Solubilization of dodac small unilamellar vesicles by sucrose esters: A fluorescence study
Author
dc.contributor.author
Becerra,
Author
dc.contributor.author
De La Nuez,
Author
dc.contributor.author
Zanocco Loyola, Antonio
Author
dc.contributor.author
Lemp Miranda, Else
Author
dc.contributor.author
Günther Sapunar, Germán
Admission date
dc.date.accessioned
2018-12-20T15:20:46Z
Available date
dc.date.available
2018-12-20T15:20:46Z
Publication date
dc.date.issued
2006
Cita de ítem
dc.identifier.citation
Colloids and Surfaces A: Physicochemical and Engineering Aspects, Volumen 272, Issue 1-2, 2018, Pages 2-7
Identifier
dc.identifier.issn
09277757
Identifier
dc.identifier.other
10.1016/j.colsurfa.2005.04.024
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/158904
Abstract
dc.description.abstract
A fluorescence method was employed to study the solubilizing interactions of several sucrose esters with Dioctadecyldimethylammonium chloride small unilamellar vesicles. In this paper we studied four different alkyl esters of sucrose, saturation and solubilization concentrations (Csat and Csol), the ester-DODAC molar ratio (Re) and bilayer/aqueous partition coefficients (K) were measured by monitoring changes in laurdan generalized polarization values. A new critical surfactant concentration at lower values than saturation concentration was observed. All critical concentrations showed linear dependence with DODAC concentration. The decrease in the length of surfactant alkyl chain (upper cmc) led to an increase in its ability to saturate and solubilize vesicles and to a decrease in its bilayer affinity. Consequently the shorter alkyl chain (lauryl sucrose ester), the higher ability to saturate and solubilize the vesicles, whereas the longer chain (stearyl sucrose ester), exhibited the h
The effect of the incorporation of the non-ionic surfactant sucrose palmitate in dioctadecyldimethylammonium chloride(DODAC) large unilamellar vesicles was studies by using several spectroscopic techniques. Significant ...
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In the present study we synthesized and purified several 6-O-sucrose monoesters by using classical synthetic methods and stereo-regioselective procedures. The compounds have different alkyl chain lengths, with the number ...