Polystyrene Homopolymer Enhances Dispersion of MWCNTs Stabilized in Solution by a PS-b-P2VP Copolymer.

Block copolymers (BCPs) have previously been identified as powerful multiwalled carbon nanotube (MWCNT) dispersants in solution. However, relatively high costs and limited dispersibility hinder the use of BCPs in large-scale practical applications. Partial replacement of BCP with a low-cost homopolymer (HP) offers a promising approach to produce cost-effective MWNCT dispersions. The effect of HP/BCP blends on MWNCT dispersion degree and stability has yet to be elucidated. In this work, we tested the hypothesis that HP-induced BCP micelle size variation affects MWCNT dispersibility. Here, blends of the BCP poly(styrene)-block-poly(2-vinylpyridine) and the HP polystyrene (PS) were applied to examine BCP micelles' size dependence on the MWCNT dispersion degree. Light microscopy results showed that using HP/BCP blends, MWCNT dispersion was enhanced by up to 263% compared to pure BCP at a constant weight ratio of BCP to MWCNTs. Based on the correlation of increased MWCNT dispersion degree with increased BCP micelle size, as revealed by dynamic light scattering, an MWCNT dispersion mechanism is proposed. The mechanism includes a rationale for the unexpected finding that HP PS swells the BCP micelle's PS corona in a good solvent for PS. Using HP to increase MWCNT dispersion is a promising approach with possible applications in the production of high-performance composite materials. This holds especially for formulations of practical relevance where often (BCP) dispersants are only one of many components in the material.

The Interfacial Assembly of Polyoxometalate Nanoparticle Surfactants.

Polyoxometalates (POMs) using {Mo72V30} as an example, dissolved in water, can interact with amine-terminated polydimethylsiloxane (PDMS-NH2) dissolved in toluene at the water/toluene interface to form POM-surfactants that significantly lower the interfacial tension and can be used to stabilize liquids via interfacial elasticity. The jamming of the POM-surfactants at the water/oil interface with consequent wrinkling occurs with a decrease in the interfacial area. The packing density of the POM-surfactants at the interface can be tuned by varying the strength of screening with the addition of cations with differing hydrated radii.

Nanoconfinement and Sansetsukon-like Nanocrawling Govern Fibrinogen Dynamics and Self-Assembly on Nanostructured Polymeric Surfaces.

Surface nanostructures are increasingly more employed for controlled protein assembly on functional nanodevices, in nanobiotechnology, and in nanobiomaterials. However, the mechanism and dynamics of how nanostructures induce order in the adsorbed protein assemblies are still enigmatic. Here, we use single-molecule mapping by accumulated probe trajectories and complementary atomic force microscopy to shed light on the dynamic of in situ assembly of human plasma fibrinogen (HPF) adsorbed on nanostructured polybutene-1 (PB-1) and nanostructured polyethylene (PE) surfaces. We found a distinct lateral heterogeneity of HPF-polymer nanostructure interface (surface occupancy, residence time, and diffusion coefficient) that allow identifying the interplay between protein topographical nanoconfinement, protein diffusion mechanism, and ordered protein self-assembly. The protein diffusion analysis revealed high-diffusion polarization without correlation to the anisotropic friction characteristic of the polymer surfaces. This suggests that HPF molecules confined on the nanosized PB-1 needle crystals and PE shish-kebab crystals, respectively, undergo partial detachment and diffuse via a Sansetsukon-like nanocrawling mechanism. This mechanism is based on the intrinsic flexibility of HPF in the coiled-coil regions. We conclude that nanostructured surfaces that encourage this characteristic surface mobility are more likely to lead to the formation of ordered protein assemblies and may be useful for advanced nanobiomaterials.

Nanocrystal Width Controls Fibrinogen Orientation and Assembly Kinetics on Poly(butene-1) Surfaces.

