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Nanozymes, as synthetic nanomaterials that catalyze the conversion of enzyme substrates to products and follow enzymatic kinetics, have emerged as powerful agents for combating oxidative stress-related diseases by scavenging reactive oxygen species (ROS). In recent years, constructing multifunctional integrated systems by integrating nanozymes with therapeutic drugs or endowing them with efficient delivery capabilities through surface functionalization strategies has become one of the cutting-edge directions. This review explores recent progress in three key surface modification approaches-chemical conjugation, physical encapsulation, and drug loading-that collectively enable synergistic therapeutic effects, precise targeting, and effective penetration of biological barriers. Chemical conjugation allows for the direct attachment of molecules to nanozyme surfaces, enhancing synergistic efficacy and targeting specificity. Physical encapsulation using mesoporous structures, hydrogels, or microneedles improves nanozyme stability, extends retention, and facilitates controlled release. Drug-loading strategies further expand the therapeutic potential by enabling co-delivery of antioxidants and other functional agents to complex pathological environments. Despite these promising advancements, challenges remain in elucidating the fundamental catalytic mechanisms of nanozymes, ensuring long-term biocompatibility, and achieving scalable clinical translation. Future efforts should focus on developing dynamically responsive systems, achieving precision catalysis, and fostering interdisciplinary integration to accelerate the evolution of nanozyme-based therapeutics. This review systematically summarizes the modification strategies from a surface perspective, offering insights for constructing multifunctional systems.
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http://dx.doi.org/10.1039/d5tb00877h | DOI Listing |
Med Oncol
September 2025
Venom and Biotherapeutics Molecules Laboratory, Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Neuropeptide Y (NPY) and the voltage-gated potassium channel Kv1.3 are closely associated with breast cancer progression and apoptosis regulation, respectively. NPY receptors (NPYRs), which are overexpressed in breast tumors, contribute to tumor growth, migration, and angiogenesis.
View Article and Find Full Text PDFDiscov Nano
September 2025
Henan Key Laboratory of Diamond Optoelectronic Materials and Devices, Key Laboratory of Integrated Circuit, Ministry of Education, School of Physics, Zhengzhou University, Zhengzhou, 450052, China.
A cost-effective and large-scale method for synthesizing ZnCoO nanoflowers with surface oxygen vacancies as electrode materials for supercapacitors is presented. The existence of oxygen vacancies on the surface of the ZnCoO nanoflowers has been confirmed through X-ray photoelectron spectroscopy (XPS). The energy bands and density of states (DOS) of ZnCoO are examined using density functional theory, revealing that treatment with NaBH reduces the band gap of ZnCoO while increasing the DOS near the Fermi level compared to pristine ZnCoO.
View Article and Find Full Text PDFAnal Sci
September 2025
Department of Chemistry, Graduate School of Advanced Science and Engineering, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, 739-8526, Japan.
Surface-enhanced Raman scattering (SERS) is a powerful analytical technique; however, its quantitative application has been limited by the instability of substrates and significant signal fluctuations. In this study, we demonstrated that 4-aminobenzenethiol (4-ATP) can be quantitatively detected through statistical analysis of SERS signal intensity distributions obtained using citrate-stabilized AuNPs, biotin-functionalized AuNPs, and gold nanoparticle (AuNP)-bound polystyrene (PS) microparticles. Raman spectra obtained in bulk aqueous solution under static conditions showed that the detection sensitivity of 4-ATP using AuNP-bound PS microparticles was approximately twice that achieved with citrate-stabilized AuNPs or biotin-modified AuNPs.
View Article and Find Full Text PDFJ Thromb Thrombolysis
September 2025
Central Laboratory of Yongchuan Hospital, Chongqing Medical University, No. 439, Xuanhua Road, Yongchuan District, Chongqing, 402160, China.
In vitro assessment of the inhibitory effect of antiplatelet drugs on platelet aggregation is frequently employed to guide personalized antiplatelet therapy in clinical practice. However, existing methods for detecting platelet aggregation rely heavily on high concentrations of exogenous agonists, which may obscure part of the inhibitory effect of antiplatelet drugs and lead to an underestimation of their effects. This study validates a novel analytical strategy for evaluating the effects of antiplatelet drugs by quantifying the microscopic three-dimensional morphological parameters of platelet aggregates formed through spontaneous aggregation on a glass surface.
View Article and Find Full Text PDFArch Microbiol
September 2025
División de Ciencias Naturales y Exactas, Departamento de Biología, Universidad de Guanajuato, Zip Code 36050, Guanajuato, Mexico.
Plasmids are fundamental to molecular biology and biotechnology, playing a crucial role in bacterial evolution. Some plasmids are linked to complex cellular dynamics, including pathogenicity islands, antibiotic resistance, and gene mobilization. This study reports the isolation and sequencing of two cryptic plasmids with different electrophoretic mobilities from the Escherichia coli clinical isolate O55.
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