Changes in phosphatidylcholine liposomes caused by a mixture of Triton X-100 and sodium dodecyl sulfate.

The mechanisms governing the interaction of equimolecular mixtures of Triton X-100 (Tx-100) and sodium dodecyl sulfate (SDS) with phosphatidylcholine liposomes were investigated. Permeability alterations were determined as a change in 5(6)-carboxyfluorescein released from the interior of vesicles and bilayer solubilization as a decrease in the static light-scattered by liposome suspensions. At subsolubilizing level, a maximum bilayer/water partitioning of surfactant mixture was reached at 30% CF release, which correlated with the increased presence of SDS in the bilayers. However, transition stages between 70% CF release and 100% light-scattering corresponded to the increased presence of Tx-100 in these structures. These findings may be correlated with the reduced deleterious effects caused by this mixture in different tissues versus pure SDS, given that the presence of Tx-100 may modulate the level of SDS partitioning in the human stratum corneum. At subsolubilizing level, the mixture showed higher affinity with bilayers than those reported for single components, whereas at solubilizing level this affinity was slightly lower and higher than those reported for Tx-100 and SDS respectively. A direct relationship was established in the initial interaction steps between the growth of vesicles, the leakage of entrapped CF and the effective molar ratio of surfactant to phospholipid in bilayers (Re). This dependence was also detected during solubilization, where the decrease in the vesicle size and in the scattered light of the system depended on the Re parameter and hence on the bilayer composition. The fact that the free surfactant concentration at subsolubilizing and solubilizing levels showed respectively lower and similar values than the critical micelle concentration (c.m.c.) of the surfactant mixture indicates that permeability alterations and solubilization were determined respectively by the action of surfactant monomer and by the formation of mixed micelles. This finding supports the generally admitted assumption, for single surfactants, that the concentration of free surfactant must reach the c.m.c. for solubilization to occur and highlights the influence of the negative synergism of this surfactant mixture on the free surfactant concentration needed to saturate or solubilize liposomes.