SOLUBILIZING EFFECTS CAUSED BY ALKYL PYRIDINIUM SURFACTANTS IN PHOSPHATIDYLCHOLINE LIPOSOMES

Citation
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
Citations number
29
Categorie Soggetti
Biology
ISSN journal
00093084
Volume
77
Issue
1
Year of publication
1995
Pages
79 - 87
Database
ISI
SICI code
0009-3084(1995)77:1<79:SECBAP>2.0.ZU;2-M
Abstract
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.