American Cyanamid Company

American Cyanamid

Tyco Group S.a.r.l.

Steven L Peake

Sivaraman Raghu

Stanley S Kaminski

Andrea Leone-Bay

Donald J Casey

Peter K Jarrett

Artun Maranci

Robert J Proverb

James S Farina

James Salvatore

A deformable surgical repair device is manufactured from a block or graft copolymer. The copolymer comprises a plurality of first linkages selected from the group consisting of glycolic acid ester and lactic acid ester linkages, and mixtures thereof, and a plurality of second linkages selected from the group consisting of 1,3-dioxan-2-one; 1,4-dioxan-2-one and .epsilon.-caprolactone linkages. The plurality of first linkages comprises at least about 50 up to about 90 mole percent of the copolymer. In an alternative Claim, the deformable surgical repair device is manufactured from a blend of a first and a second absorbable polymer. The first absorbable polymer comprises a plurality of linkages selected from the group consisting of glycolic acid ester and lactic acid ester linkages, and mixtures thereof. The second absorbable polymer comprises a plurality of linkages selected from the group consisting of 1,3-dioxan-2-one; 1,4-dioxan-2-one and .epsilon.-caprolactone linkages. The first absorbable polymer comprises at least about 50 up to about 90 weight percent of the blend. The device is useful in fracture fixation.

Deformable absorbable surgical device

A deformable surgical repair device is manufactured from a block or graft copolymer. The copolymer comprises a plurality of first linkages selected from the group consisting of glycolic acid ester and lactic acid ester linkages, and mixtures thereof, and a plurality of second linkages selected from the group consisting of 1,3-dioxan-2-one; 1,4-dioxan-2-one and .epsilon.-caprolactone linkages. The plurality of first linkages comprises at least about 50 up to about 90 mole percent of the copolymer. In an alternative claim, the deformable surgical repair device is manufactured from a blend of a first and a second absorbable polymer. The first absorbable polymer comprises a plurality of linkages selected from the group consisting of glycolic acid ester and lactic acid ester linkages, and mixtures thereof. The second absorbable polymer comprises a plurality of linkages selected from the group consisting of 1,3-dioxan-2-one; 1,4-dioxan-2-one and .epsilon.-caprolactone linkages. The first absorbable polymer comprises at least about 50 up to about 90 weight percent of the blend. The device is useful in fracture fixation.

Deformable, absorbable surgical device

Polymides are made by imidization of the product of reaction of dianhydrides with diaminobenzotrifluoride and bis(trifluoromethyl) oxydianilines. In preferred embodiments the polyimides are end capped with monoanhydride or monoamine residues.

Polyimides from diaminobenzotrifluorides

The invention relates to prepregs of fiber-reinforced thermosetting resin that have a coating comprising thermoplastic particles on one or both outer surfaces. Upon lamination of the prepregs into a composite, the layer comprising thermoplastic particles at the surface of the prepreg is formed into a discrete resin layer in the composite at the interface between fiber-reinforced thermosetting resin layers. The laminated composite materials have improved toughness and impact strength due to the thermoplastic particulate material at the interface and yet the composites still retain desired mechanical properties under hot/wet conditions.

Advance composites with thermoplastic particles at the interface between

Polyimides are made by imidization of the product of reaction of dianhydrides with diaminobenzotrifluoride and bis(trifluoromethyl) oxydianilines. In preferred embodiments the polyimides are end capped with monoanhydride or monoamine residues.

Improved heat resistant reinforced composites, including laminates, are made by impregnating reinforcing fabrics and tapes, e.g., graphite, glass, polyaramide and boron, with thermoplastic polyimides from solution in mixtures of specified solvents formulated to retard rapid evaporation and to insure high resin loading, good fiber wetting and the absence of distortion.

Process for the preparation of reinforced thermoplastic composites

This disclosure describes a novel process for the preparation of 9,10-anthracenedicarboxaldehyde by the oxidation of 9,10-bis(chloromethyl)anthracene.

Process for preparing 9,10-anthracenedicarboxaldehyde

This disclosure describes a novel process for the preparation of 2-(n-propyl)-4-methyl-5-(lower alkanoyl)imidazoles which are useful as intermediates for the preparation of anti-asthmatic agents.

Process for preparing

An improved method to prepare vinylpolystyrylpyridines comprises reacting a polymethylpyridine and an aromatic dialdehyde to form a 1:1 adduct and thereafter adding a methylvinylpyridine to terminate the adduct. Vinylpolystyrylpyridines are useful as cross-linking agents in bis-imide resin matrix compositions comprising reinforcing fillers.

Process for the prepartion of vinylpolystyrylpyridine compounds

This disclosure describes a novel process for the preparation of 1-(lower alkyl)substituted derivatives of 6-n-propyl-8-alkylimidazo[1,5-d]-as-triazin-4(3H)-ones which are useful as anti-asthmatic agents.

Process for preparing 5-imidazolyl ketones

This disclosure describes continuous epimerization-crystallization process for the isolation of [S-(R*, S*)]-1-(3-acetylthio-3-benzoyl-2-methylpropionyl)-L-proline from a diasteromeric mixture thereof with [S-(R*, R*)]-1-(3-acetylthio-3-benzoyl-2-methylpropionyl)-L-proline.

Isolation of [S-(R*,

A method for the preparation of cyclopentenones of the general formula (VIII): ##STR1## wherein n is 5-7, has been developed which proceeds via the acid catalyzed deprotection and rearrangement of novel substituted-.alpha.-hydroxymethylfurans of general formula (VII): ##STR2## wherein R is a hydroxyl protecting group, R.sub.1 and R.sub.2 are methyl or ethyl or together form --(CH.sub.2).sub.3 -- and n is as above described. Cyclopentenones of formula VIII are useful intermediates in prostaglandin analog synthesis.

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Ridgefield, CT, United States of America

Steven L Peake