From the view of biomedical relevance, it is known that a specific arrangement of surface-immobilized human plasma fibrinogen (HPF) molecules is required to retain their biological functionality. Here, we demonstrate a topographical effect of chemically identical isotactic poly(butene-1) (iPB-1) semicrystalline nanostructures on the adsorption behavior, i.e., conformation change and orientation of HPF molecules. Using the distinct crystallization of iPB-1 under different shear conditions, polymer thin films consisting of needle-like crystals (NLCs) or shish-kebab crystals (SKCs) having lateral dimension, i.e., width, smaller than or comparable to the HPF major axis, respectively, were fabricated. The protein adsorption kinetic studies by quartz crystal microbalance with dissipation (QCM-D) revealed surface-dependent packing density and assembly configuration of HPF. High-resolution imaging disclosed a "side-on" protein adsorption and anisotropic network formation on the NLCs. With a 2-fold orientation analysis performed at both "single" protein and multiprotein levels, we quantitatively proved the preferential alignment of adsorbed HPF molecules with respect to the axial direction of the NLCs. Remarkably, the iPB-1 surface with SKCs perturbed the "end-to-end" protein-protein interactions and thus hindered the network formation. The distinguished adsorption behavior of HPF molecules on iPB-1 surfaces is explained by the physical effect of crystal width, which is additionally supported by the synergistic effect of crystal curvature and aspect ratio. Our studies provide fundamental insight into purely topography-controlled self-assembly of HPF molecules, which might be further exploited in creating topographically defined implant surfaces for preventing protein aggregation related disorders.

pH-Dependent Ordered Fibrinogen Adsorption on Polyethylene Single Crystals.

Nanostructured surfaces have the potential to influence the assembly as well as the orientation of adsorbed proteins and may, thus, strongly influence the biomaterials' performance. For the class of polymeric (bio)materials a reproducible and well-characterized nanostructure is the ordered chain folded surface of a polyethylene single crystal (PE-SC). We tested the hypothesis that the trinodal-rod-shaped protein human plasma fibrinogen (HPF) adsorbs on the (001) surface of PE-SCs along specific crystallographic directions. The PE-SC samples were prepared by isothermal crystallization in dilute solution and characterized by atomic force microscopy (AFM) before as well as after HPF adsorption at different concentrations and pH values. At a physiological pH of 7.4, connected HPF molecules, or e.g., fibrils, fibril networks, or sponge-like structures, were observed on PE-SC surfaces that featured no preferential orientation. The observation of these nonoriented multiprotein assemblies was explained by predominant protein-protein interactions and limited surface diffusion. However, at an increased pH of 9.2, single HPF molecules, e.g., spherical-shaped and trinodal-rod-shaped HPF molecules as well as agglomerates, were observed on the PE-SC surface. The presence of single HPF molecules at increased pH was explained by decreased protein-protein interactions. These single trinodal-rod-shaped HPF molecules oriented preferentially along crystallographic [100] and [010] directions on the PE-SC surface which was explained by an increased amount of intermolecular bonds along these crystallographic directions with increased surface atom density. The study established that HPF molecules can align on chemically homogeneous surface topographies one order of magnitude smaller than the dimension of the protein. This advances the understanding of how to control the assembly and orientation of proteins on nanostructured polymer surfaces. Controlled protein adsorption is a crucial key to improve the surface functionality of future implants and biosensors.

Enveloping self-assembly of carbon nanotubes at copolymer micelle cores.

Carbon nanotubes (CNTs) and their polymer nanocomposites are interesting materials for future applications, for example in optics or electronics. Research faces two major challenges with these outstanding nanofillers: control over dispersion and spatial arrangement within the nanocomposite, both required to achieve optimal structure and properties of CNT-based nanocomposites. We report on novel self-assembled multiwall CNT (MWCNT)/block copolymer (BCP) nanostructures realized by patterning MWCNTs with amphilphilic diblock copolymer micelles. A high molecular weight poly(styrene)-b-poly(2-vinylpyridine) BCP which forms large micelles (250 nm) was chosen to facilitate the templating by reducing the bending energy induced in the MWCNTs. We tested the hypothesis that it is possible to use an amphiphilic BCP as a dispersing agent and its spherical micelles as a template at the same time without modification of the CNTs. In thin films of the MWCNT/BCP micelles, highly separated MWCNTs were repeatedly observed which enveloped the core of the BCP micelles, i.e., the unfunctionalized MWCNTs segregated to the interface between the two BCP phases. Depending on the size of the MWCNTs, ring-like (split-ring) or network forming structures were obtained. The MWCNT templating mechanism, i.e., the segregation to the interface, is explained by the interfacial tension within the BCP interface and the chain entropy. The reported new complex nanocomposite has potential to be applied for example as cost-effective split-ring resonators for metamaterials or for conductive polymer films with an extremely low percolation threshold.

