Self-Cross-Linkable Chitosan-Alginate Complexes Inspired by Mussel Glue Chemistry.

In this study, mussel-inspired chemistry, based on catechol-amine reactions, was adopted to develop self-cross-linkable chitosan-alginate (Chi-Alg) complexes. To do so, the biopolymers were each substituted with ∼20% catechol groups (ChiC and AlgC), and then four complex combinations (Chi-Alg, ChiC-Alg, Chi-AlgC, ChiC-AlgC) were prepared at the surface and in bulk solution. Based on QCM-D and lap shear adhesion tests, the complex with catechol only on Chi (ChiC-Alg) did not show a significant variation from the control complex (Chi-Alg).

Dopamine-Assisted Layer-by-Layer Deposition Providing Coatings with Controlled Thickness, Roughness, and Functional Properties.

In this study, dopamine-assisted deposition combined with layer-by-layer assembly was investigated as an efficient method for preparing coatings with tunable thickness, roughness, and functional properties. By this method, one can first benefit from the versatile chemistry of dopamine allowing the co-deposition of various functional materials, for example, polymers, ions, and nanoparticles, within the coating. Moreover, the layer-by-layer approach allows tuning the coating thickness and surface roughness, as well as varying the chemical composition of the coating in the vertical direction.

Parameterization of the optical constants of polydopamine films for spectroscopic ellipsometry studies.

Bio-inspired polydopamine coatings offer vast possibilities for surface modification of materials. The thickness of such nanometric coatings is usually estimated based on ellipsometry measurements. However, the complex light-absorbing nature of polydopamine is often overlooked when analyzing such data, which can result in inaccurate estimations of the coating thickness as well as the optical properties.

Cell-imprinted substrates: in search of nanotopographical fingerprints that guide stem cell differentiation.

Cell-imprinted substrates direct stem cell differentiation into various lineages, suggesting the idea of lineage-specific nanotopography. We herein examined the surface topography of five different imprinted cell patterns using AFM imaging and statistical analysis of amplitude, spatial, and hybrid roughness parameters. The results suggest that different cell imprints possess distinguished nanotopographical features.

Water vapor permeation through topical films on a moisture-releasing skin Model.

Background: Covering the skin by topical films affects the skin hydration and transepidermal water loss (TEWL). In vivo studies to investigate the water vapor permeation through topical films are complicated, expensive, ethically not preferred, and time- and labor-consuming. The objective of this study was to introduce an in vitro and subject-independent alternative evaluation method to predict the breathability of topical formulations.

Swelling Behavior, Interaction, and Electrostatic Properties of Chitosan/Alginate Dialdehyde Multilayer Films with Different Outermost Layer.

In this study, self-cross-linked chitosan/alginate dialdehyde multilayer films, capped with either alginate dialdehyde (6 layers) or chitosan (7 layers), were fabricated using the layer-by-layer method. The disruption of the electrostatic equilibrium when exposing the fabricated layers to acidic and alkaline conditions causes swelling within the film and independently in the outermost layer, showing dependence on the ionic strength. Spectroscopic ellipsometry and quartz crystal microbalance with dissipation monitoring were employed to examine the swelling behavior.

Structural Investigation of a Self-Cross-Linked Chitosan/Alginate Dialdehyde Multilayered Film with in Situ QCM-D and Spectroscopic Ellipsometry.

A chitosan/alginate dialdehyde multilayered film was fabricated using the layer-by-layer assembly method. Besides electrostatic interaction that promotes alternate adsorption of the oppositely charged polyelectrolytes, the Schiff base reaction between the amine groups on chitosan and the aldehyde groups on alginate dialdehyde provides a covalently cross-linked film, which after reduction by sodium cyanoborohydride is stable under both acidic and alkaline conditions. Moreover, the cross-linked film is responsive to changes in pH and addition of multivalent salts.

PPEGMEMA-based cationic copolymers designed for layer-by-layer assembly.

