Modulation of physical properties of reverse hexagonal mesophases: A dielectric spectroscopy study
[Display omitted] ► Three processes of the HII mesophase are detected using dielectric spectroscopy. ► Phosphatidylcholine affects the dynamic and kinetic properties of the HII matrix. ► 10wt.% phosphatidylcholine is the optimal concentration for structural stability. ► Triacylglycerol percolates an...
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Veröffentlicht in: | Journal of colloid and interface science 2013-04, Vol.396, p.178-186 |
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Format: | Artikel |
Sprache: | eng |
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► Three processes of the HII mesophase are detected using dielectric spectroscopy. ► Phosphatidylcholine affects the dynamic and kinetic properties of the HII matrix. ► 10wt.% phosphatidylcholine is the optimal concentration for structural stability. ► Triacylglycerol percolates and transfers between the HII rods.
The structural, dynamic, and kinetic aspects of the HII systems based on glycerol monooleate (GMO), phosphatidylcholine (PC), triacylglycerol (TAG), and water were investigated by dielectric spectroscopy in a frequency range of 10-2–106 Hz, and a temperature range of 290–320 K. Three distinct processes as well as a temperature-activated dc conductivity were detected and examined. These were assigned to the reorientation of the GMO polar heads, the tangential movement of counterions at the interface, the transport of TAGs through the lipids tails, and the ion mobility within the water cylinders.
Upon addition of PC, the critical temperature (T0) of the dehydration of the GMO headgroups increased. The optimal concentration found for structural stabilization of the HII mesophase was 10 wt% PC, since it imparted the strongest bonding at the interfacial layer and increased the association between the lipid tails. Within the HII cluster, TAG percolated and shifted between the hexagonal rods themselves.
The present study demonstrated the benefit of controlling the critical temperature of the HII mesophase partial dehydration and softening, as well as the percolation of TAGs. These factors influence the diffusion mode of embedded drugs in the physiological temperature range. |
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ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2012.12.067 |