WO2007113453A1 - Composites d'hydrogel absorbant - Google Patents

Composites d'hydrogel absorbant Download PDF

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Publication number
WO2007113453A1
WO2007113453A1 PCT/GB2006/001218 GB2006001218W WO2007113453A1 WO 2007113453 A1 WO2007113453 A1 WO 2007113453A1 GB 2006001218 W GB2006001218 W GB 2006001218W WO 2007113453 A1 WO2007113453 A1 WO 2007113453A1
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WO
WIPO (PCT)
Prior art keywords
absorbent
layer
hydrogel
absorbent layer
article according
Prior art date
Application number
PCT/GB2006/001218
Other languages
English (en)
Inventor
Hugh Semple Munro
Philip Andrews
Susana Saina Garcia
Original Assignee
First Water Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by First Water Limited filed Critical First Water Limited
Priority to PCT/GB2006/001218 priority Critical patent/WO2007113453A1/fr
Publication of WO2007113453A1 publication Critical patent/WO2007113453A1/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/26—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42—Use of materials characterised by their function or physical properties
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42—Use of materials characterised by their function or physical properties
    • A61L15/60—Liquid-swellable gel-forming materials, e.g. super-absorbents

Definitions

  • the present invention relates to absorbent (porous) hydrogel/foam composites, and more particularly to sheet hydrogel/hydrophilic foam composites suitable for use in wound and burn dressings and other applications where a relatively high speed of fluid uptake is required.
  • the invention also relates to processes for the manufacture of the novel hydrogel composites, and to uses of the compositions.
  • hydrogel and “hydrogel composites” used herein are not to be considered as limited to gels which contain water, but extend generally to all hydrophilic gels and gel composites, including those containing organic non-polymeric components in the absence of water.
  • WO-A-03/077964 and WO-A-04/052415 (First Water Limited), the disclosure of which is incorporated herein by reference, describes certain superabsorbent hydrogel foam compositions.
  • the composition is a flexible plasticised hydrophilic polymeric matrix.
  • a first portion of the polymeric matrix has an internal cellular structure, and a second portion has a relatively continuous internal structure.
  • the first portion is relatively porous and the second portion is relatively non-porous, relative to each other.
  • the second portion of the composition may include apertures providing fluid flow communication through the said second portion between an external surface of the said second portion and the first portion whereby the first portion of the composition can take up external water or other fluid into the cellular structure through the apertures of the said second portion.
  • compositions are preferably provided in sheet form, the portions comprising layers of the sheet.
  • the said first and second portions of the prior art compositions are preferably (although not essentially) of the same polymeric matrix material and integrally formed in a single polymerisation step.
  • a large amount of research has been conducted into unfoamed, relatively non-porous, hydrogels based on hydropbilic polymers, e.g. for use as skin adhesives for a range of applications in skin- adhesive articles. Such materials exhibit a range of properties which make them suitable for skin adhesives.
  • Representative references include PCT Patent Applications Nos.
  • compositions comprising foam and continuous portions represent a significant development in the area of absorbent hydrogels, particularly but not exclusively for use in skin adhesive applications, nevertheless there is a need for stronger materials having the desired porosity, water retention and other characteristics offered by hydrogel technology.
  • the present invention is based on our surprising finding that relatively strong absorbent hydrogel/hydrophilic foam composites (hereinafter: "absorbent hydrogel composites" or simply “hydrogel composites”) can be made in a convenient manner with very acceptable water uptake speeds.
  • the manufacturing process can be batchwise, partially continuous or continuous.
  • the absorbent hydrogel composites are prepared in sheet or layer form.
  • the hydrogels are characterised by a first hydrophilic absorbent part which has an internal cellular (e.g. foam) structure and a second absorbent part which is relatively continuous (i.e. has a relatively non- cellular internal structure). Some or all of the second part can fill some of the voids of the internal cellular structure of the first part.
  • the second part can have apertures provided therethrough, to assist uptake of water and other fluids into the first part.
  • the composites are not formed integrally together in one step from a single pre-gel mixture, but must be assembled.
  • the sheet or layer composites may be supported on a relatively strong polymeric support sheet, which may be permeable or impermeable to moisture liquid or moisture vapour.
  • the absorbent hydrogel composites can combine the requirements of good gel flexibility, good mechanical strength and good fluid absorption capacity, optionally also with tackiness to the skin.
  • an absorbent material or article comprising an absorbent hydrogel composite sheet including: an absorbent layer part having two major faces which comprises a flexible plasticised hydrophilic polymer matrix having an internal cellular structure, and a second part which comprises a flexible plasticised hydrophilic polymer matrix having a relatively continuous internal structure; wherein the second part is associated with the layer part such that the second part infiltrates some but not all of the cellular voids of the absorbent layer part over a major face of the absorbent layer part whereby some but not all of the absorbent layer part is effectively exposed for absorption of external water or other fluid through the side of the sheet corresponding to that said major face of the absorbent layer.
  • the flexible plasticised hydrophilic polymer matrix materials forming the said absorbent layer and second parts of the absorbent hydrogel composite sheet may be the same or different.
  • the absorbent layer may suitably comprise a hydrophilic polyurethane foam or a hydrogel.
  • the second part of the absorbent hydrogel composite sheet may suitably comprise a hydrogel and infiltrates some but not all of the cellular voids of the absorbent layer part.
  • the cellular voids are typically established in the solid matrix forming the absorbent layer part of the composite before ingress of a liquid pre-gel material for forming the second part of the composite. That portion of the said second part of the composite which infiltrates some but not all of the cellular voids of the absorbent layer part of the composite may be all or only some of the said second part of the composite. When it is only some of the said second part of the composite, it may preferably be continuous with the remainder of the said second part of the composite, i.e.
  • the weight of the second part of the absorbent hydrogel composite per unit area (“coat weight") is typically in the range of up to about 500 g/m 2 , for example about 50 to about 460 g/m 2 , about 150 to about 460 g/m 2 , or about 200 g/m 2 .
  • the second part of the composite is " preferably absorbent, and may in particular have a water absorption capacity generally similar to the absorbent layer part of the composite having the internal cellular structure.
  • the absorbent layer part of the hydrogel composite is effectively exposed for absorption of external water or other fluid through one side of the sheet.
  • the absorbent layer part of the hydrogel composite may be effectively exposed for absorption of external water or other fluid through the other side of the sheet, or may be effectively sealed from absorption of external water or other fluid through the other side of the sheet, or some regions of the absorbent layer part may be effectively exposed and other regions of the absorbent layer part may be effectively sealed with respect to absorption of external water or other fluid through the other side of the sheet.
  • a support layer of a polymeric material which may be, respectively, permeable to moisture liquid and/or moisture vapour, impermeable to moisture liquid and/or moisture vapour, or may have regions which are permeable to moisture liquid and/or moisture vapour and regions which are impermeable to moisture liquid and/or moisture vapour.
  • the said support layer when present, is preferably a mechanically strong polymeric supporting sheet or film. This preferably comprises a non- hydrogel polymer.
  • the said support layer may suitably comprise a backing layer of a sheet absorbent article such as a wound or burn dressing. Where such a support layer is present, one or more additional layer (e.g.
  • hydrogel material for example of the same general type as the material forming the said second part of the hydrogel composite sheet, which may if desired infiltrate some but not all of the cellular voids of the absorbent layer part) may if desired be present, between the absorbent layer part and the support layer.
  • a support layer of a polymeric material is itself novel in a more general sense in connection with foam/continuous composites of the type with which the present invention is concerned.
  • an absorbent material or article comprising an absorbent hydrogel composite sheet including: an absorbent layer part having two major faces, which comprises a flexible plasticised hydrophilic polymer matrix having an internal cellular structure, and a second part which comprises a flexible plasticised hydrophilic polymer matrix having a relatively continuous internal structure; wherein the second part is associated with the layer part such that the second part overlies a major face of the absorbent layer part such that some but not all of the absorbent layer part is effectively exposed for absorption of external water or other fluid through the side of the sheet corresponding to that major face of the absorbent layer part which is overlain by the second part, and wherein there is provided over the other major face of the layer part a support layer of a polymeric material.
