Types, Enzyme-Like Activities and Applications of Nanozyme Materials
Types, Enzyme-Like Activities and Applications of Nanozyme Materials
Nanozymes refer to nanomaterials with catalytic activities similar to natural enzymes. Under specific reaction conditions, they can mimic enzymatic functions such as peroxidase, oxidase, catalase and superoxide dismutase. Compared with natural enzymes, nanozymes usually show greater structural stability, easier modification, stronger tolerance and broader application scope. They have been widely used in biodetection, antibacterial therapy, tumor microenvironment regulation, oxidative stress research and environmental analysis.
Keywords: nanozyme; enzyme-like activity; peroxidase-like activity; oxidase-like activity; ROS regulation; biodetection
1 Conceptual Basis of Nanozymes
1.1 Basic Definition
(1) Enzyme-like catalytic materials
Nanozymes are not traditional protein enzymes, but inorganic, organic or composite nanomaterials with enzyme-like catalytic capability. Their catalytic functions usually originate from surface metal active sites, valence-state cycling, oxygen vacancies, defect structures, electron transfer capability or nanoscale confinement effects.
(2) Differences from natural enzymes
Natural enzymes have highly specific active centers and substrate-recognition structures, and their catalytic efficiency is high. However, they are relatively sensitive to temperature, pH, organic solvents and storage conditions. Nanozymes generally have lower substrate specificity than natural enzymes, but they offer stronger material stability, engineering flexibility and tolerance in complex environments.
(3) Research value
Nanozymes can combine the optical, electrical, magnetic, thermal and surface chemical properties of nanomaterials with enzyme-like catalytic functions, forming multifunctional research platforms. Their applications are not limited to single catalytic reactions, but can also extend to signal amplification, reactive oxygen species regulation, microenvironment responsiveness and multimodal therapy.
1.2 Sources of Enzyme-Like Activity
(1) Surface active sites
Nanomaterials have high specific surface area and can expose abundant active sites on their surfaces. These sites can adsorb substrates, promote electron transfer or participate in redox reactions, forming the basis of nanozyme catalytic activity.
(2) Metal valence-state cycling
Elements such as iron, copper, manganese, cerium and platinum can transform between different valence states and participate in electron transfer, free radical generation or free radical scavenging. For example, Fe²⁺/Fe³⁺, Ce³⁺/Ce⁴⁺ and Mn²⁺/Mn³⁺/Mn⁴⁺ valence-state cycles are key factors for many nanozymes showing peroxidase-like, catalase-like or superoxide dismutase-like activities.
(3) Defects and oxygen vacancies
Oxygen vacancies, lattice defects and edge sites in oxide nanomaterials can regulate the electronic structure of materials and improve their ability to activate oxygen molecules, hydrogen peroxide or free radicals. Defect engineering is therefore an important strategy for regulating nanozyme activity.
2 Main Types of Nanozyme Materials
2.1 Metal Oxide Nanozymes
(1) Iron oxide nanozymes
Iron oxide nanoparticles are among the earliest studied nanozyme materials and often show peroxidase-like activity. Under acidic conditions, iron sites can promote hydrogen peroxide decomposition and generate reactive oxygen species, making them useful for colorimetric detection, magnetic separation, antibacterial applications and tumor microenvironment responsiveness.
(2) Cerium oxide nanozymes
Cerium oxide nanoparticles have reversible Ce³⁺/Ce⁴⁺ conversion capability and often show superoxide dismutase-like, catalase-like and free radical scavenging activities. Their antioxidant properties are prominent, making them suitable for oxidative stress, inflammation models and cytoprotective studies.
(3) Manganese oxide nanozymes
Manganese oxide materials can show peroxidase-like, oxidase-like, catalase-like and glutathione-oxidation-related activities. In the tumor microenvironment, manganese-based materials can respond to hydrogen peroxide, acidic pH and reducing glutathione, and are commonly used for oxygen generation, ROS regulation and therapeutic sensitization.
(4) Copper-based oxide nanozymes
Copper oxide, cuprous oxide and other copper-based materials have strong redox activity and can be used in oxidase-like and peroxidase-like reactions, as well as antibacterial and catalytic detection systems. In biological applications, copper ion release, concentration window and cytotoxicity should be carefully considered.
