The present invention provides a bio-electrode composition including: a resin containing a urethane bond in a main chain and a silsesquioxane in a side chain; and an electro-conductive material, wherein the electro-conductive material is a polymer compound having one or more repeating units selected from fluorosulfonic acid salts shown by the following general formulae (1)-1 and (1)-2, sulfonimide salts shown by the following general formula (1)-3, and sulfonamide salts shown by the following general formula (1)-4. This can form a living body contact layer for a bio-electrode that is excellent in electric conductivity and biocompatibility, light in weight, manufacturable at low cost, and free from large lowering of the electric conductivity even when it is wetted with water or dried. The present invention also provides a bio-electrode in which the living body contact layer is formed from the bio-electrode composition, and a method for manufacturing the bio-electrode. ##STR00001##

A process for producing a polymerizable composition for optical materials of the present invention includes a step A of mixing together a polyisocyanate compound (i), a polymer (ii) represented by General Formula (ii), a photochromic compound (iii), and an internal release agent (iv), a step B of mixing a mixed solution obtained by the step A with a polythiol compound (v), and a step C of further mixing a mixed solution obtained by the step B with a polymerization catalyst (vi) so as to obtain a polymerizable composition for optical materials, wherein in the step A, the internal release agent (iv) is added so that a content thereof in the polymerizable composition for optical materials is 500 to 3,000 ppm, and in the step C, the polymerization catalyst (vi) is added so that a content thereof in the polymerizable composition for optical materials is 120 to 500 ppm.
R.sub.1A.sub.1R.sub.2A.sub.2R.sub.3].sub.n(ii).

The present disclosure relates to compositions A composition comprising a polymerization product of an anionic polysaccharide, a diisocyanate, and a linker, wherein the linker comprises i) an ether group, an ester group, or a combination thereof and, ii) a chain extender comprising a hydroxyl group, a thiol group, an amine group, or a combination thereof. The disclosure further relates to medical devices comprising the aforementioned compositions, and to methods of using the compositions and devices. More particularly, the compositions, devices and methods described herein are useful for preventing protein adhesions in vivo, particularly the Vroman effect.

The present invention provides a bio-electrode composition including: a resin containing a main chain having a urethane bond and two side chains each having a silicon-containing group; and an electro-conductive material, wherein the electro-conductive material is a polymer compound having one or more repeating units selected from fluorosulfonic acid salts shown by the following formulae (1)-1 and (1)-2, sulfonimide salts shown by the following formula (1)-3, and sulfonamide salts shown by the following formula (1)-4. This can form a living body contact layer for a bio-electrode that is excellent in electric conductivity and biocompatibility, light in weight, manufacturable at low cost, and free from large lowering of the electric conductivity even when it is wetted with water or dried. The present invention also provides a bio-electrode in which the living body contact layer is formed from the bio-electrode composition, and a method for manufacturing the bio-electrode.

Solvent-based adhesive compositions are disclosed herein. In some embodiments, the solvent-based adhesive compositions include (A) an isocyanate component comprising an isocyanate curing agent and (B) a hydroxyl component comprising a polyester polyol, a polyether polyol, and a phosphate ester compound. The isocyanate curing agent of the isocyanate component (A) crosslinks the components of the hydroxyl component. In some embodiments, the phosphate ester compound has the structure (I): (I) wherein R1 is any organic group. Methods for preparing solvent-based adhesive compositions are also disclosed. The methods include providing an isocyanate component (A) comprising an isocyanate curing agent, providing a hydroxyl component (B) comprising a polyol blend, comprising a polyester polyol and a polyether polyol, and a phosphate ester compound, curing the hydroxyl component (B) with the isocyanate component (A) at a mix ratio ((A):(B), by weight) of from 100:8 to 100:15, thereby forming the solvent-based adhesive composition.

