On the stability of the polymer brushes formed by adsorption of Ionomer Complexes on hydrophilic and hydrophobic surfaces

We have studied the effect of normal forces and shear forces on the stability and functionality of a polymer brush layer formed upon adsorption of polymeric micelles on hydrophilic and hydrophobic surfaces. The micelles consist of oppositely charged polyelectrolyte blocks (poly(acrylic acid) and poly(N-methyl 2-vinyl pyridinium iodide), and a neutral block (poly(vinyl alcohol)) or neutral grafts (poly(ethylene oxide)). The strength of the attachment of the micellar layers to various substrates was evaluated with Atomic Force Microscopy. Flow cell experiments allowed for the evaluation of long-term stability of coatings in lateral flow. Fixed angle optical reflectometry was used to quantify protein (BSA) adsorption on the micellar layers after their exposure to flow. The results show that adsorbed micellar layers are relatively weakly attached to hydrophobic surfaces and much stronger to hydrophilic surfaces, which has a significant impact on their stability. Adsorbed layers maintain their ability to suppress protein adsorption on hydrophilic surfaces but not on hydrophobic surfaces. Due to the relatively weak attachment to hydrophobic surfaces the structure of adsorbed layers may easily be disrupted by lateral forces, such that the complex coacervate-brush structure no longer exists.

Reduction of BSA adsorption by coatings, formed upon absorption of lonomer Complexes (ICs), exposed to the lateral flow (shear) strongly depends on the properties of the native substrate and composition of the ICs.Figure optionsDownload high-quality image (58 K)Download as PowerPoint slideResearch highlights
► Mechanical stability IC coatings on solid–liquid interfaces depends on properties of the native substrate.
► Under shear the complex coacervate-brush structure on hydrophilic substrate remains intact.
► Under shear the complex coacervate-brush structure on hydrophobic substrate is lost.