2.2 Noble Metal Nanozymes
(1) Gold nanomaterials
Gold nanoparticles have good surface modifiability and optical signal characteristics, and can show oxidase-like or peroxidase-like activity. They are commonly used in colorimetric detection, immunoassays, nucleic acid detection and biosensing platforms.
(2) Platinum nanomaterials
Platinum nanoparticles have strong redox catalytic capability and can show catalase-like, peroxidase-like and superoxide dismutase-like activities. They are widely used in reactive oxygen species scavenging, anti-inflammatory protection and biocatalysis research.
(3) Palladium nanomaterials
Palladium nanomaterials have good reduction catalytic capability and surface reaction activity, and can be used in redox reactions, pollutant degradation and catalytic signal amplification. Compared with platinum, palladium materials have application advantages in some reduction systems and composite catalytic systems.
2.3 Carbon-Based and Two-Dimensional Nanozymes
(1) Graphene-based materials
Graphene, graphene oxide and their composites have high specific surface area, good conductivity and modifiable surface functional groups. They can be used for substrate adsorption, electron transfer and construction of composite catalytic systems.
(2) Carbon dots
Carbon dots have small particle size, good fluorescence properties and easily functionalized surfaces. Some carbon dots can show peroxidase-like, oxidase-like or antioxidant activity and are suitable for combining fluorescence detection with catalytic signal amplification.
(3) Molybdenum disulfide materials
Molybdenum disulfide nanomaterials have a two-dimensional layered structure, active surface edges and photothermal response characteristics. They can show peroxidase-like activity and can synergize with photothermal or photocatalytic processes for detection, antibacterial and tumor therapy research.
2.4 MOF-Based and Composite Nanozymes
(1) MOF nanozymes
Metal-organic frameworks have designable metal nodes, organic ligands and pore structures. They can provide catalytic sites through metal centers and enrich substrates through their pores. MOF nanozymes are often used for reaction confinement, catalytic carriers and multifunctional composite platforms.
(2) Single-atom nanozymes
Single-atom materials use highly dispersed metal atoms as active centers, which can improve atomic utilization and catalytic selectivity. Metal-nitrogen-carbon structures are often used to mimic the active centers of natural metalloenzymes.
(3) Composite nanozymes
Composite nanozymes combine metals, oxides, carbon materials, polymers or biomolecules to achieve synergistic enzyme-like activities. For example, magnetic iron oxide combined with surface functional layers can simultaneously provide magnetic responsiveness, POD-like activity and bioconjugation capability.
3 Main Enzyme-Like Activities of Nanozymes
3.1 Peroxidase-Like Activity
(1) Reaction characteristics
Peroxidase-like activity usually refers to the ability of nanozymes to catalyze substrate oxidation in the presence of hydrogen peroxide. Common chromogenic substrates include TMB, ABTS and OPD, which produce color, fluorescence or electrochemical signal changes after reaction.
(2) Influencing factors
pH, hydrogen peroxide concentration, substrate concentration, material particle size, surface charge, metal valence state and dispersion status can all affect peroxidase-like activity. Many POD-like nanozymes show stronger activity under acidic conditions.
(3) Application value
POD-like activity is one of the most widely used types of nanozyme activity. It can be used in colorimetric detection, immunoassays, glucose detection, bacterial detection and reactive oxygen species generation in the tumor microenvironment.
3.2 Oxidase-Like Activity
(1) Reaction characteristics
Oxidase-like nanozymes can use dissolved oxygen to oxidize substrates without exogenous hydrogen peroxide, generating oxidation products or reactive oxygen species. This reaction can simplify detection systems and reduce background interference from hydrogen peroxide.
(2) Material characteristics
Gold-based, copper-based, manganese-based and some carbon-based nanomaterials often show oxidase-like activity. The adsorption, activation and electron transfer ability of material surfaces toward oxygen molecules are key determinants of activity.
(3) Application directions
Oxidase-like activity is suitable for hydrogen-peroxide-free colorimetric detection, antibacterial systems and oxidative stress model construction.
3.3 Catalase-Like Activity
(1) Reaction characteristics
Catalase-like activity refers to nanozyme-catalyzed decomposition of hydrogen peroxide into water and oxygen. This reaction can reduce hydrogen peroxide accumulation and improve hypoxic or oxidative stress environments.
