Periodic

Materials
  • ALL
  • Enzyme-like Activity
  • ALL
  • ref material application target method linear range linear range unit LOD LOD unit recovery comment
    4952 17 MoO3–x NUs biodegradation-medicated enzymatic activity-tunable molybdenum oxide nanourchins (MoO3–x NUs), which selectively perform therapeutic activity in tumor microenvironment via cascade catalytic reactions, while keeping normal tissues unharmed due to their responsive biodegradation in physiological environment
    4953 19 Cu-nanoflower@gold nanoparticles-GO NFs glucose detection
    4954 20 HMON-Au@Cu-TA photodynamic therapy (PDT) and chemodynamic therapy (CDT)
    4955 21 Fe-N/C Detection of alkaline phosphatase Alkaline phosphatase (ALP) Color 0.05-100 U/L 0.02 U/L
    4956 23 Co3O4@Co-Fe oxide double-shelled nanocages Detection acetylcholinesterase (AChE) Color 0.0008-1 mU/mL 0.0002 mU/mL
    4957 23 Co3O4@Co-Fe oxide double-shelled nanocages Detection H2O2 Color 0.02 - 600 μM 0.02 μM
    4958 24 core–shell UMOFs@Au NPs Cancer therapy
    4959 27 Cu–N–C Detection organophosphorus pesticides Color 1-300 ng/mL 0.6 ng/mL
    4960 27 Cu–N–C Detection acetylcholine Color 10-8000 μM 1.24 μM
    4961 29 PDA‐Pt‐CD@RuFc NPs Cancer therapy
    4962 31 FeS2 NPs quantitative detection of H2O2 or GSH GSH Color 0.20-3.5 μM 0.15 μM
    4963 31 FeS2 NPs quantitative detection of H2O2 or GSH H2O2 Color 2-80 μM 0.91 μM
    4964 32 Au2Pt synergistic chemodynamic therapy / phototherapy
    4965 33 Co/PMCS Sepsis Management
    4966 35 Cu5.4O USNPs exhibit cytoprotective effects against ROS-mediated damage at extremely low dosage and significantly improve treatment outcomes in acute kidney injury, acute liver injury and wound healing.
    4967 36 P-Co3O4 Detection of H2O2 and Glucose GSH Color 10-30 μM 0.69 μM
    4968 36 P-Co3O4 Detection of H2O2 and Glucose H2O2 Color 1-30 μM 0.77 μM
    4969 36 R-Co3O4 Detection of H2O2 and Glucose GSH Color 1-20 μM 0.32 μM
    4970 36 R-Co3O4 Detection of H2O2 and Glucose H2O2 Color 1-30 μM 0.43 μM
    4971 38 Pt@PCN222-Mn ROS scavenge •O2−
    4972 39 Au@Rh‐ICG‐CM Alleviate Tumor Hypoxia for Simultaneous Bimodal Imaging and Enhanced Photodynamic Therapy
    4973 40 MoS2/g-C3N4 HNs sulfide ions sensing S2- Color 0.1-10 μM 37 μM
    4974 42 Atv/PTP-TCeria NPs the sepsis-induced AKI therapy ROS Unsure
    4975 44 Sm-TCPP-Pt generating oxygen for PDT H2O2
    4976 45 Au40/γ-CD-MOF the property tuning and practical application of metal nanoclusters Color
    4977 47 CuTA ROS scavenge •O2− •OH
    4978 49 Lipo-OGzyme-AIE oxygen generation
    4979 52 EPL-coated MnO2 nanosheets (EM) CAT H2O2
    4980 54 GOx@MOF-545(Fe) glucose Color 0.5–100 μM 0.28000000000000003 μM
    4981 56 MOF-546(Fe) cascade reaction glucose
    4982 60 Cu2MoS4 (CMS)/Au Hypoxia Alleviation O2- color
    4983 61 Fe3O4-TiO2/rGO (FTG) detection and photodegradation of pesticide atrazine Color 2-20 μg/L 2.98 μg/L
    4984 63 Co-based homobimetallic hollow nanocages detection acetylcholinesterase (AChE) Color 0.0001-1 mU/mL 0.1 mU/L
    4985 64 NCNTs@MoS2 Detection of AA Ascorbic acid (AA) Color 0.2-80 μM 0.12 μM
    4986 64 NCNTs@MoS2 Detection of H2O2 H2O2 Color 2–50 μM 0.14 μM
    4987 66 Fe3O4 NP Colorimetric quantification of phenol Phenol Color 1.67-1200 μM 3.79 μM
    4988 68 Fe3O4@SiO2-NH2-Au@PdNPs Detection of Glucose glucose Color 0.010−60 μM 0.06 μM 0.93
    4989 71 Au/Co@HNCF identify the low levels of uric acid (UA) in human serum uric acid E-chem 0.1–2500 μM 0.023 μM
    4990 73 vanadium oxide nanodots (VOxNDs) Antibacterial
