The influence of co-solvents on the swelling behavior of tunable thermosensitive core-shell nanoparticle gels was investigated. The poly(methyl methacrylate) (PMMA) core and poly(2-hydroxyethyl methacrylate) (PHEMA) shell network in 1-propanol reacted differently upon the addition of three co-solvents (cyclohexane (CHX), 1,3-propanediol (PDO), and water), resulting in highly controllable swelling properties of the core-shell gels. In particular, a strongly enhanced solvation effect, called the cosolvency phenomenon, occurred even with a very small amount of water (1-3 wt%). To examine the tunability, thermo-optical analysis (TOA) and photon correlation spectroscopy (PCS) were employed. The results show that a small addition of CHX, PDO, or water induced the "lower/upper," "even/upper," and "lower/lower" volume transition temperatures (VTTs) of the core-shell networks, respectively. For theoretical treatment, a multi-component lattice theory of mixing was combined with the Flory-Rehner (F-R) chain model to calculate the net free energy of mixing. The required interaction parameters were obtained from the binary and ternary phase diagrams of the linear polymer solutions and were applied directly to the swelling calculation of the cross-linked core-shell network solutions. The calculated results corresponded well with the experimental swelling data without further adjustment.
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Pharmaceutics
November 2024
Institute for Chemical-Physical Processes, National Research Council, 56124 Pisa, Italy.
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The Avram and Stella Goldstein-Goren Department of Biotechnology Engineering, Ben-Gurion University of the Negev Beer-Sheva 84105 Israel
Droplet-based microfluidic systems have received much attention as promising tools for fabricating monodisperse microspheres of alginate solutions with high accuracy and reproducibility. The immediate and simple ionotropic gelation of alginate, its biocompatibility, and its tunability of mechanical properties make it a favorable hydrogel in the biomedical and tissue engineering fields. In these fields, micron-sized alginate hydrogel spheres have shown high potential as cell vehicles and drug delivery systems.
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February 2025
College of Physics and Energy, Fujian Provincial Solar Energy Conversion and Energy Storage Engineering Technology Research Center, Fujian Normal University, Fuzhou 350117, China; Fujian Provincial Collaborative Innovation Center for Advanced High-Field Superconducting Materials and Engineering, Fuzhou 350117, China; Fujian Provincial Key Laboratory of Quantum Manipulation and New Energy Materials, Fuzhou 350117, China. Electronic address:
Int J Biol Macromol
November 2024
Department of Polymer Science and Engineering, Chungnam National University, Daejeon 34134, Republic of Korea; Department of Materials Science and Engineering, Chungnam National University, Daejeon 34134, Republic of Korea. Electronic address:
Thermo-responsive hydrogels (thermogels), known for their sol-gel transition capabilities, have garnered significant interest for biomedical applications over recent decades. However, conventional thermogels are hindered by intrinsic physicochemical and functional limitations that impede their broader utility. This study introduces methacryl glycol chitosan (MGC) as a novel thermogel, offering enhanced functionality and addressing these limitations.
View Article and Find Full Text PDFJ Phys Chem Lett
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Thermosensitive transient receptor potential (thermoTRP) ion channels can transduce external thermal stimuli to neural electrical signals, allowing organisms to detect and respond to changes in environmental temperature. Reproducing such ionic machinery holds promise for advancing the design of highly efficient low-grade thermal energy harvesters and ultrasensitive thermal sensors. However, there still exist challenges for artificial nanofluidic architectures to achieve comparable thermoelectric performance.
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