(2) Typical materials
Platinum nanoparticles, cerium oxide, manganese dioxide and Prussian blue materials often show relatively clear catalase-like activity. Their catalytic capability is closely related to surface redox cycling.
(3) Application directions
CAT-like nanozymes can be used for antioxidant protection, tissue hypoxia improvement, tumor therapy sensitization and inflammatory microenvironment regulation. In tumor research, oxygen generation can also enhance photodynamic therapy and radiotherapy.
3.4 Superoxide Dismutase-Like Activity
(1) Reaction characteristics
SOD-like activity can catalyze the dismutation of superoxide anions and reduce free radical levels. This activity is often associated with antioxidation, anti-inflammation and cytoprotection.
(2) Typical materials
Cerium oxide, Prussian blue, platinum-based materials, manganese-based materials and some single-atom materials often show SOD-like activity. Valence-state transformation capability and defect status have major effects on free radical scavenging ability.
(3) Application directions
SOD-like nanozymes are suitable for research on oxidative stress injury, inflammatory diseases, neurodegenerative injury and tissue protection.
3.5 Multiple Enzyme-Like Activities
(1) Coexistence of activities
The same nanomaterial can show multiple enzyme-like activities under different conditions. For example, cerium oxide can show both SOD-like and CAT-like activities, while Prussian blue materials can simultaneously show POD-like, CAT-like and SOD-like activities.
(2) Environmental dependence
Multiple enzyme-like activities are highly condition-dependent. Acidic environments may enhance POD-like activity, while neutral or weakly alkaline environments are more favorable for CAT-like or antioxidant activity. When evaluating nanozymes, the reaction environment should be clearly defined.
(3) Synergistic applications
Multi-enzyme-like nanozymes can be used in cascade reactions and microenvironment-responsive therapy. For example, CAT-like activity can first generate oxygen to enhance photodynamic reactions, or GSH depletion can be combined with POD-like reactions to increase oxidative damage.
4 Strategies for Regulating Nanozyme Activity
4.1 Size and Morphology Regulation
(1) Particle size effect
Reducing particle size usually increases specific surface area and exposes more active sites. However, excessively small particles may also cause aggregation, increased toxicity or reduced stability. Activity optimization requires a balance between active-site exposure and system stability.
(2) Morphology effect
Nanosheets, nanospheres, nanorods, nanoflowers and hollow structures have different exposed crystal facets and mass-transfer characteristics. Specific crystal facets may have higher catalytic activity, so morphology regulation is a common method for improving enzyme-like activity.
(3) Pore structure effect
Mesoporous or porous structures can enhance substrate enrichment and mass transfer efficiency, making it easier for reactants to contact active sites. MOFs, mesoporous carbon and hollow materials often use this advantage to improve catalytic performance.
4.2 Surface Modification
(1) Ligand modification
Surface ligands can improve water dispersibility, reduce nonspecific adsorption and affect the ability of substrates to approach active sites. PEG, proteins, peptides, nucleic acids and small-molecule ligands are often used for biocompatibility optimization.
(2) Targeting modification
Antibodies, aptamers, peptides or small-molecule ligands can give nanozymes targeting capability, allowing them to enrich in specific cells, bacteria or tissue regions. Targeting modification is suitable for detection and therapeutic applications.
(3) Functional group regulation
Surface functional groups such as carboxyl, amine, maleimide, biotin and streptavidin can be used to conjugate antibodies, proteins, peptides or nucleic acids, enabling construction of magnetic detection probes, immunoassay platforms or targeted nanozyme systems.
4.3 Composition and Defect Engineering
(1) Element doping
Introducing hetero-elements can change electronic structure and active-site distribution, improving redox capability. Both metal and non-metal doping can be used to regulate catalytic activity.
(2) Valence-state regulation
Adjusting the valence-state ratio of metal elements can optimize electron transfer processes. For example, increasing the Ce³⁺ ratio may enhance certain antioxidant activities, while regulating Mn valence states can affect the direction of redox reactions.
(3) Defect construction
Oxygen vacancies, edge defects and lattice defects can act as active sites or electron transfer channels. Moderate defects help improve activity, while excessive defects may reduce structural stability.
5 Application Directions of Nanozymes
5.1 Biodetection
(1) Colorimetric detection
POD-like nanozymes can catalyze oxidation of chromogenic substrates and present detection results through color changes. This method is simple to operate and is suitable for detecting glucose, hydrogen peroxide, nucleic acids, proteins and pathogens.
