FIBRINOGEN ADSORPTION AND HOST TISSUE RESPONSES TO PLASMA FUNCTIONALIZED SURFACES

Citation
Lp. Tang et al., FIBRINOGEN ADSORPTION AND HOST TISSUE RESPONSES TO PLASMA FUNCTIONALIZED SURFACES, Journal of biomedical materials research, 42(1), 1998, pp. 156-163
Citations number
53
Categorie Soggetti
Materials Science, Biomaterials","Engineering, Biomedical
ISSN journal
00219304
Volume
42
Issue
1
Year of publication
1998
Pages
156 - 163
Database
ISI
SICI code
0021-9304(1998)42:1<156:FAAHTR>2.0.ZU;2-8
Abstract
The physical and chemical characteristics of material surfaces are tho ught to play important roles in biomaterial-mediated tissue responses. To understand the importance of discrete biomaterial chemical charact eristics in modifying host tissue responses, we constructed surfaces b earing different functional groups using radio frequency glow discharg e plasma polymerization. Surfaces evaluated included those having high concentrations of -OH, -NH2, -CF3, and siloxyl groups. These surfaces and polyethylene terephthalate controls were used to assess the impor tance of particular physicochemical characteristics in surface:protein :cell interactions both in vitro and in vivo. The results obtained sho w that surface functionalities do significantly affect both the adsorp tion and ''denaturation'' of adsorbed fibrinogen (which is an importan t mediator of inflammatory responses to biomaterial implants). In addi tion, these surfaces provoke different degrees of acute inflammatory r esponses. Interestingly, the amounts of ''denatured'' fibrinogen that spontaneously accumulate on the individual surfaces correlate closely with the extent of biomaterial-mediated inflammation. These results su ggest that surfaces that tend to ''irreversibly'' bind fibrinogen prom pt greater acute inflammatory responses. Unexpectedly, all test surfac es except those bearing a siloxyl group engender relatively similar bi omaterial-mediated fibrotic responses. Thus surface functionalities al one may not be sufficient to affect subsequent fibrotic responses. (C) 1998 John Wiley Rr Sons, Inc.