Design of polygalacturonate hydrogels using iron(II) as cross-linkers: A promising route to protect bioavailable iron against oxidation

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TitreDesign of polygalacturonate hydrogels using iron(II) as cross-linkers: A promising route to protect bioavailable iron against oxidation
Type de publicationJournal Article
Year of Publication2018
AuteursPoset AMaire du, Lerbret A, Zitolo A, Cousin F, Assifaoui A
JournalCARBOHYDRATE POLYMERS
Volume188
Pagination276-283
Date PublishedMAY 15
Type of ArticleArticle
ISSN0144-8617
Mots-clésGelation mechanism, Hydrogels, Iron(II), Mechanical properties, Polygalacturonate
Résumé

We designed stable and highly reproducible hydrogels by external unidirectional diffusion of Fe2+ ions into aqueous solutions of polygalacturonate (polyGal) chains. The Fe2+ ions act as cross-linkers between the Gal units in such a way that both the molar ratio R ([Fe2+]/[Galunits]=0.25) and the mesh size of the polyGal network at the local scale (zeta=75 +/- 5 angstrom) have constant values within the whole gel, as respectively determined by titration and Small Angle Neutron Scattering. From macroscopic point of view, there is a progressive decrease of polyGal concentration from the part of the gel formed in the early stages of the gelation process, which is homogeneous, transparent and whose Young modulus has a high value of similar to 10(5) Pa, up to the part of the gel formed in the late stages, which is heterogeneous, highly turbid and has a much lower Young modulus of similar to 10(3) Pa. Since the local organization of the polyGal chains remains identical all along the hydrogels, this macroscopic concentration gradient originates from the formation of heterogeneities at a mesoscopic length scale during the gelation process. In addition, X-ray Absorption Spectroscopy measurements remarkably reveal that Fe2+ ions keep their +II oxidation state in the whole gels once they have cross-linked the Gal units. These polyGal hydrogels thus protect iron against oxidation and could be used for iron fortification.

DOI10.1016/j.carbpol.2018.02.007