Issue 41, 2013

Ultrathin cellulose film coating of porous alumina membranes for adsorption of superoxide dismutase

Abstract

The non-toxic and biocompatible cellulose possesses nonspecific binding properties for many protein molecules. But its abundant inter- and intra-molecular hydrogen bonds induce spontaneous self-assembly of cellulose into a random fibrous morphology and cellulose film coating is usually just available for two-dimensional flat substrates, which severely limits its protein adsorption performance. In this study, direct self-assembly of an ultrathin cellulose film on hybrid polyelectrolyte multilayer pre-coated pore surfaces of an anodic aluminum oxide membrane was achieved through the dissolution and precipitation of cellulose from N-methylmorpholine oxide solution. Each pore channel surface pre-coated with a uniform polyelectrolyte hybrid layer (thickness ∼5.0 nm) was covered by a cellulose film (∼15.0 nm) consisting of dense cellulose nanoparticles with a diameter of 5.5 ± 1.4 nm. The three-dimensional porous structure of the aluminum oxide membrane was well-preserved and micrometre-long flexible nanotubes with an average outer diameter of ∼200 nm were obtained after further aluminum oxide template dissolution treatment in an acidic environment. Moreover, the cellulose film coated pore channel surfaces presented sufficient hydrogen bonds and exhibited a high adsorption capacity rate of ∼1.45 mg m−2 for superoxide dismutase. This facile cellulose deposition approach enabled ultrathin cellulose film coating on three-dimensional structured substrates for enhanced adsorption performance for protein molecules.

Graphical abstract: Ultrathin cellulose film coating of porous alumina membranes for adsorption of superoxide dismutase

Supplementary files

Article information

Article type
Paper
Submitted
22 May 2013
Accepted
28 Aug 2013
First published
29 Aug 2013

J. Mater. Chem. B, 2013,1, 5636-5643

Ultrathin cellulose film coating of porous alumina membranes for adsorption of superoxide dismutase

Y. Gu and J. Huang, J. Mater. Chem. B, 2013, 1, 5636 DOI: 10.1039/C3TB20725K

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