INQUISUR   21779
INSTITUTO DE QUIMICA DEL SUR
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Interaction between ascorbyl palmitate and water
Autor/es:
ERICA P. SCHULZ; LUCIANO BENEDINI; PAULA V. MESSINA; PABLO C. SCHULZ; SANTIAGO D. PALMA; DANIEL A. ALLEMANDI
Lugar:
Córdoba
Reunión:
Congreso; RICIFA 2010 1ª Reunión Internacional de Ciencias Farmacéuticas; 2010
Institución organizadora:
Universidad Nacional de Córdoba
Resumen:
This work addresses the ascorbyl palmitate (Asc16) aqueous systems. It has been studied through differential scanning calorimetry (DSC) and polarizing microscopy (PM) at different temperatures over a wide range of concentrations (weight fractions (w/w) between 0.05 and 1.0), allowing the determination of a complete phase diagram. When possible, the findings were corroborated with literature data. Systems below C≈0.48wt fraction show hydrated crystals in an isotropic liquid, which lead to a lamellar liquid crystal when heated to about 60 ◦C. Above this concentration, the phase transition occurs at about 80 ◦C, giving a cubic liquid crystal which in turn becomes lamellar liquid crystal at about 90 ◦C. The texture of this lamellar mesophase is different to that produced at lower concentrations. It has been determined, through DSC analysis of the melting peaks of water, computer simulation of the hydration of Asc16molecules and amodel of the hydrated aggregates (hydrated crystals and lamellarmesophase), that low concentration liquid crystals exist provided bulk water is present in the system. Two other kinds of water but bulk were detected: a first hydration shell, with watermolecules strongly attached by hydrogen bonds to the oxygen and hydrogen atoms of the polar headgroup, which does not melt and is then undetectable by DSC (11.47±0.95watermolecules per surfactantmolecule) and a second hydration layer containing 59±17watermolecules per surfactant one (apart fromthose in the first hydration layer). The number of water molecules in the second hydration layer decreases as the surfactant concentration increases, and vanishes at C = 0.62±0.01wt fraction (computer simulation and structure model data) or at C = 0.667±0.007 (DSC). At very high concentrations the formation of mesophases is preceded by the melting of the chains, giving a waxy texture when viewed at the polarizing microscope, maintaining the structure of crystals because the anhydrous polar bilayer remains “solid”.