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Updated: Feb 10, 2026

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Fabrication of Small Caliber Stent-grafts Using Electrospinning and Balloon Expandable Bare Metal Stents
Published on: October 26, 2016
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A Review on Phosphorylcholine-Coated Stents
Andrew L Lewis1, Peter W Stratford2
1Biocompatibles Ltd., Farnham Business Park, Weydon Lane, Farnham, Surrey, GU9 8QL, UK.
Journal of Long-Term Effects of Medical Implants
|May 19, 2018
Summary
Phosphorylcholine (PC)-coated stents improve hemocompatibility, reducing thrombosis risk. This advanced coating offers clinical advantages and serves as a platform for drug delivery to prevent restenosis.
Area of Science:
- Biomaterials Science
- Cardiovascular Medicine
- Medical Device Engineering
Background:
- Stainless steel stents are crucial after percutaneous transluminal coronary angioplasty (PTCA) to prevent arterial recoil.
- Subacute thrombosis (SAT) was a major complication, though largely mitigated by antiplatelet agents.
- Stent occlusion persists as a risk, especially for complex lesions, necessitating improved hemocompatibility.
Purpose of the Study:
- To evaluate a novel phosphorylcholine (PC)-based coating for stainless steel stents.
- To assess the hemocompatibility, biocompatibility, and clinical performance of PC-coated stents.
- To explore the potential of PC-coated stents as a platform for drug delivery.
Main Methods:
- In vitro, preclinical, and early clinical evaluations of PC-coated stents.
- Assessment of stent surface hemocompatibility and interaction with arterial tissue.
- Analysis of long-term stability and therapeutic agent loading/release capabilities.
Main Results:
- The PC-coated stent demonstrated a nonthrombogenic nature.
- Excellent acceptance by arterial tissue and long-term stability in vivo were observed.
- The coating showed potential clinical advantages over uncoated stents.
Conclusions:
- PC-coated stents exhibit favorable hemocompatibility and biocompatibility.
- The device shows promise for reducing stent occlusion and restenosis.
- PC-coated stents are a viable platform for future stent-mediated drug delivery systems.
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