  • this second aspect of the present invention is novel and inventive over the disclosure of WO-A-2004/052415, for the purpose of any jurisdictions in which that application constitutes prior art against the present application, we reserve the right to claim the second aspect of the present invention with the proviso that, when the second part of the hydrogel composite substantially entirely overlies the said major face of the layer part and some but not all of the absorbent layer part is effectively exposed for absorption of external water or other fluid by virtue of apertures provided through the second part which provide fluid flow communication through the second part between an external surface of the second part and the absorbent layer part, whereby the layer part can take up external water or other fluid into the cellular structure through the apertures of the second part, then the apertures of the second part continue through the absorbent layer part to penetrate it entirely, but without penetrating the support layer provided over the other major face of the absorbent layer part; or any modified form of this proviso that may be required by the tribunal or forum adjudicating the matter.
  • the said second part of the hydrogel composite may infiltrate some but not all of the cellular voids of the absorbent layer part, or the said second part of the hydrogel composite may be associated with the absorbent layer part in such a way - e.g. lamination, with or without intermediate adhesives or other components - that it does not infiltrate any of the cellular voids of the absorbent layer part
  • the support layer may, for example, be permeable to moisture liquid and/or moisture vapour, impermeable to moisture liquid and/or moisture vapour, or may have regions which are permeable to moisture liquid and/or moisture vapour and regions which are impermeable to moisture liquid and/or moisture vapour.
  • the said support layer when present, is preferably a mechanically strong polymeric supporting sheet or film. This preferably comprises a non-hydrogel polymer.
  • the said support layer may suitably comprise a backing layer of a sheet absorbent article such as a wound or burn dressing. Where such a support layer is present, one or more additional layer (e.g.
  • hydrogel material for example of the same general type as the material forming the said second part of the hydrogel composite sheet, which may if desired infiltrate some but not all of the cellular voids of the absorbent layer part) may if desired be present, between the absorbent layer part and the support layer.
  • the support layer is formed of any suitable material, e.g. a polymer (which may be foamed or unfoamed, or any combination thereof) such as polyurethane, or a fabric (which may comprise natural fibres, synthetic fibres or any combination thereof, and may be woven or non-woven).
  • a suitable material e.g. a polymer (which may be foamed or unfoamed, or any combination thereof) such as polyurethane, or a fabric (which may comprise natural fibres, synthetic fibres or any combination thereof, and may be woven or non-woven).
  • the support layer may have any suitable structure, e.g. a web, film, sheet, net or any combination thereof.
  • the second part of the hydrogel composite sheet overlies a major face of the absorbent layer part such that some but not all of the absorbent layer part is effectively exposed for absorption of external water or other fluid through the side of the sheet corresponding to that major face of the absorbent layer part which is overlain by the second part.
  • the expression "effectively exposed” and like expressions, used herein, means that external water or other fluid at the said side of the sheet can gain access into the cellular internal structure of the absorbent layer part of the hydrogel composite sheet for absorption into the composite sheet within an acceptable period of time and in acceptable volumes according to the intended use of the composite sheet.
  • the external water or other fluid must physically contact the absorbent layer part of the hydrogel composite sheet before any other part; for example, a thin layer of a hydrogel having a continuous internal structure or other absorbent material maybe disposed over an "effectively exposed" portion of the absorbent layer of the hydrogel composite - provided that the external water or other fluid can pass through any such thin extra layer within an acceptable period of time and in acceptable volumes according to the intended use of the composite, and thereby into the cellular internal structure of the composite sheet, then the requirements of the invention would have been fulfilled.
  • an "effectively exposed" portion of the absorbent layer part is outward facing to the side of the composite sheet through which the external water or other fluid can be absorbed - by means of three-dimensional surface and/or internal features provided on the composite sheet (such as, for example, apertures, hollows, dents, slits, slots, depressions, raised bumps, raised ridges, or any combination thereof), portions of the absorbent layer part of the hydrogel composite sheet can be effectively exposed in such a way that external water or other fluid can pass into the cellular internal structure within an acceptable period of time and in acceptable volumes according to the intended use of the composite, for example passing around surface regions of the hydrogel material constituting the second part of the composite.
  • Such three- dimensional features may advantageously invade the absorbent layer part of the composite to some extent to achieve their exposing effect. They may even penetrate the absorbent layer part of the hydrogel composite sheet entirely, particularly (as mentioned above) if a support layer is provided over the opposite major face of the composite sheet.
  • the absorbent layer part of the hydrogel composite sheet may comprise a porous foam having an internal cellular structure such that the volume ratio of cell void to matrix is greater than about 1:3, more preferably greater than about 1:1, and the second part may comprise a relatively continuous matrix, which may have substantially no cell voids or only occasional cell voids (e.g. a volume ratio of cell void to matrix less than about 1:10, for example less than about 1:20).
  • the said second part of the hydrogel composition will be referred to herein as "continuous", which expression is used in the relative sense explained above.
  • the absorbent layer part of the composite has a first water uptake rate and the second part of the composite has a second water uptake rate (disregarding any apertures or the like providing fluid flow communication).
  • the first and second water uptake rates may be generally similar. At least the first water uptake rate may be very fast, e.g. comparable with the rate of absorption of water by absorbent paper kitchen roll.
  • the absorption capacity of the hydrogel composite will generally be at least about 30% by weight (i.e. the weight of water taken up and held at saturation will be at least about 30% of the weight of the hydrogel composite used), and may be as much as about 20000%. More typically, the absorption capacity of the hydrogel composite will be between about 300% and about 10000%.
  • a skin-tacky hydrogel composite sheet according to the present invention may be used in a bioadhesive article which is adapted to be adhered to human or other mammalian skin in use.
  • Such an article typically comprises the hydrogel composite sheet as an adhesive for contacting the skin and a substrate supporting the hydrogel adhesive sheet.
  • the side of the hydrogel composite sheet through which external water or other fluid can be absorbed into the sheet typically defines the skin-contactable surface of the hydrogel composite sheet.
  • the absorbent material of the present invention absorbs moisture well into the cellular structure, while loss of moisture from the material can be restricted or controlled so that the material serves in use also as a moisture reservoir, which is beneficial to human or other mammalian skin in a range of circumstances, as discussed in more detail below.
  • the infiltration of voids of the cellular structure by the material of the relatively non-absorbent second part of the composite strengthens and reinforces the composite material, this strengthening being assisted by any support layer present.
  • a process for the preparation of an absorbent hydrogel composite sheet for use in the absorbent material or article according to the first and second aspects of the invention which comprises associating said absorbent layer and second parts of the hydrogel composite sheet together as defined in the first and second aspects, optionally with other layers or components such as, for example, any required support layer.
  • association of the parts is preferably achieved by first forming the absorbent layer part of the composite as a foam layer in the solid cured state, and subsequently applying to a surface thereof a liquid pre-gel precursor for the second part of the composite, allowing the liquid pre- gel precursor to infiltrate the pores of the absorbent layer part to a desired extent, and subsequently curing the second part to provide the composite sheet.
  • association of the parts is preferably achieved by adhering or laminating in conventional manner pre-formed areas of the second part of the composite to a pre-formed absorbent layer part of the composite (e.g. a foam layer in the solid cured state).
  • Additional hydrogel layer or area - may if desired be provided on one or both sides of the hydrogel composite sheet according to the present invention, or may be interposed between the parts of the hydrogel composite sheet according to the present invention.
  • Such other layers or areas may be foamed or unfoamed, hydrogel or non- hydrogel.
  • An additional layer of an unfoamed (continuous) hydrogel may, for example, be provided overlying the absorbent layer part of the hydrogel composite sheet, and particularly between the absorbent layer part of the hydrogel composite sheet and any support layer present.
  • the hydrogel of such an additional layer when present, may conveniently be selected from the same hydrogel materials as those from which the second part of the hydrogel composite sheet may be formed, as described herein, or from other unfoamed hydrogels as described in any of the prior art documents acknowledged herein.
