Cm. Edwards et al., NOVEL FLUORINATED SURFACTANTS FOR PERFLUOROCHEMICAL EMULSIFICATION - BIOCOMPATIBILITY ASSESSMENTS OF GLYCOSIDIC AND POLYOL DERIVATIVES, Artificial cells, blood substitutes, and immobilization biotechnology, 25(3), 1997, pp. 327-333
A novel series of fluoro-surfactants, derived from glycosides (monosac
charides) or polyols (ureas or carbamates), have been produced for use
in respiratory gas-carrying perfluorochemical emulsions. Compounds we
re synthesised via simple, but highly selective, routes using highly f
luorinated isocyanates with amino alcohols, polyethoxylated alcohols a
nd partially protected sugars at anomeric carbon; yields were 88-95%.
Resultant compounds were perfluoroalkylated with hydroxylic ''head'' g
roups. The biocompatibility of surfactants with human blood in vitro w
as assessed using a conventional haemolyis test. Compounds showing ins
ignificant haemolysis at up to 10 g l(-1) were further evaluated (i) f
or their effects on neutrophil chemiluminescence, and (ii) in a human
platelet aggregation assay. Some fluoro-surfactants inhibited spontane
ous platelet aggregation, in blood anti-coagulated with hirudin, at co
ncentrations of 0.01% (w/v), suggesting possible applications as antit
hrombotic agents.