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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. In the case when the fraction of TBCHA is equal or higher than the fraction of VCL, the microgels become almost insensitive to the temperature changes, and the amount of water inside the microgels appeared to be diminishingly small. In the opposite case, if the VCL fraction is major, the copolymer microgels preserve their softness and deformability while being adsorbed onto a solid surface. At the same time, all samples have shown a good colloidal stability and a low polydispersity in size. Thus, the presented polymerization technique is applicable for the fabrication of microgels using hydrophobic monomers, which are not accessible by conventional precipitation polymerization. We demonstrate that the mechanical properties and the temperature-responsiveness of the copolymer microgels can be precisely adjusted by the content of the hydrophobic comonomer.
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http://dx.doi.org/10.1016/j.jcis.2019.12.123 | DOI Listing |
Polymers (Basel)
August 2025
Theoretical Physics of Living Matter, Institute for Advanced Simulation, Forschungszentrum Jülich, 52425 Jülich, Germany.
Polymers and polymer composites offer versatile possibilities for engineering the physico-chemical properties of materials on micro- and macroscopic scales. This review provides an overview of polymeric and polymer-decorated particles that can serve as drug-delivery vectors: linear polymers, star polymers, diblock-copolymer micelles, polymer-grafted nanoparticles, polymersomes, stealth liposomes, microgels, and biomolecular condensates. The physico-chemical interactions between the delivery vectors and biological cells range from chemical interactions on the molecular scale to deformation energies on the particle scale.
View Article and Find Full Text PDFMolecules
July 2025
Department of Chemistry of the College of Staten Island, and The PhD Program in Chemistry of Graduate Center, The City University of New York, 2800 Victory Boulevard, Staten Island, NY 10314, USA.
Glucose-responsive insulin delivery systems that effectively regulate insulin retention and release in response to real-time fluctuation of glucose levels are highly desirable for diabetes care with minimized risk of hypoglycemia. Herein, we report a class of glucose-sensitive copolymer microgels, prepared from a simple one-pot precipitation copolymerization of 4-vinylphenylboronic acid (VPBA), 2-(dimethylamino) ethyl acrylate (DMAEA), and oligo(ethylene glycol) methyl ether methacrylate (M = 300, MEOMA), for gated glucose-responsive insulin release within the physiologically desirable glucose level range. The composition of the p(VPBA-DMAEA-MEOMA) copolymer microgels were analyzed using NMR and FTIR spectra.
View Article and Find Full Text PDFBiomacromolecules
July 2025
Department of Chemical Engineering, McMaster University, 1280 Main St. W., Hamilton, Ontario L8S 4L7, Canada.
While poly(ethylene glycol) (PEG) has been widely applied in a host of biomedical applications due to its antifouling properties, its limited potential for functionalization and emerging concerns over potential immunogenicity have inspired the development of PEG alternatives. Herein, we review the use of poly(oligo(ethylene glycol) methacrylate) (POEGMA) as a PEG alternative that can provide significantly more synthetic versatility, minimize immunogenicity, and open up additional applications (e.g.
View Article and Find Full Text PDFNanoscale
June 2025
Pharmaceutical Sciences Laboratory, Faculty of Science and Engineering, Åbo Akademi University, Biocity (3rd floor), Tykistökatu 6A, Turku FI-20520, Finland.
Cellulose nanofibers (CNFs) are renewable bionanomaterials with great utilization potential in future biomedicals. However, conventional CNF hydrogels are limited by low structural flexibility and insufficiently tunable mechanical properties, restricting their use in 3D cell culture systems. To address these limitations, we developed granular hydrogel platforms using photocurable and ionically crosslinkable methacrylated CNFs (CNFMAs) and their copolymers with polyacrylamide a dual cross-linking mechanism.
View Article and Find Full Text PDFGels
March 2025
Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore 117585, Singapore.
This study explored the formation of soft colloidal particles from a diblock ionomer (DI) with the monomeric composition (acrylonitrile)-co-(glycidyl methacrylate)-b-(3-sulfopropyl methacrylate potassium)-abbreviated as (AG)S, where x >> z > y. A colloidal dispersion was generated by introducing water into the pre-prepared DMSO solutions of DI, which led to micelle formation and subsequent coagulation. The assembly of the hydrophobic (AG) blocks was influenced by water content and chain conformational flexibility (the ability to adopt various forms of conformation).
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