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Abstract

Hydrogels Based on Polysaccharides Grafted Ferulic Acid: A Biomimetic Approach †

by
Ahdi Hadrich
,
Didier Le Cerf
,
Virginie Dulong
and
Luc Picton
*
Polymères, Biopolymères, Surfaces (PBS) UMR6270 CNRS, Université de Rouen Normandie, 76821 Mont Saint Aignan, France
*
Author to whom correspondence should be addressed.
†
Presented at the 17th International Symposium “Priorities of Chemistry for a Sustainable Development” PRIOCHEM, Bucharest, Romania, 27–29 October 2021.
Chem. Proc. 2022, 7(1), 69; https://doi.org/10.3390/chemproc2022007069
Published: 28 April 2022
(This article belongs to the Proceedings of The 17th International Symposium “Priorities of Chemistry for a Sustainable Development” PRIOCHEM)
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Versions Notes

Some cereal seeds present mucilage composed of polysaccharides bearing ferulic acid (FA) groups, which are capable of reacting in the presence of an enzyme such as laccase to generate chemical hydrogels [1]. The main idea of this work, following a biomimetic approach, is to elaborate artificial polysaccharides grafted with ferulic acid groups [2]. Various polysaccharides have been studied: anionic ones (carboxymethylpullulane (CMP) as a model, hyaluronan (HA) for application) and neutral ones (pullulan (P)). We report here the availability of the grafting, the evidence of crosslinking (Figure 1) leading to hydrogels in the presence of laccase (as a function of FA, polymer and laccase amount) and evidence of antioxidant properties of such derivatives [3].

Author Contributions

Conceptualization, all; methodology, all; software, L.P.; validation, all; formal analysis, all; investigation, all; resources, all; data curation, all; writing—original draft preparation, all; writing—review and editing, L.P.; visualization, L.P.; supervision, L.P.; project administration, V.D. and L.P.; funding acquisition, V.D. and L.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Carvajal-Millan, E.; Landillon, V.; Morel, M.H.; Rouau, X.; Doublier, J.L.; Micard, V. Arabinoxylan gels: Impact of the feruloylation degree on their structure and properties. Biomacromolecules 2005, 6, 309–317. [Google Scholar] [CrossRef] [PubMed]
  2. Dulong, V.; Hadrich, A.; Picton, L.; Le Cerf, D. Enzymatic cross-linking of carboxymethylpullulan grafted with ferulic acid. Carbohydr. Polym. 2016, 151, 78–87. [Google Scholar] [CrossRef] [PubMed]
  3. Mathew, S.; Abraham, T.E. Ferulic acid: An antioxidant found naturally implant cell walls and feruloyl esterases involved in its release and their applications. Crit. Rev. Biotechnol. 2004, 24, 59–83. [Google Scholar] [CrossRef]
Chemproc 07 00069 g001 550
Figure 1. G’ vs. time for CMP-FA for various DSFA. Laccase at 2 nkat, 20 g L−1 in polymer, 25 °C in citrate/phosphate buffer (0.1 mol L−1 pH 5.5).
Figure 1. G’ vs. time for CMP-FA for various DSFA. Laccase at 2 nkat, 20 g L−1 in polymer, 25 °C in citrate/phosphate buffer (0.1 mol L−1 pH 5.5).
Chemproc 07 00069 g001
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MDPI and ACS Style

Hadrich, A.; Le Cerf, D.; Dulong, V.; Picton, L. Hydrogels Based on Polysaccharides Grafted Ferulic Acid: A Biomimetic Approach. Chem. Proc. 2022, 7, 69. https://doi.org/10.3390/chemproc2022007069

AMA Style

Hadrich A, Le Cerf D, Dulong V, Picton L. Hydrogels Based on Polysaccharides Grafted Ferulic Acid: A Biomimetic Approach. Chemistry Proceedings. 2022; 7(1):69. https://doi.org/10.3390/chemproc2022007069

Chicago/Turabian Style

Hadrich, Ahdi, Didier Le Cerf, Virginie Dulong, and Luc Picton. 2022. "Hydrogels Based on Polysaccharides Grafted Ferulic Acid: A Biomimetic Approach" Chemistry Proceedings 7, no. 1: 69. https://doi.org/10.3390/chemproc2022007069

APA Style

Hadrich, A., Le Cerf, D., Dulong, V., & Picton, L. (2022). Hydrogels Based on Polysaccharides Grafted Ferulic Acid: A Biomimetic Approach. Chemistry Proceedings, 7(1), 69. https://doi.org/10.3390/chemproc2022007069

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