The present invention relates to a composition that can be used as or as part of a wound dressing and to wound dressings comprising the same. More specifically, the present invention relates to a composition that disrupts and kills bacteria within a biofilm and also prevents biofilm formation. The composition comprises a fibrous first component selected from the group consisting of chitosan, chitin, derivatives of chitosan, derivatives of chitin, and combinations thereof; at least one triprotic acid and at least one solubilising acid.

Glass-based particles of a biocompatible material which comprises 40 to about 80 wt % borate (B.sub.2O.sub.3) intermixed into a carrier which is an ointment, cream, or surgical glue.

Embodiments disclosed herein are directed to negative pressure treatment systems and wound dressing systems, apparatuses, and methods that may be used for the treatment of wounds. In particular, some embodiments are directed to improved wound dressings comprising a number of viewing portals that facilitate observation of wound tissue or healthy skin underlying the wound dressing. Some embodiments of the viewing portals are provided by forming through holes in internal dressing layers including absorbent material and transmission material, optionally by providing a plug material within the through holes, and by providing translucent or transparent cover layer and tissue contact layer materials.

A chemically modified cellulose/alginate co-spun (seacell) fiber, a wound dressing made therefrom and a preparation method thereof. The seacell fiber is subject to a chemical modification through which a hydrophilic carboxymethyl group is introduced into the cellulose structure making the chemically modified seacell fiber more absorbent. The modified cellulose has a degree of substitution of 0.05-0.5; the seacell fiber has a linear density of 0.5-5 dtex and a fiber length of 5-180 mm. The seacell fiber has hygroscopic and gel-forming properties, while retaining its active ingredient of algae particles.

A skin care fabric for medical, pharmaceutical or cosmetic use includes at least 80% by weight of microfibers that are a mixture of polyamide and polyester and have a diameter of less than 50 microns. Each microfiber is split to produce fine fibers closely packed in a parallel structure having a capillary effect and an abrasive effect. The fabric has a surface weight of less than 180 g/m.sup.2 and is loaded with medical, pharmaceutical or cosmetic active agents. The skin care fabric includes a warp-knitted fabric having a first surface and a second surface opposite the first surface, which is mechanically roughened and cut to become fluffy and yet short-haired and compact and resulting in a further surface enlargement of the fabric structure and a water absorbency of at least four times the surface weight of the fabric.

The present technology generally relates to products, devices, methods and systems for healing of wounds or for wound-treatment therapies. More particularly, but not by way of limitation, the present technology relates an absorbent product impregnated with photoactivatable agents, or light-absorbing molecules, as photoactivatable inserts as wound dressing that can be used together as part of negative-pressure wound therapy (NPWT) system or separately and without the NPWT system.

There is provided herein, according to an embodiment, a plasma thread application of dielectric barrier discharge, which incorporates the effectiveness of plasma in sterilization and the flexibility of thread like structure and has the malleability to be formed into any apparel design. The design of one embodiment uses a dielectric coated/insulated wire in the range of 30 to 40 awg based on the application in question. It can be used as sutures or can be woven into a material for countless bandage-like applications. The ready availability of medically approved dielectric materials is conducive to the manufacture of the same.

The present invention relates to a composition that can be used as or as part of a wound dressing and to wound dressings comprising the same. More specifically, the present invention relates to a composition that disrupts and kills bacteria within a biofilm and also prevents biofilm formation. The composition comprises a first component selected from the group consisting of chitosan, chitin, derivatives of chitosan, derivatives of chitin, and combinations thereof; at least one triprotic acid and at least one solubilising acid.

A wound dressing includes an elastic foam layer, a drape layer, and superabsorbent projections. The elastic foam layer is configured to engage a wound bed and has a first side and a second side, the second side configured to face the wound bed. The drape layer also has a first side and a second side, the second side configured to face the first side of the elastic foam layer. The elastic foam layer also has a plurality of superabsorbent projections (nodules, dots, bumps, lumps, islands, protuberances) fixed to and extending from the first side of the elastic foam layer towards the second side of the drape layer.

The disclosed technology relates to a wound dressing comprising a vertically lapped material. The disclosed technology further relates to methods and uses of the wound dressing.