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Time sequence of bl...
Time sequence of blood activation by nanoporous alumina : Studies on platelets and complement system
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- Ferraz, Natalia, 1976- (författare)
- Uppsala universitet,Ytbioteknik,Nano-biomaterial research and Tissue Culturing
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- Karlsson Ott, Marjam, 1975- (författare)
- Uppsala universitet,Ytbioteknik,Nano-biomaterial research and Tissue Culturing
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- Hong, Jaan (författare)
- Uppsala universitet,Enheten för klinisk immunologi
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(creator_code:org_t)
- 2010-03-15
- 2010
- Engelska.
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Ingår i: Microscopy research and technique (Print). - : Wiley-Liss Inc.. - 1059-910X .- 1097-0029. ; 73:12, s. 1101-1109
- Relaterad länk:
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https://urn.kb.se/re...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- In the present work the time sequence of blood activation by alumina membranes with different porosities (20 and 200 nm in diameter) was studied. The membranes were incubated with whole blood from 2 min to 4 h. Platelet adhesion and activation in addition to complement activation were monitored at different time points. Evaluation of platelet adhesion and activation was done by determining the change in platelet number and the levels of thrombospondin-1 in the fluid phase. Scanning electron microscopy studies were done to further evaluate platelet adhesion and morphology. Immunocytochemical staining was used to evaluate the presence of CD41 and CD62P antigens on the material surface. Complement activation was monitored by measuring C3a and sC5b-9 in plasma samples by means of enzyme immunoassays. Both alumina membranes displayed similar complement activation time profiles, with levels of C3a and sC5b-9 increasing with incubation time. A statistically significant difference between the membranes was found after 60 min of incubation. Platelet activation characteristics and time profile were different between the two membranes. Platelet adhesion increased over time for the 20 nm surface, while the clusters of microparticles on the 200 nm surface did not appreciably change during the course of the experiment. The release of thrombospondin-1 increased with time for both membranes, however much later for the 200 nm alumina (240 min) as compared to the 20 nm membrane (60 min). The surface topography of the alumina most probably influence protein transition rate, which in turn affects material-platelet activation kinetics.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Andra medicinska och farmaceutiska grundvetenskaper (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Other Basic Medicine (hsv//eng)
Nyckelord
- nanotopography
- biomaterial
- whole blood
- thrombospondin-1
- platelet microparticles
- Chemistry
- Kemi
- Immunologi
- Immunology
- Materialvetenskap
- Materials Science
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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