Effect of Polymer Network Architecture on Adsorption Kinetics at Liquid-Liquid Interfaces: A Comparison Between Poly(NIPAM-co-AA) Copolymer Microgels and Interpenetrating Network Microgels.

Understanding the adsorption features of polymer microgels with different chemical compositions and structures is crucial in studying the mechanisms of respective emulsion stabilization. Specifically, the use of stimuli-responsive particles can introduce new properties and broaden the application range of such complex systems. Recently, we demonstrated that emulsions stabilized by microgels composed of interpenetrating networks (IPNs) of poly-N-isopropylacrylamide (PNIPAM) and polyacrylic acid (PAA) exhibit higher colloidal stability upon heating compared to PNIPAM homopolymer and other relevant PNIPAM-based copolymer counterparts.

Polymeric Microbubble Shell Engineering: Microporosity as a Key Factor to Enhance Ultrasound Imaging and Drug Delivery Performance.

Microbubbles (MB) are widely used as contrast agents for ultrasound (US) imaging and US-enhanced drug delivery. Polymeric MB are highly suitable for these applications because of their acoustic responsiveness, high drug loading capability, and ease of surface functionalization. While many studies have focused on using polymeric MB for diagnostic and therapeutic purposes, relatively little attention has thus far been paid to improving their inherent imaging and drug delivery features.

Computer Simulations of Responsive Nanogels at Lipid Membrane.

The swelling and collapse of responsive nanogels on a planar lipid bilayer are studied by means of mesoscopic computer simulations. The effects of molecular weight, cross-linking density, and adhesion strength are examined. The conditions for collapse-mediated engulfing by the bilayer are found.

Peculiarities of Emulsions Stabilized by Stimuli-Responsive Interpenetrating Polymeric Network Microgels.

Emulsions have become a crucial product form in various industries in modern times. Expanding the class of substances used to stabilize emulsions can improve their stability or introduce new properties. Particularly, the use of stimuli-responsive microgels makes it possible to create "smart" emulsions whose stability can be controlled by changing any of the specified stimuli.

Compression and Ordering of Hollow Microgels in Monolayers Formed at Liquid-Liquid Interfaces.

Monolayers of polymer microgels with a spherical cavity adsorbed at the liquid-liquid interface were studied using mesoscopic computer simulations. One liquid, named water, was always considered as a good solvent, while the microgel solubility in the second liquid, named oil, was varied. The symmetric and asymmetric cases of vanishing and the strong differences in solubility between the network particles and the liquids were considered.

Swift Janitor: Efficient Absorption of a Minor Component from the Mixtures of Immiscible Liquids by Thermoresponsive Macroscopic and Microscopic Hydrogels.

Polymer hydrogels are known to be efficient absorbents of various aqueous solutions. Along with the hydrophilicity of the polymer network, the presence of specific functional groups is required for the absorption of respective solutes. Alternatively, a selective uptake can be realized without any specific attraction of solutes to the network, which is shown in this paper.

Morphological Transitions in Micelles of Amphiphilic Bottlebrushes upon the Adsorption and Compression at the Liquid Interface.

Densely grafted comb-like macromolecules (bottlebrushes) with alternating solvophobic and solvophilic side chains were studied in a selective solvent and at the liquid interface using mesoscopic computer simulations. The effects of backbone length and copolymer composition were considered. While self-assembly in solution revealed only spherical aggregates for all ar-chitectures studied, adsorption onto the liquid interface in particular cases resulted in morpho-logical changes, with worm-like aggregates or a continuous monolayer observed.

Swelling and Collapse of Cylindrical Polyelectrolyte Microgels.

In this study, we propose computer simulations of charged cylindrical microgels. The effects of cross-linking density, aspect ratio, and fraction of charged groups on the microgel swelling and collapse with a variation in the solvent quality were studied. The results were compared with those obtained for equivalent neutral cylindrical microgels.

Swelling, collapse and ordering of rod-like microgels in solution: Computer simulation studies.

