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.