(2) Immunoassays
Nanozymes can replace natural enzymes such as horseradish peroxidase as signal labels in immunodetection. Their strong stability and convenient storage make them suitable for constructing highly tolerant immunoassay systems.
(3) Magnetic separation detection
Fe₃O₄ magnetic nanozymes have both magnetic responsiveness and POD-like activity, enabling integrated target capture, magnetic separation and catalytic color development. They are suitable for detecting low-abundance biomarkers.
5.2 Antibacterial Applications and Biofilm Removal
(1) ROS-mediated antibacterial activity
Nanozymes with POD-like or OXD-like activity can generate reactive oxygen species such as hydroxyl radicals and superoxide anions, damaging bacterial membrane structures, proteins and nucleic acids, thereby exerting antibacterial effects.
(2) Biofilm disruption
The polysaccharide, protein and DNA matrices in biofilms reduce the penetration efficiency of traditional antibacterial agents. Nanozymes can improve biofilm removal by catalytically generating reactive oxygen species or disrupting matrix structures.
(3) Synergistic antibacterial effects
Nanozymes can be used synergistically with antibiotics, photothermal materials or photodynamic materials to reduce the dosage of single antibacterial agents and enhance inhibition of drug-resistant bacteria.
5.3 Tumor Microenvironment Regulation
(1) Hydrogen peroxide responsiveness
The tumor microenvironment often contains relatively high levels of hydrogen peroxide. POD-like nanozymes can use this feature to generate reactive oxygen species and induce oxidative damage in tumor cells.
(2) Hypoxia alleviation
CAT-like nanozymes can decompose hydrogen peroxide to generate oxygen, improving tumor hypoxia. This strategy can enhance photodynamic therapy, radiotherapy and some oxygen-dependent treatments.
(3) Redox intervention
Manganese-based, copper-based, iron-based and noble-metal nanozymes can participate in tumor redox regulation through ROS generation, GSH depletion or free radical scavenging.
5.4 Antioxidation and Inflammation Regulation
(1) Free radical scavenging
Nanozymes with SOD-like, CAT-like or multi-enzyme antioxidant activities can reduce reactive oxygen species levels and protect cells from oxidative damage.
(2) Inflammation alleviation
Oxidative stress often amplifies inflammatory signaling. Antioxidant nanozymes can indirectly inhibit inflammatory factor release and tissue injury by reducing free radical levels.
(3) Tissue protection
Cerium oxide, Prussian blue, platinum-based and manganese-based nanozymes are often used in studies related to neuroprotection, myocardial protection, renal injury protection and wound repair. In practical applications, in vivo distribution, long-term metabolism and safety should be carefully evaluated.
5.5 Environmental Analysis and Pollutant Treatment
(1) Pollutant detection
Nanozymes can be used to detect heavy metal ions, phenolic substances, pesticide residues and peroxides. Colorimetric, fluorescent and electrochemical platforms can all be combined with nanozyme catalytic reactions.
(2) Organic pollutant degradation
Some nanozymes can participate in oxidative degradation of organic pollutants through reactive oxygen species, making them suitable for water treatment and environmental catalysis research.
(3) Adaptability to complex samples
Nanozymes have strong stability and can work over relatively wide ranges of pH, temperature and ionic strength. Therefore, they have certain advantages in complex environmental samples.
6 Nanozyme Activity Evaluation and Experimental Design
6.1 Activity Evaluation Indicators
(1) Reaction rate
Reaction rate reflects the ability of nanozymes to catalyze substrate conversion and is often calculated from changes in absorbance, fluorescence intensity or electrochemical signals.
(2) Apparent kinetic parameters
Km and Vmax can be used to compare the apparent substrate affinity and catalytic capability of nanozymes. It should be noted that nanozymes are not natural enzymes, and their kinetic parameters are also affected by adsorption, diffusion, aggregation and surface reactions.
(3) Stability
Nanozyme evaluation should include thermal stability, pH stability, storage stability and cycling stability. For biological applications, the effects of serum environment, protein adsorption and ionic strength should also be evaluated.
