A new technique to obtain microporous hydrogels was realised. It permits us to obtain a microporous structure directly on the already cross-linked hydrogel. It consists in stratifying the already cross-linked hydrogel on to a filter with known porosity and forcing the CO2 bubbles, derived from the addition of HCI to a porogen salt (NaHCO3), to cross through the filter first and then the matrix. By changing the porosity of the filter, it was possible to modulate the porous morphology of the hydrogels. The polysaccharides selected were hyaluronane, alginate, and carboxymethylcellulose. The influence of the porous morphology on the physico-chemical properties of the gel has been evaluated by FT-IR, FRAP, calorimetric, water uptake, and rheological analysis. © 2004 Kluwer Academic Publishers.
Leone, G., Barbucci, R., Borzacchiello, A., Ambrosio, L., Netti, P., Migliaresi, C. (2004). Preparation and physico-chemical characterisation of microporous polysaccharidic hydrogels. JOURNAL OF MATERIALS SCIENCE. MATERIALS IN MEDICINE, 15(4), 463-467 [10.1023/B:JMSM.0000021121.91449.f4].
Preparation and physico-chemical characterisation of microporous polysaccharidic hydrogels
Leone, Gemma;Barbucci, Rolando;
2004-01-01
Abstract
A new technique to obtain microporous hydrogels was realised. It permits us to obtain a microporous structure directly on the already cross-linked hydrogel. It consists in stratifying the already cross-linked hydrogel on to a filter with known porosity and forcing the CO2 bubbles, derived from the addition of HCI to a porogen salt (NaHCO3), to cross through the filter first and then the matrix. By changing the porosity of the filter, it was possible to modulate the porous morphology of the hydrogels. The polysaccharides selected were hyaluronane, alginate, and carboxymethylcellulose. The influence of the porous morphology on the physico-chemical properties of the gel has been evaluated by FT-IR, FRAP, calorimetric, water uptake, and rheological analysis. © 2004 Kluwer Academic Publishers.File | Dimensione | Formato | |
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https://hdl.handle.net/11365/18555
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