Abstract
Porous, defective, gray cerium oxide (g-CeO2–x) microspheres 4.8 μm in size were synthesized as a multifunctional nanozyme with catalase-, peroxidase-, and oxidase-like activities by the reduction of monodisperse-porous cerium oxide (CeO2) microspheres. Higher Ce(III) atomic fraction, more oxygen vacancy, and lower oxygen content on the surface of g-CeO2–x microspheres were shown by Raman and X-ray photoelectron spectroscopy. Band gap energies of plain CeO2 and g-CeO2–x microspheres were determined as 3.0 and 2.4 eV, respectively. Reactive oxygen species (ROS) related to the enzyme-mimetic activity of g-CeO2–x microspheres were determined as singlet oxygen (1O2•) and superoxide anion (•O2–) by ESR spectroscopy. Michaelis–Menten plots sketched for catalase-, peroxidase-, and oxidase-like activities provided superior maximum substrate consumption rates for g-CeO2–x microspheres. Oxidase- and peroxidase-like activities were used for developing colorimetric and fluorometric protocols for the detection of nitrite as a common pollutant, respectively. g-CeO2–x microspheres also exhibited a photothermal response explained by enhanced light adsorption originated from more oxygen vacancies. A temperature elevation up to 19 °C was obtained under near infrared laser irradiation at 808 nm. Photothermal response accompanying with multifunctional enzyme-mimetic activities makes the porous nanozyme a promising synergistic therapy agent capable of overcoming hypoxia and generating additional ROS in a tumor microenvironment.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.