BIOCOMPATIBLE NONIONIC SURFACTANTS FOR BIOMEDICAL UTILIZATION - DOUBLE-TAILED HYDROCARBON AND OR FLUOROCARBON SYNTHETIC GLYCOLIPIDS
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PUCCI, B
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FAC SCI AVIGNON,CHIM BIOORGAN LAB,33 RUE LOUIS PASTEUR,F-84000 AVIGNON,FRANCEFAC SCI AVIGNON,CHIM BIOORGAN LAB,33 RUE LOUIS PASTEUR,F-84000 AVIGNON,FRANCE
PUCCI, B
[1
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GUEDJ, C
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FAC SCI AVIGNON,CHIM BIOORGAN LAB,33 RUE LOUIS PASTEUR,F-84000 AVIGNON,FRANCEFAC SCI AVIGNON,CHIM BIOORGAN LAB,33 RUE LOUIS PASTEUR,F-84000 AVIGNON,FRANCE
GUEDJ, C
[1
]
PAVIA, AA
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FAC SCI AVIGNON,CHIM BIOORGAN LAB,33 RUE LOUIS PASTEUR,F-84000 AVIGNON,FRANCEFAC SCI AVIGNON,CHIM BIOORGAN LAB,33 RUE LOUIS PASTEUR,F-84000 AVIGNON,FRANCE
PAVIA, AA
[1
]
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[1] FAC SCI AVIGNON,CHIM BIOORGAN LAB,33 RUE LOUIS PASTEUR,F-84000 AVIGNON,FRANCE
Two classes of double-tailed hydrocarbon and/or fluorocarbon glycolipids containing either a gluco- or a galactopyranose residue in their hydrophilic head have been synthesized. The first was obtained upon opening a maltono- or lactonolactone moiety by the amino group of glycine followed by condensation of the glycine carboxylic function with a double-chain primary amine. The second involves L-lysine in place of glycine. Formation of vesicular structures upon conventional treatment was confirmed by preliminary measurements.