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Blood-surface interaction, influencing

FTIR spectroscopy has proven to be particularly useful in gaining an understanding of the biocompatibility phenomenon. It is believed [746, 841, 856, 857] that protein adsorption is the initial step in the interaction of blood with implanted biomaterials, followed by adhesion of cells and subsequent tissue attachment. This implies that the substrate surface characteristics influence the process, which was confirmed by ATR studies of albumin adsorption on calcium phosphate bioceramics and titanium [763] and segmented polyurethane [764], albumin and fibrinogen on acetylated and unmodified cellulose [765, 766], poly(acrylic acid)-mucin bioadhesion [767], polyurethane-blood contact surfaces [768], and other proteins on poly(ester)urethane [769], polystyrene [767, 771] and poly(octadecyl methacrylate) [771] and by IRRAS study of adsorption of proteins on Cu [858]. Another branch of IR spectroscopic studies of protein adsorption relates to microbial adhesion (Section 7.8.3). [Pg.623]

Surface Tension. Interfacial surface tension between fluid and filter media is considered to play a role in the adhesion of blood cells to synthetic fibers. Interfacial tension is a result of the interaction between the surface tension of the fluid and the filter media. Direct experimental evidence has shown that varying this interfacial tension influences the adhesion of blood cells to biomaterials. The viscosity of the blood product is important in the shear forces of the fluid to the attached cells viscosity of a red cell concentrate is at least 500 times that of a platelet concentrate. This has a considerable effect on the shear and flow rates through the filter. The surface stickiness plays a role in the critical shear force for detachment of adhered blood cells. [Pg.524]

W. Norde and R. A. Gage, Interaction of bovine serum albumin and human blood plasma with PEO-tethered surfaces influence of PEO-chain length, grafting density and temperature, Langmuir 20, 4162-4167 (2004). [Pg.176]

The liposome biodistribution profile changes significantly when the vesicle surface [227-229] is coated with polymers, usually PEG. Longer blood circulation, lower liver uptake, and higher accumulation in tumors have been reported. The presence of the hydrophilic groups of PEG on the liposome surface provides electrostatic and steric repulsion between PEG-grafted liposomes. PEG molecules neutralize the surface charge of vesicles and thus prevent their opsonization. Also, liposome opsonization is reduced due to inability of opsonins to bind to hydrophilic surfaces. Moreover, the thickness of the PEG layer influences the interaction of the liposomes... [Pg.469]

A study has been carried out on the interactions of blood with plasticised poly(vinyl chloride) biomaterials in a tubular form. The influence of different factors such as the biomaterial, antithrombotic agent, blood condition and the nature of the application is represented when considering the blood response in the clinical utilisation of the plasticised PVC. The PVC was plasticised with di-(2-ethylhexyl)phthalate (DEHP) and tri-(2-ethylhexyl)trimellitate (TEHTM)and in-vitro and ex-vivo procedures used to study the biomaterial with respect to the selection of the plasticiser. The blood response was measured in terms of the measurement of fibrinogen adsorption capacity, thrombin-antithrombin III complex and the complement component C3a. X-ray photoelectron spectroscopy was used for surface characterisation of the polymers and the data obtained indicated that in comparison with DEHP-PVC, there is a higher reactivity... [Pg.113]


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Interaction blood-surface

Surfaces [influence

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