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N-acetylcysteine-loaded electrospun mats improve wound healing in mice and human fibroblast proliferation
Author(s) -
Ramin Seyedian,
Elham Shabankareh Fard,
Maryam Najafiasl,
Majid Assadi,
Sasan Zaeri
Publication year - 2020
Publication title -
doaj (doaj: directory of open access journals)
Language(s) - English
Resource type - Journals
eISSN - 2008-3874
pISSN - 2008-3866
DOI - 10.22038/ijbms.2020.41550.11078
Subject(s) - wound healing , fibroblast , in vivo , chemistry , granulation tissue , polyvinyl alcohol , in vitro , electrospinning , pharmacology , dermal fibroblast , biomedical engineering , medicine , surgery , biochemistry , biology , microbiology and biotechnology , organic chemistry , polymer
Objective(s): N-acetylcysteine (NAC) has gained attention recently in dermatology as a unique anti-oxidant. In light of progress in nanotechnological methods, it was hypothesized that loading NAC onto nanofibers would positively affect skin wound healing. The objective of this study was to fabricate NAC-loaded electrospun mats and test their effect on wound healing in vivo and in vitro .Materials and Methods: Polyvinyl alcohol (PVA)-based mats loaded with NAC at three concentrations were electrospun and characterized in terms of physicochemical properties and drug release profile. Human fibroblast cells ( in vitro ) and mouse full-thickness skin wounds ( in vivo ) were treated with mats for 5 and 14 days, respectively. Wound area, tissue histopathology, fibroblast proliferation and cellular oxidative state were evaluated. Results: Mats containing 5% PVA/NAC showed thinner fibers with suitable physicochemical properties and a sustained drug release profile. PVA/NAC (5%) mats enhanced fibroblast proliferation and attachment in vitro . The mats resulted in significant wound closure with high levels of re-epithelialization and collagen fiber synthesis on day 14 post-surgery in vivo. The mats also reduced granulation tissue and edematous stroma to a higher extent. These findings were accompanied by a significant decrease in tissue lipid peroxidation and higher superoxide dismutase activity, which may explain how NAC improved wound healing. Conclusion: We propose an NAC-loaded nanofibrous mat that takes the advantage of a porous nanoscaffold structure to release NAC in a sustained manner. This mat may be a promising candidate for further clinical evaluation.

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