    4991 75 BDD|PB nanozymes utmost sensitivity of the H2O2 sensor H2O2 E-chem 1×10-7-1×10-3 M 0.14 ± 0.02 A M -1 cm-2
    4992 76 DNA-Ag/Pt NCs detection of miRNA-21 miRNA-21 Color 1-700 pM 0.6 pM
    4993 77 TPP-MoS2 QDs mitigate AD pathology O2•- •OH H2O2
    4994 78 AuNP-ICA platform Detection of Escherichia coli O157:H7 in Milk E. coli Color 5-2.5*10^5 CFU/mL 12.5 CFU/mL 90.94
    4995 82 PNCNzyme Activating IAA to produce abundant ROS and triggering tumor cell apo-ptosis
    4996 84 Co-V MMO nanowires Antibacterial
    4997 87 CeM treatment of Alzheimer's disease
    4998 90 heteroatom-doped graphene Constructingnanozymesensorarrayfordetectingpesticides
    4999 91 Au@AgPt detection Hg2+ SERS 1-10000 nM 0.28 nM
    5000 91 Au@AgPt detection Hg2+ Color 1-100 μM 0.52 μM
    5001 92 Rhodium Anti-Inflammation and Antitumor Theranostics of Colon Diseases RONS Fluor
    5002 94 cNFs antimicrobial H2O2 Color
    5003 95 Co3O4 Detection of S. aureus S. aureus Color 10–10000 cfu/mL 8 cfu/mL
    5004 96 AuNCs detaction of tetracycline antibiotics tetracycline antibiotics Color 1-16 μM 46 nM
    5005 97 Prussian Blue detection of lactate lactate E-chem
    5006 98 Tb-OBBA-Hemin Detection and Degradation of Estrogen Endocrine Disruptors 17β-estradiol Fluor 0-100 nM 5 nM
    5007 101 CeO2 NPs protection from DEN-induced liver damage via antioxidative activity.
    5008 103 CeO2NRs-MOF the on-site determination of Cr(VI) in real water samples Cr(VI) Color 0.03−5 μM 20 nM 95%-105%
    5009 105 AU-1 exhibited excellent enzymatic activity towards the fungal cells.
    5010 106 IMSN-PEG-TI The results show that IMSN nanozyme exhibits both intrinsic peroxidase-like and catalase-like activities under acidic TME, which can decompose H2O2 into hydroxyl radicals (•OH) and oxygen (O2), respectively
    5011 108 HP-MIL-88B-BA exhibited a rapid response to glucose (10 min) glucose Color 2-100 μM 0.98 μM
    5012 109 IrOx demonstrate for the first time that iridium oxide nanoparticles (IrOx) possess acid-activated oxidase and peroxidase-like functions and wide pH-dependent catalase-like properties. Integrating of glucose oxidase (GOD) could unlock its oxidase and peroxidase activities by gluconic acid produced by catalysis of GOD towards glucose in cancer cells, and the produced H2O2 can be converted to O2 to compensate its consumption in GOD catalysis due to the catalase-like function of the nanozyme, which result in continual consumption of glucose and self-supplied substrates for generating superoxide anion and hydroxyl radical.
    5013 110 SnSe is capable of mimicking native dehydrogenases to efficiently catalyze hydrogen transfer from 1-(R)-2-(R')-ethanol groups
    5014 111 F-BS NCs virus-like F-BS NCs have been successfully constructed by simple ultrasound that possesses PA and IRT imaging capacity, by which synergetic PT and PT-enhanced nanozymatic biocatalytic cancer-combating therapy is hopeful to be realized.
    5015 112 Cerium Oxide Nanoparticles More studies looking into the therapeutic effects of cerium oxide nanoparticles in systemic conditions caused inter alia by oxidative stress, inflammation, and bacteria. Therapeutic effects of these nanoparticles in diseases that require tissue regeneration (scaffolds) need to be further explored
    5016 113 PB lactate biosensor lactate E-chem
    5017 114 Pt-carbon nanozyme The established Pt-carbon nanozyme enabled us to carry out a simultaneous favorable CAT-like activity and high-efficiency photothermal/photodynamic tumor therapy in near-infrared light.
