Marine Drugs (Feb 2023)

Enhanced Wound Healing Potential of <i>Spirulina platensis</i> Nanophytosomes: Metabolomic Profiling, Molecular Networking, and Modulation of HMGB-1 in an Excisional Wound Rat Model

  • Hanan Refai,
  • Amira A. El-Gazar,
  • Ghada M. Ragab,
  • Doaa H. Hassan,
  • Omar S. Ahmed,
  • Rehab A. Hussein,
  • Samah Shabana,
  • Pierre Waffo-Téguo,
  • Josep Valls,
  • Asmaa K. Al-Mokaddem,
  • Heba Mohammed Refat M. Selim,
  • Einas Mohamed Yousef,
  • Sahar K. Ali,
  • Ahmed Salman,
  • Hagar B. Abo-Zalam,
  • Rofida Albash

DOI
https://doi.org/10.3390/md21030149
Journal volume & issue
Vol. 21, no. 3
p. 149

Abstract

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Excisional wounds are considered one of the most common physical injuries. This study aims to test the effect of a nanophytosomal formulation loaded with a dried hydroalcoholic extract of S. platensis on promoting excisional wound healing. The Spirulina platensis nanophytosomal formulation (SPNP) containing 100 mg PC and 50 mg CH exhibited optimum physicochemical characteristics regarding particle size (598.40 ± 9.68 nm), zeta potential (−19.8 ± 0.49 mV), entrapment efficiency (62.76 ± 1.75%), and Q6h (74.00 ± 1.90%). It was selected to prepare an HPMC gel (SPNP-gel). Through metabolomic profiling of the algal extract, thirteen compounds were identified. Molecular docking of the identified compounds on the active site of the HMGB-1 protein revealed that 12,13-DiHome had the highest docking score of −7.130 kcal/mol. SPNP-gel showed higher wound closure potential and enhanced histopathological alterations as compared to standard (MEBO® ointment) and S. platensis gel in wounded Sprague-Dawley rats. Collectively, NPS promoted the wound healing process by enhancing the autophagy process (LC3B/Beclin-1) and the NRF-2/HO-1antioxidant pathway and halting the inflammatory (TNF-, NF-κB, TlR-4 and VEGF), apoptotic processes (AIF, Caspase-3), and the downregulation of HGMB-1 protein expression. The present study’s findings suggest that the topical application of SPNP-gel possesses a potential therapeutic effect in excisional wound healing, chiefly by downregulating HGMB-1 protein expression.

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