A. Delamaza et Jl. Parra, SOLUBILIZING EFFECTS CAUSED BY ALKYL PYRIDINIUM SURFACTANTS IN PHOSPHATIDYLCHOLINE LIPOSOMES, Chemistry and physics of lipids, 77(1), 1995, pp. 79-87
The solubilization of neutral and electrically charged liposomes by a
series of alkyl pyridinium surfactants (alkyl chain lengths C-10-C-14)
was investigated. Solubilization was detected as a decrease in static
light-scattering of liposome suspensions. Two parameters were regarde
d as corresponding to the effective surfactant/lipid molar ratios at w
hich the surfactant saturated the liposomes Re-sat and led to a comple
te solubilization of these structures Re-sol. From these parameters th
e corresponding surfactant partition coefficients were determined. The
Re and K parameters fell as the surfactant alkyl chain length decreas
ed or both the critical micellar concentration (CMC) and the hydrophil
ic/lipophilic balance (HLB number) increased, regardless of the bilaye
rs electrical charge. Thus, although decyl-pyridiniumm bromide (DePB)
showed the highest ability for saturation and solubilization of bilaye
rs, its concentration was always higher than that needed for dodecyl-p
yridinium bromide (DoPB) and tetradecyl-pyridinium bromide (TePB), the
last one being the most active. These results emphasize the influence
of the hydrophilic/lipophilic balance of these surfactants on liposom
e solubilization and the minor influence of the electrostatic factors
in this process.