Abstract

We report the ability of cellulose to support cells without the use of matrix ligands on the surface of the material, thus creating a two-component system for tissue engineering of cells and materials. Sheets of bacterial cellulose, grown from a culture medium containing Acetobacter organism were chemically modified with glycidyltrimethylammonium chloride or by oxidation with sodium hypochlorite in the presence of sodium bromide and 2,2,6,6-tetramethylpipiridine 1-oxyl radical to introduce a positive, or negative, charge, respectively. This modification process did not degrade the mechanical properties of the bulk material, but grafting of a positively charged moiety to the cellulose surface (cationic cellulose) increased cell attachment by 70% compared to unmodified cellulose, while negatively charged, oxidised cellulose films (anionic cellulose), showed low levels of cell attachment comparable to those seen for unmodified cellulose. Only a minimal level of cationic surface derivitisation (ca 3% degree of substitution) was required for increased cell attachment and no mediating proteins were required. Cell adhesion studies exhibited the same trends as the attachment studies, while the mean cell area and aspect ratio was highest on the cationic surfaces. Overall, we demonstrated the utility of positively charged bacterial cellulose in tissue engineering in the absence of proteins for cell attachment.

Highlights

  • Damaged tissues and organs are a costly problem in healthcare, which, in some cases, cannot be addressed using traditional medical intervention (Song and Ott 2011)

  • We demonstrated the utility of positively charged bacterial cellulose in tissue engineering in the absence of proteins for cell attachment

  • Cellulose surfaces were rendered positively charged by nucleophilic substitution of alkali activated 1° alcohol groups with an epoxide bearing a quaternary ammonium group (GTMAC), or negatively charged by controlled oxidation using the well-studied tetramethylpipiridine 1-oxyl (TEMPO)/NaOCl/NaBr system (Scheme 1)

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Summary

Introduction

Damaged tissues and organs are a costly problem in healthcare, which, in some cases, cannot be addressed using traditional medical intervention (Song and Ott 2011). The addition of ligands or peptides may be achieved by passive adsorption (simplest method) (Cutler and Garcıa 2003), or more complex routes such as incorporation into the polymer backbone (Schmedlen et al 2002), at the ends of the polymer chains (Hersel et al 2003), or functionalised on the material surfaces (Wan et al 2004). These approaches involve complex chemistries, or costly crosslinking reagents that are unstable after a short period of time, adding cost and complexity to production. Concerns may arise pertaining to transmission of pathogens, such as including prions

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