4.7 Article

Silk fibroin nanoparticles enhance quercetin immunomodulatory properties in DSS-induced mouse colitis

Journal

INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 606, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ijpharm.2021.120935

Keywords

Inflammatory bowel disease; Silk fibroin nanoparticles; Quercetin; Anti-inflammatory; Drug loading

Funding

  1. European Commission ERDF/FEDER Operational Programme `Murcia' CCI [2007ES161PO001, 14-20/20]
  2. Junta de Andalucia [CTS164]
  3. Instituto de Salud Carlos III [PI19/01058]
  4. Spanish MINECO [CTQ201787708-R]
  5. ERDF/FEDER Operational Programme 'Murcia' CCI [2007ES161PO001, 14-20/20]

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Inflammatory bowel disease (IBD) is a chronic inflammatory disorder with limited effectiveness in current pharmacological treatments. Research suggests that loading quercetin in silk fibroin nanoparticles may have anti-inflammatory effects and serve as a promising treatment for IBD.
Inflammatory bowel disease (IBD) is a chronic and idiopathic inflammatory disorder affecting the gastrointes-tinal tract. The pharmacological treatments used currently for its treatment lack efficacy, so new therapeutic strategies should be developed. In this context, flavonoids loaded in biopolymeric nanoparticles can be considered as novel promising candidates. The aim of the present study was to evaluate the intestinal anti-inflammatory effects of quercetin when is administered loaded in silk fibroin nanoparticles (QSFN) in the dextran sulphate sodium experimental model of mouse colitis, which displays some similarities to human IBD. Previously characterized quercetin-loaded silk fibroin nanoparticles (QSFN). QSFN showed a reversible aggre-gation profile induced by the acidification of the solution but did not affect the loaded quercetin. Daily administration of QSFN significantly reduced disease activity index values compared to the control colitic group. This beneficial effect was not only corroborated by the histological examination of the colonic specimens but also the improvement of the colonic expression of the different proinflammatory cytokines (Tnf-alpha, Il-1 beta, Il-6, Mcp-1, Icam-1, Nlrp3 and iNOS). Therefore, these data suggest that QSFN could be a promising alternative to current treatments as a drug delivery system for IBD treatment.

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