Journal
SOFT MATTER
Volume 5, Issue 23, Pages 4823-4834Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b907596h
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Funding
- Commonwealth of Australia
- National Science Foundation/Department of Energy [CHE-0535644]
- U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
- Australian Research Council Federation Fellowship
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The thermal and lyotropic liquid crystalline phase behaviour of a series of amide and monoethanolamide amphiphiles with isoprenoid-type hydrocarbon chains has been investigated. The amphiphilic nature of these molecules combined with their ability to form nanostructured self-assemblies makes them ideal candidates as delivery vehicles of bioactive molecules. For both families of molecules, increased branching in the hydrophobic chain, associated with increasing chain length, results in a decreased melting point. The melting points of the amides are significantly higher than their monoethanolamide homologues. Interestingly, both hexahydrofarnesoyl (H-farnesoyl) and phytanoyl monoethanolamide exhibit a glass transition temperature at around -72 degrees C to -74 degrees C. H-Farnesoyl and phytanoyl monoethanolamide form lyotropic liquid crystalline phases in water, whilst H-farnesoyl and phytanoyl amide form a spontaneous emulsion at the amphiphile-water interface. In particular, at room temperature H-farnesoyl and phytanoyl monoethanolamide form the Schwarz diamond (Q(II)(D)) and the Schoen gyroid (Q(II)(G)) bicontinuous cubic phases which are retained down to temperatures as low as 1 degrees C. Furthermore, phytanoyl monoethanolamide displays a Q(II)(D), Q(II)(G) and inverse hexagonal phase (H-II) at physiological temperature. Both phytanoyl and H-farnesoyl monoethanolamide form mesoporous cubic phases at room temperature that are easily dispersed into cubosomes. The robust nature of the nanostructured phase formation of these two monoethanolamides over a wide range of temperatures makes them ideal candidates for a variety of applications.
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