US2020324021A1PendingUtilityA1

3D Printed Scaffold Structures and Methods of Fabrication

Assignee: UNIV MARYLANDPriority: Apr 11, 2019Filed: Apr 13, 2020Published: Oct 15, 2020
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-modified
What 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.

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