  • Such additional layer(s), when present, may be associated with the essential components of the hydrogel composite sheet in any suitable manner.
  • the means of association include infiltration where appropriate, lamination where appropriate, or in some cases an absorbent bilayer or multi-layer component can be prepared in one procedure as an integral unitary material, using the methods described in WO-A-03/77964 and WO-A-2004/052415.
  • a scrim material may be present, suitably within any one or more relatively continuous hydrogel layers that are present in the material or article according to the present invention.
  • a scrim material may be formed of a material that is natural in origin, synthetic in origin, or partly natural and partly synthetic.
  • the scrim may suitably be in the form of a net or a woven or non-woven fabric.
  • Preferred scrims include those formed from polyolefins, polyamides, polyacrylates, or polyesters, for example non-wovens or nets.
  • the crim material may, for example, comprise sodium polyacrylate fibres, such as those commercially available under the tradename OasisTM from Acordis Technical Absorbents Limited.
  • the scrim is preferably provided by introducing it into a laid down (e.g.
  • the absorbent hydrogel composite sheet of the material or article of the first aspect of the present invention may preferably consist essentially of: (a) the absorbent layer part, the second part disposed on some but not all of one major face of the absorbent layer (optionally with three-dimensional surface features, e.g. selected from depressions, slits, crosses or any combination thereof provided on said major face), and a support layer adhered to the other major face of the absorbent layer; or (b) as (a) and an additional continuous hydrogel layer disposed between the absorbent layer and the support layer; or
  • hydrogel components of the embodiments (a) to (j) above are associated together by any means within the options provided for in the first and second embodiments of the present invention defined above.
  • Curing of a pre-gel can suitably be by polymerisation, although evaporation of a solvent from a liquid pre-gel which comprises an organic solvent solution of a pre-formed polymer - to leave behind a dry residue of the polymer - is not excluded from the ambit of the word "curing" as used herein.
  • the absorbent layer part of the hydrogel composite for use in the present invention may thus generally be prepared by a process which comprises polymerising a polymerisable mixture comprising a hydrophilic monomer selected from monomers and monomer mixtures, wherein the polymerisable mixture includes introduced gas bubbles, as described in WO-A-03/077964 and WO-A-2004/052415.
  • Any polymerisation step in the manufacture of the composite hydrogel sheet or component parts thereof is preferably a free radical polymerisation performed in air using a polymerisation inducing device such as a heat, light (e.g. UV light) or other radiation source which is in relative motion with respect to the polymerisable mixture.
  • a polymerisation inducing device such as a heat, light (e.g. UV light) or other radiation source which is in relative motion with respect to the polymerisable mixture.
  • a moving line-wise polymerisation procedure can take place, rather than the static batchwise procedures available from the prior art.
  • the polymerisable mixture or composite of pre-formed part (e.g. cured foamed component) and polymerisable pre-gel (herein generically. "polymerisable material”) is laid down in sheet or layer form on a suitable support arrangement for the polymerisation procedure.
  • the support arrangement comprises a structure which underlies and supports a sheet material adapted to receive the laid down polymerisable material, the sheet material being removable from the underlying structure, e.g. after completion of polymerisation, and the said projections extending from the upper surface of the sheet material.
  • the sheet material may have a non-stick surface, so that it may easily be removed from the hydrogel composition after completion of polymerisation.
  • the sheet material is preferably adapted to constitute a release layer in conventional manner, for protecting the polymerised hydrogel composite sheet prior to use.
  • hydrogel composite is prepared by adhesion or lamination of pre-formed hydrogel parts together.
  • the resultant hydrogel composite and the release layer may be maintained in contact with each other in a subsequent process for manufacturing an article including the hydrogel composite.
  • a further release layer may suitably be applied to the exposed surface of the freshly prepared hydrogel composite, to protect the same for storage or transportation. At the times of subsequent processing and use, the relevant release layer is peeled away and may be discarded.
  • any required three-dimensional surface and/or internal features of the hydrogel composite or any part thereof may suitably be formed simultaneously with, or after, formation of the polymer matrix of the said part or simultaneously with, or after, formation of the composite sheet itself.
  • Such features may, for example, be formed by moulding, punching, cutting, slicing and/or pressing, in conventional manner.
  • Component parts of the composite can be associated with one another in conventional manner (e.g. using adhesives or other conventional bonding methods), or parts (e.g. layers) can be formed in situ on other component parts.
  • apertures and similar features can be formed in situ during any polymerisation reaction using an appropriately shaped underlying support sheet of the support arrangement for the pre-gel material, as described in more detail in WO-A- 2004/052415.
  • the absorbent hydrogel composites used in this invention may be electrically conductive and constitute a skin-contactable, preferably adhesive, portion of a biomedical electrode. Such a hydrogel composition will typically provide good current dispersion over the skin-electrode interface.
  • a biomedical electrode comprising an electrically conductive current distribution member adapted for electrical connection to an electrical apparatus, and an electrically conductive skin contactable portion in association with the electrically conductive current distribution member, whereby electrical current can flow between the electrical apparatus and a wearer's skin when the electrode is in use, wherein the electrically conductive skin contactable portion comprises an absorbent hydrogel composite or a hydrogel/release layer combination according to the first or second aspect of the present invention or prepared according to the third aspect of the present invention.
  • the electrically conductive skin contactable portion is in sheet or layer form. The side of the composite through which external water or other fluid can be absorbed will preferably form the skin-contactable surface of the electrically conductive skin contactable portion.
  • a bioadhesive wound or burn dressing typically comprises an absorbent member adapted to contact a wearer's skin in the location of a wound or burn, and a sheet backing member supporting the absorbent member, the sheet backing member including a portion which extends beyond the absorbent member and defines a skin-directed surface which carries a pressure- sensitive adhesive for securement of the dressing to the wearer's skin.
  • a wound or burn dressing which comprises an absorbent member adapted to contact a wearer's skin in the location of a wound or burn, and a sheet backing member supporting the absorbent member, the sheet backing member including a portion which extends beyond the absorbent member and defines a skin-directed surface which carries a pressure-sensitive adhesive for securement of the dressing to the wearer's skin, wherein the absorbent member comprises an absorbent hydrogel composite or a hydrogel/release layer combination according to the first or second aspect of the present invention or prepared according to the third aspect of the present invention.
  • the absorbent member is in sheet or layer form. The side of the composite through which external water or other fluid can be absorbed will preferably form the skin-contactable surface of the absorbent member.
  • the sheet backing member is formed of any suitable material, e.g. a polymer (which may be foamed or unfoamed, or any combination thereof) such as polyurethane, or a fabric (which may comprise natural fibres, synthetic fibres or any combination thereof, and may be woven or non- woven).
  • the sheet backing member may have any suitable structure, e.g. a web, film, sheet, net or any combination thereof.
  • the sheet backing member in this wound and burn dressing aspect of the invention is preferably the support member part of the absorbent material of the first or second aspect of the present invention, simply dimensioned so as to extend beyond the absorbent member which comprises the absorbent hydrogel composite sheet according to the invention.
  • the pressure-sensitive adhesive is any suitable skin-compatible adhesive, e.g. a known acrylic- based polymeric pressure-sensitive adhesive; or a bioadhesive hydrogel or gel or a bioadhesive porous plasticised hydrophilic polymer having an internal cellular structure, such as those described in the PCT Patent Applications mentioned above.
  • the internal cellular structure of the absorbent layer part may be closed-cell throughout, open- cell throughout, or may have regions of closed-cell structure and regions of open-cell structure.
  • an open-cell structure is preferred, as it will absorb fluid at a faster initial rate than a closed-cell structure, by reason of the interconnection of the internal cells.
  • the second part or any additional continuous layer of the hydrogel composite sheet may suitably be in the form of a layer of the sheet, which may be of the same or different material to the absorbent layer.
  • the layers may be infiltrated together, as described above, or may be laminated together, optionally with intermediate bonding media.