    5018 115 CuO-C-dots determination of glucose glucose E-chem 0.5-2-5 mM 0.2 mM 88%-94%
    5019 117 Au/Fe-MOF prostate specific antigen E-chem 0.001-100 ng/mL 0.13 pg/mL
    5020 118 Au@Au-aptamer HIF-1α Color 0.3-200 ng/L 0.2 ng/L 97.2-101.3%
    5021 119 ZIF-67 L-Cys Fluor 0.05-6 μM 31 nM 98-103%
    5022 120 Fe3O4-Au@Ag CaMV35S gene E-chem 1x10-16-1x10-10 M 1.26x10-17 M
    5023 121 CeO2/C nanowires glucose Color 1-100 μM 0.69 μM
    5024 123 Cu‐HNCS Tumor parallel catalytic therapy
    5025 124 PPy@MnO2-BSA T1-MRI-guided combined photothermal therapy (PTT) and photodynamic therapy (PDT) of tumors
    5026 125 Ag@Au core/shell TNPs glucose Color 1-30 mM 1 mM 90.2-103%
    5027 126 Ab2-MSN-PQQ prostate specific antigen Color 0.005-0.5 ng/mL 1 pg/mL
    5028 127 GOx-MnO2/HMME Magnetic resonance imaging and anti-tumor efficiency in vitro and in vivo
    5029 128 BNS-CDs H2O2 Color 3-30 μM 0.8 μM 92.7-108.3% Smartphone colorimetric determination
    5031 129 CoFe-LDH/CeO2 H2O2 Color 0.01-1 mM 0.003 mM
    5030 129 CoFe-LDH/CeO2 glucose Color 0.05-2 mM 0.015 mM
    5032 130 Ru4PCVs A new type of catalytic micro-compartment with multi-functional activity
    5033 134 CTF-1 determination of rutin in tablets and in Flos Sophorae Immaturus rutin CL 0.03–0.25 μmol·L−1 0.015 μmol·L−1 The CL system gave a linear response to the concentration of rutin in the range of 0.03–0.25 μmol·L−1 with a limit of detection of 0.015 μmol·L−1.
    5034 134 CTF-1 determination of rutin in tablets and in Flos Sophorae Immaturus rutin CL 0.03–0.25 μmol·L−1 0.015 μmol·L−1
    5035 137 Zr-MOF Quantification and discrimination of phosphorylated proteins α-casein Color 0.17-5 μg/mL 0.16 μg/mL
    5036 137 Zr-MOF Quantification and discrimination of phosphorylated proteins α-casein Color 0.17-5 μg/mL 0.16 μg/mL Further, the absorbance at 652 nm is linearly decreased with the increased levels of α-CS ranging from 0.17 to 5.0 μg/mL (Fig. 4B). The equation can be written as A = −0.0554[α-CS] (μg/mL) + 0.4119 (R2 = 0.996). The limit of detection (LOD) is calculated to be 0.16 μg/mL based on S/N = 3.
    5037 138 Ru@CeO2 YSNs Cancer therapy
    5039 139 AuNFs/Fe3O4@ZIF-8-MoS2 Electrochemical detection of H2O2 released from cells H2O2 E-chem 15-120 mM 0.9 μM One was from 5 μM to 15 mM with a linear regression equation of I(μA) = 0.0171C(μM) + 16.6 (R2 = 0.990) (Fig. 4d), and the other was from 15 mM to 120 mM with a linear regression equation of I(μA) = 0.00417C(μM) + 191 (R2 = 0.993) (Fig. 4e). The reason for two linear regions was probably caused by the different H2O2 absorption and activation behavior on AuNFs/Fe3O4@ZIF-8-MoS2 hybrid catalyst under different H2O2 concentration [4].
