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Impact of Glucose on the Nanostructure and Mechanical Properties of Calcium-Alginate Hydrogels

Lopez-Sanchez, Patricia, 1977 (author)
Chalmers tekniska högskola,Chalmers University of Technology,Chalmers University of Technology, Sweden
Assifaoui, Ali (author)
Université Bourgogne Franche-Comté,University of Burgundy - Franche-Comté,Université de Bourgogne Franche-Comté, Sweden
Cousin, Fabrice (author)
Université Paris-Saclay,University Paris-Saclay,Université Paris-Saclay, France
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Moser, Josefine (author)
RISE,Jordbruk och livsmedel,RISE Research Institutes of Sweden
Bonilla, Mauricio R. (author)
Basque Center for Applied Mathematics (BCAM),Basque Center for Applied Mathematics, Spain
Ström, Anna, 1976 (author)
Chalmers tekniska högskola,Chalmers University of Technology,Chalmers University of Technology, Sweden
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 (creator_code:org_t)
2022-01-22
2022
English.
In: Gels. - : MDPI AG. - 2310-2861. ; 8:2
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Alginate is a polysaccharide obtained from brown seaweed that is widely used in food, pharmaceutical, and biotechnological applications due to its versatility as a viscosifier and gelling agent. Here, we investigated the influence of the addition of glucose on the structure and mechanical properties of alginate solutions and calcium-alginate hydrogels produced by internal gelation through crosslinking with Ca2+ . Using1H low-field nuclear magnetic resonance (NMR) and small angle neutron scattering (SANS), we showed that alginate solutions at 1 wt % present structural hetero-geneities at local scale whose size increases with glucose concentration (15–45 wt %). Remarkably, the molecular conformation of alginate in the gels obtained from internal gelation by Ca2+ crosslinking is similar to that found in solution. The mechanical properties of the gels evidence an increase in gel strength and elasticity upon the addition of glucose. The fitting of mechanical properties to a poroelastic model shows that structural changes within solutions prior to gelation and the increase in solvent viscosity contribute to the gel strength. The nanostructure of the gels (at local scale, i.e., up to few hundreds of Å) remains unaltered by the presence of glucose up to 30 wt %. At 45 wt %, the permeability obtained by the poroelastic model decreases, and the Young’s modulus increases. We suggest that macro (rather than micro) structural changes lead to this behavior due to the creation of a network of denser zones of chains at 45 wt % glucose. Our study paves the way for the design of calcium-alginate hydrogels with controlled structure for food and pharmaceutical applications in which interactions with glucose are of relevance.

Subject headings

NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Kemiteknik -- Polymerteknologi (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Chemical Engineering -- Polymer Technologies (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Materialteknik -- Annan materialteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Materials Engineering -- Other Materials Engineering (hsv//eng)

Keyword

Alginate
Glucose
Poroelasticity
Hydrogels
Crosslinking
Mechanical properties
SANS
Structure

Publication and Content Type

art (subject category)
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