Copolymers Of 2-hydroxyethyl Methacrylate Research Articles

Poly (acrylic acid-co-2-hydroxyethyl methacrylate)-grafted gum ghatti hydrogel for capturing heavy metal ions

In this work, a facile route is explored for the synthesis of a novel polymer composite-based hydrogel (PC-hydrogel). The ratio of 2-(Hydroxyethyl) methacrylate (HEMA) and acrylic acid (AA) is optimized first based on Fourier transform infra-red spectroscopy, swelling ratio (SR%) and surface negative charge (PZC). Results indicate that PC-hydrogel composed of copolymer of HEMA: AA in 1:4 ratio is optimized, for grafting on Gum ghatti (Gg) during free-radical graft copolymerization process. Among all other possible combination of HEMA: AA, 1:4 ratio grafted Gg is termed as PC-hydrogel [Poly (AA-co-HEMA)-g-Gg]. PC-hydrogel exhibited negative surface charge over a wide range of pH owing to increase in AA. The swelling (g/g) and water retention ratio (%) of the prepared hydrogel have been found to be 342.6, 385 & 412.6 g/g and 74.83, 65.30 & 57.86 % in grey, tap and distilled water respectively. Furthermore, PC-hydrogel is applied for capturing Cu2+ and Co2+ ions in aqueous phases. Experimental results showed that adsorption process was pH-dependent, and the maximum capturing of Cu2+ and Co2+ was observed at neutral pH 7. Among different adsorption isotherms models like Langmuir, Freundlich, and Temkin models, experimental data fitted closely with the Langmuir adsorption model showing a maximum adsorption capacity of 381.67 and 328.94 mg/g for Cu2+ and Co2+ respectively. The capturing of metal ion followed pseudo-second-order rate model [rate constant k = 1.7 x 10−4 for Cu2+ and 1.5 x 10−4 for Co2+ g/(mg.min)]. The PC-hydrogel property retained its uptake capacity of metal ions up to the three successive adsorption−desorption cycles, and exhibited higher selectivity towards Cu2+ and Co2+ and other (NaCl, MgCl2, CaCl2) coexisting ions.

Hydrogels in Biomedicine: Granular Controlled Release Systems Based on 2-Hydroxyethyl Methacrylate Copolymers. A Review

The article analyzes and summarizes the latest achievements in the field of polymer systems for controlled release devices based on hydrogel materials. Possible directions of drug delivery are presented, including the use of granular hydrogels, which work on the principle of drug sorption − release in the body. The research on the synthesis regularities, structure, properties, and prospects for the use of granular hydrogels based on 2-hydroxyethyl methacrylate (HEMA) and its copolymers, in particular with polyvinylpyrrolidone (PVP), as systems for the controlled release of substances, in particular, drugs, is analyzed.

Technological features of the formation of film products from modified hydrogels by the centrifugal method

Processing of polymers and composites based on them by centrifugal molding is important for production the bodies of revolution, which are used in various industries. This article analyzes the centrifugal molding and presents the results of research about new areas of such materials applications. For instance as method for the hydrogel films production of materials based on copolymers of 2-hydroxyethyl methacrylate (HEMA) with polyvinylpyrrolidone (PVP), including filled hydrogels, which can be applicable in medicine, electrical and tool engineering.

Thermodynamics of interactions and structural peculiarities of interpenetrating polymer networks based on polyurethane and copolymer of 2-hydroxyethyl methacrylate with methacryloyloxyethylphosphorylcholine

