Paul Rouxhet

Collagen films adsorbed on native and oxidized poly(ethylene terephtalate): morphology after drying

The collagen layer formed by adsorption of collagen on native (PETn) and surface oxidized poly(ethylene terephtalate) (PETox) was studied by X-ray photoelectron spectroscopy and atomic force microscopy (AFM). On PETox, for adsorption times up to a few hours. the collagen molecules form a network, the nodes of which seem to be responsible for a dot-like morphology, On PETn, at very short adsorption times and consequently low surface coverages, the adsorbed molecules are displaced by the AFM tip. This effect reveals lower interactions between the collagen and the surface after drying compared to PETox. At higher coverages, the surface morphology is similar to that obtained for PETox. After an adsorption time of 24 h, an aggregation of collagen molecules is observed for both substrates. The results are discussed with regard to the interactions between collagen and the substrate in water, the events occurring during the drying process and the mobility of collagen molecules in the dry state, (C) 2001 Elsevier Science B.V. All rights reserved.

Fabrication of surfaces with bimodal roughness through polyelectrolyte/colloid assembly

From bioengineering to optics and electronics, a great deal of work has been conducted on the development of new materials with structured surfaces. A large range of methods has been used, such as plasma etching, electron beam and colloidal lithography (Denis et al., 2002), electrical deposition (Yang et al., 2009), phase separation (Dekeyser et al., 2004) and polyelectrolyte assembly in order to produce structured surfaces (Agheli et al., 2006). The combination of different methods is also more and more explored. Schaak et al. (2004) described a simple approach to achieve colloidal assembly on a patterned template obtained by lithography. Densely packed layers of colloidal particles can be produced by lifting a substrate vertically from a suspension (Fustin et al., 2004; Li J. et al., 2007) or by spin coating (Yang et al., 2009). Colloidal lithography utilizes the ability of particles to adhere on oppositely charged surfaces (Johnson & Lenhoff, 1996; Hanarp et al., 2001, 2003)), possibly using surface modification by inorganic or organic polyelectrolytes. The surface coverage is influenced by several factors: ionic strength, particle size and time. The adhesion of microbial cells on various substrates was also achieved by surface treatments with inorganic or organic polycations (Changui et al., 1987; Van haecht et al., 1985) or with positively charged colloidal particles (Boonaert et al., 2002). A review on colloidal lithography and biological applications was published recently (Wood, 2007). Adsorption of polyelectrolytes is influenced by ionic strength, pH and the polyelectrolyte characteristics (molecular mass, charge density) (Lindquist & Stratton, 1976; Davies et al., 1989; Choi & Rubner, 2005). At low ionic strength, highly charged polyelectrolytes adopt extended conformations and are fairly rigid due to the strong repulsion between charged units. The maximum adsorbed amount and the adsorbed layer thickness do not vary markedly according to molecular weight. As the salt concentration is increased and the electrostatic intrachain repulsion is decreased, the polyelectrolyte becomes more coiled. In this case, the maximum amount adsorbed (expressed in mass) increases as a function of molecular weight (Roberts, 1996; Lafuma, 1996; Claesson et al., 2005; Boonaert et al., 1999). Build up of polyelectrolyte films may be achieved using layer-by-layer assembly through alternating adsorption of oppositely charged polyelectrolytes (Decher & Hong, 1991).