AJP - Heart Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Heart Circ Physiol 259: H1527-H1532, 1990;
0363-6135/90 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Carr, M. E.
Right arrow Articles by Hauge, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Carr, M. E., Jr
Right arrow Articles by Hauge, Y.

AJP - Heart and Circulatory Physiology, Vol 259, Issue 5 1527-H1532, Copyright © 1990 by American Physiological Society


ARTICLES

Enhancement of red cell washout from blood clots by alteration of gel pore size and red cell flexibility

M. E. Carr Jr and Y. Hauge
Department of Pathology, Medical College of Virginia, Richmond.

Plasma clots formed in the presence of erythrocytes have pores large enough to allow significant perfusion induced washout of red cells. Erythrocyte washout is a function of gel pore size and erythrocyte flexibility. This study evaluated the possibility of increasing cell washout by enhancing gel pore size and/or erythrocyte flexibility. Addition of increasing concentrations of Dextran 40 resulted in gels composed of large fibers with large intervening pores. Gel fiber mass-to-length ratios increased from 2.6 to 8.1 x 10(13) Da/cm as Dextran 40 concentration increased from 0 to 12 mg/ml. Over the same dextran concentration range, perfusion measurements revealed an increase in gel pore diameter from 1.4 to 3.5 x 10(-4) cm and an increase in erythrocyte washout from 8.2 to 30.4% during a 1.5 gel volume exchange. Pentoxifylline was added to blood to enhance erythrocyte flexibility. Whereas turbidity measurements indicated minimal direct impact of pentoxifylline (50 micrograms/ml) on fibrin assembly or structure, perfusion measurements indicated an increase in erythrocyte washout from 8.1 to 13.4% after a 1.5 gel volume exchange. Efforts to evaluate pentoxifylline effects at higher concentrations were hampered by decreased adhesion of the gel to the sides of the perfusion chamber. These results indicate that it may be possible to enhance erythrocyte washout and thereby increase diffusion and perfusion of materials through in situ clots.





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online