Polymer microgels have proven to be highly promising macromolecular objects for a wide variety of applications. In particular, the soft particles of an anisotropic (rod-like) shape are of special interest because of their potential use in tissue engineering or materials design. However, a little is known about the physical behavior of such microgels in solution, which inspired us to study them using mesoscopic computer simulations.

Correction: Effect of network topology and crosslinker reactivity on microgel structure and ordering at liquid-liquid interface.

Correction for 'Effect of network topology and crosslinker reactivity on microgel structure and ordering at liquid-liquid interface' by Rustam A. Gumerov , , 2022, , 3738-3747, https://doi.org/10.

Effect of network topology and crosslinker reactivity on microgel structure and ordering at liquid-liquid interface.

Polymer microgels synthesized were studied at a liquid-liquid interface mesoscopic computer simulations and compared to microgels with ideal (diamond-like) structure. The effect of crosslinkers reactivity ratio on the single particle morphology at the interface and monolayer behavior was examined. It was demonstrated that single particles deform into an explicit core-corona morphology when adsorbed at the interface.

Tuning the Elasticity of Nanogels Improves Their Circulation Time by Evading Immune Cells.

Peptide receptor radionuclide therapy is used to treat solid tumors by locally delivering radiation. However, due to nephro- and hepato-toxicity, it is limited by its dosage. To amplify radiation damage to tumor cells, radiolabeled nanogels can be used.

Rigid-to-Flexible Transition in a Molecular Brush in a Good Solvent at a Semidilute Concentration.

The structures of a molecular brush in a good solvent are investigated using synchrotron small-angle X-ray scattering in a wide range of concentrations. The brush under study, PPOx--PPrOx, features a relatively long poly(2-isopropenyl-2-oxazoline) (PPOx) backbone and short poly(2--propyl-2-oxazoline) (PPrOx) side chains. As a solvent, ethanol is used.

Self-assembly of miktoarm palm tree-like star copolymers in a selective solvent.

Amphiphilic miktoarm star copolymers with one long solvophobic arm (a "stem") and several short solvophilic arms (the "leaves") were studied in a selective solvent using mesoscopic computer simulations. The conventional morphologies (spherical, cylindrical and vesicular) as well as the mixed ones were obtained. However, the resulting diagram of states appeared to be different from the diagram of the linear diblock copolymer with the analogous composition.

Controlling microgel deformation deposition method and surface functionalization of solid supports.

Soft matter at solid-liquid interfaces plays an important role in multiple scientific disciplines as well as in various technological fields. For microgels, representing highly interesting soft matter systems, we demonstrate that the preparation method, i.e.

Metal Coordination Induces Phase Segregation in Amphipolar Arborescent Copolymers with a Core-Shell-Corona Architecture.

Arborescent copolymers with a core-shell-corona (CSC) architecture were synthesized and the topology of the molecules was challenged (constrained) through intramolecular interactions, resulting in phase separation breaking the symmetry of radial density. The inner poly(2-vinylpyridine) shell of these arborescent polystyrene--[poly(2-vinylpyridine)--polystyrene] molecules can self-assemble by binding metallic salts and acids in apolar and intermediate-polarity solvents. Upon loading with HAuCl, the characteristics of the polymer templates govern the "loading sites" of the metal within the molecules.

Scavenging One of the Liquids versus Emulsion Stabilization by Microgels in a Mixture of Two Immiscible Liquids.

It is known that microgels can serve as soft, permeable and stimuli-responsive alternative of solid colloidal particles to stabilize oil-water emulsions. The driving force for the adsorption of the microgels on interface of two immiscible liquids is a shielding of unfavorable oil-water contacts by adsorbed subchains, that is, the decrease of the surface tension between the liquids. Such phenomenon usually proceeds if volume fractions of the two liquids are comparable with each other and the microgel concentration is not high enough.

Compression and Ordering of Microgels in Monolayers Formed at Liquid-Liquid Interfaces: Computer Simulation Studies.

