Process for making absorbent bioactive wettable medical fabric

Claim 2

A process for making an absorbent, bioactive wettable medical fabric comprising the steps of: (a) applying to a non-woven cellulosic-containing substrate (1) a bioactive amount of a bioactive silyl quaternary amine compounds have the formula: ##STR6## wherein R is an alkyl of 11 to 22 carbon atoms and R 1 is a bromine or chlorine; and (2) a wettable hydrophilic coupling amount of an organosilicone terpolymer of the formula: ##STR7## wherein R is hydrogen or methyl, the sum of a+b is in the range of 5 to 200, x is 10 to 50,000, y is 1 to x and z is 1 to 0.05x provided that the sum of y+z is ≦0.75x; and (b) heating the thus coated substrate from step (a) to dry the substrate and fix the microbiocide and hydrophilic coupling agent to said substrate, thereby producing bacteriocidal substantially non-leachable and non-flammable finish which is substantive on said substrate.

Claim 3

The process of claim 1 wherein the microbiocide and the hydrophilic coupling agent are applied together in the same pad bath.

Claim 4

The process of claim 2 wherein said pad bath is an aqueous solution containing from about 0.2 to about 1.1 weight percent of the bioactive agent (1) and from about 0.5 to about 1.5 weight percent of the hydrophilic coupling agent (2).

Claim 5

The process of claim 1 wherein step (b) is conducted at a temperature in the range of about 280° F. to about 360° F.

Claim 6

The process of claim 1 wherein said non-woven substrate is composed of at least about 80 weight percent cellulose.

Claim 7

The process of claim 5 wherein said non-woven substrate contains from about 80 to 85 weight percent cellulose bonded with about 15 to about 20 weight percent acrylic resin binder.

Claim 8

The process of claim 3 or 4 wherein said non-woven substrate is composed of at least about 80 weight percent cellulose.

Claim 9

The process of claim 7 wherein said non-woven substrate contains from about 80 to 85 weight percent cellulose bonded with about 15 to about 20 weight percent acrylic resin binder.

Claim 10

The process of claim 1, 2, 3, 4 or 6 wherein said microbiocide (1) is 3-(trimethoxysilyl)-propyloctadecyl dimethyl ammonium chloride and said hydrophilic coupling agent (2) is an organosilicone terpolymer of the formula: ##STR8## wherein R is hydrogen or methyl, the sum of a+b is in the range of 5 to 200, x is 50 to 300, y is 1 to 0.25x and z is 1 to 0.5x, provided that the sum of y+z is ≦0.25x.

Claim 11

A process for making an absorbent, bioactive, wettable medical fabric comprising the steps of: (A) applying to a non-woven substrate containing at least about 80% cellulose an aqueous solution containing: (i) a bioactive amount of 3-(trimethoxysilyl)-propyloctadecyl dimethyl ammonium chloride, and (ii) a hydrophilic coupling amount of an organosilicone terpolymer of the formula: ##STR9## wherein R is hydrogen or methyl, the sum of a+b is in the range of 5 to 200, x is 50 to 300, y is 1 to 0.25x and z is 1 to 0.5x, provided that the sum of y+z is ≦0.25x; and (B) heating the thus applied substrate of step (A) at a temperature in the range of about 280° F. to about 360° F. for a period of time sufficient to dry the applied aqueous solution and to attach the microbiocide (i) and hydrophilic coupling agent (ii) to the cellulose fibers of the substrate such that components (i) and (ii) are substantially non-leachable from the substrate, the resulting fabric being bacteriocidal, substantially non-leachable, non-cytotoxic, substantially completely non-flammable and static resistant and capable of absorbing body fluids.

Claim 12

A process for making an absorbent, bioactive, wettable medical fabric comprising the steps of: (A) applying to a non-woven substrate containing at least about 80% cellulose an aqueous solution containing: (i) a bioactive amount of 3-(trimethoxysilyl)-propyloctadecyl dimethyl ammonium chloride, and (ii) a hydrophilic coupling amount of an organosilicone terpolymer of the formula: ##STR9## wherein R is hydrogen or methyl, the sum of a+b is in the range of 5 to 200, x is 50 to 300, y is 1 to 0.25x and z is 1 to 0.5x, provided that the sum of y+z is ≦0.25x; and (B) heating the thus applied substrate of step (A) at a temperature in the range of about 280° F. to about 360° F. for a period of time sufficient to dry the applied aqueous solution and to attach the microbiocide (i) and hydrophilic coupling agent (ii) to the cellulose fibers of the substrate such that components (i) and (ii) are substantially non-leachable from the substrate, the resulting fabric being bacteriocidal, substantially non-leachable, non-cytotoxic, substantially completely non-flammable and static resistant and capable of absorbing body fluids.

Claim 13

The process of claim 10 wherein the aqueous solution contains from about 0.2 to about 1.1 weight percent of component (i) and about 0.5 to about 1.5 weight percent of component (ii).

Claim 14

The process of claim 10 or 11 wherein said substrate contains from about 80 to about 85 weight percent cellulose bonded with about 15 to about 20 weight percent acrylic resin binder.

Claim 15

The absorbent, bioactive wettable medical fabric produced by the process of claim 10.