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Carvacrol-Loaded Phytosomes for Enhanced Wound Healing: Molecular Docking, Formulation, DoE-Aided Optimization, and in vitro/in vivo Evaluation

BACKGROUND: Despite recent advances in wound healing products, phytochemicals have been considered promising and attractive alternatives. Carvacrol (CAR), a natural phenolic compound, has been reported to be effective in wound healing. PURPOSE: This work endeavored to develop novel CAR-loaded phytos...

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Autores principales: Tafish, Ahmed Mowafy, El-Sherbiny, Mohamed, Al‐Karmalawy, Ahmed A, Soliman, Osama Abd El-Azeem, Saleh, Noha Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578319/
https://www.ncbi.nlm.nih.gov/pubmed/37849641
http://dx.doi.org/10.2147/IJN.S421617
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author Tafish, Ahmed Mowafy
El-Sherbiny, Mohamed
Al‐Karmalawy, Ahmed A
Soliman, Osama Abd El-Azeem
Saleh, Noha Mohamed
author_facet Tafish, Ahmed Mowafy
El-Sherbiny, Mohamed
Al‐Karmalawy, Ahmed A
Soliman, Osama Abd El-Azeem
Saleh, Noha Mohamed
author_sort Tafish, Ahmed Mowafy
collection PubMed
description BACKGROUND: Despite recent advances in wound healing products, phytochemicals have been considered promising and attractive alternatives. Carvacrol (CAR), a natural phenolic compound, has been reported to be effective in wound healing. PURPOSE: This work endeavored to develop novel CAR-loaded phytosomes for the enhancement of the wound healing process. METHODS: Molecular docking was performed to compare the affinities of the different types of phospholipids to CAR. Phytosomes were prepared by three methods (thin-film hydration, cosolvency, and salting out) using Lipoid S100 and Phospholipon 90H with three levels of saturation percent (0%, 50%, and 100%), and three levels of phospholipid molar percent (66.67%, 75%, and 80%). The optimization was performed using Design Expert where particle size, polydispersity index, and zeta potential were chosen as dependent variables. The optimized formula (F1) was further investigated regarding entrapment efficiency, TEM, (1)H-NMR, FT-IR, DSC, X-RD, in vitro release, ex vivo permeation, and stability. Furthermore, it was incorporated into a hydrogel formulation, and an in vivo study was conducted to investigate the wound-healing properties of F1. RESULTS: F1 was chosen as the optimized formula prepared via the thin-film hydration method with a saturation percent and a phospholipid molar percent of zero and 66.67, respectively. TEM revealed the spherical shape of phytosomal vesicles with uniform size, while the results of (1)H-NMR, FT-IR, DSC, and X-RD confirmed the formation of the phytosomal complex. F1 demonstrated a higher in vitro release and a slower permeation than free CAR. The wound area of F1-treated animals showed a marked reduction associated with a high degree of collagen fiber deposition and enhanced cellular proliferation. CONCLUSION: F1 can be considered as a promising remedy for the enhancement of wound healing and hence it would be hoped to undergo further investigation.
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spelling pubmed-105783192023-10-17 Carvacrol-Loaded Phytosomes for Enhanced Wound Healing: Molecular Docking, Formulation, DoE-Aided Optimization, and in vitro/in vivo Evaluation Tafish, Ahmed Mowafy El-Sherbiny, Mohamed Al‐Karmalawy, Ahmed A Soliman, Osama Abd El-Azeem Saleh, Noha Mohamed Int J Nanomedicine Original Research BACKGROUND: Despite recent advances in wound healing products, phytochemicals have been considered promising and attractive alternatives. Carvacrol (CAR), a natural phenolic compound, has been reported to be effective in wound healing. PURPOSE: This work endeavored to develop novel CAR-loaded phytosomes for the enhancement of the wound healing process. METHODS: Molecular docking was performed to compare the affinities of the different types of phospholipids to CAR. Phytosomes were prepared by three methods (thin-film hydration, cosolvency, and salting out) using Lipoid S100 and Phospholipon 90H with three levels of saturation percent (0%, 50%, and 100%), and three levels of phospholipid molar percent (66.67%, 75%, and 80%). The optimization was performed using Design Expert where particle size, polydispersity index, and zeta potential were chosen as dependent variables. The optimized formula (F1) was further investigated regarding entrapment efficiency, TEM, (1)H-NMR, FT-IR, DSC, X-RD, in vitro release, ex vivo permeation, and stability. Furthermore, it was incorporated into a hydrogel formulation, and an in vivo study was conducted to investigate the wound-healing properties of F1. RESULTS: F1 was chosen as the optimized formula prepared via the thin-film hydration method with a saturation percent and a phospholipid molar percent of zero and 66.67, respectively. TEM revealed the spherical shape of phytosomal vesicles with uniform size, while the results of (1)H-NMR, FT-IR, DSC, and X-RD confirmed the formation of the phytosomal complex. F1 demonstrated a higher in vitro release and a slower permeation than free CAR. The wound area of F1-treated animals showed a marked reduction associated with a high degree of collagen fiber deposition and enhanced cellular proliferation. CONCLUSION: F1 can be considered as a promising remedy for the enhancement of wound healing and hence it would be hoped to undergo further investigation. Dove 2023-10-12 /pmc/articles/PMC10578319/ /pubmed/37849641 http://dx.doi.org/10.2147/IJN.S421617 Text en © 2023 Tafish et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Tafish, Ahmed Mowafy
El-Sherbiny, Mohamed
Al‐Karmalawy, Ahmed A
Soliman, Osama Abd El-Azeem
Saleh, Noha Mohamed
Carvacrol-Loaded Phytosomes for Enhanced Wound Healing: Molecular Docking, Formulation, DoE-Aided Optimization, and in vitro/in vivo Evaluation
title Carvacrol-Loaded Phytosomes for Enhanced Wound Healing: Molecular Docking, Formulation, DoE-Aided Optimization, and in vitro/in vivo Evaluation
title_full Carvacrol-Loaded Phytosomes for Enhanced Wound Healing: Molecular Docking, Formulation, DoE-Aided Optimization, and in vitro/in vivo Evaluation
title_fullStr Carvacrol-Loaded Phytosomes for Enhanced Wound Healing: Molecular Docking, Formulation, DoE-Aided Optimization, and in vitro/in vivo Evaluation
title_full_unstemmed Carvacrol-Loaded Phytosomes for Enhanced Wound Healing: Molecular Docking, Formulation, DoE-Aided Optimization, and in vitro/in vivo Evaluation
title_short Carvacrol-Loaded Phytosomes for Enhanced Wound Healing: Molecular Docking, Formulation, DoE-Aided Optimization, and in vitro/in vivo Evaluation
title_sort carvacrol-loaded phytosomes for enhanced wound healing: molecular docking, formulation, doe-aided optimization, and in vitro/in vivo evaluation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578319/
https://www.ncbi.nlm.nih.gov/pubmed/37849641
http://dx.doi.org/10.2147/IJN.S421617
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