## Abstract Percutaneous medical devices are integral in the management and treatment of disease. The space created between the skin and the device becomes a haven for bacterial invasion and biofilm formation and results in infection. We hypothesize that sealing this space via integration of the sk
A model for studying epithelial attachment and morphology at the interface between skin and percutaneous devices
β Scribed by Negar G. Knowles; Yuko Miyashita; Marcia L. Usui; Andrew J. Marshall; Annalisa Pirrone; Kip D. Hauch; Buddy D. Ratner; Robert A. Underwood; Philip Fleckman; John E. Olerud
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 172 KB
- Volume
- 74A
- Category
- Article
- ISSN
- 1549-3296
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β¦ Synopsis
Abstract
Percutaneous devices are indispensable in modern medicine, yet complications from their use result in significant morbidity, mortality, and cost. Bacterial biofilm at the device exit site accounts for most infections in shortβterm devices. We hypothesize that advanced biomaterials can be developed that facilitate attachment of skin cells to percutaneous devices, forming a seal to preclude bacterial invasion. To study the skin/biomaterial interface systematically, we first identified biomaterials with physical properties compatible with histological processing of skin. Second, we developed an organ culture system to study skin response to implants. Organ cultures implanted with porous poly(2βhydroxyethyl methacrylate) [poly(HEMA)] or polytetrafluoroethylene (PTFE) could easily be evaluated histologically with preservation of the skin/biomaterial interface. Epithelial cells migrated down the cut edges of the biomaterial in a pattern seen in marsupialization of percutaneous devices in vivo. This in vitro model maintains skin viability and allows histologic evaluation of the skin/biomaterial interface, making this a useful, inexpensive testβbed for studies of epidermal attachment to modified biomaterials. Β© 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2005
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