Interpenetrating polymer networks based on biocompatible components – polyurethane and copolymer of 2-hydroxyethyl methacrylate with methacryloyloxyethylyphosphorylcholine (HEMA-MPC) were synthesized and thermodynamic parameters of interactions in the system and morphology were investigated. The thermodynamic parameters of interactions between polymer components of the IPNs were calculated based on sorption isotherms of methylene chloride vapors by samples of the created polymer systems. It is shown that MPC plays the role of a compatibilizer in the system, increasing the thermodynamic compatibility between polyurethane and the HEMA-MPC copolymer at small amounts of the copolymer in the IPNs. As the amount of copolymer HEMA-MPC in the IPNs increases, the value of the free energy of the polyurethane and copolymer mixing shifts to the positive value, which is associated with the formation of ionic clusters of MPC. This may mean that with an increasing amount of the MPC in the system, interactions between the negatively charged phosphoryl groups and the positively charged nitrogen atom of various MPC polymer chains occur, i.e., the part of intermolecular interactions (polyurethane and copolymer) decreases, while the part of intramolecular interactions (between different groups of MPC) increases. The results of the morphology investigations of the IPN samples are consistent with the data of the thermodynamic compatibility study of polymers during the formation of the IPNs. With a significant increase in the positive values of the free energy of the polyurethane and copolymer mixing in the IPNs with 41 % and 51 % of the copolymer content, a significant phase separation is observed in the IPNs, with phase inclusions ranging from 1 to 5 mm.

Features of the Formation of a Reinforcing Coating on Hydrogel Membranes Based on Polyvinylpyrrolidone Copolymers

This paper presents the study results of formation features of composite hydrogel/polyamide membranes obtained by modification of hydrogel films based on 2-hydroxyethylmethacrylate (HEMA) and polyvinylpyrrolidone (PVP) copolymers. The formation process of composite two-layer membranes was carried out in two stages: obtaining hydrogel membrane substrates followed by their modification with an ultra-thin layer based on a mixture of polyamide (PA) with PVP. The main task of the work was to investigate the possibility of forming a modifying PA/PVP coating on the surface of hydrogel films and to obtain composite hydrogel membranes with the required strength and osmotic permeability based on them. For the formation of composite two-layer membranes, PVP with MM = 12 × 103 g/mol and MM = 360 × 103 g/mol were used. Additional use of PVP in the modifying solution contributes to the process of its penetration into the hydrogel substrate. Together with the formation of a reinforcing layer, this ensures the obtainment of hydrogel films of increased strength, with the possibility of directional regulation of their diffusion permeability. It was found that the main factors affecting the nature of the interaction between the layers of the obtained composite films, as well as their physico-mechanical and sorption–diffusion properties, are the HEMA:PVP ratio in the original polymer–monomer composition (PMC), the formulation of the reinforcing layer, the duration of the modification process and the molecular weight of PVP in PMC and in the modifying solution. The strength and water content of two-layer composite hydrogel/polyamide membranes, as well as their salt and water permeability coefficients, are the highest in the case of using high-molecular weight PVP (MMPVP = 360 × 103 g/mol) and low-molecular weight (MMPVP = 12 × 103 g/mol) during the synthesis of the hydrogel substrate to obtain a PA-6/PVP solution for forming a reinforcing layer.

Lens epithelial cell response to polymer stiffness and polymer chemistry.

Posterior capsule opacification (PCO) is the most common complication of cataract surgery, and intraocular lens (IOL) implantation is the standard of care for cataract patients. Induction of post-operative epithelial-mesenchymal transition (EMT) in residual lens epithelial cells (LEC) is the main mechanism by which PCO forms. Previous studies have shown that IOLs made with different materials have varying incidence of PCO. The aim of this paper was to study the interactions between human (h)LEC and polymer substrates. Polymers and copolymers of 2-hydroxyethyl methacrylate (HEMA) and 3-methacryloxypropyl tris (trimethylsiloxy) silane (TRIS) were synthesized and evaluated due to the clinical use of these materials as ocular biomaterials and implants. The chemical properties of the polymer surfaces were evaluated by contact angle, and polymer stiffness and roughness were measured using atomic force microscopy. In vitro studies showed the effect of polymer mechanical properties on the behavior of hLECs. Stiffer polymers increased α-smooth muscle actin expression and induced cell elongation. Hydrophobic and rough polymer surfaces increased cell attachment. These results demonstrate that attachment of hLECs on different surfaces is affected by surface properties in vitro, and evaluating these properties may be useful for investigating prevention of PCO.

