Other

Allied Corporation

Ecoplastics Limited

Medipro Sciences Limited

G-nano, LLC

University of Toronto

Peroxco Incorporated

Solarchem Corporation

James E Guillet

Gad Friedman

Dennis C Smith

Douglas G Murray

Anthony E Redpath

Ilse Treurnicht

Dan Ervin

Ervin Dan

D Gary Murray

Maria Nowakowska

Hamid Bakhtiyari

Michael Heskins

Kevin C Kohler

Ruey S Li

There are provided internally cross-linked, stables polymeric materials, in the form of substantially spherical particles, each particle consisting essentially of a single macromolecule. They have the unusual property of being soluble or dispersible in a liquid medium without significantly increasing the viscosity of the medium, rendering them potentially useful in imaging applications such as ink jet printers. They can be prepared by dissolving polymeric material in a solvent system to form a solution of the polymeric material at a concentration therein of less than the critical concentration for the polymer, causing the polymeric material to contract into an approximately spheroidal conformation in solution, cross-linking the polymeric material in solution in said spheroidal conformation so assumed, and recovering stable, cross-linked approximately spheroidal polymeric particles from the solution.

Cross-linked polymeric nanoparticles and metal nanoparticles derived therefrom

Novel antenna polymers characterized by a polymeric background of a biodegradable water soluble polymer and chromophores chemically bonded to the polymeric background have been found to be useful as photocatalysts in aqueous media. On completion of the desired photochemical reaction, the residual medium can safely be discharged to the natural environment as the catalyst residues undergo biodegradation to form environmentally harmless products.

Water soluble biodegradable polymeric photocatalysts

There are provided internally cross-linked, stable polymeric materials, in the form of substantially spherical particles, each particle consisting essentially of a single macromolecule. They have the unusual property of being soluble or dispersible in a liquid medium without significantly increasing the viscosity of the medium, rendering them potentially useful in imaging applications such as ink jet printers. They can be prepared by dissolving polymeric material in a solvent system to form a solution of the polymeric material at a concentration therein of less than the critical concentration for the polymer, causing the polymeric material to contract into an approximately spheroidal conformation in solution, cross-linking the polymeric material in solution in said spheroidal conformation so assumed, and recovering stable, cross-linked approximately spheroidal polymeric particles from the solution.

Hydrogen peroxide is produced by a process which uses solid, insoluble, supported anthraquinone as catalyst. The supported anthraquinone is converted to supported anthrahydroquinone utilizing soluble reducing agentsor by hydrogenation with a hydrogen-donating organic substrate such as an alcohol, followed by reaction with oxygen, to regenerate anthraquinone and to form hydrogen peroxide, which can be solvent extracted from the solid catalyst.

Production of hydrogen peroxide

Hydrogen peroxide is produced by a process which uses as catalyst a polymer which has anthraquinone/anthrahydroquinone groups attached to it, and which exhibits differential solubility in water. The polymer is water soluble under one set of conditions, e.g. temperature range, but insoluble under another set of such conditions. Accordingly, the polymer bound anthrahydroquinone groups are oxidized in aqueous solution to form anthraquinone groups and hydrogen peroxide, which dissolves in the aqueous medium. Then the conditions, e.g. temperature, are changed to precipitate the polymer, which can readily be separated off, ready for re-use.

Aqueous phase production of hydrogen peroxide and catalysts for use

A photoactivatable drug delivery system is provided, in which a drug is combined e.g. by covalent bonding, incorporation in a matrix or encapsulation, with a photosensitive macromolecule. In combination, the drug is inert. The macromolecule is large enough to prevent migration of the combination within the body, so that the combination can be implanted at a location of maximum effectiveness. The drug is released from the combination, in therapeutically active form, upon appropriate irradiation.

Drug delivery systems

Hydrogen peroxide is produced by a process which uses solid, insoluble, supported anthraquinone as catalyst. The catalyst is reduced to supported anthrahydroquinone using a hydrogen-donating organic substrate such as an alcohol, followed by reaction with oxygen, suitably photochemical reaction, to regenerate anthraquinone and to form hydrogen peroxide, which can be solvent extracted from the solid catalyst.