  • the absorbent layer part is preferably pre-formed as described in the prior art mentioned above.
  • the absorbent hydrogel composite sheet consists essentially of the absorbent layer and the infiltrated relatively non-absorbent second part
  • the absorbent layer is formed in such a way that substantially no "draining" of the foamed (gassed) pre-gel takes place, as described in WO-A-03/077964 and WO-A-2004/052415, so that the formation of a relatively continuous (non-absorbent) portion adjacent the foamed layer is minimised.
  • the infiltrated relatively non-absorbent part can then be formed on the absorbent layer as described in more detail below.
  • the absorbent hydrogel composite sheet comprises the absorbent layer, the infiltrated relatively non-absorbent part, and a further relatively non-absorbent part (e.g. layer) overlying the absorbent layer
  • the absorbent layer may be formed in such a way that "draining" of the foamed (gassed) pre-gel takes place, so that a relatively continuous (non- absorbent) portion adjacent the foamed layer is simultaneously formed, which can the serve as the further relatively non-absorbent layer overlying the absorbent layer.
  • the infiltrated relatively non-absorbent part would be formed on the absorbent portion of the resulting material as described in more detail below.
  • the lamination can be accomplished in generally conventional manner, typically by using the typical inherent tackiness of plasticised hydrogels or by using an intermediate bonding adhesive between the parts (e.g. a conventional acrylic adhesive), or a combination of both.
  • the hydrogel composite sheet preferably includes a non-hydrogel support layer (e.g. of polyurethane or the like) associated with the side opposite to the side from which water can be absorbed (the latter side being typically the skin-contacting side).
  • the composite is preferably protected before use by the skin-contacting side being in contact with a protective release layer, for example siliconised plastic or paper.
  • the hydrogel composite may be provided, for example, in partially finished form in the form of a sheet having first and second major hydrogel faces, i.e. with no support layer, both of said hydrogel faces being in contact with a protective release layer, for example siliconised plastic or paper.
  • the support layer is preferably a backing member for the article, e.g. a backing member forming part of a wound or burn dressing, a biomedical electrode or another article.
  • a bioadhesive hydrogel layer is to be provided in use between the article and the skin of a patient.
  • Such articles are exemplified below (see “Applications").
  • the hydrogel composition may be present in the form of a sheet having a woven or non-woven fabric, or a net, embedded therein.
  • the hydrogel sheets may typically have a substantially uniform thickness.
  • the hydrogel sheets may typically have a thickness in the range of about 0.5 mm to about 10 mm.
  • the hydrogel composition may suitably be in the form of a sheet having a mean basis weight of hydrogel in the range of about 0.1 kg/m 2 to about 2.5 kg/m 2 .
  • the water may be present in any suitable amount.
  • the typical range of water content is between 0 and about 95% by weight of the hydrogel.
  • the hydrogel composition may conveniently be classified as “high water content” or “low water content”.
  • high water content refers particularly to hydrogel compositions comprising more than about 40% by weight of water, more particularly above about 50% by weight, and most preferably between about 60% and about 95% by weight.
  • low water content refers particularly to hydrogel compositions comprising up to about 40% by weight of water.
  • any three-dimensional surface features of the hydrogel composite are preferably formed by moulding at the stage of preparation of the composite sheet, or alternatively by stamping, punching and/or cutting a pre-assembled flat composite sheet, using a conventional stamping, punching and/or cutting apparatus.
  • the flat composite sheet is preferably formed initially with a uniform layer of the hydrogel for providing the second part of the composite disposed over the full area of the face of the absorbent layer through which it is desired that external water or other fluid is to be capable of being absorbed.
  • the process of stamping, punching and/or cutting the flat composite sheet to form the three-dimensional surface features typically breaks the uniform layer of the hydrogel and thereby creates the effective exposure of the underlying absorbent layer, in accordance with the invention.
  • the methods for preparing the composite material and articles of the present invention typically use liquid pre-gel deposition methods such as casting, injecting, drop application or printing (e.g. screen printing or gravure printing) and subsequent curing, in combination with conventional liquid shaping methods such as moulding, and/or mechanical forming of solid pre- formed sheet components (e.g. punching, stamping and/or cutting), to form single layers, a partially assembled layer structure or the completely assembled layer structure, and if necessary subsequently associating component parts together and/or forming parts or layers from liquid pre-gel materials by similar methods in situ on pre-formed component parts and subsequent curing.
  • liquid pre-gel deposition methods such as casting, injecting, drop application or printing (e.g. screen printing or gravure printing) and subsequent curing, in combination with conventional liquid shaping methods such as moulding, and/or mechanical forming of solid pre- formed sheet components (e.g. punching, stamping and/or cutting), to form single layers, a partially assembled layer structure or the completely assembled layer structure, and if necessary subsequently associ
  • the surface features of the hydrogel sheet are preferably provided in a grid or array across the surface of the hydrogel composite.
  • any apertures may preferably be spaced far enough apart from each other to effectively restrict granulation (scab formation) between adjacent apertures when in contact with a wound.
  • the surface features e.g. depressions, apertures, etc.
  • the surface features are preferably tapered so that their external ends are somewhat (e.g. between about 20% and about 1000%) wider than their internal ends.
  • the surface features can preferentially permit fluid flow from the wearer's skin to the absorbent layer of the hydrogel composite, in comparison to the reverse direction. Fluid flow in the reverse direction would tend to close the internal end of the aperture, obstructing the flow. Such a one-way effect assists in preventing leakage of fluid from the absorbent layer of the hydrogel, when in use it functions as a fluid reservoir.
  • the density of the hydrogel composites of the present invention can be selected within a wide range, according to the materials used and the manufacturing conditions. Generally speaking, the bulk density of the total hydrogel composite may be in the range of about 0.05 to about 1.5g/cm 3 , more typically in the range of about 0.3 to about 0.8g/cm 3 .
  • the water activity of the hydrogel composites of the present invention typically lies within the range of 0 to about 0.96, as measured by an AquaLab Series 3TE water activity meter.
  • the water uptake rate of the absorbent layer and the second or any additional continuous parts of the hydrogel composites of the present invention typically lies within the range of at least about 2 ⁇ l/s, more preferably between about 2 and about lOO ⁇ l/s, as measured by the technique of applying a 5 ⁇ l drop of water from a syringe onto the face of the sheet hydrogel and measuring the reduction in volume of the drop over a period of 0.1s starting from contact between the drop and the hydrogel, and extrapolating to a rate expressed as volume per second, the measurements being made using a Scientific and Medical Products DATIlOO dynamic contact angle analyser.
  • a water uptake rate of, say, 25 ⁇ l/s indicates complete absorption of the applied water in 0.2s.
  • the absorption capacity of the hydrogel composite will generally be between about 30% and about 20000%. More typically, the absorption capacity of the hydrogel composite will be between about 300% and about 10000%.
  • the preferred hydrogel composition of the present invention comprises a plasticised three- dimensional matrix of cross-linked polymer molecules, and has sufficient structural integrity to be self-supporting even at very high levels of internal water content, with sufficient flexibility to conform to the surface contours of the human skin.
  • the hydrogel composition preferably has sufficient bioadhesion to adhere to the skin under all skin and moisture conditions likely to be encountered during use.
  • Our PCT Patent Application No. WO-00/45864 describes a method whereby the skin adhesion performance of the hydrogel can be predicted and thereby tailored to particular applications.
  • the hydrogel composites with which the present invention is concerned generally comprise, in addition to the cross-linked polymeric network, an aqueous plasticising medium and, where electrical conductivity is required, at least one electrolyte.
  • the materials and processing methods used are normally chosen to provide a suitable balance of adhesive and electrical properties for the desired application.
  • the hydrogel component material may, for example, be a polymer of one or more ionic and/or non-ionic monomer.
