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Peptide-Based Hydrogel for Nanosystems Encapsulation: the Next Generation of Localized Delivery Systems for the Treatment of Intestinal Inflammations.
Andretto, Valentina; Rosso, Annalisa; Zilio, Serena; Sidi-Boumedine, Jacqueline; Boschetti, Gilles; Sankar, Sharanya; Buffier, Marie; Miele, Adriana Erica; Denis, Morgane; Choffour, Pierre-Antoine; Briançon, Stéphanie; Nancey, Stéphane; Kryza, David; Lollo, Giovanna.
Afiliación
  • Andretto V; Univ Lyon, Université Claude Bernard Lyon 1, CNRS, LAGEPP UMR 5007, 43 Boulevard du 11 Novembre 1918, Villeurbanne, F-69622, France.
  • Rosso A; Univ Lyon, Université Claude Bernard Lyon 1, CNRS, LAGEPP UMR 5007, 43 Boulevard du 11 Novembre 1918, Villeurbanne, F-69622, France.
  • Zilio S; Univ Lyon, Université Claude Bernard Lyon 1, CNRS, LAGEPP UMR 5007, 43 Boulevard du 11 Novembre 1918, Villeurbanne, F-69622, France.
  • Sidi-Boumedine J; SATT, Ouest Valorisation, 14C Rue du Patis Tatelin, Renne, 35708, France.
  • Boschetti G; Univ Lyon, Université Claude Bernard Lyon 1, CNRS, LAGEPP UMR 5007, 43 Boulevard du 11 Novembre 1918, Villeurbanne, F-69622, France.
  • Sankar S; Department of Gastroenterology, Lyon Sud Hospital, Hospices Civil de Lyon and CIRI, Lyon, 69495, France.
  • Buffier M; 3-D Matrix Europe SAS, Medical Technology, Caluire-et-Cuire, 69300, France.
  • Miele AE; 3-D Matrix Europe SAS, Medical Technology, Caluire-et-Cuire, 69300, France.
  • Denis M; Univ Lyon, Université Claude Bernard Lyon 1, CNRS, ISA UMR 5280, 5 rue de la Doua, Villeurbanne, F-69100, France.
  • Choffour PA; Dept Biochemical Sciences, Sapienza University of Rome, P.le Aldo Moro 5, Rome, I-00185, Italy.
  • Briançon S; Univ Lyon, Université Claude Bernard Lyon, INSERM 1052, CNRS 5286, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Lyon, 69008, France.
  • Nancey S; Antineo, R&D Department, Lyon, 69008, France.
  • Kryza D; Antineo, R&D Department, Lyon, 69008, France.
  • Lollo G; Univ Lyon, Université Claude Bernard Lyon 1, CNRS, LAGEPP UMR 5007, 43 Boulevard du 11 Novembre 1918, Villeurbanne, F-69622, France.
Adv Healthc Mater ; 13(16): e2303280, 2024 06.
Article en En | MEDLINE | ID: mdl-38445812
ABSTRACT
Conventional 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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos / Hidrogeles Límite: Animals Idioma: En Revista: Adv Healthc Mater Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos / Hidrogeles Límite: Animals Idioma: En Revista: Adv Healthc Mater Año: 2024 Tipo del documento: Article País de afiliación: Francia