Interactions between bilayer membranes and latex

Citation
Am. Carmona-ribeiro et Md. Lessa, Interactions between bilayer membranes and latex, COLL SURF A, 153(1-3), 1999, pp. 355-361
Citations number
21
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
ISSN journal
09277757 → ACNP
Volume
153
Issue
1-3
Year of publication
1999
Pages
355 - 361
Database
ISI
SICI code
0927-7757(19990815)153:1-3<355:IBBMAL>2.0.ZU;2-G
Abstract
The interaction between sulfate polystyrene latex and bilayer vesicles is d escribed from the point of view of membrane-induced latex deflocculation an d theoretical colloid stability for bilayer-covered particles from a DLVO m odel without free parameters. Unilamellar cationic or anionic vesicles were prepared from dioctadecyldimethylammonium bromide (DODAB) or asolecithin ( ASO), respectively, and allowed to interact with sulfate polystyrene micros pheres of several sizes. Mean zeta-average diameters for latex particles in the interacting mixtures decreases as a function of interaction time betwe en sulfate polystyrene particles and asolecithin vesicles attaining a final size compatible with a negatively charged asolecithin monolayer deposited onto the anionic latex surface. In contrast to the ASO behaviour, the catio nic DODAB was previously reported to deposit as a bilayer onto the sulfate latex. The occurrence of an ordered amphiphile assembly deposited onto the latex is highly dependent on the proportion of total surface areas for vesi cles and particles. From zeta-potential measurements and a DLVO model, theo retical colloid stabilities are calculated as a function of monovalent salt concentration or particle size and found to be much higher than experiment ally measured stabilities. DLVO expectations are not fulfilled in spite of the presumably ideal nature of the bilayer-covered polystyrene microsphere as a colloid. (C) 1999 Elsevier Science B.V. All rights reserved.