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May 17, 2026The International Journal of Lower Extremity Wounds0 citations

Topical Application of Sepia Ink Extract-Loaded Phytosome on Mouse Skin Injury Accelerates Wound Healing: A Histopathological, Immunohistochemical, and Biochemical Study

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IAIslam Ahmed AbdelmawgoodFAFatma AlshakmakHSHader I. Sakr

Key Points

  • This research aims to assess the wound healing efficacy of sepia ink extract and its nanoparticle-loaded phytosome in a murine model.
  • Mice were divided into five groups for treatment with sepia ink extract and phytosomes after inducing skin wounds.
  • Wound healing rates were evaluated through histopathological, immunohistochemical, and biochemical analyses.
  • The impact on oxidative stress and inflammation markers was measured post-treatment.
  • SIE-NP significantly improved the wound healing rate compared to SIE alone (p<0.01).
  • Both treatments reduced malondialdehyde levels and increased antioxidants like catalase and glutathione (p<0.05).
  • Treatment lowered inflammatory markers (TNF-α, IL-6) and decreased caspase 3 expression, indicating reduced apoptosis (p<0.01).

Abstract

Sepia officinalis ink contains bioactive secondary metabolites abundant in melanin granules, has extensive medicinal properties and is commonly utilized in the prevention of different diseases. This research examined the topical wound healing efficacy of sepia ink extract (SIE) and SIE- Nanoparticle-loaded phytosome (SIE-NP) in a murine model of excisional wound healing. Mice were divided into five groups, all groups were anesthetized, and excisional skin wounds were established using a biopsy punch, except the control group. Both SIE and SIE-NP significantly improved the wound healing rate; nevertheless, the effect of SIE-NP was more pronounced. Treatment with SIE and SIE-NP accelerated the wound healing process by mitigating oxidative stress, evidenced by a reduction in malondialdehyde levels and an enhancement in antioxidants levels, including catalase and glutathione. SIE and SIE-NP attenuated oxidative stress-induced DNA fragmentation in wound tissue. Additionally, they reduced the levels of inflammatory markers, such as TNF-α and IL-6, myeloperoxidase activity, and the infiltration of inflammatory cells in the skin tissue. Furthermore, SIE and SIE-NP reduced histopathological abnormalities and concentration of fragmented DNA and elevated nitric oxide levels and collagen content. Moreover, SIE and SIE-NP decreased apoptosis by lowering caspase 3 expression. The data indicate that SIE and SIE-NP expedited wound healing via their antioxidant, anti-inflammatory, and anti-apoptotic characteristics.

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Cite This Study

Abdelmawgood et al. (2026) studied this question.

synapsesocial.com/papers/6a095c6d7880e6d24efe2867https://doi.org/10.1177/15347346261448965
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