Absorbable implant materials having controlled porosity
AssigneeJohnson & Johnson Medical, Inc.
InventorsJames McGregor, Paul W. Watt, Nicholas D. Light, Wilson Harvey
Life of this patent
Estimating the term…
Loading patent…
AssigneeJohnson & Johnson Medical, Inc.
InventorsJames McGregor, Paul W. Watt, Nicholas D. Light, Wilson Harvey
Estimating the term…
Absorbable implant materials having controlled porosity are formed by a method comprising the steps of: providing a dispersion of a bioabsorbable polymer, such as collagen, in a first solvent, such as water; adding particles of a second material, e.g. frozen water droplets or ice particles to the dispersion; followed by freezing the dispersion to form a frozen dispersion having the particles embedded therein, and removing both the first solvent and the second material from the frozen dispersion by freeze-drying or solvent extraction to leave the porous implant material. The invention also encompasses the use of such implant materials for wound healing applications.
A method of making a bioabsorbable material having interconnecting pores comprising the steps of:
Dependencies are inferred from the claim text.
No related US applications are recorded in the indexed filing history.
Drawings are temporarily unavailable. Open the PDF at USPTO
Materials characterised by their function or physical properties , e.g. injectable or lubricating compositions, shape-memory materials, surface…:…
Use of materials characterised by their function or physical properties: porous materials, e.g. foams or sponges
Use of materials characterised by their function or physical properties: specially adapted to be resorbable inside the body
Materials characterised by their function or physical properties , e.g. injectable or lubricating compositions, shape-memory materials, surface…:…
Term ended 28 May 2016 (estimated)
USPTO file history isn’t available for this patent, so only indexed dates are shown.
The present invention relates to bioabsorbable materials having controlled porosity. The materials are especially suitable for use as implants or dressings in wound healing applications.
A number of attempts have been made to fashion solid, bioabsorbable implant and/or dressing materials for application to wounds to protect the wounds and assist wound healing and tissue regeneration.
A solid wound implant material should preferably include the properties of gradual, controllable degradation and absorption in situ as the wound heals, low antigenicity, mechanical strength, conformability, and optimised porosity. The controlled porosity is important because the healing of wounds depends on the production by the wound of substantial quantities of matrix materials and granulation tissue involving the migration of fibroblast cells and connective tissue into the implant.
Specific embodiments of the present invention will now be described further, by way of example, with reference to the accompanying figures, in which:
FIG. 1 shows a scanning electron micrograph of a collagen sponge implant material obtained by a prior art method;
FIG. 2 shows a scanning electron micrograph, on the same scale as FIG. 1, of a collagen sponge implant obtained by a process according to the present invention;
Fibrous collagen was obtained from bovine hides in pure form as an insoluble slurry in water, as described in U.S. Pat. No. 4,320,201 and U. Pat. No. 3,823,212, the entire contents of which are hereby expressly incorporated by reference. The fibrous slurry is made basic with sodium hydroxide to pH 9.0, and water is added to adjust the solids concentration to 5% by weight.
The aqueous dispersion of collagen fibers is then diluted to 0.5% solids. A cross-linker, HMDI (hexamethylene diisocyanate), is added in an amount corresponding to 5%by weight of the collagen in the dispersion with mixing, and the mixture is then snap frozen in a blast freezer. The frozen dispersion is then dried by freeze drying under standard conditions.
A cross-section through a collagen sponge made in this way is shown in FIG. 1. It can be seen that the sponge comprises interconnected pores. The median pore size is approximately 0.1 mm.