Masumi Villeneuve

Differential conformational behaviors of α-mycolic acids in Langmuir monolayers and computer simulations

Phase diagrams of Langmuir monolayers of alpha-mycolic acids (alpha-MAs) from representative slow growing mycobacteria were intensively analyzed over a range of temperatures, by using so-called type-1 alpha-MAs having two cis-cyclopropyl groups from Mycobacterium tuberculosis, Mycobacterium kansasii and Mycobacterium avium-intracellulare complex (MAC) and type-3 alpha-MA, having one cis-cyclopropyl and one cis-double bond from Mycobacterium bovis BCG and MAC. Their intrachain groups are either cis-cyclopropyl or cis-double bond but the methylene chain segment lengths vary greatly. However, their monolayer features were alike: at lower temperatures and surface pressures, the molecules seemed to be in folded conformations, requiring larger mean molecular areas, whereas at higher temperatures and surface pressures, to be in extended conformations, requiring smaller average molecular areas approximately equivalent to cross sectional area of two hydrocarbon chains in a condensed film. In phase diagrams, the region for the folded forms of alpha-MAs was very limited, in contrast to the previously established behavior of ketomycolates, where complete folding predominated. Easy conversion of folded to extended conformations was indicated by thermodynamic studies of the Langmuir monolayer results and computer simulations.

Effect of equimolar salt to decyltrimethylammonium decyl sulfate on vesicle formation and surface adsorption.

The aqueous solution of mixture of sodium decyl sulfate (SDeS) and decyltrimethylammonium bromide (DeTAB) has been found to form equilibrium multilamellar vesicles (MLV) spontaneously. We measured the surface tension of the aqueous solution of 1:1 mixture of SDeS and DeTAB as a function of temperature T at various molalities m under atmospheric pressure. The surface density, the entropy of adsorption and the entropy of vesicle formation are evaluated and compared with those of the decyltrimethylammonium decyl sulfate (DeTADeS) aqueous solution system to investigate the role of small counterions in the mechanism of equilibrium vesicle formation. The saturated surface density Gamma (H,C ) vs T curve of the SDeS/DeTAB system sits below that of the DeTADeS system. Therefore, sodium and bromide ions are negatively adsorbed and nevertheless, they neutralize the electric charge of the decyl sulfate ion DeS(-) and the decyltrimethylammonium ion DeTA(+) to some extent to weaken the electrostatic attraction between the polar head groups in the adsorbed film. The net surfactant concentration required for vesicle formation was larger in the SDeS/DeTAB system. Hence, the electrostatic attraction between the polar head groups of the surfactant ions which is one of the major driving forces for vesicle formation is weakened by the presence of the counterions Na(+) and Br(-). Small but distinct changes in the surface density and the entropies of MLV formation of the SDeS/DeTAB system from those of the DeTADeS system were also found.

A carbosilane dendrimer and a silacyclopentadiene analog carrying peripheral lactoses as drug-delivery systems

A carbosilane dendrimer (4a) and its silacyclopentadiene analog (4b), both functionalized with lactoses, were tested for their abilities to act as drug-delivery systems. The critical micelle concentrations of 4a and 4b were measured using the drop-volume method in water and were 1.7 and 2.9 μM, respectively, suggesting that they could act as aggregates of glycoclusters. The amounts of the hydrophobic dye Orange OT loaded onto aqueous micelles of 4a and 4b and the stabilities of the dye/micelle complexes were determined by extracting the dyes from the complexes into chloroform. The particle sizes were measured for the loaded micelles by dynamic light scattering. Transfer of the dye from the micelles to peanut agglutinin was observed by fluorescence microscopy. Given the abilities of micelles of 4a and 4b to bind and release Orange OT, these glycocluster micelles may find use as drug-delivery systems.

Adsorption of polyprotic acid at the water/air interface

A rigorous thermodynamic treatment appropriate for surface adsorption from mixed aqueous solution of alkali and polyprotic acid was derived. Those equations were applied to mixed aqueous solution/air systems of alkali metal hydroxide and FeIII complex with ethylenediamine- N, N, N′,N′-tetraacetate (Fe-EDTA). Surface density of each species arising from Fe-EDTA was separately evaluated, and thus, surface activity of Fe-EDTA was studied, especially its dependence on pH and how it is influenced by the counter cations. Fe-EDTA was positively adsorbed at the water/air interface at very low pHs and negatively at high pHs. The pH range of positive adsorption of Fe-EDTA with potassium ion, as a counter ion, was wider than that with sodium ion. Thus, potassium ion, a structure breaker, tended to smooth surface adsorption of Fe-EDTA at the water/air interface, whereas sodium ion, a structure maker, tended to withdraw Fe-EDTA from the interfacial region.