This proposal is directed toward testing hypotheses that can lead to improved polyurethane materials form cardiovascular and other implant devices. Embolic problems with artificial hearts, the proposed use of polyurethane vascular grafts, and the failure of pacemaker leads all point to the need for improved polyurethanes. The central hypothesis of this proposal is that poly(ether urethanes) (PEU's) with surfaces rich in hydrocarbon or fluorocarbon moieties might demonstrate minimal platelet interaction in arterial flows, a reduced tendency to calcify, and a reduced susceptibility to biodegradation. The research proposed has five major components: (1) the synthesis, purification and bulk characterization of PEU's with hydrocarbon or fluorocarbon surfaces; (2) the analysis of the surface structure of these materials in the hydrated and dehydrated condition by ESCA, SIMS and contact angle methods; (3) in vitro studies of the biodegradation of these PEU's directed toward testing out many of the hypotheses formulated about the breakdown mechanism; (4) in vitro modelling of the propensity towards calcification based upon SIMS analysis of the calcium binding ability of PEU surfaces; and (5) biological studies, primarily with external collaborators, including protein adsorption, cell interaction, in vitro laser emboli detection and ex vivo evaluation of platelet interaction using a baboon model.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL025951-08
Application #
3338383
Study Section
Surgery and Bioengineering Study Section (SB)
Project Start
1981-04-01
Project End
1990-03-31
Budget Start
1988-04-01
Budget End
1989-03-31
Support Year
8
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Simonovsky, Felix I; Porter, Stephen C; Ratner, Buddy D (2005) Synthesis of segmented poly(ether urethane)s and poly(ether urethane urea)s incorporating various side-chain or backbone functionalities. J Biomater Sci Polym Ed 16:267-84
Ratner, B D (2000) Blood compatibility--a perspective. J Biomater Sci Polym Ed 11:1107-19
Horbett, T A; Cooper, K W; Lew, K R et al. (1998) Rapid postadsorptive changes in fibrinogen adsorbed from plasma to segmented polyurethanes. J Biomater Sci Polym Ed 9:1071-87
Ratner, B D (1995) Surface modification of polymers: chemical, biological and surface analytical challenges. Biosens Bioelectron 10:797-804
Ertel, S I; Ratner, B D; Kaul, A et al. (1994) In vitro study of the intrinsic toxicity of synthetic surfaces to cells. J Biomed Mater Res 28:667-75
Perez-Luna, V H; Horbett, T A; Ratner, B D (1994) Developing correlations between fibrinogen adsorption and surface properties using multivariate statistics. Student Research Award in the Doctoral Degree Candidate Category, 20th annual meeting of the Society for Biomaterials, Boston, MA, April 5-9, 1994. J Biomed Mater Res 28:1111-26
Tyler, B J; Ratner, B D (1993) Variations between Biomer lots. 2: The effect of differences between lots on in vitro enzymatic and oxidative degradation of a commercial polyurethane. J Biomed Mater Res 27:327-34
Haycox, C L; Ratner, B D (1993) In vitro platelet interactions in whole human blood exposed to biomaterial surfaces: insights on blood compatibility. J Biomed Mater Res 27:1181-93
Slack, S M; Horbett, T A (1992) Changes in fibrinogen adsorbed to segmented polyurethanes and hydroxyethylmethacrylate-ethylmethacrylate copolymers. J Biomed Mater Res 26:1633-49
Chinn, J A; Posso, S E; Horbett, T A et al. (1992) Postadsorptive transitions in fibrinogen adsorbed to polyurethanes: changes in antibody binding and sodium dodecyl sulfate elutability. J Biomed Mater Res 26:757-78

Showing the most recent 10 out of 20 publications