6.2 Control of Experimental Conditions
(1) pH conditions
Different enzyme-like activities have different pH dependence. POD-like activity is often stronger under acidic conditions, while CAT-like and antioxidant activities are usually closer to neutral physiological environments. Reaction pH should be clearly specified, and simple comparisons across different conditions should be avoided.
(2) Substrate concentration
Excessively high substrate concentration may cause auto-oxidation or nonspecific reactions, while excessively low concentration may result in insufficient signal. Chromogenic substrate, hydrogen peroxide and nanozyme concentrations all need to be optimized through pilot experiments.
(3) Dispersion stability
Aggregation reduces effective surface area and changes catalytic results. Before nanozyme testing, particle size distribution, Zeta potential and dispersion stability should be evaluated, especially in salt solutions, culture media and serum systems.
7 Nanozyme Material Selection
7.1 Nanozyme Material Types, Activity Characteristics and Application Scenarios
Nanozyme Material Type | Cat. No. | Product Name | Grade & Purity | Enzyme-Like Activity and Functional Features | Applicable Research Directions |
MnO₂ nanomaterial | Molybdenum Disulfide Nanoparticles | BioReagent,1 mg/mL, dispersion solvent: pure water, particle size: ~100 nm | Redox activity, CAT-like/oxidase-like functions | ROS regulation, tumor microenvironment, oxidative stress research | |
CeO₂ nanomaterial | Cerium Oxide Nanoparticles | BioReagent,1 mg/mL, dispersion solvent: ultrapure water, particle size: 2~5 nm | SOD-like, CAT-like and oxidase-like activities | Antioxidation, inflammation models, oxidative injury protection | |
MoS₂ nanomaterial | Molybdenum Disulfide Nanoparticles | BioReagent,1 mg/mL, dispersion solvent: pure water, particle size: ~100 nm | POD-like activity, photothermal/catalytic synergistic features | Biodetection, antibacterial research, tumor therapy research | |
Peroxide nanomaterial | Zinc Peroxide Nanoparticles | BioReagent,10 mg/mL, dispersion solvent: Absolute Ethanol, particle size: 40-50 nm | ROS release and oxidative stress regulation | Tumor therapy, antibacterial applications, oxidative stress induction | |
Peroxide nanomaterial | Calcium Peroxide Nanoparticles | BioReagent,5 mg/mL, dispersion solvent: Absolute Ethanol, particle size: 60-70 nm | Oxygen/ROS release-related function | Hypoxia regulation, tumor microenvironment, oxidative stress research | |
HfO₂ nanomaterial | Hafnium oxid Nanoparticles | BioReagent,4 mg/mL, dispersion solvent: ultrapure water, particle size: ~50 nm | High-Z element, ROS sensitization-related function | Radiosensitization, ROS-related biomedical research | |
Prussian blue nanomaterial | PVP-modified Prussian Blue Nanoparticles | BioReagent,0.25 mg/mL, dispersion solvent: ultrapure water, particle size: <100 nm | POD-like, CAT-like and SOD-like activities | Antioxidation, inflammation regulation, biodetection | |
Prussian blue nanomaterial | Citrate-modified Prussian Blue Nanoparticles | BioReagent,1 mg/mL, dispersion solvent: ultrapure water, particle size: <100 nm | Multi-enzyme-like activity, free radical scavenging | Oxidative stress, neuroprotection, inflammation models | |
Prussian blue nanomaterial | Cesium-doped Prussian Blue Nanoparticles | BioReagent,1 mg/mL, dispersion solvent: ultrapure water, particle size: <50 nm | Prussian blue framework catalysis and ion-doping regulation | Antioxidation, ion response, nanocatalysis research | |
MOF-based nanomaterial | Ce/Zr-MOF Nanoparticles | BioReagent,particle size: 300nm | Metal-node catalysis, porous structure loading | MOF nanozymes, catalytic carriers, ROS regulation | |
MOF-based nanomaterial | Cu-Co bimetallic MOF Nanoparticles | BioReagent,particle size: 150nm | Cu/Co bimetallic synergistic catalysis | MOF nanozymes, POD-like catalysis, biodetection | |
Fe₃O₄ magnetic nanomaterial | Ferromagnetic nanoparticles | Solid powder | POD-like activity, magnetic response | Preparation of magnetic composites | |
Fe₃O₄ magnetic nanomaterial | Ferromagnetic nanoparticles | Iron concentration:1 mg/mL | POD-like activity, controllable particle size | Magnetic nanozyme construction | |
