Electrostatic Potential Analysis in Polyelectrolyte Brush-Grafted Microchannels Filled with Polyelectrolyte Dispersion

In this study, the model framework that includes almost all relevant parameters of interest has been developed to quantify the electrostatic potential and charge density occurring in microchannels grafted with polyelectrolyte brushes and simultaneously filled with polyelectrolyte dispersion. The brush layer is described by the Alexander-de Gennes model incorporated with the monomer distribution function accompanying the quadratic decay. Each ion concentration due to mobile charges in the bulk and fixed charges in the brush layer can be determined by multi-species ion balance. We solved 2-dimensional Poisson–Nernst–Planck equations adopted for simulating electric field with ion transport in the soft channel, by considering anionic polyelectrolyte of polyacrylic acid (PAA). Remarkable results were obtained regarding the brush height, ionization, electrostatic potential, and charge density profiles with conditions of brush, dispersion, and solution pH. The Donnan potential in the brush channel shows several times higher than the surface potential in the bare channel, whereas it becomes lower with increasing PAA concentration. Our framework is fruitful to provide comparative information regarding electrostatic interaction properties, serving as an important bridge between modeling and experiments, and is possible to couple with governing equations for flow field.

Chitosan: An Overview of Its Properties and Applications

Chitosan has garnered much interest due to its properties and possible applications. Every year the number of publications and patents based on this polymer increase. Chitosan exhibits poor solubility in neutral and basic media, limiting its use in such conditions. Another serious obstacle is directly related to its natural origin. Chitosan is not a single polymer with a defined structure but a family of molecules with differences in their composition, size, and monomer distribution. These properties have a fundamental effect on the biological and technological performance of the polymer. Moreover, some of the biological properties claimed are discrete. In this review, we discuss how chitosan chemistry can solve the problems related to its poor solubility and can boost the polymer properties. We focus on some of the main biological properties of chitosan and the relationship with the physicochemical properties of the polymer. Then, we review two polymer applications related to green processes: the use of chitosan in the green synthesis of metallic nanoparticles and its use as support for biocatalysts. Finally, we briefly describe how making use of the technological properties of chitosan makes it possible to develop a variety of systems for drug delivery.

Chitosan: A Versatile Polymer for 21st Century

Chitosan arouses large interest due to its properties and possible applications. Every year the number of publications and patents based on this polymer increases. Chitosan exhibits poor solubility in neutral and basic media limiting its use in such conditions. Another serious obstacle is directly related to its natural origin. Chitosan is not a single polymer with a defined structure but a family of molecules with differences in their composition, size, and monomer distribution. These properties have a fundamental effect on the biological and technological performance of the polymer. Moreover, some of the biological properties claimed are discrete. In this review, we discuss how chitosan chemistry can solve the problems related to its poor solubility and can boost the polymer properties. We focus on some of the main biological properties of chitosan and the relationship with the physicochemical properties of the polymer. Then, we visit two polymer applications related to green processes: the use of chitosan in the green synthesis of metallic na-noparticles and its use as support in biocatalyst. Finally, we briefly describe how making use of the technological properties of chitosan it is possible to develop a variety of systems for drug delivery

Thermo-Rheological and Shape Memory Properties of Block and Random Copolymers of Lactide and ε-Caprolactone

Biodegradable block and random copolymers have attracted numerous research interests in different areas, due to their capability to provide a broad range of properties. In this paper, an efficient strategy has been reported for preparing biodegradable PCL-PLA copolymers with improved thermal, mechanical and rheological properties. Two block-copolymers are synthesized by sequential addition of the cyclic esters lactide (L-LA or D,L-LA) and ε-caprolactone (CL) in presence of a dimethyl(salicylaldiminato)aluminium compound. The random copolymer of L-LA and CL was synthetized by using the same catalyst. Chain structure, molar mass, thermal, rheological and mechanical properties are characterized by NMR, SEC, TGA, DSC, Rheometry and DMTA. Experimental results show that by changing the stereochemistry and monomer distribution of the copolymers it is possible to obtain a variety of properties. Promising shape-memory properties are also observed in the di-block copolymers characterized by the co-crystallization of CL and L-LA segments. These materials show great potential to substitute oil-based polymers for packaging, electronics, and medicine applications.

Profilin 1 Controls the Assembly, Organization, and Dynamics of Leading Edge Actin Structures Through Internetwork Competition and Collaboration

How actin monomers are distributed to different networks remains poorly understood. One emerging concept is that the monomer pool is limited and heterogenous, causing biased assembly and internetwork competition. However, most knowledge regarding monomer distribution comes from studies where competing networks are discrete. In metazoans, many actin-based structures are complex, containing competing networks that overlap and are functionally interdependent. Addressing how monomers control the assembly and organization of these complex structures is critical to understanding how actin functions in cells. Here, we identify the monomer-binding protein profilin 1 (PFN1) as a major determinant of actin assembly, organization, and network homeostasis in mammalian cells. At the leading edge, PFN1 controls the localization and activity of the assembly factors Arp2/3 and Mena/VASP, with discrete stages of internetwork competition and collaboration occurring at different PFN1 concentrations. This causes substantial changes to leading edge actin architecture and the types of structures that form there.

Surfactants in systems with oil and water, including microemulsions

The solubilization of small amounts of nonpolar oil by surfactant micelles was described in Chapter 9. In the present chapter surfactant behaviour in systems (such as emulsions) that contain comparable amounts of water and oil are considered. Above the critical aggregation concentration surfactant distribution between the oil and water is partly determined by the preferred curvature of the aggregates present, although surfactant ‘monomer’ distribution is unrelated to where the aggregates reside. The formation of microemulsion droplets in so-called Winsor systems is described, as are the concomitant changes in oil/water interfacial tension, which become ultralow and pass through a minimum. Microemulsion droplets, like micelles, are dynamic structures, and aspects of drop dynamics are introduced. In the Appendix some methods for the determination of the size of microemulsion droplets, including conventional and dynamic light scattering and small angle neutron scattering, are described.

Solvent-control over monomer distribution in the copolymerization of 2-oxazolines and the effect of a gradient structure on self-assembly

The effect of a polymerization solvent on the monomer distribution in gradient copolymers is demonstrated and the effect of the monomer gradient on the copolymer self-assembly behavior is shown.