Supple tissue dressing assemblies, systems, and methods formed from hydrophilic polymer sponge structures such as chitosan
Supple tissue dressing assemblies are formed from hydrophilic polymer sponge structures, such as chitosan. The supple tissue dressing assemblies are characterized by suppleness or multi-dimensional flexibility. The assemblies can be flexed, bent, folded, twisted, and even rolled upon itself before and during use, without creasing, cracking, fracturing, otherwise compromising the integrity and mechanical and/or therapeutic characteristics of the assemblies.
1 . A supple sponge structure adapted for placement in contact with animal tissue comprising a biocompatible hydrophilic polymer solution that has undergone phase separation by freezing and drying into a form, the form having, when dry, a Gurley stiffness value (in units of milligrams) of not greater than about 5000.
2 . A supple sponge structure according to claim 1 , wherein the form has, when dry, a Gurley stiffness value (in units of milligrams) of not greater than about 2000.
3 . A supple sponge structure according to claim 2 , wherein the form has, when dry, a dry suppleness-to strength ratio of not greater than about 210, the dry suppleness-to-strength ratio comprising a ratio between the Gurley stiffness value (in units of milligrams) and tensile strength (in units of Newtons).
4 . A supple sponge structure according to claim 1 , wherein the form has, when dry, a Gurley stiffness value (in units of milligrams) of not greater than about 1000.
5 . A supple sponge structure according to claim 4 , wherein the form has, when dry, a dry suppleness-to strength ratio of not greater than about 210, the dry suppleness-to-strength ratio comprising a ratio between the Gurley stiffness value (in units of milligrams) and tensile strength (in units of Newtons).
6 . A supple sponge structure according to claim 1 , wherein the form has, when dry, having an initial sponge density that is, after drying, increased to a densified sponge density by application of mechanical pressure.
7 . A supple sponge structure according to claim 6 , wherein the densified sponge density comprises about 0.1 g/cm 3 to about 0.5 g/cm 3 .
8 . A supple sponge structure according to claim 7 , wherein the densified sponge density comprises about 0.2 g/cm 3 .
9 . A supple sponge structure according to claim 6 , wherein the form has, when dry, a dry suppleness-to-density ratio of not greater than about 50,000, the dry suppleness-to-density ratio comprising a ratio between the Gurley stiffness value (in units of milligrams) and the densified sponge density (in units of g/cm 3 ).
10 . A supple sponge structure according to claim 9 , wherein the dry suppleness-to-density ratio is not greater than about 20,000.
11 . A supple sponge structure according to claim 9 , wherein the dry suppleness-to-density ratio is not greater than about 10,000.
12 . A supple sponge structure according to claim 1 , wherein the form, when dry, has a sponge thickness of not greater than about 8 mm.
13 . A supple sponge structure according to claim 1 , wherein the form, when dry, has an initial sponge thickness of not greater than about 8 mm that is, after drying, increased to a densified sponge thickness of about 0.1 g/cm 3 to about 0.5 g/cm 3 by application of mechanical pressure.
14 . A supple sponge structure according to claim 1 , wherein the form, after drying, is subject to a mechanical softening process.
15 . A supple sponge structure according to claim 1 , wherein the biocompatible hydrophilic polymer solution comprises a chitosan material.
16 . A method comprising
providing a supple sponge structure as defined in claim 1 , and
placing the supple sponge structure in contact with animal tissue.
17 . A method of making the supple sponge structure as defined in claim 1 comprising
providing the biocompatible hydrophilic polymer solution,
phase separating the hydrophilic polymer solution into the form by freezing from a room temperature to a freezing temperature at an overall cooling rate that is less than about 0.5° C./min, and drying the form.
18 . A supple sponge structure adapted for placement in contact with animal tissue comprising a biocompatible hydrophilic polymer solution that has undergone phase separation by freezing and drying into a form, the form having, when dry, a resistance to flexure expressed as a Gurley stiffness value (in units of milligrams), a tensile strength (in units of Newtons), and dry suppleness-to strength ratio comprising a ratio between Gurley stiffness value and the tensile strength, the dry suppleness-to-strength ratio being not greater than about 210.
19 . A supple sponge structure according to claim 18 , wherein the form has, when dry, having an initial sponge density that is, after drying, increased to a densified sponge density of between about 0.1 g/cm 3 and about 0.5 g/cm 3 by application of mechanical pressure.
20 . A supple sponge structure according to claim 18 , wherein the form, after drying, is subject to a mechanical softening process.
21 . A supple sponge structure according to claim 18 , wherein the biocompatible hydrophilic polymer solution comprises a chitosan material.
22 . A method comprising
providing a supple sponge structure as defined in claim 18 , and
placing the supple sponge structure in contact with animal tissue.
