Thin film
US-2024352668-A1 · Oct 24, 2024 · US
US12576181B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12576181-B2 |
| Application number | US-201916548402-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 22, 2019 |
| Priority date | Jun 16, 2009 |
| Publication date | Mar 17, 2026 |
| Grant date | Mar 17, 2026 |
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The present invention provides a hemostatic porous sponge comprising a matrix of a fibrous biomaterial and particles of a fluid absorbing, particulate material adhered to said matrix material, a method of producing these sponges and their use for wound healing.
Opening claim text (preview).
The invention claimed is: 1 . A hemostatic porous sponge having a first, injury-facing side, and an oppositely disposed second side, the hemostatic porous sponge comprising: a fibrous biomaterial matrix formed of a fibrous biomaterial comprising gelatin or collagen, the fibrous biomaterial matrix being present in an amount of 1% to 50% of the porous sponge in a dried state (w/w %); an adhesive layer continuously coated on the first, injury-facing side of the sponge, the adhesive layer comprising a cross-linkable synthetic polymer comprising succinimidyl groups; and a supporting layer provided on the second side of the sponge, the supporting layer being an active hemostatic layer having a greater tensile strength than the fibrous biomaterial matrix, wherein the sponge is configured to absorb fluid from a site of injury. 2 . The sponge according to claim 1 , wherein said adhesive layer comprises a bioresorbable polymer. 3 . The sponge according to claim 1 , wherein the adhesive layer further comprises a cross-linkable component that cross-links with the synthetic polymer comprising succinimidyl groups under reaction enabling conditions. 4 . The sponge according to claim 1 being freeze-dried or air-dried. 5 . The sponge according to claim 1 , wherein said supporting layer comprises a bioresorbable polymer. 6 . The sponge according to claim 1 , wherein said supporting layer has a greater density than the matrix material. 7 . The sponge according to claim 1 , wherein the polymer is a hydrophilic polymer. 8 . The sponge according to claim 1 , wherein the adhesive layer comprises only one synthetic polymer. 9 . The sponge according to claim 1 , wherein the polymer comprises active side groups for cross-linking and adherence to a tissue. 10 . A method of treating an injury comprising administering a hemostatic porous sponge to a site of injury, the hemostatic porous sponge having a first, injury-facing side, and an oppositely disposed second side and comprising: a matrix of a fibrous biomaterial comprising gelatin or collagen; an adhesive layer continuously coated on a first injury facing side of the sponge, the adhesive layer comprising a synthetic polymer comprising succinimidyl groups; and a supporting layer provided on the second side of the sponge, the supporting layer being an active hemostatic layer having a greater tensile strength than the fibrous biomaterial matrix, wherein the sponge is configured to absorb fluid from the site of injury. 11 . The method according to claim 10 , wherein said injury comprises a wound, a hemorrhage, damaged tissue and/or bleeding tissue. 12 . The method according to claim 10 , wherein the polymer is a hydrophilic polymer. 13 . The method according to claim 10 , wherein the adhesive layer comprises only one synthetic polymer. 14 . The method according to claim 10 , wherein the polymer comprises active side groups for cross-linking and adherence to a tissue. 15 . A hemostatic porous sponge having a first, injury-facing side, and an oppositely disposed second side, the hemostatic porous sponge comprising: a fibrous biomaterial matrix formed of a fibrous biomaterial comprising gelatin or collagen, the fibrous biomaterial matrix being present in an amount of 1% to 50% of the porous sponge in a dried state (w/w %); and an adhesive layer consisting of a first cross-linkable component and a second cross-linkable component configured to cross-link with the first cross-linkable component under reaction enabling conditions.
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