Interactions of novel, nonhemolytic surfactants with phospholipid vesicles
- PMID: 17516668
- DOI: 10.1021/la063700b
Interactions of novel, nonhemolytic surfactants with phospholipid vesicles
Abstract
PEG-12-acyloxystearates constitute a novel class of pharmaceutical solubilizers and are synthesized from polyethylene glycol and 12-hydroxystearic acid, which has been esterified with a second acyl chain. The hemolytic activity of these surfactants decreases drastically with increasing pendant acyloxy chain length, and surfactants with an acyloxy chain of 14 carbon atoms or more are essentially nonhemolytic. In this paper, the interactions of PEG-12-acyloxystearates (acyloxy chain lengths ranging from 8 to 16 carbon atoms) with phosphatidylcholine vesicles, used as a model system for erythrocyte membranes, were studied in search of an explanation for the large variations in hemolytic activity. Surfactant-induced alterations of membrane permeability were investigated by studying the leakage of vesicle-entrapped calcein. It was found that all of the surfactants within the series interact with the vesicle membranes and cause slow leakage at elevated surfactant concentrations, but with large variations in leakage kinetics. The initial leakage rate decreases rapidly with increasing pendant acyloxy chain length. After prolonged incubation, on the other hand, the leakage is not a simple function of acyloxy chain length. The effect of the surfactants on membrane integrity was also investigated by turbidity measurements and cryo-transmission electron microscopy. At a surfactant/lipid molar ratio of 0.4, the vesicle membranes are saturated with surfactant. When the surfactant/lipid molar ratio is further increased, the vesicle membranes are progressively solubilized into mixed micelles. The rate of this process decreases strongly with increasing acyloxy chain length. When comparing the results of the different experiments, it can be concluded that there is no membrane permeabilization below saturation of the vesicle membranes. The large variations in the kinetics suggest that several steps are involved in the mechanism of leakage induced by PEG-12-acyloxystearates and that their relative rates vary with acyloxy chain length. The slow kinetics may in part be explained by the low critical micelle concentrations (CMCs) exhibited by the surfactants. The CMCs were found to be in the range of 0.003-0.025 microM.
Similar articles
-
Interactions between nonionic Triton X surfactants and cholesterol-containing phosphatidylcholine liposomes.J Colloid Interface Sci. 2006 Oct 1;302(1):335-40. doi: 10.1016/j.jcis.2006.06.028. Epub 2006 Jun 23. J Colloid Interface Sci. 2006. PMID: 16839562
-
Impact of membrane cholesterol content on the resistance of vesicles to surfactant attack.Langmuir. 2005 Oct 25;21(22):9843-9. doi: 10.1021/la050568r. Langmuir. 2005. PMID: 16229500
-
Role of hydrophobic interactions in the adsorption of poly(ethylene glycol) chains on phospholipid membranes investigated with a quartz crystal microbalance.J Phys Chem B. 2009 Mar 19;113(11):3365-9. doi: 10.1021/jp810304f. J Phys Chem B. 2009. PMID: 19227992
-
Interactions of surfactants with lipid membranes.Q Rev Biophys. 2008 Aug-Nov;41(3-4):205-64. doi: 10.1017/S0033583508004721. Q Rev Biophys. 2008. PMID: 19079805 Review.
-
The relationship between the chain length of non-ionic surfactants and their hemolytic action on human erythrocytes.Comp Biochem Physiol C Pharmacol Toxicol Endocrinol. 1999 Oct;124(2):117-20. doi: 10.1016/s0742-8413(99)00057-2. Comp Biochem Physiol C Pharmacol Toxicol Endocrinol. 1999. PMID: 10622426 Review.
Cited by
-
Investigation of the adsorption of PEG1500-12-acyloxystearate surfactants onto phospholipid bilayers: an ellipsometry and cryo-TEM study.Biophys J. 2007 Dec 15;93(12):4300-6. doi: 10.1529/biophysj.107.109900. Epub 2007 Aug 31. Biophys J. 2007. PMID: 17766340 Free PMC article.
-
Lateral membrane organization as target of an antimicrobial peptidomimetic compound.Nat Commun. 2023 Jul 7;14(1):4038. doi: 10.1038/s41467-023-39726-5. Nat Commun. 2023. PMID: 37419980 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources