Eobania vermiculata whole-body muscle extract-loaded chitosan nanoparticles enhanced skin regeneration and decreased pro-inflammatory cytokines in vivo.


Journal

Journal of nanobiotechnology
ISSN: 1477-3155
Titre abrégé: J Nanobiotechnology
Pays: England
ID NLM: 101152208

Informations de publication

Date de publication:
13 Oct 2023
Historique:
received: 20 08 2023
accepted: 04 10 2023
medline: 1 11 2023
pubmed: 13 10 2023
entrez: 12 10 2023
Statut: epublish

Résumé

Usually, wounds recover in four to six weeks. Wounds that take longer time than this to heal are referred to as chronic wounds. Impaired healing can be caused by several circumstances like hypoxia, microbial colonization, deficiency of blood flow, reperfusion damage, abnormal cellular reaction and deficiencies in collagen production. Treatment of wounds can be enhanced through systemic injection of the antibacterial drugs and/or other topical applications of medications. However, there are a number of disadvantages to these techniques, including the limited or insufficient medication penetration into the underlying skin tissue and the development of bacterial resistance with repeated antibiotic treatment. One of the more recent treatment options may involve using nanotherapeutics in combination with naturally occurring biological components, such as snail extracts (SE). In this investigation, chitosan nanoparticles (CS NPs) were loaded with an Eobania vermiculata whole-body muscle extract. The safety of the synthesized NPs was investigated in vitro to determine if these NPs might be utilized to treat full-skin induced wounds in vivo. SEM and TEM images showed uniformly distributed, spherical, smooth prepared CS NPs and snail extract-loaded chitosan nanoparticles (SE-CS NPs) with size ranges of 76-81 and 91-95 nm, respectively. The zeta potential of the synthesized SE-CS NPs was - 24.5 mV, while that of the CS NPs was 25 mV. SE-CS NPs showed a remarkable, in vitro, antioxidant, anti-inflammatory and antimicrobial activities. Successfully, SE-CS NPs (50 mg/kg) reduced the oxidative stress marker (malondialdehyde), reduced inflammation, increased the levels of the antioxidant enzymes (superoxide dismutase and glutathione), and assisted the healing of induced wounds. SE-CS NPs (50 mg/kg) can be recommended to treat induced wounds safely. SE was composed of a collection of several wound healing bioactive components [fatty acids, amino acids, minerals and vitamins) that were loaded on CS NPs. The nanostructure enabled bioactive SE components to pass through cell membranes and exhibit their antioxidant and anti-inflammatory actions, accelerating the healing process of wounds. Finally, it is advised to treat rats' wounds with SE-CS NPs.

Sections du résumé

BACKGROUND BACKGROUND
Usually, wounds recover in four to six weeks. Wounds that take longer time than this to heal are referred to as chronic wounds. Impaired healing can be caused by several circumstances like hypoxia, microbial colonization, deficiency of blood flow, reperfusion damage, abnormal cellular reaction and deficiencies in collagen production. Treatment of wounds can be enhanced through systemic injection of the antibacterial drugs and/or other topical applications of medications. However, there are a number of disadvantages to these techniques, including the limited or insufficient medication penetration into the underlying skin tissue and the development of bacterial resistance with repeated antibiotic treatment. One of the more recent treatment options may involve using nanotherapeutics in combination with naturally occurring biological components, such as snail extracts (SE). In this investigation, chitosan nanoparticles (CS NPs) were loaded with an Eobania vermiculata whole-body muscle extract. The safety of the synthesized NPs was investigated in vitro to determine if these NPs might be utilized to treat full-skin induced wounds in vivo.
RESULTS RESULTS
SEM and TEM images showed uniformly distributed, spherical, smooth prepared CS NPs and snail extract-loaded chitosan nanoparticles (SE-CS NPs) with size ranges of 76-81 and 91-95 nm, respectively. The zeta potential of the synthesized SE-CS NPs was - 24.5 mV, while that of the CS NPs was 25 mV. SE-CS NPs showed a remarkable, in vitro, antioxidant, anti-inflammatory and antimicrobial activities. Successfully, SE-CS NPs (50 mg/kg) reduced the oxidative stress marker (malondialdehyde), reduced inflammation, increased the levels of the antioxidant enzymes (superoxide dismutase and glutathione), and assisted the healing of induced wounds. SE-CS NPs (50 mg/kg) can be recommended to treat induced wounds safely. SE was composed of a collection of several wound healing bioactive components [fatty acids, amino acids, minerals and vitamins) that were loaded on CS NPs.
CONCLUSIONS CONCLUSIONS
The nanostructure enabled bioactive SE components to pass through cell membranes and exhibit their antioxidant and anti-inflammatory actions, accelerating the healing process of wounds. Finally, it is advised to treat rats' wounds with SE-CS NPs.

Identifiants

pubmed: 37828599
doi: 10.1186/s12951-023-02143-3
pii: 10.1186/s12951-023-02143-3
pmc: PMC10571447
doi:

Substances chimiques

Chitosan 9012-76-4
Antioxidants 0
Cytokines 0
Anti-Inflammatory Agents 0
Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

373

Informations de copyright

© 2023. BioMed Central Ltd., part of Springer Nature.

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Auteurs

Alyaa Farid (A)

Biotechnology Department, Faculty of Science, Cairo University, Giza, Egypt. alyaafarid@cu.edu.eg.

Adham Ooda (A)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Ahmed Nabil (A)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Areej Nasser (A)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Esraa Ahmed (E)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Fatma Ali (F)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Fatma Mohamed (F)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Habiba Farid (H)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Mai Badran (M)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Mariam Ahmed (M)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Mariam Ibrahim (M)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Mariam Rasmy (M)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Martina Saleeb (M)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Vereena Riad (V)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Yousr Ibrahim (Y)

Biotechnology/Biomolecular Chemistry Program, Faculty of Science, Cairo University, Giza, Egypt.

Neveen Madbouly (N)

Zoology Department, Faculty of Science, Cairo University, Giza, Egypt.

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Classifications MeSH