramides. The process involves: (a) heating of a thermotropic liquid crystalline polymer to above its melting transition temperature; (b) passing said molten polymer through an extrusion chamber equipped with an extrusion capillary of an aspect ratio of greater than about 1 and less than about 15 to form a filament; (c) winding the filament on to a bobbin at a low tension and draw-down ratio of at least about 4; and (d) heat treating the filament directly on the bobbin at suitable temperature and pressure conditions for a sufficient period of time. The filaments so formed are of at least 50 denier per filament (dpf) and feature essentially uniform molecular orientation across the cross-section. The heat-treated filaments feature remarkably good tensile properties retaining at least 80 to 90 percent of the properties expected of conventional low denier (5 to 10 dpf) filaments.

Process for direct on-bobbin heat treating of high denier filaments of

A process for making a transparent film comprising a liquid crystalline polymer, and a transparent film made thereby having high barrier properties. In this process, the LCP is dissolved in an appropriate solvent, then cast into a film at ambient or near-ambient temperatures. The film optionally may be dried at elevated temperatures and/or reduced pressures to remove the solvent. The film is then annealed at a temperature between the glass transition temperature (T.sub.g) and the melting point temperature (T.sub.m) of the polymer. The result is a highly transparent film having liquid crystalline morphology and high barrier properties.

high barrier transparent films

A miscible blend comprising from about 5 to about 95 weight percent of a polybenzimidazole and from about 95 to about 5 weight percent of a polyamide-imide having fluorine-containing linking groups, total weight percent of the two polymers being 100. A process for preparing the blends comprises dissolving in a mutual solvent from about 5 to about 95 weight percent of the aromatic polybenzimidazole to about 95 to about 5 weight percent of the polyamide-imide having fluorine-containing linking groups, based on the total weight of those polymers and subsequently evaporating the solvent, thereby producing a dried blend of a polybenzimidazole and a polyamide-imide having fluorine-containing linking groups. The blends, particularly in the form of films, fibers or fibrets, may be post-treated with heat or sulfuric acid in order to minimize their shrinkage when subsequently subjected to heat and in order to increase their resistance to solvents and acid. The polyamide-imides having fluorine-containing linking groups are prepared by forming the polycondensation product of one or more aromatic diamines, one or more trifunctional acid anhydride monomers, and one or more tetrafunctional aromatic dianhydrides, at least one of said monomers containing the group ##STR1## linking two aromatic moieties, wherein R is CF.sub.3 or phenyl.

Miscible blends of polybenzimidazoles and polyamide-imides having

A compatible polymer blend containing a polyacetal, a hydroxylated polyacetal, polypropylene, and an acid-grafted polyolefine such as a muconic acid-polypropylene graft copolymer. The polyacetal is preferably a polyoxymethylene polymer such as Celcon.RTM.. The preferred hydroxylated polyacetal is one having a structure very similar to the polyacetal. The invention also includes a process for forming a compatible blend containing polypropylene and polyacetal by melt mixing polypropylene and polyacetal with an acid grafted polyolefin and hydroxylated polyacetal.

Growing community of inventors

Summit, NJ, United States of America

Michael L Jaffe