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Processing of degradable ulvan 3D porous structures for biomedical applications
Author(s) -
Alves Anabela,
Sousa Rui A.,
Reis Rui L.
Publication year - 2013
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.34403
Subject(s) - materials science , biomaterial , porosity , scanning electron microscope , biomedical engineering , degradation (telecommunications) , chemical engineering , polysaccharide , morphology (biology) , nanotechnology , composite material , chemistry , computer science , biochemistry , biology , medicine , telecommunications , engineering , genetics
Abstract The interest in ulvan within a biomedical framework increases as the knowledge of this polysaccharide evolves. Ulvan has been recently proposed as a potential biomaterial, and structures based on this polysaccharide are now being studied for different biomedical applications. In this work, a novel porous structure based on cross‐linked ulvan was designed and characterized. Its mechanical performance, water‐uptake ability and weight loss were assessed, morphology analyzed through scanning electron microscopy, and morphometric parameters quantified by microcomputed tomography. Cell viability and cell proliferation were evaluated in order to estimate the cytotoxicity of these structures and respective degradation products. Produced ulvan structures revealed remarkable ability to uptake water (up to ∼ 2000% of its initial dry weight) and are characterized by a highly porous and interconnected structure. Furthermore, these ulvan structures underwent nontoxic degradation, and cells remained viable through the time of culture. These results position ulvan structures as prospective blocks that can be further functionalized in order to acquire the desired stability and needed biological interactivity to be used as tissue‐engineered structures. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2013.

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