  • a suitable ionic monomer will be water soluble and may be selected from: 2-acrylamido-2- methylpropane sulphonic acid or an analogue thereof or one of its salts (e.g. an ammonium or alkali metal salt such as a sodium, potassium or lithium salts); acrylic acid or an analogue thereof or one of its salts (e.g. an alkali metal salt such as a sodium, potassium or lithium salt); and/or a polymerisable sulphonate or a salt thereof (e.g. an alkali metal salt such as a sodium, potassium or lithium salt), more particularly acrylic acid (3-sulphopro ⁇ yl) ester or an analogue thereof, or a salt thereof.
  • analogue in this context refers particularly to substituted derivatives of 2-acrylamido-2-methylpropane sulphonic acid, of acrylic acid or of acrylic acid
  • a further category of ionic monomer that may be mentioned is a monomer/comonomer pair consisting of a first monomer comprising one or more pendant anionic group and a second monomer comprising one or more pendant cationic group, the relative amounts of the said monomers in the pair being such that the anionic groups and cationic groups are present in essentially equimolar quantities.
  • the said anionic and cationic groups may be selected from groups which are salts of acid groups and groups which are salts of basic groups.
  • the pendant groups in the first monomer are preferably the sodium, potassium, calcium, lithium and/or ammonium (individually or in any combination of one or more) salts of carboxylic acid, phosphoric acid and/or sulphonic acid. Sulphonic acid groups are most preferred.
  • the pendant groups in the second monomer are preferably quaternary ammonium salts of halide (for example chloride), sulphate and/or hydroxide. Chloride and sulphate are most preferred.
  • a particularly preferred ionic monomer is a sodium salt of 2-acrylamido-2-methylpropane sulphonic acid, commonly known as NaAMPS, which is available commercially at present from Lubrizol as either a 50% aqueous solution (reference code LZ2405) or a 58% aqueous solution (reference code LZ2405A) and/or acrylic acid (3-sulphopropyl) ester potassium salt, commonly known as SPA or SPAK.
  • SPA or SPAK is available commercially in the form of a pure solid from Raschig.
  • a suitable non-ionic monomer may preferably be water soluble and be selected from acrylamide or a mono- or di-N-alkylacrylamide or an analogue thereof.
  • analogue in this in this context refers to non-ionic water soluble monomers containing an alkyl or substituted alkyl group linked to a carbon-carbon double bond via an amido or alkylamido (-
  • CO.NH- or -CO.NR- function.
  • Examples of such analogues include diacetone acrylamide (N- l,l-dimethyl-3-oxobutyl-acrylamide), vinyl lactams, N-alkylated acrylamides, N,N-dialkylated acrylamides, N-vinyl pyrrolidone, N-acryloyl morpholine and any mixture thereof (particularly
  • Optional substituents of the monomers used to prepare the hydrogels used in the present invention may preferably be selected from substituents which are known in the art or are reasonably expected to provide polymerisable monomers which form hydrogel polymers having the properties necessary for the present invention.
  • Suitable substituents include, for example, lower (Cl to C6) alkyl, hydroxy, halo and amino groups.
  • cross-linking agents are suitably used to provide the necessary mechanical stability and to control the adhesive properties of the hydrogel.
  • the amount of cross-linking agent required will be readily apparent to those skilled in the art such as from about 0.01% to about 0.5%, particularly from about 0.05% to about 0.4%, most particularly from about 0.08% to about 0.3%, by weight of the total polymerisation reaction mixture.
  • Typical cross-linkers include tripropylene glycol diacrylate, ethylene glycol dimethacrylate, triacrylate, polyethylene glycol diacrylate (polyethylene glycol (PEG) molecular weight between about 100 and about
  • the one or more organic plasticiser when present, may suitably comprise any of the following either alone or in combination: at least one polyhydric alcohol (such as glycerol, polyethylene glycol, or sorbitol), at least one ester derived therefrom, at least one polymeric alcohol (such as polyethylene oxide) and/or at least one mono- or poly-alkylated derivative of a polyhydric or polymeric alcohol (such as alkylated polyethylene glycol).
  • Glycerol is the preferred plasticiser.
  • An alternative preferred plasticiser is the ester derived from boric acid and glycerol.
  • the organic plasticiser may comprise up to about 45% by weight of the hydrogel composition.
  • Any compatible surfactant may optionally be used as an additional ingredient of the hydrogel composition.
  • Surfactants can lower the surface tension of the mixture before polymerisation and thus aid processing.
  • Non-ionic, anionic and cationic surfactants are preferred.
  • the surfactant ideally comprises any of the surfactants listed below either alone or in combination with each other and/or with other surfactants.
  • the total amount of surfactant, if present, is suitably up to about 10% by weight of the hydrogel composition, preferably from about 0.05% to about 4% by weight.
  • Non-ionic Surfactants Suitable non-ionic surfactants include, but are not limited to, those selected from the group consisting of the condensation products of a higher aliphatic alcohol, such as a fatty alcohol, containing about 8 to about 20 carbon atoms, in a straight or branched chain configuration, condensed with about 3 to about 100 moles, preferably about 5 to about 40 moles and most preferably about 5 to about 20 moles of ethylene oxide.
  • a higher aliphatic alcohol such as a fatty alcohol, containing about 8 to about 20 carbon atoms, in a straight or branched chain configuration
  • Examples of such non-ionic ethoxylated fatty alcohol surfactants are the TergitolTM 15-S series from Union Carbide and
  • BrijTM surfactants from ICI. TergitolTM 15-S surfactants include Cn-Ci 5 secondary alcohol polyethyleneglycol ethers. BrijTM 58 surfactant is polyoxyethylene(20) cetyl ether, and BrijTM 76 surfactant is polyoxyethylene(l 0) stearyl ether.
  • non-ionic surfactants include, but are not limited to, those selected from the group consisting of the polyethylene oxide condensates of one mole of alkyl phenol containing from about 6 to 12 carbon atoms in a straight or branched chain configuration, with about 3 to about 100 moles of ethylene oxide.
  • non- ionic surfactants are the IgepalTM CO and CA series from Rhone-Poulenc.
  • IgepalTM CO surfactants include nonylphenoxy poly(ethyleneoxy) ethanols.
  • IgepalTM CA surfactants include octylphenoxy poly(ethyloneoxy) ethanols.
  • non-ionic surfactants include, but are not limited to, those selected from the group consisting of block copolymers of ethylene oxide and propylene oxide or butylene oxide.
  • non-ionic block copolymer surfactants are the Pluronic and TetronicTM series of surfactants from BASF.
  • PluronicTM surfactants include ethylene oxide- propylene oxide block copolymers.
  • TetronicTM surfactants include ethylene oxide-propylene oxide block copolymers.
  • the balance of hydrophobic and hydrophilic components within the surfactant together with the molecular weight are found to be important. Suitable examples are Pluronic L68 and Tetronic 1907. Particularly suitable examples are Pluronic L64 and Tetronic 1107.
  • non-ionic surfactants include, but are not limited to, those selected from the group consisting of sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters and polyoxyethylene stearates.
  • fatty acid ester non- ionic surfactants are the SpanTM, TweenTM, and MyrjTM surfactants from ICI.
  • SpanTM surfactants include Ci 2 -Ci 8 sorbitan monoesters.
  • TweenTM surfactants include poly(ethylene oxide) C 12 -C 18 sorbitan monoesters.
  • MyrjTM surfactants include poly(ethylene oxide) stearates.
  • Anionic surfactants normally include a hydrophobic moiety selected from the group consisting of (about C 6 to about C 2 o) alkyl, alkylaryl, and alkenyl groups and an anionic group selected from the group consisting of sulfate, sulfonate, phosphate, polyoxyethylene sulfate, polyoxyethylene sulfonate, polyoxyethylene phosphate and the alkali metal salts, ammonium salts, and tertiary amino salts of such anionic groups.
  • Anionic surfactants which can be used in the present invention include, but are not limited to. those selected from the group consisting of (about Cg to about C 20 ) alkyl or alkylaryl sulfates or sulfonates such as sodium lauryl sulfate (commercially available as PolystepTM B-3 from Srepan Co.) and sodium dodecyl benzene sulfonate, (commercially available as SiponateTM DS-IO from Rhone-Poulenc); polyoxyethylene (about C 6 to about C 2 o) alkyl or alkylphenol ether sulfates with the ethylene oxide repeating unit in the surfactant below about 30 units, preferably below about 20 units, most preferably below about 15 units, such as PolystepTM B-I commercially available from Stepan Co.
