Abstract

There is currently a huge need for new, improved therapeutic approaches for the treatment of chronic wounds. One promising strategy is to develop wound dressings capable of modulating the chronic wound environment (e.g., by controlling the high levels of reactive oxygen species (ROS) and proteases). Here, we selected the thiol-containing amino acid cysteine to endow wood-derived cellulose nanofibrils (CNF) with bioactivity toward the modulation of ROS levels and protease activity. Cysteine was covalently incorporated into CNF and the functionalized material, herein referred as cys-CNF, was characterized in terms of chemical structure, degree of substitution, radical scavenging capacity, and inhibition of protease activity. The stability of the thiol groups was evaluated over time, and an in vitro cytotoxicity study with human dermal fibroblasts was performed to evaluate the safety profile of cys-CNF. Results showed that cys-CNF was able to efficiently control the activity of the metalloprotease collagenase and to inhibit the free radical DPPH (1,1-Diphenyl-2-picrylhydrazyl radical), activities that were correlated with the presence of free thiol groups on the nanofibers. The stability study showed that the reactivity of the thiol groups challenged the bioactivity over time. Nevertheless, preparing the material as an aerogel and storing it in an inert atmosphere were shown to be valid approaches to increase the stability of the thiol groups in cys-CNF. No signs of toxicity were observed on the dermal fibroblasts when exposed to cys-CNF (concentration range 0.1–0.5 mg/mL). The present work highlights cys-CNF as a promising novel material for the development of bioactive wound dressings for the treatment of chronic wounds.

Highlights

  • Cutaneous wound healing is a well-orchestrated process consisting of four overlapping phases: hemostasis, inflammation, proliferation, and remodeling

  • Chronic wounds remain in the inflammatory phase, where elevated levels of reactive oxygen species (ROS), pro-inflammatory cytokines, and degradative proteases result in reduced concentrations of growth factors and proteinase inhibitors, and an imbalance in the wound equilibrium [2]

  • The thiol content and the radical scavenging properties of the cys-cellulose nanofibrils (CNF) suspension were measured by the Ellman assay and the Diphenyl-2-picrylhydrazyl radical (DPPH) assay, respectively, over a time period of 30 days to evaluate the stability of the thiol group in the cys-CNF suspension and the correlation to its radical scavenging capacity

Read more

Summary

Introduction

Cutaneous wound healing is a well-orchestrated process consisting of four overlapping phases: hemostasis, inflammation, proliferation, and remodeling. Wood-derived cellulose nanofibrils (CNF) comprise individual fibrils that are 2–10 nm in diameter and several micrometers in length, typically forming 20–60 nm thick aggregates [8] Characteristics such as being a renewable material, not being of animal origin, having tuneable properties in terms of surface chemistry, aspect ratio and form, and being produced in a process that can be scaled-up industrially have contributed to the increased interest in using CNF for biomedical applications [5,9]. We selected the amino acid cysteine as an active molecule to endow CNF with bioactivity and for the first time investigate the potential of the functionalized CNF material to modulate the chronic wound environment in vitro. CNF was investigated in an in vitro cytotoxicity study with human dermal fibroblasts

Chemicals and Reagents
Characterization of the Molecular Structure
Degree of Substitution
Thiol Group Content
Radical Scavenging Capacity
Evaluation of the Material Interactions with the Metalloprotease Collagenase
Evaluation of Protease Inhibition
Evaluation of Protease Entrapment
Material Stability over Time
Cell Culture
Cytotoxicity Assessment
Statistical Analysis
Material Characterization
Determined
Radical Scavenging Activity
Interactions with the Metalloprotease Collagenase
Representative
Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call