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Published on: August 12, 2014
Uropathogen interaction with the surface of urological stents using different surface properties
Dirk Lange1, Chelsea N Elwood, Kenny Choi
1Stone Centre at Vancouver General Hospital, Department of Urologic Sciences, University of British Columbia, Vancouver, Canada.
The Journal of Urology
|July 24, 2009
Summary
Heparin coating did not reduce bacterial adherence to ureteral stents. Drug-eluting stents and the Polaris stent demonstrated better resistance to common uropathogens compared to standard stents.
Area of Science:
- Urology
- Biomaterials Science
- Infectious Diseases
Background:
- Ureteral stents are prone to infection and encrustation.
- Bacterial adherence is a primary concern for stent-associated complications.
- Heparin coating is a novel approach to mitigate bacterial adherence.
Purpose of the Study:
- To evaluate the efficacy of heparin coating on ureteral stents against bacterial adherence.
- To assess the impact of heparin coating on the physical properties of ureteral stents.
- To compare heparin-coated stents with existing stent technologies.
Main Methods:
- In vitro testing of heparin-coated (Radiance) and non-coated ureteral stents.
- Evaluation of adherence for common uropathogens (E. coli, K. pneumoniae, E. faecalis, S. aureus, P. aeruginosa) over 7 days.
- Assessment of stent physical properties including radial, tensile, and coil strength.
Main Results:
- Heparin coating did not significantly decrease bacterial adherence compared to control stents.
- The Polaris stent exhibited superior resistance to Klebsiella, Pseudomonas, and Enterococcus adherence.
- Drug-eluting Triumph stents showed broad-spectrum bacterial resistance, except against Pseudomonas and Enterococcus.
Conclusions:
- Heparin coating is ineffective in reducing bacterial adherence to ureteral stents.
- Drug-eluting stents and the Polaris stent offer improved protection against bacterial colonization.
- Further research into advanced stent coatings and designs is warranted to prevent stent-associated infections.