We have synthesized three PPEGMEMA-based cationic copolymers with similar amine contents but with systematic variation in the average length of the PEG side chains. The positively charged copolymers were paired with alginate to fabricate layer-by-layer assembled multilayered films. It was demonstrated that the polymeric design, in terms of the systematic variation in the average length of the PEG units, affects the polyelectrolyte multilayer growth mechanism and can be used to tune the structural properties and the water content of the layers.

The Hofmeister series: Specific ion effects in aqueous polymer solutions.

Specific ion effects in aqueous polymer solutions have been under active investigation over the past few decades. The current state-of-the-art research is primarily focused on the understanding of the mechanisms through which ions interact with macromolecules and affect their solution stability. Hence, we herein first present the current opinion on the sources of ion-specific effects and review the relevant studies.

An engineered cell-imprinted substrate directs osteogenic differentiation in stem cells.

A cell-imprinted poly(dimethylsiloxane)/hydroxyapatite nanocomposite substrate was fabricated to engage topographical, mechanical, and chemical signals to stimulate and boost stem cell osteogenic differentiation. The physicochemical properties of the fabricated substrates, with nanoscale resolution of osteoblast morphology, were probed using a wide range of techniques including scanning electron microscopy, atomic force microscopy, dynamic mechanical thermal analysis, and water contact angle measurements. The osteogenic differentiation capacity of the cultured stem cells on these substrates was probed by alizarin red staining, ALP activity, osteocalcin measurements, and gene expression analysis.

Thermo-responsive diblock and triblock cationic copolymers at the silica/aqueous interface: A QCM-D and AFM study.

The properties of synthesized diblock poly(N-isopropylacrylamide)-poly((3-acrylamidopropyl)trimethylammonium chloride) and triblock methoxy-poly(ethylene glycol)-poly(N-isopropylacrylamide)-poly((3-acrylamidopropyl)trimethylammonium chloride) cationic copolymers at the silica/aqueous interface are investigated using quartz crystal microbalance with dissipation monitoring (QCM-D) and atomic force microscopy (AFM). Moreover, dynamic light scattering is employed to assess the copolymers in terms of the hydrodynamic size and interchain aggregation. Although viscoelastic Voigt modeling of the QCM-D data suggests a comparable layer thickness for the copolymers on the silica surface, the AFM imaging and colloidal probe measurements reveal significant differences in surface coverage and thickness of the layers, which are discussed and compared with respect to the stabilization effect by the hydrophilic poly(ethylene glycol) block.

Hofmeister Effect on PNIPAM in Bulk and at an Interface: Surface Partitioning of Weakly Hydrated Anions.

The effect of sodium fluoride, sodium trichloroacetate, and sodium thiocyanate on the stability and conformation of poly(N-isopropylacrylamide), in bulk solution and at the gold-aqueous interface, is investigated by differential scanning calorimetry, dynamic light scattering, quartz crystal microbalance, and atomic force microscopy. The results indicate a surface partitioning of the weakly hydrated anions, i.e.

Hofmeister effect on thermo-responsive poly(propylene oxide): Role of polymer molecular weight and concentration.

Although a vast amount of research has been dedicated to investigate the Hofmeister effect on the stability of polymer solutions, a clear understanding of the role of polymer properties in this phenomenon is still missing. Here, the Hofmeister effect of NaCl (destabilizing) and NaSCN (stabilizing) salts on aqueous solutions of poly(propylene oxide) (PPO) is studied. Four different molecular weights of PPO were investigated, to determine how the variation in the polymer coil size affects the Hofmeister effect.

Hofmeister effect of salt mixtures on thermo-responsive poly(propylene oxide).

The Hofmeister series is a classification of ions regarding their ability to stabilize or destabilize aqueous solutions of proteins, polymers and other molecules which are partly miscible with water. In this study, we employ differential scanning calorimetry to investigate how the stability of aqueous solutions of poly(propylene oxide) is affected by mixtures of ions with different location in the Hofmeister series. Our results show that the Hofmeister effects of pure salt species are not always linearly additive and that the relative effect of some ions can be reversed depending on the composition of the salt mixture as well as by the absolute and relative concentration of the different species.