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Designing coatings and films that can protect surfaces is important in a wide variety of applications from corrosion prevention to anti-fouling. These systems are challenging from a modeling perspective because they are invariably multicomponent, which quickly leads to an expansive design space. At a minimum, the system has a substrate, a film (often composed of a polymeric material), a ubiquitous carrier solvent, which may be either a vapor or liquid phase, and one or more contaminants. Each component has an impact on the effectiveness of coating. This paper focuses on films that are used as a barrier to surface contamination, but the results also extend to surface coatings that are designed to extract a low density species from the fluid phase as in liquid chromatography. A coarse-grained model is developed using Yukawa potentials that encompasses both repulsive and attractive interactions among the species. Classical density functional theory calculations are presented to show how contaminant adsorption is controlled by the molecular forces in the system. Two specific vectors through the parameter space are considered to address likely experimental manipulations that change either the solvent or the polymer in a system. We find that all the adsorption results can be unified by considering an appropriate combination of molecular parameters. As a result, these calculations provide a link between molecular interactions and film performance and may serve to guide the rational design of films. [ABSTRACT FROM AUTHOR]

We investigate diffusion in fluids near surfaces that may be coated with polymer films. We first consider diffusion in hard sphere fluids near a planar hard wall. We specifically consider color diffusion, where hard spheres are labeled A or B but are otherwise identical in all respects. In this inhomogeneous fluid, we consider a surface reaction–diffusion problem. At the left wall, a particle of species A is converted to one of species B upon a wall collision. At the opposing wall, the reverse reaction takes place: B → A. Using molecular dynamics simulation, we study the steady state of this system. We demonstrate that in the homogeneous region, a diffusing particle is subject to an equilibrium oscillatory force, the solvation force, that arises from the interfacial structuring of the fluid at the wall. For the hard sphere/hard wall system, the solvation force can be determined in various ways. We use the solvation force [the potential of mean force (PMF)] to solve the continuum diffusion equation. This provides an adequate and accurate description of the reaction–diffusion problem. The analysis is then extended to consider both color diffusion in the presence of a slowly varying one-body field such as gravity and a more applied problem of diffusion of free species through a surface film consisting of tethered chains. In both cases, the PMF experienced by the free particles is affected, but the diffusion problem can be treated in the same way as for the simpler hard sphere color diffusion case. [ABSTRACT FROM AUTHOR]

Encapsulation of drugs within nanocarriers that selectively target malignant cells promises to mitigate side effects of conventional chemotherapy and to enable delivery of the unique drug combinations needed for personalized medicine. To realize this potential, however, targeted nanocarriers must simultaneously overcome multiple challenges, including specificity, stability and a high capacity for disparate cargos. Here we report porous nanoparticle-supported lipid bilayers (protocells) that synergistically combine properties of liposomes and nanoporous particles. Protocells modified with a targeting peptide that binds to human hepatocellular carcinoma exhibit a 10,000-fold greater affinity for human hepatocellular carcinoma than for hepatocytes, endothelial cells or immune cells. Furthermore, protocells can be loaded with combinations of therapeutic (drugs, small interfering RNA and toxins) and diagnostic (quantum dots) agents and modified to promote endosomal escape and nuclear accumulation of selected cargos. The enormous capacity of the high-surface-area nanoporous core combined with the enhanced targeting efficacy enabled by the fluid supported lipid bilayer enable a single protocell loaded with a drug cocktail to kill a drug-resistant human hepatocellular carcinoma cell, representing a 10(6)-fold improvement over comparable liposomes.

We study the interaction between a flat surface and a contaminant solution. The surface is protected by a grafted polymer layer. Our primary interest is to better understand and elucidate the effect of simple molecular interactions on the contamination and decontamination of the surface through molecular diffusion. These interactions manifest themselves in the potential of mean force that the contaminant molecule experiences as it diffuses across the grafted polymer layer. For simplicity, we consider that all interactions are of the hard-sphere type. The size of the contaminant molecule is the same as that of the solvent as well as the individual polymer segment. Despite these simplifications, the analysis offers important physical insights and a qualitative description of the contamination and decontamination processes. [ABSTRACT FROM AUTHOR]

In the research conducted the liquid-liquid phase separation with lysozyme is studied. It is suggested that molecular volume and second viral coefficient are important to know the phase behavior of solutions.

Electrokinetic phenomena play an important role for the transport in submicrometer-size channels since the electric double layers formed at the walls can occupy a substantial part of the channel volume. This presents a theoretical difficulty and specific problems are usually treated numerically or not comprehensively. In our work we present a theoretical model that allows one to obtain analytical expressions for the transport of fluid (electro-osmotic flow), ions (electric current), and dissolved charged molecules (analytes). The model is based on the weak double layer approximation and has a wide range of validity. An important feature of this theoretical approach is that it is applicable not only to symmetric but also to asymmetric 2:1 and 1:2 electrolytes which exhibit very interesting properties in nanoscale channels. The possibility of affecting the wall electrokinetic ζ potential by applying a transverse voltage bias is analyzed. This transverse bias is used in an attempt to control the transport in the channel and such devices are often called “fluidic field-effect transistors.” Our model quantifies the effect of the voltage bias on the ζ potential of the channel wall and therefore can be used for prediction of transport and optimization of separations in such fluidic devices. [ABSTRACT FROM AUTHOR]