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The efficient capture and immobilization of radioiodine (I, IO) is of great importance in radioactive waste management. Here, a CuO-loaded three-dimensional bulk cationic hydrogel composite (CuO@CH) was successfully prepared by simple redox reactions and UV photopolymerization, which realized the rapid enrichment and efficient immobilization of I and IO. The adsorption experiments showed that the maximum adsorption capacity of CuO@CH for I in the solution at pH = 3 reached 416.5 mg/g, and the adsorption capacity of IO in the solution at pH = 6 could reach 313.4 mg/g. It exhibited extremely fast adsorption kinetics for I and IO. In addition, CuO@CH also exhibited efficient I and IO removal from simulated high-level liquid waste. The rapid capture and effective immobilization of radioiodine (I, IO) were realized by the electrostatic interaction of -N(CH) groups in CuO@CH with I and IO, as well as the chemical reactions between CuO and I. The bulk cationic hydrogel composite explored the multifunctional role toward fast, high adsorption capability and easy handling, highlighting its superiority compared to the powder adsorbent, which renders it a potential adsorbent for the removal of radioactive iodine (I, IO) in nuclear wastewater treatment.
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http://dx.doi.org/10.1021/acsami.3c04816 | DOI Listing |
Colloids Surf B Biointerfaces
September 2025
Department of Medicine and Health Sciences "V. Tiberio", University of Molise, Via De Sanctis, Campobasso, 86100, Italy. Electronic address:
Four different biomedical patches were bioprinted using nanocomposite hydrogels of sodium alginate/gelatin, sodium alginate/gelatin/indocyanine green freely dispersed, sodium alginate/gelatin/empty liposomes and sodium alginate/gelatin/indocyanine green loaded liposomes. Quasi-static and dynamic nanoindentations of the patch surfaces were performed to examine the effect of the single component on the mechanical response. The combination of results suggests that the mechanical structure of the gels is strongly influenced by crosslinking and the liposomes incorporating dye.
View Article and Find Full Text PDFLangmuir
September 2025
Department of Materials Science and Engineering, Drexel University, Philadelphia, Pennsylvania 19104, United States.
The surfaces of 1D layered lepidocrocite-structured titanates (1DLs) are negatively charged due to an oxygen-to-titanium atomic ratio >2. This, and their layered structure, allow for facile ion exchange and high colloidal stability, demonstrated by ζ-potentials of ≈ -85 mV at their unadjusted pH of ≈10.4.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, Kraków 30-387, Poland.
The multifunctional systems presented here introduce an innovative and deeply thought-out approach to the more effective and safer use of temozolomide (TMZ) in treating glioma. The developed hydrogel-based flakes were designed to address the issues of local GBL therapy, bacterial neuroinfections, and the bleeding control needed during tumor resection. The materials obtained comprise TMZ and vancomycin (VANC) loaded into cyclodextrin/polymeric capsules and embedded into gelatin/hyaluronic acid/chitosan-based hydrogel films cross-linked with genipin.
View Article and Find Full Text PDFBiomed Eng Lett
September 2025
Department of Mechanical Engineering, University of Nevada, Las Vegas, Las Vegas, NV 89154 USA.
Alginate is known to readily aggregate and form a physical gel when exposed to cations, making it a promising material for bioprinting applications. Alginate and its derivatives exhibit viscoelastic behavior due to the combination of solid and fluid components, necessitating the characterization of both elastic and viscous properties. However, a comprehensive investigation into the time-dependent viscoelastic properties of alginate hydrogels specifically optimized for bioprinting is still lacking.
View Article and Find Full Text PDFEur J Pharm Sci
September 2025
Department of Medicinal Chemistry, Uppsala University, SE-75123 Uppsala, Sweden. Electronic address:
Subcutaneous (SC) injection is the primary alternative to oral administration for therapeutic proteins and peptides. However, bioavailability and absorption rate are often variable and difficult to predict. Therefore, there is a need for new biorelevant and predictive SC in vitro methods.
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