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Updated: May 15, 2026

Vascular Gene Transfer from Metallic Stent Surfaces Using Adenoviral Vectors Tethered through Hydrolysable Cross-linkers
Published on: August 12, 2014
Bioactive coronary stent coating based on layer-by-layer technology for siRNA release.
S Hossfeld1, A Nolte, H Hartmann
1NMI-Natural and Medical Sciences Institute at the University of Tuebingen, Reutlingen, Germany.
This study developed drug-eluting stents with small interfering RNA (siRNA) nanoplexes using layer-by-layer technology for improved vascular regeneration. The innovative stent coatings demonstrated effective siRNA delivery to cells and artery walls with good hemocompatibility.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Cardiovascular Research
Background:
- Percutaneous transluminal coronary angioplasty (PTCA) is used to treat stenotic coronary arteries.
- Drug-eluting stents (DESs) improve outcomes but can be enhanced for better vascular regeneration.
- Small interfering RNA (siRNA) delivery via stents is a promising approach.
Purpose of the Study:
- To develop and evaluate layer-by-layer (LbL) coated coronary stents incorporating siRNA nanoplexes (NPs).
- To assess the stability, cellular uptake, and ex vivo delivery of siRNA NPs from the stent coatings.
- To evaluate the hemocompatibility of the developed bioactive stent coatings.
Main Methods:
- Fabrication of hyaluronic acid/chitosan (HA/Chi) multilayer films with incorporated chitosan-siRNA NPs using LbL technology.
- Characterization of coating thickness and stability using quartz crystal microbalance, fluorescence microscopy, and scanning electron microscopy.
- In vitro assessment of NP uptake by endothelial cells and ex vivo NP transfer into porcine artery walls; hemocompatibility testing.
Main Results:
- Homogeneous HA/Chi and Chi-siRNA NP coatings were successfully fabricated on stents.
- Coatings remained stable after sterilization and stent expansion.
- In vitro studies showed endothelial cell uptake of NPs, and ex vivo studies demonstrated NP transfer into porcine artery walls.
- The developed coatings exhibited good hemocompatibility.
Conclusions:
- Chitosan-siRNA NPs can be effectively incorporated into HA/Chi multilayer films using LbL technology.
- The developed coatings facilitate siRNA NP delivery to endothelial cells in vitro and artery walls ex vivo.
- These bioactive coatings show potential as an innovative tool for coronary stent applications.
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