An anti-swelling chitosan-based hydrogel driven by balance of hydrophilic segment and hydrophobic segment strategy for underwater detection of human motion

Hydrogel-based flexible strain sensors have gained rapid development. However, most of traditional hydrogels were prone to undergo swelling behavior underwater as solvent molecules continuously penetrated, which limited their application scenarios. To make up this deficiency, a chitosan-based anti-swelling hydrogel cross-linked by ionic liquid are presented. The hydrogel is consisted of chitosan (CS) and copolymer of acrylic acid (AA), 2-hydroxyethyl methacrylate (HEMA), butyl acrylate (BA) and dimethylaminoethyl methacrylate maleate (DMAEMA-MA). The P(HEMA-BA-AA)/ILs/CS hydrogel exhibited excellent anti-swelling properties driven by balance of hydrophilic segment and hydrophobic segment strategy (equilibrium swelling rate of −3.79 % in water for 100 days). The ionic liquid was introduced into the hydrogel system as cross-linking agent, which could effectively prevent the loss of conductivity of the hydrogel after soaking in water. The synergy effect chain entanglement, H-bonds and electrostatic interactions endowed the hydrogel with excellent mechanical property. Surprisingly, the modulus and toughness of the hydrogel were significantly boosted after a week of submersion. Thus, this anti-swelling hydrogel was employed as wireless strain sensor, which implemented underwater motion monitoring and safety alarms. It is expected that the anti-swelling hydrogel driven by balance of hydrophilic and hydrophobic effects would inspire the development of underwater sensors.

Synthesis and Characterization of Poly Styrene-Co-Poly 2-Hydroxyethylmethacrylate (HEMA) Copolymer and an Investigation of Free-Radical Copolymerization Propagation Kinetics by Solvent Effects

Synthesis and Characterization of Poly Styrene-Co-Poly 2-Hydroxyethylmethacrylate (HEMA) Copolymer and an Investigation of Free-Radical Copolymerization Propagation Kinetics by Solvent Effects

Dual stimuli-responsive delivery system for self-regulated colon-targeted delivery of poorly water-soluble drugs

Inflammatory bowel disease (IBD) are chronic inflammatory conditions which cause significant patient morbidity. Local drug delivery to the colon can improve treatment efficacy and reduce side effects associated with IBD treatment. Smart drug delivery systems are designed to regulate the release of therapeutic agents at the desired site of action. pH-responsive drug carriers have been previously utilised for improved oral drug delivery beyond stomach harsh conditions. Additionally, the colon possesses a diverse microbiome secreting bioactive molecules e.g., enzymes, that can be exploited for targeted drug delivery. We herein synthesised and characterised a 2-hydroxyethyl methacrylate and methacrylic acid copolymer, crosslinked with an azobenzyl crosslinker, that displayed pH- and enzyme-responsive properties. The swelling and drug release from hydrogel were analysed in pH 1.2, 6.5 and 7.4 buffers, and in the presence of rat caecal matter using metronidazole and mesalamine as model BCS Class I and IV drugs, respectively. Swelling studies displayed pH-responsive swelling behaviour, where swelling was maximum at pH 7.4 and minimum at pH 1.2 (69 % versus 32 %). Consequently, drug release was limited in gastric and small intestinal conditions but increased significantly when exposed to colonic conditions containing caecal matter. This system displays promising capacity for achieving colon-targeted drug delivery with enhanced dissolution of poorly water-soluble drugs for local treatment of IBD and other colon-targeted therapies.

Molecular Dynamics Simulation of Hydrogels Based on Phosphorylcholine-Containing Copolymers for Soft Contact Lens Applications.

