US2020324021A1PendingUtilityA1
3D Printed Scaffold Structures and Methods of Fabrication
Est. expiryApr 11, 2039(~12.7 yrs left)· nominal 20-yr term from priority
B33Y 70/10A61L 27/58A61L 27/3813A61L 27/54A61L 2430/04A61L 27/60A61L 27/52B33Y 70/00B29L 2031/7532B33Y 80/00B33Y 10/00B29C 64/112A61L 2430/34A61L 27/26B29K 2995/0056A61L 27/3641A61L 2300/414B29K 2105/0061A61L 2300/41A61L 2300/406A61F 2/186
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Claims
Abstract
An implantable scaffold device comprises a non-biodegradable backbone and a biodegradable dermal compartment comprising live cells. Method of fabricating implantable devices via 3D printing using a synthetic ink formulation coprinted with a biodegradable bioink.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . An implantable scaffold device comprising a non-biodegradable support portion and a biodegradable dermal portion.
2 . The scaffold device of claim 1 , wherein said support portion comprises a first hydrogel and said dermal portion comprises a second hydrogel.
3 . The scaffold device of claim 2 , wherein said first hydrogel comprises a polymer material selected from the group consisting of a polyether, a polyacrylamide, a polyvinyl, a polyacrylate, and mixtures thereof.
4 . The scaffold device of claim 1 , wherein said dermal portion comprises a biopolymer.
5 . The scaffold device of claim 4 , wherein said biopolymer is selected from the group consisting of collagen, gelatin, silk fibroin, fibrin, elastin, chitosan, hyaluronic acid, and alginate.
6 . The scaffold device of claim 4 , wherein said dermal portion comprises gelatin methacrylate. The scaffold device of claim 1 , wherein said dermal portion comprises autologous cells of a subject.
8 . The scaffold device of claim 1 , wherein said scaffold is fabricated via three-dimensional (3D) printing.
9 . The scaffold device of claim 1 , wherein said dermal portion further comprises a population of fibroblasts and/or a population of keratinocytes.
10 . The scaffold device of claim 1 , further comprising an epidermal portion, said support portion intermediate said epidermal portion and said dermal portion.
11 . The scaffold device of claim 10 , wherein said epidermal portion comprises a population of keratinocytes.
12 . The scaffold device of claim 10 , wherein said epidermal portion comprises a therapeutic agent.
13 . The scaffold device of claim 12 , wherein said therapeutic agent is selected from the group consisting of an antibiotic, an anti-inflammatory, a proangiogenic, and a growth hormone.
14 . The scaffold device of claim 1 , which is a nipple-areola complex implant.
15 . A method of 3D printing an implantable scaffold device, comprising the step of coprinting a non-biodegradable support portion using a synthetic ink formulation and a biodegradable dermal portion using a biodegradable bioink formulation.
16 . The method of claim 15 , wherein said synthetic ink formulation comprises a polymer material selected from the group consisting of a polyether, a polyacrylamide, a polyvinyl, a polyacrylate, and mixtures thereof
17 . The method of claim 15 , wherein said bioink formulation comprises a biopolymer selected from the group consisting of collagen, gelatin, silk fibroin, fibrin, elastin, chitosan, hyaluronic acid, and alginate.
18 . The method of claim 15 , wherein said synthetic ink formulation comprises a thickener.
19 . The method of claim 15 , wherein said bioink formulation comprises a population of fibroblasts and/or a population of keratinocytes.
20 . The method of claim 15 , wherein said implantable scaffold device is configured as a nipple-areola complex.Join the waitlist — get patent alerts
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