Volume 104, Issue 7 pp. 1668-1679
Original Article

Thermo-responsive hydrogels from cellulose-based polyelectrolytes and catanionic vesicles for biomedical application

Gesmi Milcovich

Gesmi Milcovich

Department of Chemical and Pharmaceutical Sciences, University of Trieste, via L. Giorgieri 1, Trieste, I-34127 Italy

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Filipe Antunes

Filipe Antunes

Chemistry Department, University of Coimbra, Coimbra, 3004-535 Portugal

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Samuel Golob

Samuel Golob

Department of Chemical and Pharmaceutical Sciences, University of Trieste, P.le Europa, 1, Trieste, I-34127 Italy

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Rossella Farra

Rossella Farra

Department of Engineering and Architecture, University of Trieste, Trieste, I-34127 Italy

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Mario Grassi

Corresponding Author

Mario Grassi

Department of Engineering and Architecture, University of Trieste, Trieste, I-34127 Italy

Correspondence to. Mario Grassi; e-mail: [email protected]Search for more papers by this author
Dario Voinovich

Dario Voinovich

Department of Chemical and Pharmaceutical Sciences, University of Trieste, P.le Europa, 1, Trieste, I-34127 Italy

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Gabriele Grassi

Gabriele Grassi

Department of Life Sciences, University Hospital of Cattinara, Trieste, 34100 Italy

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Fioretta Asaro

Fioretta Asaro

Department of Chemical and Pharmaceutical Sciences, University of Trieste, via L. Giorgieri 1, Trieste, I-34127 Italy

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First published: 03 March 2016
Citations: 17

Abstract

In this study, negatively charged catanionic vesicles/hydrophobically modified hydroxyethylcellulose polymers thermo-responsive hydrogels have been fabricated. Vesicular aggregates were found to act as multifunctional junctions for networking of modified-cellulose water solutions. The contributions of the electrostatic and hydrophobic interactions were evaluated by changing either vesicles composition or the polymer hydrophobic substitution. Thermal-induced size and lamellarity of hydrogel-enclosed vesicles were detected, with further polygonal shape changes induced by cellulose-based polymer addition. The thermal transition was also found to tune hydrogel mechanical behaviour. The network formation was further assessed through molecular insights, which allow to determine the arrangement of the polymer chains on the vesicles' surface. The examined systems exhibited interesting thermo-responsive characteristics. Thus, vesicularly cross-linked hydrogels herein presented can offer a wide variety of applications, i.e. in biomedical field, as multi-drug delivery systems, thanks to their ability to provide for different environments to guest molecules, comprising bulk water, vesicles' interior and bilayers, sites on polymeric chains. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 1668–1679, 2016.

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