Monolayers of polymer microgels adsorbed at the liquid interfaces were studied by dissipative particle dynamics simulations. The results demonstrated that the compressibility of the monolayers can be widely tuned by varying the cross-linking density of the microgels and their (in)compatibility with the immiscible liquids. In particular, the compression of the monolayers (increase of 2D concentration of the microgels) leads to the decrease of their lateral size.

Amphiphilic PVCL/TBCHA microgels: From synthesis to characterization in a highly selective solvent.

Thermoresponsive copolymer microgels based on the biocompatible monomer N-vinylcaprolactam (VCL) and the hydrophobic comonomer 4-tert-butylcyclohexylacrylate (TBCHA) with highly tunable comonomers ratio were for the first time synthesized by miniemulsion polymerization. Their physical properties in aqueous solution and at the solid interface were characterized using dynamic light scattering (DLS), atomic force microscopy (AFM) and dissipative particle dynamics (DPD) simulations. The results show a significant decrease of the swelling rate of the obtained microgels with an increase of the amount of the hydrophobic comonomer.

Effect of the 3D Swelling of Microgels on Their 2D Phase Behavior at the Liquid-Liquid Interface.

We investigate soft, temperature-sensitive microgels at fluid interfaces. Though having an isotropic, spherical shape in bulk solution, the microgels become anisotropic upon adsorption. The structure of microgels at interfaces is described by a core-corona morphology.

Deformation of Microgels at Solid-Liquid Interfaces Visualized in Three-Dimension.

Solid-liquid interfaces play an important role for functional devices. Hence, a detailed understanding of the interaction of soft matter objects with solid supports and of the often concomitant structural deformations is of great importance. We address this topic in a combined experimental and simulation approach.

Enhanced catalyst performance through compartmentalization exemplified by colloidal l-proline modified microgel catalysts.

Exploring and controlling chemical reactions in compartments opens new platforms for designing bioinspired catalysts and energy-autonomous systems. Aqueous polymer networks or hydrogels serve as a perfect model for biological tissues, allowing systematic investigations of chemical transformations in compartments. Herein, we report the synthesis of a versatile, colloidal microgel catalyst containing covalently bound l-proline as an organocatalyst.

Amphiphilic microgels adsorbed at oil-water interfaces as mixers of two immiscible liquids.

Amphiphilic microgels adsorbed at an oil-water interface were studied by means of dissipative particle dynamics (DPD) simulations. The hydrophobic (A) and hydrophilic (B) monomer units in the polymer network are considered to be randomly distributed. Effects of the crosslinking density, interfacial tension between the liquids, their selectivity as solvents towards species A and B, and the degree of incompatibility between the A and B units on the internal microgel structure and distribution of the liquids are considered.

Nanogels and Microgels: From Model Colloids to Applications, Recent Developments, and Future Trends.

Nanogels and microgels are soft, deformable, and penetrable objects with an internal gel-like structure that is swollen by the dispersing solvent. Their softness and the potential to respond to external stimuli like temperature, pressure, pH, ionic strength, and different analytes make them interesting as soft model systems in fundamental research as well as for a broad range of applications, in particular in the field of biological applications. Recent tremendous developments in their synthesis open access to systems with complex architectures and compositions allowing for tailoring microgels with specific properties.

Amphiphilic Arborescent Copolymers and Microgels: From Unimolecular Micelles in a Selective Solvent to the Stable Monolayers of Variable Density and Nanostructure at a Liquid Interface.

Amphiphilic arborescent block copolymers of two generations (G2 and G3) and polymer microgels, obtained via cross-linking of diblock copolymers, were studied in a selective solvent and at liquid interface via dissipative particle dynamics (DPD) simulations. Depending on the primary structure, single arborescent macromolecules in selective solvent can have both core-corona and multicore structures. Self-assembly of the G2, G3, and microgels in the selective solvent is compared with equivalent linear diblock copolymers.