The structure and dynamics of copolymers of 2-hydroxyethyl methacrylate (HEMA) with 2-methacryloyloxyethyl phosphorylcholine (MPC) were studied by molecular dynamics simulations. In total, 20 systems were analyzed. They differed in numerical fractions of the MPC in the copolymer chain, equal to 0.26 and 0.74, in the sequence of mers, block and random, and the water content, from 0 to 60% by mass. HEMA side chains proved relatively rigid and stable in all considered configurations. MPC side chains, in contrast, were mobile and flexible. Water substantially influenced their dynamics. The copolymer swelling caused by water resulted in diffusion channels, pronounced in highly hydrated systems. Water in the hydrates existed in two states: those that bond to the polymer chain and the free one; the latter was similar to bulk water but with a lower self-diffusion coefficient. The results proved that molecular dynamics simulations could facilitate the preliminary selection of the polymer materials for specific purposes before their synthesis.

Exploration of Optimal Reaction Conditions for Constructing Hydrophobic Polymers with Low Deformation to Facilitate the Dimensional Stability of Laminated Bamboo Lumber.

The environmental moisture changes would result in the deformation and cracking of laminated bamboo lumber (LBL) easily due to the unreleased internal stress, leading to poor durability. In this study, a hydrophobic cross-linking polymer with low deformation was successfully fabricated and introduced in the LBL by polymerization and esterification to improve its dimensional stability. In an aqueous solution, the 2-hydroxyethyl methacrylate (HEMA) and Maleic anhydride (MAh) were employed as the base compounds for synthesizing the copolymer of 2-hydroxyethyl methacrylate and maleic acid (PHM). The hydrophobicity and swelling performance of the PHM was adjusted by controlling the reaction temperatures. PHM-modified LBL's hydrophobicity as indicated by the contact angle, increased from 58.5° to 115.2°. The anti-swelling efficiency was also improved. Moreover, multiple characterizations were applied to clarify the structure of PHM and its bonding linkages in LBL. This study demonstrates an efficient avenue to facilitate the dimensional stability of LBL by PHM modification and sheds new light on the efficient utilization of LBL using a hydrophobic polymer with low deformation.

Preparation of bamboo-derived structured cellulose and its evaluation as resin composite materials

Bamboo, a highly productive and renewable resource, shows a high strength among other biomass resources. Composites of lignocellulose with a polymer are attracting attention as a new material for buildings and furniture according to recent demands for sustainable development goals (SDGs). The present report describes the first preparation of a composite with resin using an organosolv technique with water and 1-butanol solvent as pre-treatment of bamboo.Organosolv treatment at 453 K selectively removed lignin and hemicellulose from bamboo without causing over-decomposition of cellulose. The delignified bamboo was impregnated with a copolymer of methyl methacrylate and hydroxyethyl methacrylate using a decompressed method. The structure of the bamboo-derived cellulose piece remained the same as it was after polymer impregnation without any molding process. Amount of the polymer impregnated into the bamboo after organosolv was significantly greater (34%) than that without organosolv.Impregnated state in the delignified bamboo was evaluated using morphological observations and determination of the properties of mesopores, which formed in the gap between cellulose microfibrils during organosolv. Results indicated that the composite of bamboo-derived structured cellulose with the co-polymer was prepared successfully, and the vascular bundles, including cell walls as well as parenchyma cells, were impregnated with the resin. Compressive strength of impregnated delignified bamboo was evaluated and found to be 12.7 MPa.

Structural Features of 4-VP-HEMA-SiO<sub>2</sub> Hybrid Membranes and Their Proton Conductivity

Hybrid organic-inorganic membranes based on tetraethoxysilane and orthophosphoric acid-doped copolymers of 4-vinylpyridine (4-VP) and 2-hydroxyethyl methacrylate (HEMA) were formed by the sol-gel synthesis method. The membranes are characterized by high values of exchange capacity and proton conductivity. An increase in the proton conductivity of hybrid organo-inorganic membranes compared to the initial copolymer can be associated with the generation of water of crystallization during the formation of a silicon dioxide fragment, which follows from quantum-chemical modeling of the local structure of the membrane, which includes an organic part from the copolymerization product of 4-VP with HEMA (44 atoms) and an inorganic part of 27 atoms, repeating the structure of the silicon dioxide block.