  • alkyl or alkylaryl sulfates or sulfonates such as sodium lauryl sulfate (commercially available as PolystepTM B-3 from Srepan Co
  • Cationic surfactants useful in the present invention include, but are not limited to, those selected from the group consisting of quaternary ammonium salts in which at least one higher molecular weight group and two or three lower molecular weight groups are linked to a common nitrogen atom to produce a cation, and wherein the electrically-balancing anion is selected from the group consisting of a halide (bromide, chloride, etc.), acetate, nitrite, and lower alkosulfate (methosulfate etc.).
  • a halide bromide, chloride, etc.
  • acetate acetate
  • nitrite nitrite
  • lower alkosulfate methosulfate etc.
  • the higher molecular weight substituent(s) on the nitrogen is/are often (a) higher alkyl grou ⁇ (s), containing about 10 to about 20 carbon atoms, and the lower molecular weight substituents may be lower alkyl of about 1 to about 4 carbon atoms, such as methyl or ethyl, which may be substituted, as with hydroxy, in some instances.
  • One or more of the substituents may include an aryl moiety or may be replaced by an aryl, such as benzyl or phenyl.
  • the surfactant comprises at least one propylene oxide/ethylene oxide block copolymer, for example such as that supplied by BASF PIc under the trade name Pluronic P65 or L64.
  • the hydrogel components of the present invention may include one or more additional ingredients, which may be added to the pre-polymerisation mixture or the polymerised product, at the choice of the skilled worker.
  • additional ingredients are selected from additives known in the art, including, for example, water, organic plasticisers, surfactants, polymers, electrolytes, pH regulators, colorants, chloride sources, bioactive compounds, personal and body care agents, and mixtures thereof.
  • the polymers can be natural polymers (e.g. xanthan gum), synthetic polymers (e.g. polyoxypropylene-polyoxyethylene block copolymer or poly-(methyl vinyl ether alt maleic anhydride)), or any combination thereof.
  • bioactive compounds we mean any compound or mixture included within the hydrogel for some effect it has on living systems as opposed to the hydrogel, whether the living system be bacteria or other microorganisms or higher animals such as the intended user of articles incorporating the hydrogel.
  • a biocidal biaoactive compound that may particularly be mentioned is citric acid.
  • Additional polymer(s), typically rheology modifying polymer(s), may be incorporated into the polymerisation reaction mixture at levels typically up to about 10% by weight of total polymerisation reaction mixture, e.g. from about 0.2% to about 10% by weight.
  • Such polymer(s) may include polyacrylamide, poly-NaAMPS, polyethylene glycol (PEG), polyvinylpyrrolidone (PVP) or carboxymethyl cellulose.
  • a particularly preferred application is in the field of biomedical skin electrodes.
  • chloride ions are required to be present in order for the electrode to function.
  • Potassium chloride and sodium chloride are commonly used.
  • any compound capable of donating chloride ions to the system may be used, for example, lithium chloride, calcium chloride, magnesium chloride or ammonium chloride.
  • the amount that should be added is dependent on the electrical properties required and is typically about 0.5-8% by weight.
  • an electrolyte e.g, a salt such as a chloride as mentioned above or another salt such as a nitrate, for example sodium or calcium nitrate
  • an electrolyte e.g, a salt such as a chloride as mentioned above or another salt such as a nitrate, for example sodium or calcium nitrate
  • the composite sheets according to the present invention are used in biomedical electrodes in generally conventional manner, as will be readily understood by those skilled in this art.
  • Such biomedical electrodes may include electrodes (suitably in patch form) for diagnostic, stimulation, therapeutic and electrosurgical use.
  • the hydrogel composites according to the present invention will typically provide good current dispersion over the skin-electrode interface, leading to potential benefits through reduction of electrical hot-spots.
  • bioactive compounds such as antimicrobial agents (e.g. citric acid, stannous chloride), enzymes, compounds providing a heating or cooling sensation to a patient's body, dermatologically active compounds and, for drug delivery applications, pharmaceutically active agents, the latter being designed to be delivered either passively (e.g. transdermally) or actively (e.g. iontophoretically) through the skin.
  • the composites may optionally contain topical, transdermal or iontophoretic agents and excipients.
  • the composites may contain penetration- enhancing agents to assist the delivery of water or active agents into the skin.
  • penetration-enhancing agents for use in such applications include methyl oleic acid, isopropyl myristate, AzoneTM, TranscutolTM and N-methyl pyrrolidone.
  • the additional ingredient may comprise an antimicrobial agent stable against light and radiation, comprising an effective amount of antimicrobial metal (e.g. silver) ions and stabilizing halide (e.g. chloride) ions, wherein the halide is present in an excess (preferably in a substantial molar excess such as around 500-fold excess) with respect to the amount of metal ions.
  • antimicrobial metal e.g. silver
  • stabilizing halide e.g. chloride
  • the hydrogel components of the composites of the present invention preferably consist essentially of a cross-linked hydrophilic polymer of a hydrophilic monomer and optionally one or more comonomer, together with water and/or one or more organic plasticiser, and optionally together with one or more additives selected from surfactants, polymers, pH regulators, electrolytes, chloride sources, bioactive compounds and mixtures thereof, with less than about 10% by weight of other additives.
  • hydrogel composites described herein may suitably be used in a range of skin contact or covering applications where the composite is brought into contact either with skin or with an intermediary member which interfaces between the composite and the skin.
  • the composite may be unsupported or may be supported on a part of a larger article for some specific use, e.g. a support or backing structure.
  • the materials and articles may suitably be in the form of sheets, coatings or membranes.
  • Applications include patches, tapes, bandages, devices and dressings of general utility or for specific uses, including without limitation biomedical, skin care, personal and body care, palliative and veterinary uses such as, for example, skin electrodes for diagnostic (e.g. ECG), stimulation (e.g. TENS), therapeutic (e.g.
  • defibrillation or electrosurgical (e.g. electrocauterisation) use
  • dressings and reservoirs for assisting wound and burn healing, wound and burn management, skin cooling, skin moisturizing, skin warming, aroma release or delivery, decongestant release or delivery, pharmaceutical and drug release or delivery, perfume release or delivery, fragrance release or delivery, scent release or delivery, and other skin contacting devices such as absorbent pads or patches for absorbing body fluids (e.g. lactation pads for nursing mothers), hairpiece adhesives and clothing adhesives; and adhesive flanges and tabs for fecal collection receptacles, ostomy devices and other incontinence devices.
  • body fluids e.g. lactation pads for nursing mothers
  • hairpiece adhesives and clothing adhesives e.g. lactation pads for nursing mothers
  • adhesive flanges and tabs for fecal collection receptacles, ostomy devices and other incontinence devices.
  • the hydrogel composites in accordance with the present invention enable a high degree of water and aqueous fluid retention. This has considerable advantages in certain important applications, for example in the treatment of wounds and burns (where an aqueous environment is advantageous for wound healing and reduced scarring), and in skin care more generally.
  • Figures 1 to 10 illustrate in transverse cross-section the internal layer structure of various absorbent hydrogel materials according to the present invention
  • Figure 11 illustrates in transverse cross-section a starting multi-layer structure from which an alternative absorbent hydrogel material according to the present invention can be formed
  • Figure 12 illustrates in transverse cross-section the step of forming three-dimensional surface features on the structure of Figure 11
  • Figure 13 illustrates in transverse cross-section the absorbent hydrogel material resulting from the step of Figure 12
  • the absorbent hydrogel layer part of the composite is represented by the numeral 1
  • the continuous second hydrogel part by the numeral 2
  • the relatively strong support layer e.g. of polyurethane film or polyurethane film/foam or other non-hydrogel polymer material
  • any additional continuous hydrogel layer by the numeral 4.