23 . A method of making the supple sponge structure as defined in claim 18 comprising
providing the biocompatible hydrophilic polymer solution,
phase separating the hydrophilic polymer solution into the form by freezing from a room temperature to a freezing temperature at an overall cooling rate that is less than about 0.5° C./min, and drying the form.
24 . A supple sponge structure adapted for placement in contact with animal tissue comprising a biocompatible hydrophilic polymer solution that has undergone phase separation by freezing and drying into a form, the form having, when dry, a resistance to flexure expressed as a Gurley stiffness value (in units of milligrams), the form further having, when dry, an initial sponge density that is, after drying, increased to a densified sponge density of between about 0.1 g/cm 3 and about 0.5 g/cm 3 by application of mechanical pressure, the form further having, when dry, a dry stiffness-to-strength ratio of not greater than about 50,000, the dry suppleness-to-density ratio comprising a ratio between the Gurley stiffness value (in units of milligrams) and the densified sponge density (in units of g/cm 3 ).
25 . A supple sponge structure according to claim 24 , wherein the dry suppleness-to-density ratio is not greater than about 20,000.
26 . A supple sponge structure according to claim 24 , wherein the dry suppleness-to-density ratio is not greater than about 10,000.
27 . A supple sponge structure according to claim 24 , wherein the form, after drying, is subject to a mechanical softening process.
28 . A supple sponge structure according to claim 24 , wherein the biocompatible hydrophilic polymer solution comprises a chitosan material.
29 . A method comprising
providing a supple sponge structure as defined in claim 24 , and
placing the supple sponge structure in contact with animal tissue.
30 . A method of making the supple sponge structure as defined in claim 24 comprising
providing the biocompatible hydrophilic polymer solution,
phase separating the hydrophilic polymer solution into the form by freezing from a room temperature to a freezing temperature at an overall cooling rate that is less than about 0.5° C./min, and drying the form.
31 . A supple sponge structure adapted for placement in contact with animal tissue comprising a biocompatible hydrophilic polymer solution that has undergone phase separation by freezing and drying into an initial form having, after drying, a width and a length, the initial form being characterized by a suppleness that allows rolling the initial form upon itself without fracture into a roll form having a diameter less than either the width or the length.
32 . A supple sponge structure according to claim 31 , wherein the initial form has thickness of between 0.25 mm and about 4 mm.
33 . A supple sponge structure according to claim 32 , wherein the initial form has a thickness of about 0.9 mm.
34 . A supple sponge structure according to claim 31 , wherein the initial form, after drying, is subject to a mechanical softening process.
35 . A supple sponge structure according to claim 31 , wherein the biocompatible hydrophilic polymer solution comprises a chitosan material.
36 . A method comprising
providing a supple sponge structure as defined in claim 31 , and
placing the supple sponge structure in contact with animal tissue.
37 . A method of making the supple sponge structure as defined in claim 31 comprising
providing the biocompatible hydrophilic polymer solution,
phase separating the hydrophilic polymer solution into the initial form by freezing from a room temperature to a freezing temperature at an overall cooling rate that is less than about 0.5° C./min, and drying the initial form.
38 . A supple sponge structure adapted for placement in contact with animal tissue comprising a biocompatible hydrophilic polymer solution that has undergone phase separation by freezing into a form from room temperature to a freezing temperature at an overall cooling rate that is less than about 0.5° C./min.
39 . A supple sponge structure according to claim 38 , wherein, after freezing and drying, the form has an initial density that is compressed to an increased density by application of mechanical pressure.
40 . A supple sponge structure according to claim 38 , wherein, after phase separation and drying, the form has an initial density that is compressed to an increased density of about 0.1 g/cm 3 to about 0.5 g/cm 3 .
41 . A supple sponge structure according to claim 38 , wherein the form, after phase separation and drying, is mechanically softened.
42 . A supple sponge structure according to claim 38 , wherein the form, after phase separation and drying, comprises a resistance to flexure, measured in Gurley Units (in milligrams), that is less than about 5000.
43 . A supple sponge structure according to claim 38 , wherein the form comprises a structure formed by a combined spherulitic and lamella nucleation of crystalline ice.
44 . A supple sponge structure according to claim 38 , wherein the form, after drying, is compressed by application of mechanical pressure to a thickness of about 0.9 mm.
45 . A supple sponge structure as defined in claim 38 , wherein the biocompatible hydrophilic polymer solution comprises chitosan.
46 . A method comprising
providing a supple sponge structure as defined in claim 38 , and
placing the supple sponge structure in contact with animal tissue.
47 . A method of making a supple sponge structure adapted for placement in contact with animal tissue comprising
providing a biocompatible hydrophilic polymer solution,
phase separating the hydrophilic polymer solution into a form by freezing from a room temperature to a freezing temperature at an overall cooling rate that is less than about 0.5° C./min, and drying the form.