Sulfonic Cryogels as Innovative Materials for Biotechnological Applications: Synthesis, Modification, and Biological Activity.

Polymeric hydrogels based on sulfo-containing comonomers are promising materials for biotechnological application, namely, for use as a system for delivering water and minerals during seed germination in conditions of an unstable moisture zone. In this work, cryogels based on 3-sulfopropyl methacrylate and 2-hydroxyethyl methacrylate copolymers were obtained by the cryotropic gelation method. The morphology, specific surface area, and swelling behaviors of cryogels are found to depend on the total concentration of monomers in the reaction system and the content of the gel fraction in cryogels. Cryogels formed in the presence of nanodiamonds are shown to exhibit high biological activity during the germination of Lepidium sativum L. variety Ajur seeds, which manifests itself by stimulating seed germination and a significant increase in the raw weight of sprouts. These results indicate that sulfonic cryogels have a high potential to improve seed germination and plant growth, proving that such cryogels can be used as environmentally friendly materials for agricultural applications.

Room-Temperature Self-Healable Blends of Waterborne Polyurethanes with 2-Hydroxyethyl Methacrylate-Based Polymers.

The design of self-healing agents is a topic of important scientific interest for the development of high-performance materials for coating applications. Herein, two series of copolymers of 2-hydroxyethyl methacrylate (HEMA) with either the hydrophilic N,N-dimethylacrylamide (DMAM) or the epoxy group-bearing hydrophobic glycidyl methacrylate were synthesized and studied as potential self-healing agents of waterborne polyurethanes (WPU). The molar percentage of DMAM or GMA units in the P(HEMA-co-DMAMy) and P(HEMA-co-GMAy) copolymers varies from 0% up to 80%. WPU/polymer composites with a 10% w/w or 20% w/w copolymer content were prepared with the facile method of solution mixing. Thanks to the presence of P(HEMA-co-DMAMy) copolymers, WPU/P(HEMA-co-DMAMy) composite films exhibited surface hydrophilicity (water contact angle studies), and tendency for water uptake (water sorption kinetics studies). In contrast, the surfaces of the WPU/P(HEMA-co-GMAy) composites were less hydrophilic compared with the WPU/P(HEMA-co-DMAMy) ones. The room-temperature, water-mediated self-healing ability of these composites was investigated through addition of water drops on the damaged area. Both copolymer series exhibited healing abilities, with the hydrophilic P(HEMA-co-DMAMy) copolymers being more promising. This green healing procedure, in combination with the simple film fabrication process and simple healing triggering, makes these materials attractive for practical applications.

Precision syntheses of poly(NIPAM-alt-HEMA) and effects of the alternating sequence on thermoresponsive behaviors in water

An alternating copolymer of 2-hydroxyethyl methacrylate and N-isopropylacrylamide was synthesized via cyclopolymerization of a divinyl monomer and aminolysis transformation for studies of the sequence-dependent thermal responsiveness in water.

Combinational Growth Factor and Gas Delivery for Thrombosis Prevention.

Cardiovascular stents enable the rapid re-endothelialization of endothelial cells (ECs), and the constant suppression of smooth muscle cell (SMC) proliferation has been proved to effectively prevent thrombosis. However, the development and application of such stents are still insufficient due the delayed re-endothelialization progress, as well as the poor durability of the SMC inhibition. In this paper, we developed a mussel-inspired coating with the ability for the dual delivery of both growth factor (e.g., platelet-derived growth factor, PDGF) and therapeutic gas (e.g., nitric oxide, NO) for thrombosis prevention. We firstly synthesized the mussel-inspired co-polymer (DMHM) of dopamine methacrylamide (DMA) and hydroxyethyl methacrylate (HEMA) and then coated the DMHM on 316L SS stents combined with CuII. Afterwards, we immobilized the PDGF on the DMHM-coated stent and found that the PDGF could be released in the first 3 days to enhance the recruitment, proliferation, and migration of human umbilical vein endothelial cells (HUVECs) to promote re-endothelialization. The CuII could be "sealed" in the DMHM coating, with extended durability (2 months), with the capacity for catalyzed NO generation for up to 2 months to suppress the proliferation of SMCs. Such a stent surface modification strategy could enhance the development of the cardiovascular stents for thrombosis prevention.

