Host cell oxidative responses can alter biomaterials and influence their long-term success. The initial reaction of neutrophils and monocytes with materials may influence the course of the inflammatory response. Previous work in our group has shown that both whole blood and monocytes from females showed a stronger oxidative burst to poly(dimethyl siloxane) PDMS than did whole blood and monocytes from males. The inflammatory response in male and female Balb/c mice to subcutaneous PDMS is being evaluated in an ongoing study. ESCA and SIMS will be used to characterize the PDMS materials.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001296-16
Application #
6345065
Study Section
Project Start
2000-09-01
Project End
2001-08-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
16
Fiscal Year
2000
Total Cost
$2,454
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
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