J. Cao et Se. Rittgers, PARTICLE MOTION WITHIN IN-VITRO MODELS OF STENOSED INTERNAL CAROTID AND LEFT ANTERIOR DESCENDING CORONARY-ARTERIES, Annals of biomedical engineering, 26(2), 1998, pp. 190-199
Asymmetric 75% and 95% area reduction, transparent Sylgard stenotic mo
dels were operated under internal carotid artery (ICA) (Womersley para
meter, alpha=5.36, Re-mean =213 and 180, respectively, and Re-peak=734
and 410, respectively) and left anterior descending coronary artery (
LAD) flow wave forms (alpha=2.65, Re-mean=59 and 57, respectively, and
Re-peak= 137 and 94, respectively) to evaluate the effect of these co
nditions on particle residence times downstream of the stenoses. Amber
lite particles (1.05 g/cm(3), 400 mu m) were added to the fluid to sim
ulate platelets and their motion through the stenotic region and were
traced using a laser Light sheet flow visualization method with pseudo
-color display. Two-dimensional (2D) particle motions were recorded an
d particle washout in the stenotic throat and downstream section were
computed for all cases. All four model cases demonstrated jetting thro
ugh the stenosis which followed an arching pattern around a large sepa
ration zone downstream. Considerable mixing was observed within these
vortex regions during high flow phases. particle washout profiles show
ed no clear trend between the degrees of stenosis although particles d
ownstream of the stenoses tended to remain longer for LAD conditions.
The critical washout cycle (1% of particles remaining downstream of th
e stenosis), however, was longer for the 95% stenoses cases under each
flow condition due to the larger protected region immediately downstr
eam and maximal for the LAD 95% case. Results of this study suggest th
at particle residence times downstream of 75% and 95% stenoses (simila
r to 3-6 s for ICA and similar to 8-10 s for LAD) exceed the minimum t
ime for platelet adhesion (similar to 1s) for at least 1% of cells and
, thus, may be sufficient to initiate thrombus formation under resting
conditions. (C) 1998 Biomedical Engineering Society.