Long-term clinical results of vessels treated with coronary stents to date show that restenosis still occurs frequently. Despite enormous progress in stent design, stent surfaces and the use of drug-eluting stents, the overall incompatibility of the implant with the vessel wall cells is too high.
The project aims to prevent leukocyte-endothelial cell adhesion, a key mechanism of restenosis. This will be achieved by temporally and spatially restricted, specific reduction of the surface receptors ICAM1, VCAM1, and E-selectin on endothelial cells using RNAi-based specific receptor knockdown. The siRNA envisaged in the project already showed very good receptor knock-down results in vitro.
For therapeutic success, continuous RNAi transfection of endothelial cells in vivo for several weeks is additionally required. To achieve this goal, cell-compatible, controllable drug transporters must be developed. These will simultaneously serve to stabilize RNA in blood and improve transfection efficiency, i.e., RNA uptake and action in cells.
In addition, the project calls for the first development of a coronary stent that can prevent the development of restenosis by controlled release of stabilized, complexed RNA over several weeks. This approach would be more effective and gentle than currently used therapies.
To optimize all of these steps, the project was divided into technological areas to allow simultaneous optimization by the project partners:
The combination of individually optimized modules should enable rapid establishment of the RNA stent as a product. The knowledge gained from the optimizations of the individual modules should also enable the rapid adaptation of the RNA stent assembly to therapeutic requirements.
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Summary: During the course of the project, new stent designs were investigated and first functional samples were produced. By reducing surface charges, the aggregation of the RNA nanoparticles could be greatly reduced and the uptake into the cell improved. While maintaining the stability of the RNA nanoplexes, the release of RNA into cells could be significantly improved, thereby increasing the transfection efficiency in endothelial cells. Different layer systems for immobilization and time-controlled release of RNA nanoplexes could be established. Analytical methods for the measurement of layer formation and degradation were established.