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Published on: September 9, 2011
A Technology for Anti-Thrombogenic Drug Coating of Small-Diameter Biodegradable Vascular Prostheses
L V Antonova1, E O Krivkina2, M A Rezvova3
1Head of the Laboratory of Cell Technologies, Department of Experimental Medicine; Research Institute for Complex Issues of Cardiovascular Diseases, 6 Sosnovy Blvd, Kemerovo, 650002, Russia.
Developing anti-thrombogenic drug coatings for biodegradable vascular prostheses improved hemocompatibility but increased stiffness. This technology enhances graft performance by reducing platelet aggregation and protein adhesion.
Area of Science:
- Biomaterials Science
- Vascular Surgery
- Drug Delivery Systems
Background:
- Biodegradable porous scaffolds are crucial for vascular prostheses.
- Developing effective anti-thrombogenic coatings is essential for graft success.
- Current prostheses face challenges with thrombosis and hemocompatibility.
Purpose of the Study:
- To create a technology for anti-thrombogenic drug coating on biodegradable scaffolds.
- To assess the physicomechanical and hemocompatible properties of coated vascular prostheses.
- To evaluate the efficacy of unfractionated heparin and iloprost coatings.
Main Methods:
- Emulsion electrospinning used to create prostheses from polyhydroxybutyrate/valerate and polycaprolactone.
- Incorporation of growth factors and chemoattractants within the scaffolds.
- Hydrogel coating with polyvinylpyrrolidone for drug complexation and binding.
- Application of unfractionated heparin and iloprost as anti-thrombogenic agents.
Main Results:
- Coated prostheses showed a 5.8-fold increase in Young's modulus, indicating enhanced stiffness.
- Platelet aggregation decreased 3.3-fold compared to unmodified controls.
- The drug-coated surface resisted platelet and blood protein adhesion.
Conclusions:
- Drug coating significantly improved the anti-thrombogenic properties of biodegradable vascular prostheses.
- The addition of unfractionated heparin and iloprost enhanced graft hemocompatibility.
- Increased stiffness was observed as a consequence of the drug coating modification.
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