  • the illustrated absorbent hydrogel composite sheets consist essentially of:
  • the support layer 3 may optionally (not shown) be of greater dimension that the absorbent hydrogel composite of layer 1 and part 2, in order to create an adhesive bordered overlay, e.g. in a wound or burn dressing.
  • Layer 1 is moulded to create surface features 5 (indentations and ridges), and the hydrogel part 2 is impregnated into the ridge portions of the surface features 5, leaving the absorbent hydrogel material of layer 1 in the indentations effectively exposed to absorb external water from the skin-contacting side (the lower side as drawn).
  • This arrangement is suitably manufactured by letting a liquid pre-gel precursor for 2 infiltrate into the cellular voids of layer 1 in the ridge portions 5, and then curing the pre-gel to form the component 2.
  • FIG 2 as for Figure 1, with additionally an additional relatively non-absorbent layer 4 between layers 1 and 3.
  • Layer 4 is preferably infiltrated into cellular voids in the upper portion of layer 1.
  • the additional layer 4 serves to lock away excess moisture absorbed into the absorbent layer 1 (e.g. excess wound exudate when the composite is used in a wound or burn dressing).
  • the support layer 3 may optionally (not shown) be of greater dimension that the absorbent hydrogel composite of layer 1 and part 2, in order to create an adhesive bordered overlay, e.g. in a wound or burn dressing.
  • Hydrogel part 2 is impregnated as islands into discrete portions of the flat skin-contacting side (the lower side as drawn) of layer 1, leaving intermediate regions of the layer 1 effectively exposed to absorb external water from that side.
  • This arrangement is suitably manufactured by letting a liquid pre-gel precursor for 2 infiltrate into the cellular voids of regions of layer 1 on the lower side as drawn, and then curing the pre-gel to form the component part 2.
  • FIG 4 As for Figure 3, with additionally an additional relatively non-absorbent layer 4 between layers 1 and 3.
  • Layer 4 is preferably infiltrated into cellular voids in the upper portion of layer 1.
  • the additional layer 4 serves to lock away excess moisture absorbed into the absorbent layer 1 (e.g. excess wound exudate when the composite is used in a wound or burn dressing).
  • layer 1, part 2 and layer 3, with layers 1 and 3 optionally associated together via an intermediate adhesive may optionally (not shown) be of greater dimension that the absorbent hydrogel composite of layer 1 and part 2, in order to create an adhesive bordered overlay, e.g. in a wound or burn dressing.
  • the coat weight of the part 2 may suitably be about 200 g/m 2 .
  • the part 2 may optionally contain an internal scrim, as described above.
  • hydrogel part 2 Prior to applying layer 3, hydrogel part 2 is initially infiltrated as a full covering layer over the flat skin-contacting side (the lower side as drawn) of layer 1, and apertures 6 are cut fully through the layers 1 and 2 to create a "foam net", leaving the internal walls of the apertures in the interior of layer 1 effectively exposed to absorb external water from the skin-contacting side. After the through-apertures 6 have been formed, the layer 3 is applied into association with the upper side of layer 1.
  • FIG 6 as for Figure 5, with additionally an additional relatively non-absorbent layer 4 between layers 1 and 3.
  • Layer 4 is preferably infiltrated into cellular voids in the upper portion of layer 1, prior to cutting the aperture, so that the apertures 6 penetrate fully through layers 1, 2 and 4.
  • the additional layer 4 serves to lock away excess moisture absorbed into the absorbent layer 1 (e.g. excess wound exudate when the composite is used in a wound or burn dressing).
  • the support layer 3 may optionally (not .shown) be of greater dimension that the absorbent hydrogel composite of layer 1 and part 2, in order to create an adhesive bordered overlay, e.g. in a wound or burn dressing.
  • Layer 1 is moulded to create surface features 5' (indentations), and the hydrogel part 2 is impregnated and filled (e.g. poured) into the indentations 5', providing a fiat skin-contacting side (the lower side as drawn) and leaving the absorbent hydrogel material of layer 1 between the indentations effectively exposed to absorb external water from that skin-contacting side.
  • This arrangement is suitably manufactured by letting a liquid pre-gel precursor for 2 infiltrate into the cellular voids of layer 1 in the indentations 5', as well as fill the indentations 5', and then curing the pre-gel to form the component 2.
  • Layer 4 is preferably infiltrated into cellular voids in the upper portion of layer 1.
  • the additional layer 4 serves to lock away excess moisture absorbed into the absorbent layer 1 (e.g. excess wound exudate when the composite is used in a wound or burn dressing).
  • layer 1 , part 2 and layer 3, with layers 1 and 3 optionally associated together via an intermediate adhesive (not shown).
  • the support layer 3 may optionally (not shown) be of greater dimension that the absorbent hydrogel composite of layer 1 and part 2, in order to create an adhesive bordered overlay, e.g. in a wound or burn dressing.
  • the coat weight of the part 2 may suitably be about 200 g/m 2 .
  • the part 2 may optionally contain an internal scrim, as described above. Slits 7, optionally linear, curved or a combination, and optionally parallel, non-parallel, randomly oriented, intersecting or any combination thereof (e.g.
  • the support layer 3 may optionally (not shown) be of greater dimension that the absorbent hydrogel composite of layer 1 and part 2, in order to create an adhesive bordered overlay, e.g. in a wound or burn dressing.
  • the coat weight of the part 2 where it is applied may suitably be about 200 g/m 2 .
  • the part 2 may optionally contain an internal scrim, as described above.
  • Hydrogel part 2 is impregnated as islands into discrete portions of the flat skin-contacting side (the lower side as drawn) of layer 1, leaving intermediate openings or apertures which cause the regions of the layer 1 at those places to be effectively exposed to absorb external water from that side. The openings or apertures facilitate the passage of wound exudate or other fluids into the layer 1.
  • This arrangement is suitably manufactured by printing a liquid pre-gel precursor for 2 onto the relevant face of the layer 1 (the lower side as drawn ) so as to infiltrate into the cellular voids of regions of layer 1, and then curing the pre-gel to form the component 2.
  • Figure 11 illustrates in transverse cross-section a starting multi-layer structure from which an alternative absorbent hydrogel material according to the present invention can be formed.
  • This comprises layer 1, part 2 as a layer over substantially the entire lower side of the layer 1 as drawn (the skin-contacting side) and layer 3, with layers 1 and 3 optionally associated together via an intermediate adhesive (not shown).
  • the coat weight of the part 2 may suitably be about 200 g/m 2 .
  • the part 2 may optionally contain an internal scrim, as described above.
  • This arrangement is suitably manufactured by letting a liquid pre-gel precursor for 2 infiltrate into the cellular voids of regions of layer 1 on the lower side as drawn, optionally with the scrim if desired, and then curing the pre-gel to form the part 2 as a layer over substantially the entire lower side of the layer 1
  • part 2 optionally encapsulating with the scrim if desired, can be pre-formed as a layer and laminated to the lower side of layer 1 as drawn, in conventional manner.
  • Figure 12 illustrates in transverse cross-section the step of forming three-dimensional surface features on the structure of Figure 11.
  • a conventional die 8 punches through the layer of hydrogel 2 from the side which is to form the skin-contacting side of the finished product (the lower side as drawn), moving in the direction of the arrows. This punching can optionally take place at the same time as the shape of the desired final article is cut in the sheet.
  • the die 8 is then withdrawn in the reverse direction.
  • Figure 13 illustrates in transverse cross-section the absorbent hydrogel material resulting from the step of Figure 12 after withdrawal of the die.
  • Apertures 9 have been punched through the hydrogel part 2, typically with some local deformation of the surface around the apertures 9. These apertures 9 cause the underlying regions of the layer 1 at those places to be effectively exposed to absorb external water from the skin-contacting side. The openings or apertures facilitate the passage of wound exudate or other fluids into the layer 1.