Correlation between multiple chemical modification strategies on graphene or graphite and physical/electrical properties

Chemical modifications of carbon based materials are often used to improve their dispersion in polymer matrix and increase the nanocomposite electrical properties. This work concerned the control of graphene and graphite physical and chemical structure thanks to different chemical modification (oxidation, copolymer functionalization and reduction). This article exposes a complete study of different chemical modifications impact on graphene and graphite microstructure, chemical structure, and its relative electrical property. A first oxidation step by Hummers or nitric acid method was necessary to further graft a copolymer of methyl methacrylate and hydroxyethyl methacrylate via a versatile “grafting onto” covalent functionalization. Hummers’ and nitric acid methods were considered as strong and soft oxidation treatments, respectively. Reduction steps were also performed using hydrazine or thermal treatments to recover high electrical conductivity. Chemical modifications of graphene and graphite were characterized by X-ray diffraction, Raman spectroscopy, thermogravimetric analysis, Fourier transform infrared spectroscopy and pyrolysis–gas chromatography–mass spectrometry. Moreover, a new method for the electrical measurement of the modified particles is presented in this work. This measurement requires adhesive tape and an electrical circuit with a diode using the four probes protocol, it allows the evaluation of the electrical conductivity of the graphene and graphite samples in powder state. Finally, the electrical resistances of the different graphene and graphite submitted to all the chemical treatments are reported.

Properties of Solutions of Amphiphilic Diblock and Random Copolymers of 2-Perfluorohexylethyl Methacrylate and 2-Hydroxyethyl Methacrylate and Coatings Based on Them

Properties of Solutions of Amphiphilic Diblock and Random Copolymers of 2-Perfluorohexylethyl Methacrylate and 2-Hydroxyethyl Methacrylate and Coatings Based on Them

Understanding dexamethasone kinetics in the rabbit tear fluid: Drug release and clearance from solution, suspension and hydrogel formulations

Rapid precorneal loss of topically applied eye drops limits ocular drug absorption. Controlling release and precorneal residence properties of topical formulations may improve ocular drug bioavailability and duration of action. In this study, we evaluated in vivo ocular pharmacokinetics of dexamethasone in rabbits after application of a drug solution (0.01%), suspension (Maxidex® 0.1%), and hydrogels of 2-hydroxyethyl methacrylate (HEMA) and acrylic acid (AAc) copolymers. The rabbits received a single eyedrop (solution or suspension) or dexamethasone-loaded hydrogel topically. Dexamethasone in tear fluid was sampled with glass capillaries and quantitated by LC-MS/MS. Higher dexamethasone exposure (AUC) in the tear fluid was observed with the suspension (≈3.6-fold) and hydrogel (12.8-fold) as compared to the solution. During initial 15 min post-application, the highest AUC of dissolved dexamethasone was seen after hydrogel application (368 min*µg/mL) followed by suspension (109.9 min*µg/mL) and solution (28.7 min*µg/mL. Based on kinetic simulations, dexamethasone release from hydrogels in vivo and in vitro is comparable. Our data indicate that prolonged exposure of absorbable dexamethasone in tear fluid is reached with hydrogels and suspensions. Pharmacokinetic understanding of formulation behavior in the lacrimal fluid helps in the design of dexamethasone delivery systems with improved ocular absorption and prolonged duration of action.