DocumentCode
2748457
Title
Molecularly engineered hydrogels for implant biocompatibility
Author
Abraham, Sheena ; Brahim, Sean ; Guiseppi-Elie, Anthony
Author_Institution
Center for Bioelectronics, Biosensors & Biochips, Virginia Commonwealth Univ., Richmond, VA, USA
Volume
2
fYear
2004
fDate
1-5 Sept. 2004
Firstpage
5036
Lastpage
5039
Abstract
The biocompatibility of biosmart polymer membranes synthesized from cross-linkable (2-hydroxyethyl methacrylate) (HEMA) and tetraethylene glycol diacrylate and containing different mole-percent polyethylene glycol methacrylate (PEGMA) and methacryloyloxyethyl phosphorylcholine (MPC), a phosphorylcholine-containing co-monomer, was investigated. The cytotoxicity (cell viability and proliferation) and the adhesion of extra cellular matrix proteins to these hydrogel surfaces were separately tested. Cell proliferation assays were conducted by cultivating human skeletal muscle fibroblasts onto the surfaces of these polymeric membranes prepared by in-situ polymerization in chemically derivatized 8-well cell-culture plates. The compositions containing MPC and PEGMA concentrations greater than 1.0 and 0.05 mole% respectively demonstrated good protein adhesion and cell viability (>90%) of human muscle fibroblast cells. Morphological deviances and partial colonization of the hydrogel surface has been noticed and suggests good compatibility of hydrogels for cellular viability but restricted proliferation. It is well known that the adsorption of proteins onto biomaterial surfaces modulates the cellular interaction with these surfaces. The extent of adsorption of fluorescein labeled proteins (laminin, collagen, and fibronectin) onto these polymer membrane surfaces was evaluated by measuring the resultant fluorescence intensity using a confocal fluorescence scanner.
Keywords
adhesion; biomedical materials; cellular biophysics; fluorescence; membranes; molecular biophysics; polymer gels; polymerisation; proteins; biomaterial surfaces; biosmart polymer membranes; cell proliferation; cell viability; collagen; confocal fluorescence scanner; cross-linkable (2-hydroxyethyl methacrylate); cytotoxicity; extracellular matrix protein adhesion; fibronectin; fluorescein labeled proteins; fluorescence intensity; human skeletal muscle fibroblasts; implant biocompatibility; in-situ polymerization; laminin; methacryloyloxyethyl phosphorylcholine; molecularly engineered hydrogels; polyethylene glycol methacrylate; tetraethylene glycol diacrylate; Adhesives; Biomembranes; Fibroblasts; Fluorescence; Humans; Implants; Muscles; Polymers; Proteins; Surface morphology; Biocompatibility; Biosmart polymers; Cell Proliferation; Hydrogels; Implantable materials; Protein Adsorption;
fLanguage
English
Publisher
ieee
Conference_Titel
Engineering in Medicine and Biology Society, 2004. IEMBS '04. 26th Annual International Conference of the IEEE
Conference_Location
San Francisco, CA
Print_ISBN
0-7803-8439-3
Type
conf
DOI
10.1109/IEMBS.2004.1404392
Filename
1404392
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