Stroke, Vol 19, 1470-1476, Copyright © 1988 by American Heart Association
T Okada, DH Bark and MR Mayberg
Polymeric drug delivery systems that allow the application of substances to
a localized region for specified periods of time have been developed. A
model for intravascular thrombosis in the rat common carotid artery was
established using a combination of balloon catheter endothelial injury with
1-hour occlusion of the vessel. After endothelial injury in 11
Sprague-Dawley rats, the adventitial surface of the carotid artery was
exposed to the polymer polyvinyl alcohol (PVA) containing heparin and was
compared with exposure to PVA alone in the contralateral (control) vessel.
Subsequent determinations of the coagulation parameters systemic
prothrombin and partial thromboplastin times showed no systemic effect of
heparin. All 11 control vessels demonstrated complete or partial
thrombosis, whereas only one of 11 heparin/PVA-treated vessels showed a
small thrombus. Morphometric analysis of the cross-sectional thrombus:
lumen ratio in 10 rats showed a significant reduction (p less than 0.005)
in thrombus size for treated vessels (4.1 +/- 9.6%) compared with control
vessels (60.2 +/- 25.8%). Scanning electron microscopy verified the absence
of thrombus in the treated vessels despite complete endothelial
desquamation. In a second group of eight rats, endothelial injury without
occlusion did not cause thrombosis in treated or control arteries. The
coagulation parameters for this group of eight unoccluded rats were
similarly unaffected by heparin/PVA treatment. Our observations suggest
that a localized antithrombotic effect of heparin can be achieved without
systemic anticoagulation using a polymeric drug delivery system. This
technique may be applied to a variety of surgical and nonsurgical clinical
conditions.
ARTICLES
Local anticoagulation without systemic effect using a polymer heparin delivery system
Department of Neurosurgery, University of Washington, Seattle.
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