Peptide‐Based Hydrogel for Nanosystems Encapsulation: the Next Generation of Localized Delivery Systems for the Treatment of Intestinal Inflammations

Author:

Andretto Valentina1,Rosso Annalisa1,Zilio Serena12,Sidi‐Boumedine Jacqueline1,Boschetti Gilles3,Sankar Sharanya4,Buffier Marie4,Miele Adriana Erica56,Denis Morgane78,Choffour Pierre‐Antoine8,Briançon Stéphanie1,Nancey Stéphane3,Kryza David19,Lollo Giovanna1ORCID

Affiliation:

1. Univ Lyon Université Claude Bernard Lyon 1 CNRS LAGEPP UMR 5007, 43 Boulevard du 11 Novembre 1918 Villeurbanne F‐69622 France

2. SATT Ouest Valorisation 14C Rue du Patis Tatelin Renne 35708 France

3. Department of Gastroenterology Lyon Sud Hospital Hospices Civil de Lyon and CIRI Lyon 69495 France

4. 3‐D Matrix Europe SAS Medical Technology Caluire‐et‐Cuire 69300 France

5. Univ Lyon, Université Claude Bernard Lyon 1 CNRS ISA UMR 5280, 5 rue de la Doua Villeurbanne F‐69100 France

6. Dept Biochemical Sciences Sapienza University of Rome P.le Aldo Moro 5 Rome I‐00185 Italy

7. Univ Lyon Université Claude Bernard Lyon INSERM 1052, CNRS 5286, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon Lyon 69008 France

8. Antineo R&D Department Lyon 69008 France

9. Hospices Civils de Lyon Lyon 69437 France

Abstract

AbstractConventional therapies for inflammatory bowel diseases are mainly based on systemic treatments which cause side effects and toxicity over long‐term administration. Nanoparticles appear as a valid alternative to allow a preferential accumulation in inflamed tissues following oral administration while reducing systemic drug exposure. To increase their residence time in the inflamed intestine, the nanoparticles are here associated with a hydrogel matrix. A bioadhesive peptide‐based hydrogel is mixed with nanoemulsions, creating a hybrid lipid‐polymer nanocomposite. Mucopenetrating nanoemulsions of 100 nm are embedded in a scaffold constituted of the self‐assembling peptide hydrogel product PuraStat. The nanocomposite is fully characterized to study the impact of lipid particles in the hydrogel structure. Rheological measurements and circular dichroism analyses are performed to investigate the system's microstructure and physical properties. Biodistribution studies demonstrate that the nanocomposite acts as a depot in the stomach and facilitates the slow release of the nanoemulsions in the intestine. Efficacy studies upon oral administration of the drug‐loaded system show the improvement of the disease score in a mouse model of intestinal inflammation.

Funder

Agence Nationale de la Recherche

Publisher

Wiley

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