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Low Temperature Dissolution of Yeast Chitin-Glucan Complex and Characterization of the Regenerated Polymer
Publication . Araújo, Diana; Delgado Alves, Vitor; Marques, Ana C.; Fortunato, Elvira; Reis, Maria A.M.; Freitas, Filomena
Chitin-glucan complex (CGC) is a copolymer composed of chitin and glucan moieties
extracted from the cell-walls of several yeasts and fungi. Despite its proven valuable properties, that
include antibacterial, antioxidant and anticancer activity, the utilization of CGC in many applications
is hindered by its insolubility in water and most solvents. In this study, NaOH/urea solvent systems
were used for the first time for solubilization of CGC extracted from the yeast Komagataella pastoris.
Di erent NaOH/urea ratios (6:8, 8:4 and 11:4 (w/w), respectively) were used to obtain aqueous
solutions using a freeze/thaw procedure. There was an overall solubilization of 63–68%, with the
highest solubilization rate obtained for the highest tested urea concentration (8 wt%). The regenerated
polymer, obtained by dialysis of the alkali solutions followed by lyophilization, formed porous
macrostructures characterized by a chemical composition similar to that of the starting co-polymer,
although the acetylation degree decreased from 61.3% to 33.9–50.6%, indicating that chitin was
converted into chitosan, yielding chitosan-glucan complex (ChGC). Consistent with this, there was
a reduction of the crystallinity index and thermal degradation temperature. Given these results, this
study reports a simple and green procedure to solubilize CGC and obtain aqueous ChGC solutions
that can be processed as novel biomaterials
Novel hydrogels based on yeast chitin-glucan complex: Characterization and safety assessment
Publication . Araújo, Diana; Delgado Alves, Vitor; Lima, Sofia A.C.; Reis, Salette; Freitas, Filomena; Reis, Maria A.M.
Chitin-glucan complex (CGC) was used for the first time for the preparation of hydrogels. Alkali solvent systems, NaOH and KOH solutions, either at 1 or 5 mol/L, were used for CGC dissolution using a freeze-thaw procedure (freezing at −20 °C and thawing at room temperature; four cycles). The CGC solutions thus obtained were subjected to dialysis that induced the spontaneous gelation of the biopolymer, yielding translucid hydrogels with a yellowish coloration. Although all CGC hydrogels exhibited porous microstructures, high water content (above 97%) and good mechanical properties, their morphology, viscoelastic properties and texture were influenced by the type of solvent system used for CGC dissolution, as well as by their ionic strength. The K-based hydrogels presented a less compact network with larger pores and exhibited lower elastic properties. The Na-based hydrogels, on the other hand, exhibited a denser structure with smaller pores and a stiffer gel structure. These results show that it is possible to prepare CGC hydrogels with differing characteristics that can be suitable for different applications. Furthermore, all hydrogels were non-cytotoxic towards L929 fibroblasts and HaCaT keratinocytes. This study demonstrates CGC can be used to prepare biocompatible hydrogels with properties render them promising biomaterials
Chitin-glucan complex – Based biopolymeric structures using biocompatible ionic liquids
Publication . Ferreira, Inês C.; Araújo, Diana; Voisin, Pierre; Delgado Alves, Vitor; Rosatella, Andreia A.; Afonso, Carlos A.M.; Freitas, Filomena; Neves, Luísa A.
This work explores the novelty of dissolving chitin-glucan complex (CGC), from two fungal strains, Komagataella pastoris (CGCP) and Aspergillus niger (CGCKZ) (KiOnutrime-CG™), using biocompatible ionic liquids (ILs). Three cholinium-based ILs were tested, choline acetate, choline propionate and choline hexanoate. Although all tested ILs resulted in the dissolution of the co-polymer at a concentration of 5 % (w/w), distinct polymeric structures, films or gels, were obtained from CGCP and CGCKZ, respectively. CGCP films were dense, flexible and elastic, with high swelling capacity (> 200 %). The IL anion alkyl chain length influenced the polymeric structures’ properties, namely, the CGCP films elongation at break and swelling degree. CGCKZ resulted in weak gels. For both polymeric structures, exposure to the ILs under the dissolution conditions caused significant changes in the co-polymers’ chemical structure, namely, reduction of their glucan moiety and reduction of the degree of acetylation, thus yielding chitosan-glucan complexes (ChGC) enriched in glucosamine (53.4 ± 0.3–60.8 ± 0.3 %)
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Funding agency
Fundação para a Ciência e a Tecnologia
Funding programme
OE
Funding Award Number
PTDC/EME-MFE/71960/2006