Electrospinning of aligned fibers with adjustable orientation using auxiliary electrodes.

A conventional electrospinning setup was upgraded by two turnable plate-like auxiliary high-voltage electrodes that allowed aligned fiber deposition in adjustable directions. Fiber morphology was analyzed by scanning electron microscopy and attenuated total reflection Fourier transform infrared spectroscopy (FTIR-ATR). The auxiliary electric field constrained the jet bending instability and the fiber deposition became controllable. At target speeds of 0.9 m s-1 90% of the fibers had aligned within 2°, whereas the angular spread was 70° without the use of auxiliary electrodes. It was even possible to orient fibers perpendicular to the rotational direction of the target. The fiber diameter became smaller and its distribution narrower, while according to the FTIR-ATR measurement the molecular orientation of the polymer was unaltered. This study comprehensively documents the feasibility of directed fiber deposition and offers an easy upgrade to existing electrospinning setups.

Modeling the saturation of detergent association in mixed liposome systems.

Cells tune the lipid types present in their membranes to adjust for thermal and chemical stability, as well as to promote association and dissociation of small molecules and bound proteins. Understanding the influence of lipid type on molecule association would open doors for targeted cell therapies, in particular when molecular association is observed in the presence of competing membranes. For this reason, we modeled and experimentally observed the association of a small molecule with two membrane types present by measuring the association of the detergent Triton X-100 with two types of liposomes, egg phosphatidylcholine (ePC) liposomes and egg phosphatidic acid (ePA) liposomes, at varying ratios. We called this mixed liposomes, as each liposome population was formed from a different lipid type. Absorbance spectrometry was used to observe the stages of detergent association with mixed liposomes and to determine the detergent concentration at which the liposomes were fully saturated. A saturation model was also derived that predicts the detergent associated with each liposome type when the lipid bilayers are fully saturated with detergent. The techinical input parameters for the model are the detergent to lipid ratio and the relative absorbance intensity for each of the pure liposome species at saturation. With that, the association of detergent with any mixture of those liposome types at saturation can be determined.

Lipid shape determination of detergent solubilization in mixed-lipid liposomes.

The effects of lipid charge and head group size on liposome partitioning by detergents is an important consideration for applications such as liposomal drug delivery or proteoliposome formation. Yet, the solubilization of mixed-lipid liposomes, those containing multiple types of lipids, by detergents has received insufficient attention. This study examines the incorporation into and subsequent dissolution of mixed-lipid liposomes comprised of both egg phosphatidylcholine (ePC) and egg phosphatidic acid (ePA) by the detergent Triton-X100 (TX). Liposomes were prepared with mixtures of the two lipids, ePC and ePA, at molar ratios from 0 to 1, then step-wise solubilized with TX. Changes in turbidity, size distribution, and molar heat power at constant temperature throughout the solubilization process were assessed. The data suggest that the difference in lipid shapes (shape factors = 0.74 and 1.4 [1,2]) affects packing in membranes, and hence influences how much TX can be incorporated before disruption. As such, liposomes containing the observed ratios of ePA incorporated higher concentrations of TX before initiating dissolution into detergent and lipid mixed-micelles. The cause was concluded to be increased mismatching in the bilayer from the conical shape of ePA compared to the cylindrical shape of ePC. Additionally, the degree to which ePA is approximated as conical versus cylindrical was modulated with pH. It was confirmed that less conical ePA behaved more similarly to ePC than more conical ePA. The understanding gained here on lipid shape in liposome incorporation of TX enables research to use in vitro liposomes that more closely mimic native membranes.