Abstract

Among nanocelluloses, bacterial nanocellulose (BNC) has proven to be a promising candidate in a range of biomedical applications, from topical wound dressings to tissue-engineering scaffolds. Chemical modifications and incorporation of bioactive molecules have been obtained, further increasing the potential of BNC. This study describes the incorporation of vancomycin and ciprofloxacin in BNC and in modified BNC to afford bioactive BNCs suitable for topical wound dressings and tissue-engineering scaffolds. BNC was modified by grafting glycidylmethacrylate (GMA) and further cross-linking with ethylene glycol dimethacrylate (EGDMA) with the formation of stable C–C bonds through a radical Fenton-type process that involves generation of cellulose carbon centred radicals scavenged by methacrylate structures. The average molar substitution degree MS (MS = methacrylate residue per glucose unit, measured by Fourier transform infrared (FT–IR) analysis) can be modulated in a large range from 0.1 up to 3. BNC-GMA, BNC-EGDMA and BNC-GMA-EGDMA maintain the hydrogel status until MS reaches the value of 1. The mechanical stress resistance increase of BNC-GMA and BNC-GMA-EGDMA of MS around 0.8 with respect to BNC suggests that they can be preferred to BNC for tissue-engineering scaffolds in cases where the resistance plays a crucial role. BNC, BNC-GMA, BNC-EGDMA and BNC-GMA-EGDMA were loaded with vancomycin (VC) and ciprofloxacin (CP) and submitted to release experiments. BNC-GMA-EGDMA of high substitution degree (0.7–1) hold up to 50 percentage of the loaded vancomycin and ciprofloxacin amount, suggesting that they can be further investigated for long-term antimicrobial activity. Furthermore, they were not colonized by Staphylococcus aureus (S.A.) and Klebsiella pneumonia (K.P.). Grafting and cross-linking BNC modification emerges from our results as a good choice to improve the BNC potential in biomedical applications like topical wound dressings and tissue-engineering scaffolds.

Highlights

  • Nanocelluloses (NCs), namely cellulose-based materials with peculiar physicochemical properties, appear as a new option offering a wide range of specific applications quite different from cellulose

  • This study describes the incorporation of vancomycin and ciprofloxacin in bacterial nanocellulose (BNC) and in modified BNC to afford bioactive BNCs suitable for topical wound dressings and tissue-engineering scaffolds

  • BNC was modified by grafting glycidylmethacrylate (GMA) and further cross-linking with ethylene glycol dimethacrylate (EGDMA) with the formation of stable C–C bonds through a radical Fenton-type process that involves generation of cellulose carbon centred radicals scavenged by methacrylate structures

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Summary

Introduction

Nanocelluloses (NCs), namely cellulose-based materials with peculiar physicochemical properties, appear as a new option offering a wide range of specific applications quite different from cellulose. The aim of this study is to provide bioactive BNCs in the form of hydrogel, suitable for tissue engineering, regenerative medicine and wound dressing. GMA-grafted and EGDMA-cross-linked BNCs of peculiar chemical and mechanical properties were obtained by a surface modification that maintained the original network structure of BNC. As concerns this last aspect, our study can be positioned in a relationship with BNC nanocomposites processing techniques that allow the incorporation of functional nanoreinforcements, nanofillers and additional phases without disturbing the original network structure of BNC [15]. BNC and GMA-grafted and EGDMA-cross-linked BNCs were made bioactive by loading the antibiotics vancomycin and ciprofloxacin. The broad-spectrum antibiotic ciprofloxacin has been used as model drug for BCN-cyclodextrin adduct to form drug-nanocarrier systems [24]

Materials and Methods
Grafting of BNC
Grafting and Cross-Linking of BNC
Mechanical Properties
Adsorption and Release Experiments
2.10. Antibacterial Activity Tests
Results
Adsorption and Release
Antibacterial Activity Tests
4. Discussion
Full Text
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