Platelet adhesion and activation on a shielded plasma gradient prepared on polyethylene

Biomaterials

Volumn 23, Issue 3, 2002, Pages 757-766

  Spijker, Hetty T ^a   Bos, Rolf ^a   Busscher, Henk J ^a   Van Kooten, Theo G ^a   Van Oeveren, Wim ^a  

^a UNIVERSITY OF GRONINGEN   (Netherlands)

Author keywords

Activation; Adhesion; Platelets; Wettability gradients

Indexed keywords

BLOOD; CHEMICAL ACTIVATION; DIFFUSION; HYDROPHOBICITY; POLYETHYLENES; POLYMERS;

PLATELETS; THROMBOGENIC EFFECTS;

BIOMATERIALS;

FIBRINOGEN RECEPTOR; OXYGEN; POLYETHYLENE; POLYMER;

ANTICOAGULATION; ARTICLE; BLOOD CLOTTING; CONTROLLED STUDY; HUMAN; HUMAN CELL; HYDROPHILICITY; HYDROPHOBICITY; HYSTERESIS; IMMERSION; PRIORITY JOURNAL; THROMBOCYTE ACTIVATION; THROMBOCYTE ADHESION; THROMBOCYTE STRUCTURE; THROMBOGENICITY; WETTABILITY;

BIOCOMPATIBLE MATERIALS; BLOOD PHYSIOLOGY; BLOOD PLATELETS; CELL MEMBRANE; FACTOR X; FACTOR XA; HUMANS; MICROSCOPY, ELECTRON, SCANNING; PLATELET ACTIVATION; PLATELET ADHESIVENESS; POLYETHYLENE; SURFACE PROPERTIES;

EID: 0036132492     PISSN: 01429612     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0142-9612(01)00181-8     Document Type: Article

References (30)

1. Assessment of material-induced procoagulant activity by a modified Russel viper venom coagulation time test
2. In vitro comparative evaluation under static conditions of the hemocompatibility of four types of tubing for cardiopulmonary bypass
3. Human plasma fibrinogen adsorption and platelet adhesion to polystyrene
4. The role of surface energy on thrombogenesis
5. Preparation and characterization of chemical gradient surfaces and their application for the study of cellular interaction phenomena
6. Protein exchange reactions on solid surfaces studied with a wettability gradient method
7. A new technique to prepare gradient surfaces using density gradient solutions
8. Studies of surface activated coagulation: Antisera binding onto methyl gradients on silicon incubated in human plasma in vitro
9. Protein adsorption on gradient surfces on polyethylene prepared in a shielded gas plasma
10. Platelet adhesion onto wettability gradient surfaces in the absence and presence of plasma proteins
11. Molecular barriers to biomaterial thrombosis by modification of surface proteins with polyethylene glycol
12. Differential surface binding of albumin, immunoglobulin G and fibrinogen
13. Protein and detergent interaction phenomena on solid surfaces with gradients in chemical composition
14. Interaction of two oral streptococcal strains with physico-chemically characterized fluorosilane diffusion gradient surfaces
15. Aging effects of repeatedly glow-discharged polyethylene: Influence on contact angle, infrared absorption, elemental surface composition, and surface topography
16. Changes in the platelet membrane glycoprotein IIb/IIIa complex during platelet activation
17. Interactions between whole blood and hydrophilic or hydrophobic glass surfaces: Kinetics of cell adhesion
18. Platelet and monoclonal antibody binding to fibrinogen adsorbed on glow-discharge-deposited polymers
19. Plasma protein adsorption and platelet adhesion onto comb-like PEO gradient surfaces
20. Cell and platelet adhesions on plasma glow discharge-treated poly(lactide-co-glycolide)
21. The platelet membrane glycoprotein IIb-IIIa complex
22. The molecular basis of platelet function
23. Clues for understanding the sturcture and function of a prototypic human integrin: The platlet glycoprotein IIb/IIIa complex
24. Additional glycoprotein defects in Bernard-Souliers syndrome: Confirmation of genetic basis by parental analysis
25. Receptor patching and capping of platelet membranes induced by monoclonal antibodies
26. Redistribution of GPIb-IX and GPIIb-IIIa during spreading of discoid platelets
27. Whole blood platelet aggregation in humans and animals: A comparative study
28. Protease-activated receptor 1 is the primary mediator of thrombin-stimulated platelet procoagulant activity
29. Inconsequentiality of surface properties for initial platelet adhesion
30. Plasma-treated PET surfaces improve the biocompatibility of human endothelial cells