Fe₃O₄ magnetic nanomaterial | Ferromagnetic nanoparticles | Solid powder | POD-like activity | Magnetic catalytic materials | |
Fe₃O₄ magnetic nanomaterial | Ferromagnetic nanoparticles | Iron concentration:1 mg/mL | POD-like activity, cationic surface | Nucleic acid adsorption, cell delivery, catalytic detection | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 15nm avg. part. size(TEM), streptavidin functionalized, 1mg/mL in H₂O | POD-like activity, biotin-streptavidin recognition | Biotinylated molecule capture, magnetic detection | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 15nm avg. part. size(TEM), 5mg/mL in H₂O | POD-like activity | Basic magnetic nanozyme model | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 5nm avg. part. size(TEM), 5mg/mL in chloroform | POD-like activity, small-size effect | Oil-phase systems, surface modification | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 15nm avg. part. size(TEM), PEG functionalized, 1mg/mL in H₂O | POD-like activity, PEG stabilization | Biocompatible magnetic nanozymes | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 5mg/mL in chloroform | POD-like activity | Oil-phase dispersion, material modification | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 10nm avg. part. size(TEM), 5mg/mL in chloroform | POD-like activity | Oil-phase nanozymes, surface modification | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 15nm avg. part. size(TEM), 5mg/mL in toluene | POD-like activity | Non-aqueous dispersion, catalytic material construction | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 20nm avg. part. size(TEM), streptavidin functionalized, 1mg/mL in H₂O | POD-like activity, specific capture | Immunoassays, biotinylated probe detection | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 10nm avg. part. size(TEM), streptavidin functionalized, 1mg/mL in H₂O | POD-like activity, bioconjugation | Magnetic immunodetection | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 15nm avg. part. size(TEM), amine functionalized, 1mg/mL in H₂O | POD-like activity, amine coupling | Protein coupling, nanoprobe construction | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 10nm avg. part. size(TEM), rhodamine B functionalized, 1mg/mL in H₂O | POD-like activity, fluorescent tracing | Imaging-catalysis composite research | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 25nm avg. part. size(TEM), amine functionalized, 1mg/mL in H₂O | POD-like activity, surface coupling | Biolabeling, magnetic catalysis | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 15nm avg. part. size(TEM), carboxylic acid functionalized, 5mg/mL in H₂O | POD-like activity, carboxyl coupling | Antibody coupling, colorimetric detection | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 25nm avg. part. size(TEM), 5mg/mL in toluene | POD-like activity | Non-aqueous catalytic materials | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 30nm avg. part. size(TEM), 5mg/mL in H₂O | POD-like activity, enhanced magnetic response | Magnetic separation, catalytic detection | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 30nm avg. part. size(TEM), 5mg/mL in toluene | POD-like activity | Hydrophobic nanozyme systems | |
Iron oxide nanomaterial | Iron oxide (II,III), nanoparticles | 30nm avg. part. size(TEM), streptavidin functionalized, 1mg/mL in H₂O | POD-like activity, bioaffinity recognition | Magnetic immunoassays | |
Platinum-based nanomaterial | Platinum nanoparticles | 1% on Titania(anatase)(surfactant and reactant-free),≤100nm | CAT-like, oxidase-like and POD-like activities | Catalysis, ROS scavenging, antioxidant research | |
Platinum-based nanomaterial | Platinum nanoparticles, pure, (<20nm) in water at 30mg/L (surfactant and reactant-free, stabilized with <0.01 mmol/l of citrate) | pure,<20nm in water at 30mg/Lsurfactant and reactant-free, stabilized with <0.01 mmol/l of citrate | Multi-enzyme-like activity, noble-metal catalysis | Biocatalysis, antioxidation, detection | |
Platinum-based nanomaterial | Platinum nanoparticles | 10% on Titaniaanatasesurfactant and reactant-free | Supported noble-metal catalysis | Photocatalysis/redox catalysis | |
