TY - JOUR
T1 - Development and characterization of a biomimetic coating for percutaneous devices
AU - Trent, Alexis
AU - Van Dyke, Mark E.
N1 - Funding Information:
The authors would like to thank the following funding sources: Department of Defense Congressionally Directed Medical Research Programs (CDMRP) , grant number W81XWH-15-1-0343 ; and Virginia Tech-Initiative for Maximizing Student Development (IMSD) , grant number R25GM072767-10 . We also thank Dr. Alan Esker and Candace Wall for access and training on the goniometer. We provide thanks to undergraduates Kevin Tong, Aaron Giuffre, and Kyle Brown for assisting on this project. In addition, we thank Stephen McCartney and Jay Tuggle for training on the AFM and XPS respectively, and access to the Nanoscale Characterization and Fabrication Lab (NCFL). The authors are also thankful to the Van Dyke lab group, in particular Michele Waters, Marc Thompson, and Nils Potter for their assistance, and our grant collaborators, Dr. Sujee Jeyapalina, and Brian Bennett at the University of Utah for assistance in implementing the HaCaT cell assays, involucrin staining technique, and providing the HaCaT cells.
Funding Information:
The authors would like to thank the following funding sources: Department of Defense Congressionally Directed Medical Research Programs (CDMRP), grant number W81XWH-15-1-0343; and Virginia Tech-Initiative for Maximizing Student Development (IMSD), grant number R25GM072767-10. We also thank Dr. Alan Esker and Candace Wall for access and training on the goniometer. We provide thanks to undergraduates Kevin Tong, Aaron Giuffre, and Kyle Brown for assisting on this project. In addition, we thank Stephen McCartney and Jay Tuggle for training on the AFM and XPS respectively, and access to the Nanoscale Characterization and Fabrication Lab (NCFL). The authors are also thankful to the Van Dyke lab group, in particular Michele Waters, Marc Thompson, and Nils Potter for their assistance, and our grant collaborators, Dr. Sujee Jeyapalina, and Brian Bennett at the University of Utah for assistance in implementing the HaCaT cell assays, involucrin staining technique, and providing the HaCaT cells.
Publisher Copyright:
© 2019 Elsevier B.V.
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Percutaneous osseointegrated prosthetics (POP), which consist of a metallic post attached to the bone that extends outward through the skin to connect to an external prosthesis, have become a clinically relevant option to replace the typical socket-residual limb connection. POP devices offer several advantages such as mechanical off-loading of soft tissues, direct force transfer to the musculoskeletal system, greater proprioception, and overall improvement in limb kinesis compared to a socket system. However, POP devices create several challenges including epidermal downgrowth, increased infection risk, and mechanical tearing at the skin-implant interface. To address these issues, biomimetic surfaces and coatings have been developed in an attempt to create an infection-free and cohesive interface between POP devices and skin. The fingernail is a prime example of a natural system with a skin interface that is both mechanically and biologically stable. Exploiting keratins’ previously demonstrated tissue compatibility and creating a biomimetic coating for POP devices that can imitate the human fingernail, and demonstrating its ability to promote a stable interface with skin tissue is the goal of this work. Silane coupling aided in producing a coating on titanium substrates consisting of human keratin proteins. Several combinations of silane and keratin derivatives were investigated, and in general showed a nano-scale coating thickness that supported skin cell (i.e. fibroblast and keratinocyte) adhesion. Initial enzyme-mediated degradation resistance was also demonstrated, but the coatings appeared to degrade at long time periods. Importantly, keratinocytes showed a stable phenotype with no indication of wound healing-like activity. These data provide justification to further explore keratin biomaterials for POP coatings that may stabilize the implant-skin interface.
AB - Percutaneous osseointegrated prosthetics (POP), which consist of a metallic post attached to the bone that extends outward through the skin to connect to an external prosthesis, have become a clinically relevant option to replace the typical socket-residual limb connection. POP devices offer several advantages such as mechanical off-loading of soft tissues, direct force transfer to the musculoskeletal system, greater proprioception, and overall improvement in limb kinesis compared to a socket system. However, POP devices create several challenges including epidermal downgrowth, increased infection risk, and mechanical tearing at the skin-implant interface. To address these issues, biomimetic surfaces and coatings have been developed in an attempt to create an infection-free and cohesive interface between POP devices and skin. The fingernail is a prime example of a natural system with a skin interface that is both mechanically and biologically stable. Exploiting keratins’ previously demonstrated tissue compatibility and creating a biomimetic coating for POP devices that can imitate the human fingernail, and demonstrating its ability to promote a stable interface with skin tissue is the goal of this work. Silane coupling aided in producing a coating on titanium substrates consisting of human keratin proteins. Several combinations of silane and keratin derivatives were investigated, and in general showed a nano-scale coating thickness that supported skin cell (i.e. fibroblast and keratinocyte) adhesion. Initial enzyme-mediated degradation resistance was also demonstrated, but the coatings appeared to degrade at long time periods. Importantly, keratinocytes showed a stable phenotype with no indication of wound healing-like activity. These data provide justification to further explore keratin biomaterials for POP coatings that may stabilize the implant-skin interface.
KW - Biomimetic
KW - Coating
KW - Keratin
KW - Osseointegrated
KW - Percutaneous
KW - Prosthetic
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UR - http://www.scopus.com/inward/citedby.url?scp=85069605955&partnerID=8YFLogxK
U2 - 10.1016/j.colsurfb.2019.110351
DO - 10.1016/j.colsurfb.2019.110351
M3 - Article
C2 - 31326624
AN - SCOPUS:85069605955
VL - 182
JO - Colloids and Surfaces B: Biointerfaces
JF - Colloids and Surfaces B: Biointerfaces
SN - 0927-7765
M1 - 110351
ER -