Basic research
Biocompatibility of phosphorylcholine coated stents in normal
porcine coronary arteries
D M Whelan, W J van der Giessen, S C Krabbendam, E A van Vliet, P D Verdouw, P W Serruys, H M M van Beusekom
Department of
Cardiology, Thoraxcenter, Erasmus University Rotterdam, PO Box 1738, 3000 DR Rotterdam, The Netherlands
Correspondence to: Dr van der Giessen email: vandergiessen{at}card.azr.nl
Accepted 19 October
1999
OBJECTIVE
To improve the biocompatibility of stents using
a phosphorylcholine coated stent as a form of biomimicry.
INTERVENTIONS
Implantation of phosphorylcholine coated
(n = 20) and non-coated (n = 21) stents was performed in the
coronary arteries of 25 pigs. The animals were killed after five days
(n = 6), four weeks (n = 7), and 12 weeks (n = 8), and the
vessels harvested for histology, scanning electron microscopy, and morphometry.
MAIN OUTCOME MEASURES
Stent performance was assessed by
studying early endothelialisation, neointima formation, and vessel wall
reaction to the synthetic coating.
RESULTS
Stent thrombosis did not occur in either group.
Morphometry showed no significant differences between the two study
groups at any time point. At five days both the coated and non-coated stents were equally well endothelialised (91% v
92%, respectively). At four and 12 weeks there was no difference
in intimal thickness between the coated and non-coated stents. Up to 12 weeks postimplant the phosphorylcholine coating was still discernible
in the stent strut voids, and did not appear to elicit an adverse
inflammatory response.
CONCLUSION
In this animal model the phosphorylcholine
coating showed excellent blood and tissue compatibility, unlike a
number of other polymers tested in a similar setting. Given that the
coating was present up to 12 weeks postimplant with no adverse tissue
reaction, it may be a potential candidate polymer for local drug delivery.
Keywords: phosphorylcholine; stents; coatings; biocompatible materials
© 2000 by Heart
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