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Herein, we report the design and synthesis of bio-degradable porous polyurethane hydrogels by a green, solvent-free, one-pot technique that can withstand physiological mechanical loads and aid in tissue regeneration. The hydrophilic/hydrophobic nature of the hydrogel was tuned using diols such as polycaprolactone diol (PCL) and polycarbonate diol (PCD), in combination with polyethylene glycol (PEG, MW ≈ 4000 g mol), 4,4'-methylene bis(cyclohexyl isocyanate) (HMDI) and hexanetriol (HT), which served as crosslinking agents. The structural characterizations of the hydrogels were performed using FT-IR as well as H and C high resolution magic angle spinning nuclear magnetic resonance (HR-MAS) spectroscopy. The utilization of various diols in the synthesis of the hydrogels enabled precise control over crystallinity, pore sizes, and customization of mechanical and degradation properties. These hydrogels exhibited tensile strength in the range of 0.22-1.48 MPa, while their compressive strength varied from 0.92 to 29.3 MPa. degradation profiles in the presence and absence of the enzyme Amano lipase PS revealed that the degradation process is contingent upon the specific diol present in the hydrogel. Furthermore, preliminary biological experiments confirmed the biocompatibility of the gels, indicating their potential as suitable substrates for drug delivery applications. This diverse library of gels can be shaped into specific forms, highlighting their promising applications as scaffolds and implants in drug delivery systems and tissue engineering.
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http://dx.doi.org/10.1039/d5tb00928f | DOI Listing |
J Mater Chem B
September 2025
Polymer Science and Engineering, CSIR-National Chemical Laboratory, Pune, India.
Herein, we report the design and synthesis of bio-degradable porous polyurethane hydrogels by a green, solvent-free, one-pot technique that can withstand physiological mechanical loads and aid in tissue regeneration. The hydrophilic/hydrophobic nature of the hydrogel was tuned using diols such as polycaprolactone diol (PCL) and polycarbonate diol (PCD), in combination with polyethylene glycol (PEG, MW ≈ 4000 g mol), 4,4'-methylene bis(cyclohexyl isocyanate) (HMDI) and hexanetriol (HT), which served as crosslinking agents. The structural characterizations of the hydrogels were performed using FT-IR as well as H and C high resolution magic angle spinning nuclear magnetic resonance (HR-MAS) spectroscopy.
View Article and Find Full Text PDFBiomaterials
February 2026
The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325035, China; Oujiang Laboratory (Zhejiang Lab for Regenerative Medicine, Vision and Brain Health), State Key Laboratory of Macromolecular Drugs and Large-scale Preparation, School of Pharmaceutical Science, Wenzhou Medi
Parkinson's disease (PD) is one of the most common age-related neurodegenerative diseases. Currently, the treatment of PD is mainly based on surgery and medication, and there is a pressing necessity to develop a new generation of strategies incorporating biomaterials for treating PD. Herein, an antioxidative injectable chitosan hydrogel crosslinked with tannic acid-modified dialdehyde polyurethane nanoparticles (TA@DAP) to target RIPK1 is produced for ameliorating PD.
View Article and Find Full Text PDFACS Sens
August 2025
Department of Chemical Engineering, Guangdong Technion-Israel Institute of Technology, 241 Daxue Road, Shantou, Guangdong 515063, China.
Long-term, high-fidelity electrophysiological monitoring requires epidermal electrodes that simultaneously offer conformability, breathability, and mechanical durability─attributes rarely achieved in current designs─through a scalable, simple, and low-cost fabrication strategy. We report a 5.2-μm-thick, transparent, air- and vapor-permeable "tattoo" electrode that adheres to the human skin through water-activated hydrogen bonding provided by a NaCl/glycerol/water hydrating solution, echoing the mechanism of temporary tattoos.
View Article and Find Full Text PDFBiomacromolecules
August 2025
State Key Laboratory of Polymer Science and Technology, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, P.R. China.
Injectable hydrogels have been widely studied because of their high adaptability to bleeding wounds. However, due to the contradictory demands for hydrogel network before and after injection, it is still difficult to develop a hemostatic injectable hydrogel with sufficient mechanical properties and convenient operation, while the complex microenvironment of wounds also requires the hydrogel to have multibiological functions besides rapid hemostasis. In this work, a polyurethane (PU)-based hemostatic injectable hydrogel is designed and constructed by introducing a tetrahydroxy compound containing a Schiff base and a dihydroxy compound containing catechol into the network.
View Article and Find Full Text PDFJ Biol Eng
July 2025
Department of Medical Oncology, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, Chengdu, 610041, China.
Unlabelled: This study reports the development of a thermoresponsive hydrogel composed of poly(N-isopropylacrylamide)-modified polyurethane (PNIPAM-PU) and carboxymethyl cellulose (CMC) for the controlled delivery of gemcitabine (GEM) in esophageal cancer treatment. Characterization by XRD and FTIR confirmed successful synthesis and structural integrity. The drug loading capacities were 76.
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