Silylation of bacterial cellulose to design membranes with intrinsic anti-bacterial properties

Carbohydr Polym. 2019 Sep 15:220:71-78. doi: 10.1016/j.carbpol.2019.05.009. Epub 2019 May 13.

Abstract

In this work, we report a convenient method of grafting non-leachable bioactive amine functions onto the surface of bacterial cellulose (BC) nanofibrils, via a simple silylation treatment in water. Two different silylation protocols, involving different solvents and post-treatments were envisaged and compared, using 3-aminopropyl-trimethoxysilane (APS) and (2-aminoethyl)-3-aminopropyl-trimethoxysilane (AEAPS) as silylating agents. In aqueous and controlled conditions, water-leaching resistant amino functions could be successfully introduced into BC, via a simple freeze-drying process. The silylated material remained highly porous, hygroscopic and displayed sufficient thermal stability to support the sterilization treatments generally required in medical applications. The impact of the silylation treatment on the intrinsic anti-bacterial properties of BC was investigated against the growth of Escherichia coli and Staphylococcus aureus. The results obtained after the in vitro studies revealed a significant growth reduction of S. aureus within the material.

Keywords: Aminosilane; Anti-bacterial; Bacterial cellulose; Nanocellulose; Silylation.

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Biomedical and Dental Materials* / chemistry
  • Biomedical and Dental Materials* / pharmacology
  • Cellulose / pharmacology*
  • Escherichia coli / drug effects
  • Gluconacetobacter / metabolism*
  • Membranes / chemistry*
  • Nanofibers* / chemistry
  • Nanofibers* / therapeutic use
  • Silanes / chemistry*
  • Staphylococcus aureus / drug effects

Substances

  • Anti-Bacterial Agents
  • Biomedical and Dental Materials
  • Silanes
  • Cellulose