The invention disclosed is a hydrogel-forming wound dressing or skin coating material suitable for household and veterinary use, consisting substantially entirely of wound-compatible and skin-compatible ingredients and comprising a first hydrophilic polymer, selected from polymers or copolymers of acrylic acid, polymers or copolymers of methacrylic acid, polymers or copolymers of itaconic acid, polymers or copolymers of maleic acid and polymers or copolymers of 3-butene-1,2,3-tricarboxylic acid, or combinations thereof, a second hydrophilic polymer which is capable of interacting with the first polymer to produce, upon drying, a hydrogel of improved water resistance and film forming properties relative to the first polymer alone and water. This material is film forming and substantially transparent but capable of being made opaque.

Method of making a hydrogel-forming wound dressing or skin coating

The invention disclosed is a hydrogel-forming wound dressing or skin coating material suitable for household and veterinary use, consisting substantially entirely of wound-compatible and skin-compatible ingredients and comprising a first hydrophilic polymer, selected from polymers or copolymers of acrylic acid, polymers or copolymers of methacrylic acid, polymers or copolymers of itaconic acid, polymers or copolymers of maleic acid and polymers or copolymers of 3-butene-1,2,3-tricarboxylic acid, or combinations thereof, a second hydrophilic polymer which is capable of interacting with the first polymer to produce, upon drying, a hydrogen of improved water resistance and film forming properties relative to the first polymer alone and water. This material is film forming and substantially transparent but capable of being made opaque.

Hydrogel-forming wound dressing or skin coating material

Condensation copolymers such as polyesters are rendered photodegradable, by subjecting them to conditions under which they undergo ester interchange effectively causing polymer chain scission, in the presence of a keto carbonyl containing compound having chemical groups reactive with the condensation polymer products formed by the ester interchange. The compound reacts chemically with the polymer products to reform the high molecular weight condensation copolymer, but with the keto carbonyl groups chemically linked into the polymer chains to confer photodegradability thereon.

Production of photodegradable polyester plastics

Polymers of fluorene containing compounds which form crosslinked networks are found to provide useful negative photoresists which are sensitive in the ultraviolet wavelength range of between about 200 nm to 300 nm. When used in negative photoresist compositions, these fluorene compounds produce a high resolution and thus higher information density in microcircuits manufactured using these photoresists.

Fluorene containing compounds and negative photoresist compositions

A novel class of copolymeric negative photoresists is provided whose sensitivity is based upon the presence of .alpha.-chloro ketone moieties. The general structure for the monomers from which the copolymers can be formed is: ##STR1## where R is a substituent selected from 1 to 6 carbon alkyl and halogen substitutes alkyl, phenyl, and halogen substituted phenyl and napthyl and the comonomers are comonomers selected from the group consisting of 1-4 carbon alkyl acrylates and methacrylates, styrene vinyl toluene and vinyl acetate and may include additionally other comonomers that are compatible and have the polymerizable &gt;C.dbd.C&lt; group. The copolymers form crosslinked networks and provide useful negative photoresists which are sensitive in the ultraviolet wavelength range of between about 200 nm to 300 nm. When used in negative photoresist compositions, these chloro vinyl methyl ketone containing compounds produce a high resolution and thus higher information density in microcircuits manufactured using these photoresists.

Negative photoresists of .alpha.-chlorovinyl methyl ketone copolymers

Photochemical reactions are conducted using polymer beads arranged as a monolayer, e.g. floating on the surface of a moving body of water. The polymer bead is impregnated with a reactant, floated on the water or otherwise exposed as a monolayer in direct sunlight so as to expose the reactant to solar radiation, collected at a downstream location, treated to remove product from the polymer, and then the bead can be recycled. The process can be used to collect and store solar energy in chemical form, or for conducting photochemical synthesis to produce useful chemical products.

Photochemical reactions for commercial synthesis

Photoresist materials that are sensitive in suitable range including the 200 nm to 300 nm ultraviolet radiation range are provided which permit relatively higher resolution and thus a higher information density in microcircuits. The positive photoresist materials are copolymers of

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Don Mills, Canada

James E Guillet