Fluorinated vs hydrogenated surfactants in mixtures with valinomycin--the Langmuir monolayer study

Broniatowski, M; Vila-Romeu, N; Dynarowicz-Łatka, P

HERO ID

4936698

Reference Type

Journal Article

Year

2010

Language

English

PMID

20176461

HERO ID 4936698
In Press No
Year 2010
Title Fluorinated vs hydrogenated surfactants in mixtures with valinomycin--the Langmuir monolayer study
Authors Broniatowski, M; Vila-Romeu, N; Dynarowicz-Łatka, P
Journal Colloids and Surfaces B: Biointerfaces
Volume 77
Issue 2
Page Numbers 298-300
Abstract Selected fluorinated and hydrogenated surfactants, namely a semifluorinated alkane (SFA): 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10-henicosafluorononacosane (F10H19), two long chain alcohols: 18,18,18,17,17,16,16,15,15,14,14,13,13,12,12,11,11-heptadecafluorooctadecane-1-ol (F8H10OH) and octadecane-1-ol (C18OH) and with two long chain thiols of the analogous apolar part structure to the above-mentioned alcohols, i.e.: 18,18,18,17,17,16,16,15,15,14,14,13,13,12,12,11,11-heptadecafluorooctadecane-1-thiol (F8H10SH) and octadecane-1-thiol (C18SH) have been tested in mixtures with valinomycin as potential artificial matrixes for its immobilization. The thermodynamic analysis (DeltaG(exc)vsX(val) plots) based on surface pressure-area isotherm registration for particular valinomycin/surfactant mixtures, complemented with BAM images of the films structure indicate that only fluorinated surfactants are suitable materials for valinomycin incorporation as they form homogeneous miscible monolayers at X(val) below 0.5.
Doi 10.1016/j.colsurfb.2010.01.027
Pmid 20176461
Wosid WOS:000276753600024
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English