Hesperidin - loaded PVA/alginate hydrogel: targeting NFκB/iNOS/COX-2/TNF-α inflammatory signaling pathway

Front Immunol. 2024 Apr 15:15:1347420. doi: 10.3389/fimmu.2024.1347420. eCollection 2024.

Abstract

Introduction: Skin injuries represent a prevalent form of physical trauma, necessitating effective therapeutic strategies to expedite the wound healing process. Hesperidin, a bioflavonoid naturally occurring in citrus fruits, exhibits a range of pharmacological attributes, including antimicrobial, antioxidant, anti-inflammatory, anticoagulant, and analgesic properties. The main objective of the study was to formulate a hydrogel with the intention of addressing skin conditions, particularly wound healing.

Methods: This research introduces a methodology for the fabrication of a membrane composed of a Polyvinyl alcohol - Sodium Alginate (PVA/A) blend, along with the inclusion of an anti-inflammatory agent, Hesperidin (H), which exhibits promising wound healing capabilities. A uniform layer of a homogeneous solution comprising PVA/A was cast. The process of crosslinking and the enhancement of hydrogel characteristics were achieved through the application of gamma irradiation at a dosage of 30 kGy. The membrane was immersed in a Hesperidin (H) solution, facilitating the permeation and absorption of the drug. The resultant system is designed to deliver H in a controlled and sustained manner, which is crucial for promoting efficient wound healing. The obtained PVA/AH hydrogel was evaluated for cytotoxicity, antioxidant and free radical scavenging activities, anti-inflammatory and membrane stability effect. In addition, its action on oxidative stress, and inflammatory markers was evaluated on BJ-1 human normal skin cell line.

Results and discussion: We determined the effect of radical scavenging activity PVA/A (49 %) and PVA/AH (87%), the inhibition of Human red blood cell membrane hemolysis by PVA/AH (81.97 and 84.34 %), hypotonicity (83.68 and 76.48 %) and protein denaturation (83.17 and 85.8 %) as compared to 250 μg/ml diclofenac (Dic.) and aspirin (Asp.), respectively. Furthermore, gene expression analysis revealed an increased expression of genes associated with anti-oxidant and anti-inflammatory properties and downregulated TNFα, NFκB, iNOS, and COX2 by 67, 52, 58 and 60%, respectively, by PVA/AH hydrogel compared to LPS-stimulated BJ-1 cells. The advantages associated with Hesperidin can be ascribed to its antioxidant and anti-inflammatory attributes. The incorporation of Hesperidin into hydrogels offers promise for the development of a novel, secure, and efficient strategy for wound healing. This innovative approach holds potential as a solution for wound healing, capitalizing on the collaborative qualities of PVA/AH and gamma irradiation, which can be combined to establish a drug delivery platform for Hesperidin.

Keywords: biomaterial hydrogel; gamma irradiation; hesperidin; hydrogel; wound dressing; wound healing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alginates* / chemistry
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / pharmacology
  • Antioxidants / chemistry
  • Antioxidants / pharmacology
  • Cyclooxygenase 2 / metabolism
  • Hesperidin* / chemistry
  • Hesperidin* / pharmacology
  • Humans
  • Hydrogels* / chemistry
  • Inflammation / drug therapy
  • NF-kappa B* / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Polyvinyl Alcohol* / chemistry
  • Signal Transduction / drug effects
  • Tumor Necrosis Factor-alpha* / metabolism
  • Wound Healing / drug effects

Substances

  • Hesperidin
  • Polyvinyl Alcohol
  • Alginates
  • NF-kappa B
  • Tumor Necrosis Factor-alpha
  • Hydrogels
  • Anti-Inflammatory Agents
  • Cyclooxygenase 2
  • Nitric Oxide Synthase Type II
  • Antioxidants

Grants and funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.