Wound dressing material

Claim 2

A wound dressing material comprising a sheet of a synthetic plastics material which is permeable to water vapour and to air, having on one side a surface for application to a wound, and immediately behind the said surface a low density cellular region having a structure of collapsed, open cells which intercommunicate with one another, and a more dense region behind the cellular region, and an intermediate region in which there is a gradual transition from the cellular region to the more dense region, so that on contact with liquid exudate from a wound, the dressing material will absorb a limited amount of exudate into the cellular region but prevent it from passing right through the dressing material.

Claim 3

A wound dressing material according to claim 1, wherein the synthetic plastics material is polyurethane.

Claim 4

A wound dressing material according to claim 2, wherein the synthetic plastics material is the product of polymerisation of a polyoxyethylene polyol with a polyisocyanate in the presence of a cross-linking agent or catalyst which is reactive with the isocyanate groups, without any substantial amount of water present.

Claim 5

A wound dressing material according to claim 3, wherein the cross-linking agent or catalyst contains in its molecule two or more amine and/or hydroxyl groups which are reactive with the isocyanate groups.

Claim 6

A wound dressing material according to claim 3, wherein the catalyst is dimethylethanolamine.

Claim 7

A wound dressing material according to claim 3, wherein the polyol is a polyoxyethylene glycol having a weight average molecular weight of approximately 3000.

Claim 8

A wound dressing material according to claim 3, wherein the polyisocyanate is toluene di-isocyanate.

Claim 9

A wound dressing material according to claim 1, and which has been prepared from a formulation comprising the following composition by weight: Polyoxyethylene glycol (m.wt 3500): 100 parts Dimethylethanolamine: 0.1-1.0 parts Silicone oil: 1-10 parts Toluene di-isocyanate: 25-50 parts

Claim 10

A wound dressing material according to claim 1, which is prepared by a process comprising the steps of mixing a polyoxyethylene polyol with a polyisocyanate and, if desired, a surfactant with agitation to form an aerated creamy mix, incorporating a catalyst which is reactive with the isocyanate groups or a cross-linking agent in the mix, spreading the mix onto a smooth glazed release paper to form a sheet of a predetermined uniform thickness, and allowing the mix to polymerize at a temperature not higher than 25° C., with the exclusion of any substantial amount of water from the mix during the said steps.

Claim 11

A method for treating wounds, which comprises: applying to a wound said side surface of the wound dressing material of claim 1.

Claim 12

A sterile wound dressing material comprising a pliable sheet of a synthetic plastics material which is permeable to water vapor and to air and impermeable to liquids, having on one side a surface for application to a wound, and immediately behind the said surface a low density collapsed cellular region having a structure of collapsed, open cells which intercommunicate with one another, and a more dense region behind the ceullular region, and an intermediate region in which there is a gradual transition from the collapsed cellular region to the more dense region, so that on contact with liquid exudate from a wound, the collapsed cellular region of the dressing material will expand and absorb a limited amount of exudate but the dense region will prevent the exudate from passing right through the dressing material.

Claim 13

A sterile wound dressing material comprising a pliable sheet of a synthetic plastics material which is permeable to water vapor and to air and impermeable to liquids, having on one side a surface for application to a wound, and immediately behind the said surface a low density collapsed cellular region having a structure of collapsed, open cells which intercommunicate with one another, and a more dense region behind the ceullular region, and an intermediate region in which there is a gradual transition from the collapsed cellular region to the more dense region, so that on contact with liquid exudate from a wound, the collapsed cellular region of the dressing material will expand and absorb a limited amount of exudate but the dense region will prevent the exudate from passing right through the dressing material.

Claim 14

A wound dressing material according to claim 11, and further comprising a smooth glazed release paper applied to said surface for application to a wound.

Claim 15

A wound dressing material according to claim 11, which is free from toxic cyanate or amine residues.

Claim 16

A method for treating wounds which comprises applying to a wound said side surface of the wound dressing material of claim 11.

Claim 17

A sterile wound dressing material according to claim 1, which is made by a process comprising the steps of mixing a polyoxyethylene polyol with a polyisocyanate to form a aerated creamy mix, spreading the mix onto a smooth glazed release paper to form a sheet of a predetermined uniform thickness, curing the sheet under substantially anhydrous conditions at a temperature below 10° C., thereby allowing the sheet to rise and cure to form a non-rigid foamed region which consists of open cells which communicate with one another and allowing the foamed region to collapse.

Claim 18

A sterile wound dressing material comprising a pliable sheet of a synthetic plastics material which is permeable to water vapor and to air and impermeable to liquids, having on one side a surface for application to a wound, and immediately behind said surface a low density collapsed cellular region which constitutes the majority of the cross-sectional area of the sheet, said collapsed cellular region having a structure of collapsed, open cells which intercommunicate with one another, and a more dense region behind the cellular region, and an intermediate cellular region in which there is a gradual transition from the collapsed cellular region to the more dense region, so that on contact with liquid exudate from a wound, the collapsed cellular region of the dressing material will expand and absorb a limited amount of exudate but the dense cellular region will prevent the exudate from passing right through the dressing material.

Claim 19

A sterile wound dressing material comprising a pliable sheet of a synthetic plastics material which is permeable to water vapor and to air and impermeable to liquids, having on one side a surface for application to a wound, and immediately behind said surface a low density collapsed cellular region which constitutes the majority of the cross-sectional area of the sheet, said collapsed cellular region having a structure of collapsed, open cells which intercommunicate with one another, and a more dense region behind the cellular region, and an intermediate cellular region in which there is a gradual transition from the collapsed cellular region to the more dense region, so that on contact with liquid exudate from a wound, the collapsed cellular region of the dressing material will expand and absorb a limited amount of exudate but the dense cellular region will prevent the exudate from passing right through the dressing material.

Claim 20

A wound dressing material according to claim 16, wherein said collapsed open cells have substantially the configuration shown in the Figure of the drawing.

Claim 21

A wound dressing material according to claim 16, having substantially the configuration shown in the Figure of the drawing.