Gold Nanoparticle Layers on Polystyrene Microspheres of Controlled Structure and Electrokinetic Properties

Formation of positively charged gold nanoparticle layers on polystyrene microparticles (PSMs600) was studied using the electrokinetic and the concentration depletion methods based on atomic force microscopy (AFM) and scanning electron microscopy (SEM) imaging. Primarily, the dependence of electrophoretic mobility of microparticles on the gold nanoparticle concentration in the suspension was measured. These results were quantitatively interpreted in terms of the three-dimensional electrokinetic model. This allowed to derive a formula for calculating the coverage of nanoparticles under in situ conditions whose validity was confirmed by direct SEM imaging of deposited gold nanoparticles (AuNPs). Additionally, the maximum coverage of gold nanoparticles for various ionic strengths was determined using a concentration depletion method based on AFM imaging of residual particles deposited on the silica substrate. The maximum coverage increased with ionic strength attaining a value of 0.35 for the ionic strength of 3 × 10^–3 M. This effect was attributed to the decreasing range of lateral electrostatic interactions among deposited particles. The electrokinetic properties of the gold nanoparticle layers were also evaluated in pH cycling experiments that confirmed their stability. Beyond significance to basic science, the new data acquired in this work confirm the feasibility of preparing gold nanoparticle layers on polymer microparticles characterized by a controlled structure, coverage, and electrokinetic properties

Monolayers of Poly(styrene/α-<i>tert</i>-butoxy-ω-vinylbenzyl-polyglycidol) Microparticles Formed by Controlled Self-Assembly with Potential Application as Protein-Repelling Substrates

The kinetics of the self-assembly of poly­(styrene/α-<i>tert</i>-butoxy-ω-vinylbenzyl-polyglycidol) microparticles on poly­(allylamine hydrochloride)-derivatized silicon/silica substrate was determined by direct AFM imaging and streaming potential (SP) measurements. The kinetic runs acquired under diffusion-controlled transport were quantitatively interpreted in terms of the extended random sequential adsorption (RSA) model. This allowed confirmation of a core/shell morphology of the microparticles. The polyglycidol-rich shell of thickness equal to 25 nm exhibited a fuzzy structure that enabled penetration of particles into each other resulting in high coverage inaccessible for ordinary microparticles. The SP measurements interpreted by using the 3D electrokinetic model confirmed this microparticle structure. Additionally, the acid–base characteristics of the microparticle monolayers were determined for a broad pH range. By using the streaming potential measurements, human serum albumin (HSA) adsorption on the microparticle monolayers was investigated under in situ conditions. It was confirmed that the protein adsorption was considerably lower than for the reference case of bare silicon/silica substrate under the same physicochemical conditions. This effect was attributed to the presence of the shell diminishing the protein/microparticle physical interactions