Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: unknown, P. 159096 - 159096
Published: Dec. 1, 2024
Language: Английский
Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: unknown, P. 159096 - 159096
Published: Dec. 1, 2024
Language: Английский
Journal of Controlled Release, Journal Year: 2025, Volume and Issue: 378, P. 1061 - 1079
Published: Jan. 5, 2025
Language: Английский
Citations
2Bioactive Materials, Journal Year: 2024, Volume and Issue: 42, P. 284 - 298
Published: Sept. 4, 2024
Language: Английский
Citations
12Journal of Nanobiotechnology, Journal Year: 2025, Volume and Issue: 23(1)
Published: Feb. 20, 2025
The advent of nanozymes has revolutionized approaches to cancer diagnosis and therapy, introducing innovative strategies that address the limitations conventional treatments. Nanozyme nanostructures with enzyme-mimicking catalytic abilities exhibit exceptional stability, biocompatibility, customizable functions, positioning them as promising tools for theranostics. By emulating natural enzyme reactions, can selectively target eradicate cells, minimizing harm adjacent healthy tissues. Nanozymes also be functionalized specific targeting ligands, allowing precise delivery regulated release therapeutic agents, improving treatment effectiveness reducing adverse effects. However, issues such selectivity, regulatory compliance remain critical challenges clinical application nanozymes. This review provides an overview nanozymes, highlighting their unique properties, various classifications, activities, diverse applications in strategic oncological deployment could profoundly impact future advancements personalized medicine, recent progress prospective directions enzyme-mimetic treatment. summarizes
Language: Английский
Citations
1Nano Letters, Journal Year: 2024, Volume and Issue: 24(45), P. 14337 - 14345
Published: Oct. 29, 2024
Nanomaterials with peroxidase-like activity and photothermal conversion efficiency have garnered significant attention for their ability to generate cytotoxic hydroxyl radicals provide synergistic therapeutic effects. Selecting nanozymes suitable properties carriers is crucial maximizing efficacy. While the mucin family known its mucoadhesive, glycosylated structures that enhance drug bioavailability targeting, potential in remains underexplored. Here, we utilize mucin-2 facilitate osmium nanoclusters (Os@Mucin), creating protein-corona-like nanozymes. This configuration bestows Os@Mucin excellent (769 U/mg) (22.83%, 808 nm). Mucin-2 promotes Os uptake by cells, allowing exhibit tumor environment-responsive activity, further enhanced under conditions targeted cytotoxicity
Language: Английский
Citations
4Polyoxometalates, Journal Year: 2025, Volume and Issue: 4(1), P. 9140074 - 9140074
Published: March 1, 2025
In recent years, polyoxometalates have been systematically studied in the treatment of diabetes, tumor, cancer, inflammation and other diseases vitro vivo, their main therapeutic mechanisms are related to generation reactive oxygen species causing oxidative stress. The site production is mitochondria, therefore, mechanism may be mitochondrial biosynthesis. This paper describes one diabetes mellitus, which involves increase species, resulting stress; at same time, preliminarily as antioxidants antitumor mellitus tumors, antioxidant properties provide an additional possibility for future a drug disease treatment; on basis study stress biomolecule due it, associating therapy actually closely through biosynthesis regulation relationship between mitochondria its impact three aspects order in-depth role drugs aspects.
Language: Английский
Citations
0International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: unknown, P. 139704 - 139704
Published: Jan. 1, 2025
Language: Английский
Citations
0Advanced Healthcare Materials, Journal Year: 2025, Volume and Issue: unknown
Published: March 19, 2025
Abstract The cGAS‐STING signaling pathway is a pivotal immune response mechanism that bridges tumor and cell interactions. This study describes multifunctional LPDAM nanoplatform integrating Lapachone, polydopamine (PDA), Mn 2+ , which synergistically kills cells activates the pathway, thereby inducing DC maturation T activation to achieve potent antitumor immunity. In microenvironment, Lapachone generates H 2 O via NAD(P)H:quinone oxidoreductase 1 (NQO1 enzyme), while catalyze conversion into •OH through chemodynamic effects (CDT). photothermal (PTT) of PDA further amplify this cascade reaction, producing reactive oxygen species (ROS) damage mitochondria release mitochondrial DNA (mtDNA). released mtDNA enhances sensitivity cGAS mtDNA, leading robust Concurrently, photothermal‐induced immunogenic death (ICD) promotes d endritic ( DCs) maturation, strengthening responses. Moreover, ⁺ also serves as contrast agent for T1‐weighted magnetic resonance imaging (MRI), offering precise visualization. demonstrates facilitates Lapachone/CDT/PTT synergistic therapy under MRI guidance, showcasing its potential an innovative strategy combined immunotherapy in clinical oncology.
Language: Английский
Citations
0Biomaterials, Journal Year: 2025, Volume and Issue: 319, P. 123199 - 123199
Published: Feb. 20, 2025
Language: Английский
Citations
0Journal of Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 681, P. 148 - 158
Published: Nov. 23, 2024
Language: Английский
Citations
1Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: unknown, P. 159096 - 159096
Published: Dec. 1, 2024
Language: Английский
Citations
1