Mesoscopic and microscopic investigation on poly(vinyl alcohol) hydrogels in the presence of sodium decylsulfate

TitleMesoscopic and microscopic investigation on poly(vinyl alcohol) hydrogels in the presence of sodium decylsulfate
Publication TypeArticolo su Rivista peer-reviewed
Year of Publication2007
AuthorsMangiapia, G., Ricciardi Rosa, Auriemma F., De Rosa C., Celso F.L., Triolo R., Heenan R.K., Radulescu A., Tedeschi A.M., D'Errico G., and Paduano L.
JournalJournal of Physical Chemistry B
Volume111
Pagination2166-2173
ISSN15206106
KeywordsCrosslinking, Hydrogel membranes, Hydrogels, Molecular Structure, neutron scattering, Polyvinyl alcohols, Sodium decylsulfate, Solutions, Surface active agents, Surfactant micelles
Abstract

The structure of poly(vinyl alcohol) (PVA) hydrogels formed as a result of freeze/thaw treatments of aqueous solutions of the polymer (11 wt % PVA) in the freshly prepared state is analyzed through the combined use of small (SANS) and ultrasmall (USANS) angle neutron scattering techniques. The structure of these hydrogels may be described in terms of polymer rich regions, with dimensions of the order of 1-2 μm, dispersed in a water rich phase, forming two bicontinuous phases. The PVA chains in the polymer rich phase form a network where the cross-linking points are mainly crystalline aggregates of PVA having average dimensions of ∼45 Å. The structural organization of freeze/thaw PVA hydrogel membranes does not change either after rehydration of dried gels or in the presence of a tensile force. Finally, addition of surfactant micelles inside the gel provides a formulation with both hydrophobic and hydrophilic regions, which demonstrates the potential of the system for drug delivery. Both SANS and EPR measurements show that sodium decylsulfate (C10OS) micelles do not significantly interact with the PVA gel. Variation of the gel structure by the number of freeze/thaw cycles should modulate the rate of release of an active constituent, for example, in a dermal patch. © 2007 American Chemical Society.

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URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-33947431956&doi=10.1021%2fjp0663107&partnerID=40&md5=ec1679f82917166bdc47e4a695e1e533
DOI10.1021/jp0663107