Functionally adapted surfaces on a silicone keratoprosthesis

Citation
S. Langefeld et al., Functionally adapted surfaces on a silicone keratoprosthesis, INT J ARTIF, 22(4), 1999, pp. 235-241
Citations number
21
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology
Journal title
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS
ISSN journal
03913988 → ACNP
Volume
22
Issue
4
Year of publication
1999
Pages
235 - 241
Database
ISI
SICI code
0391-3988(199904)22:4<235:FASOAS>2.0.ZU;2-L
Abstract
Background. Silicone intraocular lenses as well as silicone sponges and enc ircling bands on the bulbar surface are widely used and are well tolerated. The aim of this project is a new one-piece silicone keratoprosthesis with enhanced cell adhesion in the haptic region to optimize the keratoprosthesi s stability. These investigations show how enhanced profileration of conjun ctival fibroblasts and, therefore, improved tissue compatibility can be ach ieved by hydrophilizing and by protein immobilisation on a hydrophobic sili cone surface. This allows a combination of desired chemical and mechanical properties of the silicone bulk material with surfaces of improved tissue c ompatibility. Methods. Silicone foils with surface modifications of different kinds were tested. Experiments were done using cell cultures with murine fibroblasts L -929 and human conjuctival fibroblasts. Cytotoxicity assays were carried ou t with cells grown on the material in direct contact, as well as in indirec t contact, with extracts (EN 30993-5). Viability stains by means of fluores ceindiacetate and ethidiumbromide together with morphology analyses by hema laun-staining were performed. Results. For the unmodified and modified foils themselves and their extract s any negative influence on cell cultures of murine and human cells could b e excluded. There was a gradual improvement of cell morphology, spreading a nd proliferation dependent on the degree of surface modification. Covalentl y immobilised fibronectin showed the best results in contrast to adsorptive binding. Conclusions. Silicone surfaces can be modified chemically with bioactive pr oteins. These modifications are cell compatible and do not result in toxic reactions. The degree and type of silicone hydrophilization results in impr oved development of cell morphology, spreading and proliferation. Even bett er results are obtained after covalent binding of bioactive proteins like f ibronectin. Improved biocompatibility with enhanced cellular overgrowth has been demonstrated in vitro for the modified silicone of the haptic region. We believe that this type of modification will help in reducing extrusion problems observed with former keratoprostheses.