  • a precursor solution comprising 70 parts by weight of a 58% aqueous solution of the sodium salt of acrylamidomethylpropanesulphonic acid (NaAMPS, LZ2405 Lubrizol), 30 parts glycerol and 0.14 parts of a 1 to 10 (by weight) mixture of Daracure 1173 photoinitiator (Ciba Speciality Chemicals) and IRR280 cross-linker (PEG400 diacrylate, UCB Chemicals) was dispensed from a slot die 120mm wide at a coat weight of 200g/m 2 onto a moving web of a 562B medical grade hydrophilic foam sample from Rynel supported on a web of siliconised paper (Cotek) moving at 7m/s and cured with a NUVA Solo 30 medium pressure mercury arc lamp (GEW).
  • NaAMPS sodium salt of acrylamidomethylpropanesulphonic acid
  • glycerol glycerol
  • IRR280 cross-linker PEG400 diacrylate, UCB Chemical
  • a 1 ml drop of saline was absorbed in less than 5s. Larger volumes of liquid for example 5 to 10 ml absorbed into 40cm 2 of the above hydrogel/foam composite is largely held within the structure such that the liquid cannot be squeezed out. This is not the case when 5 to 10 ml of saline is absorbed into the foam only.
  • a precursor solution comprising 70 parts by weight of a 58% aqueous solution of the sodium salt of acrylamidomethylpropanesulphonic acid (NaAMPS, LZ2405 Lubrizol), 30 parts glycerol and 0.14 parts of a 1 to 10 (by weight) mixture of Daracure 1173 photoinitiator (Ciba Speciality Chemicals) and IRR280 cross-linker (PEG400 diacrylate, UCB Chemicals) was dispensed from a slot die 120mm wide at a coat weight of 450g/m 2 onto a moving web of a 562B medical grade hydrophilic foam sample from Rynel supported on a web of siliconised paper (Cotek) moving at 7m/s and cured with a NUVA Solo 30 medium pressure mercury arc lamp (GEW).
  • NaAMPS sodium salt of acrylamidomethylpropanesulphonic acid
  • glycerol glycerol
  • IRR280 cross-linker PEG400 diacrylate, UCB
  • a 1 ml drop of saline was absorbed in less than 5s. Larger volumes of liquid for example 5 to 10 ml absorbed into 40cm 2 of the above hydrogel/foan ⁇ composite is largely held within the structure such that the liquid cannot be squeezed out. This is not the case when 5 to 10 ml of saline is absorbed into the foam only.
  • the present invention makes available absorbent hydrogels with useful capacity to absorb potentially large quantities of liquids at an acceptable speed for many uses. Moreover, the hydrogels can be made conveniently and efficiently.

Abstract

L'invention concerne un matériau ou article absorbant comprenant une feuille composite d'hydrogel absorbant. La feuille comprend une partie couche absorbante présentant deux faces principales qui comprennent une matrice polymère hydrophile plastifiée souple possédant une structure cellulaire interne, et une seconde partie qui comprend une matrice polymère hydrophile plastifiée souple présentant une structure interne relativement continue. La seconde partie peut être associée à la partie couche de sorte que la seconde partie s'infiltre dans une partie mais pas dans l'ensemble des vides cellulaires de la partie couche absorbante sur une face principale de la partie couche absorbante. Dans une variante, la seconde partie peut être associée à la partie couche de sorte que la seconde partie recouvre une face principale de la partie couche absorbante. Du fait de ladite disposition, une partie, mais pas l'ensemble de la partie couche absorbante, est efficacement exposée pour l'absorption d'eau externe ou d'un autre liquide par le côté de la feuille correspondant à ladite face principale de la couche absorbante.
PCT/GB2006/001218 2006-04-03 2006-04-03 Composites d'hydrogel absorbant WO2007113453A1 (fr)

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WO2010086457A1 (fr) 2009-02-02 2010-08-05 Bsn Medical Gmbh Pansement, son procédé de fabrication et son utilisation pour le soin de plaies
WO2010000450A3 (fr) * 2008-07-03 2010-10-14 Paul Hartmann Ag Pansement à matrice d'hydrogel
US20110280926A1 (en) * 2008-07-03 2011-11-17 Martin Junginger Wound dressing
US8097272B2 (en) 2000-12-07 2012-01-17 Systagenix Wound Management (Us), Inc. Layered materials for use as wound dressings
GB2522178A (en) * 2013-11-12 2015-07-22 First Water Ltd Multilayer composition
US9579413B2 (en) 2009-12-24 2017-02-28 Paul Hartmann Ag Hydrogel matrix having improved adhesive properties

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WO1992003172A1 (fr) * 1990-08-17 1992-03-05 Sebapharma Gmbh & Co. Systeme de pansement
US5846214A (en) * 1996-03-29 1998-12-08 Nichiban Company Limited PVA hydrogel, hydrogel laminate using the same and hydrogel wound-dressing material using the same
WO2000006214A1 (fr) * 1998-07-31 2000-02-10 First Water Limited Compositions bioadhesives et electrodes biomedicales les contenant
GB2369799A (en) * 2000-12-07 2002-06-12 Johnson & Johnson Medical Ltd Layered materials
WO2003077964A1 (fr) * 2002-03-11 2003-09-25 First Water Limited Hydrogels absorbants
WO2003092756A1 (fr) * 2002-04-30 2003-11-13 Her Majesty The Queen, In Right Of Canada, As Represented By The Minister Of National Defence Of Her Majesty's Canadian Government Pansement synthetique a couches multiples et a caracteristiques refroidissantes
WO2004052415A1 (fr) * 2002-12-12 2004-06-24 First Water Limited Compositions d'hydrogels absorbants
EP1658865A1 (fr) * 2004-11-23 2006-05-24 First Water Limited Composites d'hydrogel absorbantes

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Publication number Priority date Publication date Assignee Title
WO1992003172A1 (fr) * 1990-08-17 1992-03-05 Sebapharma Gmbh & Co. Systeme de pansement
US5846214A (en) * 1996-03-29 1998-12-08 Nichiban Company Limited PVA hydrogel, hydrogel laminate using the same and hydrogel wound-dressing material using the same
WO2000006214A1 (fr) * 1998-07-31 2000-02-10 First Water Limited Compositions bioadhesives et electrodes biomedicales les contenant
GB2369799A (en) * 2000-12-07 2002-06-12 Johnson & Johnson Medical Ltd Layered materials
WO2003077964A1 (fr) * 2002-03-11 2003-09-25 First Water Limited Hydrogels absorbants
WO2003092756A1 (fr) * 2002-04-30 2003-11-13 Her Majesty The Queen, In Right Of Canada, As Represented By The Minister Of National Defence Of Her Majesty's Canadian Government Pansement synthetique a couches multiples et a caracteristiques refroidissantes
WO2004052415A1 (fr) * 2002-12-12 2004-06-24 First Water Limited Compositions d'hydrogels absorbants
EP1658865A1 (fr) * 2004-11-23 2006-05-24 First Water Limited Composites d'hydrogel absorbantes

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8097272B2 (en) 2000-12-07 2012-01-17 Systagenix Wound Management (Us), Inc. Layered materials for use as wound dressings
WO2010000450A3 (fr) * 2008-07-03 2010-10-14 Paul Hartmann Ag Pansement à matrice d'hydrogel
US20110280926A1 (en) * 2008-07-03 2011-11-17 Martin Junginger Wound dressing
AU2009265996B2 (en) * 2008-07-03 2014-10-16 Paul Hartmann Ag Wound dressing
US10130521B2 (en) * 2008-07-03 2018-11-20 Paul Hartmann Ag Wound dressing
WO2010086457A1 (fr) 2009-02-02 2010-08-05 Bsn Medical Gmbh Pansement, son procédé de fabrication et son utilisation pour le soin de plaies
US9579413B2 (en) 2009-12-24 2017-02-28 Paul Hartmann Ag Hydrogel matrix having improved adhesive properties
GB2522178A (en) * 2013-11-12 2015-07-22 First Water Ltd Multilayer composition
GB2522178B (en) * 2013-11-12 2018-07-18 First Water Ltd Multilayer composition

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