##STR00001##

A resin composition comprises a base resin containing an urethane (meth)acrylate oligomer, a monomer having a phenoxy group, and a photopolymerization initiator, and hydrophobic inorganic oxide particles, wherein the viscosity is 300 mPa.Math.s or more and 4200 mPa.Math.s or less at 45 C. and the content of the monomer having a phenoxy group is 1% by mass or more and 30% by mass or less based on the total amount of the base resin.

Low-friction fluorinated coatings are disclosed herein. A preferred low-friction material contains a low-surface-energy fluoropolymer having a surface energy between about 5 mJ/m.sup.2 to about 50 mJ/m.sup.2, and a hygroscopic material that is covalently connected to the fluoropolymer in a triblock copolymer, such as PEG-PFPE-PEG. The material forms a lubricating surface layer in the presence of humidity. An exemplary copolymer comprises fluoropolymers with average molecular weight from 500 g/mol to 20,000 g/mol, wherein the fluoropolymers are (,)-hydroxyl-terminated and/or (,)-amine-terminated, and wherein the fluoropolymers are present in the triblock structure T-(CH.sub.2CH.sub.2O)CH.sub.2CF.sub.2O(CF.sub.2CF.sub.2O).sub.m(CF.sub.2O).sub.nCF.sub.2CH.sub.2(OCH.sub.2CH.sub.2).sub.p-T where T is a hydroxyl or amine terminal group, p=1 to 50, m=1 to 100, and n=1 to 100. The copolymer also contains isocyanate species and polyol or polyamine chain extenders or crosslinkers possessing a functionality of preferably 3 or greater. These durable, solvent-resistant, and transparent coatings reduce insect debris following impact.

Low-friction fluorinated coatings are disclosed herein. A preferred low-friction material contains a low-surface-energy fluoropolymer having a surface energy between about 5 mJ/m.sup.2 to about 50 mJ/m.sup.2, and a hygroscopic material that is covalently connected to the fluoropolymer in a triblock copolymer, such as PEG-PFPE-PEG. The material forms a lubricating surface layer in the presence of humidity. An exemplary copolymer comprises fluoropolymers with average molecular weight from 500 g/mol to 20,000 g/mol, wherein the fluoropolymers are (,)-hydroxyl-terminated and/or (,)-amine-terminated, and wherein the fluoropolymers are present in the triblock structure T-(CH.sub.2CH.sub.2O)CH.sub.2CF.sub.2O(CF.sub.2CF.sub.2O).sub.m(CF.sub.2O).sub.nCF.sub.2CH.sub.2(OCH.sub.2CH.sub.2).sub.p-T where T is a hydroxyl or amine terminal group, p=1 to 50, m=1 to 100, and n=1 to 100. The copolymer also contains isocyanate species and polyol or polyamine chain extenders or crosslinkers possessing a functionality of preferably 3 or greater. These durable, solvent-resistant, and transparent coatings reduce insect debris following impact.

The present disclosure relates to compositions A composition comprising a polymerization product of an anionic polysaccharide, a diisocyanate, and a linker, wherein the linker comprises i) an ether group, an ester group, or a combination thereof and, ii) a chain extender comprising a hydroxyl group, a thiol group, an amine group, or a combination thereof. The disclosure further relates to medical devices comprising the aforementioned compositions, and to methods of using the compositions and devices. More particularly, the compositions, devices and methods described herein are useful for preventing protein adhesions in vivo, particularly the Vroman effect.

A self-restoring polyurethane-based polymer obtained by polymerization of a composition containing an aromatic disulfide diol represented by Chemical Formula, HOAr.sub.1SSAr.sub.2OH, an alicyclic polyisocyanate, and a polyol. Ar.sub.1 and Ar.sub.2 each are independently a substituted or unsubstituted C.sub.6-C.sub.30 arylene group. The composition satisfies Equation, 0.1M.sub.[disulfide]/M.sub.[OH]. M.sub.[disulfide] is a total mole number of the aromatic disulfide diol in the composition, and M.sub.[OH] is a total mole number of the aromatic disulfide diol and the polyol in the composition.