Platinum-based nanomaterial | Platinum nanoparticles | 10% on carbon blacksurfactant and reactant-free | Supported Pt catalytic activity | Electrocatalysis, redox research | |
Platinum-based nanomaterial | Platinum nanoparticles | 5% on carbon black (surfactant and reactant-free) | Supported Pt catalytic activity | Catalytic materials, redox systems | |
Platinum-based nanomaterial | Platinum nanoparticles, pure | pure, <20nm in water at 100mg/Lsurfactant and reactant-free, stabilized with < 0.01 mmol/l of citrate | CAT-like, POD-like and oxidase-like activities | Antioxidation, biodetection, ROS regulation | |
Platinum-based nanomaterial | Platinum nanoparticles | 20% on carbon blacksurfactant and reactant-free | High-loading Pt catalysis | Electrocatalysis, nanocatalysis research | |
Platinum-based nanomaterial | Platinum nanoparticles, pure | pure, <20nm in isopropanol at 100mg/Lsurfactant and reactant-free | Noble-metal multi-enzyme-like catalysis | Non-aqueous catalysis, material modification | |
Platinum-based nanomaterial | Platinum nanoparticles | 30% on carbon blacksurfactant and reactant-free | High-loading Pt catalysis | Electrocatalysis, oxygen reduction-related research | |
Platinum-based nanomaterial | Platinum nanoparticles | 10% on Titaniaanatase/rutilesurfactant and reactant-free | Pt/TiO₂ composite catalysis | Photocatalysis, ROS generation research | |
Platinum-based nanomaterial | Platinum nanoparticles | 1% on Titaniaanatase/rutilesurfactant and reactant-free | Pt/TiO₂ composite catalysis | Photocatalysis, redox catalysis | |
Platinum-based nanomaterial | Platinum Nanoparticles [PtNP: 2-3 nm (gum Arabic)] |
| Small-size Pt multi-enzyme-like activity | Antioxidation, ROS scavenging, biocatalysis | |
Palladium-based nanomaterial | Palladium nanoparticles entrapped in aluminum hydroxide matrix | 0.5wt% loading | Noble-metal catalysis, supported nanocatalysis | Catalytic reactions, nanocomposites | |
Palladium-based nanomaterial | Palladium nanoparticles, pure | pure, <20nm in water at 100mg/Lsurfactant and reactant-free, stabilized with < 0.01 mmol/l of citrate | Redox catalysis, enzyme-like catalysis potential | Catalytic detection, noble-metal nanozyme research | |
Palladium-based nanomaterial | Palladium nanoparticles, pure | pure, <20nm in water at 500mg/Lsurfactant and reactant-free, stabilized with < 0.01 mmol/l of citrate | Redox catalysis | High-concentration catalytic systems, material preparation | |
Palladium-based nanomaterial | Palladium nanoparticles, pure | pure, 50-70nm in acetone at 100mg/Lsurfactant and reactant-free | Noble-metal catalysis | Non-aqueous catalysis, material composites | |
Palladium-based nanomaterial | Palladium nanoparticles, pure | pure, <20nm in acetone at 100mg/Lsurfactant and reactant-free | Noble-metal catalysis | Hydrophobic systems, nanocatalysis | |
Gold-based nanomaterial | Gold nanoparticles | Particle size: 20nm, solvent: ultrapure water, OD: >0.75 | Surface plasmon effect, catalytic enhancement | Colorimetric detection, biolabeling, sensing | |
Gold-based nanomaterial | Gold nanoparticles | Laser liquid phase preparation, high purity, reactant free, 10nm, 0.05mg/ml in H2O,OD 1,PDI<0.2 | Gold surface catalysis and signal amplification | Biosensing, immunodetection | |
Gold-based nanomaterial | Gold nanoparticles | A stable suspension with a diameter of 40nm, OD 1, in citrate buffer solution | Colorimetric signal, surface catalysis | Colloidal gold detection, nanoprobe construction |
Nanozyme research focuses on matching material composition, surface sites, enzyme-like activities and application environments. By rationally selecting material types, controlling dispersion systems, optimizing surface functionalization and establishing standardized activity evaluation conditions, nanozymes can be further advanced in biodetection, antibacterial applications, tumor microenvironment regulation, antioxidant protection and environmental analysis.
For more related articles, please see below:
[1] Silver Nanomaterials for Biological Applications
[2] Application of Nanomaterials in Wastewater Treatment
[3] Application of Nanomaterials in Photoacoustic Imaging
[4] Chemical Synthesis Methods of Nanomaterials
[5] Silica-Coated Gold Nanoparticles: Surface Chemistry, Properties, Benefits, and Applications