    5038 139 AuNFs/Fe3O4@ZIF-8-MoS2 Electrochemical detection of H2O2 released from cells H2O2 E-chem 5-15000 μM 0.9 μM
    5040 140 Fe3+/AMP CPs cascade reaction
    5041 141 CDAu detection of Pb(II) Pb(II) Color 0.0005–0.46 μM 0.25 nM
    5042 141 CDAu detection of Pb(II) Pb(II) Color 0.0005–0.46 μM 0.25 nM Thus, a new and highly sensitive synergetic catalytic fluorescence method for the determination of 0.0005–0.46 μmol/L Pb(II) was established, with a detection limit of 0.25 nmol/L,
    5043 142 CDs conformational transition of pDNA
    5044 144 Au21Pd79 glucose detection glucose Color 5-400 μM 0.85 μM
    5045 145 Ag/ZnMOF detection of bleomycin bleomycin E-chem 0.5-500 nM 0.18 nM Photoelectrochemical
    5046 145 Ag/ZnMOF detection of bleomycin bleomycin E-chem 0.5-500 nM 0.18 nM
    5047 147 Fe3O4@Cu/GMP pollutant removal
    5048 148 AgNP@CD Detection of H2O2 and Glucose Glucose Color 1-600 μM 10 nM
    5049 148 AgNP@CD Detection of H2O2 and Glucose H2O2 Color 0.01-9 μM 9 nM
    5050 149 NiO detection of P(III) P(III) Fluor 0-10 mM 1.46 μM
    5051 150 Co3O4 NPs detection of L-Ascorbic acid L-Ascorbic acid Color 0.01-0.35 mM 3.91 μM
    5052 150 Co3O4@β-CD NPs detection of L-Ascorbic acid L-Ascorbic acid Color 0.01-0.6 mM 1.09 μM 96.8% - 113.0%
    5053 150 Co3O4@β-CD NPs detection of L-Ascorbic acid L-Ascorbic acid Color 0.01-0.6 mM 1.09 μM 96.8% - 113.0% Besides, in order to investigate the precision of Co3O4@β-CD NPs detection method, recovery experiments were made by adding a serious of AA solution with different concentration. As shown in Table S3, the average recovery of all the samples was range from 96.8% to 113.0%.
    5054 151 Hf-DBP-Fe Cancer therapy
    5055 154 GOD/hPB@gellan Cancer therapy
    5056 155 Au NCs-ICG Cancer therapy
    5057 156 Au@NH2-MIL-125(Ti) Colorimetric detection of H2O2 and cysteine H2O2 Color 2–10 μM 0.24 μM
    5058 156 Au@NH2-MIL-125(Ti) Colorimetric detection of Hg2+ Hg2+ Color 1-5 μM 0.1 μM 104.1±3.03
    5059 156 Au@NH2-MIL-125(Ti) Colorimetric detection of Hg2+ cysteine Color 1–10 μM 0.14 μM 93.8±3.23
    5060 156 Au@NH2-MIL-125(Ti) Colorimetric detection of Hg2+ Hg2+ Color 1-5 μM 0.1 μM 104.1±3.03 104.1±3.03 at 3μM; 91.56±2.03 at 6μM; 106.9±2.53 μM
    5061 156 Au@NH2-MIL-125(Ti) Colorimetric detection of Hg2+ cysteine Color 1–10 μM 0.14 μM 93.8±3.23 93.8±3.23 at4.0 μM; 100.3 ±5.62 at 7.0 μM; 103.5±6.13 at 9.0 μM
    5062 157 PEG/Ce-Bi@DMSN in vitro photothermal-enhanced nanocatalytic therapeutic efficacy
    5063 158 AgPd@BSA/DOX Ag/Pd bimetal nanozyme with enhanced catalytic and photothermal effects for ROS/hyperthermia/chemotherapy triple-modality antitumor therap
    5064 159 Au@Pt Au@Pt nanozymes were introduced to develop a low-cost, rapid, visual and highly sensitive immunochromatographic assay for streptomycin detection streptomycin Color 0.06 ng/ml
    5065 159 Au@Pt Au@Pt nanozymes were introduced to develop a low-cost, rapid, visual and highly sensitive immunochromatographic assay for streptomycin detection streptomycin Color 0.06 ng/ml The qualitative LOD was 0.1 ng mL−1 by the naked eye, and the quantitative LOD was 0.06 ng mL−1.
    5066 160 Fe-N-C It is interesting that Fe-N-C not only demonstrated the similar function of CYP3A4 in the metabolization of 1,4-DHP but also had avery high level of similarity in inhibiting interactions with other drugs
    5067 161 CeO2/Mn3O4 Nanocrystals Epitaxially Strained CeO2 /Mn3 O4 Nanocrystals as an Enhanced Antioxidant for Radioprotection
    5069 162 Ir@MnFe2O4 NPs A mitochondria-targeting magnetothermogenic nanozyme for magnetinduced synergistic cancer therapy antitumor
    5068 162 Ir@MnFe2O4 NPs A mitochondria-targeting magnetothermogenic nanozyme for magnetinduced synergistic cancer therapy
    5070 164 PBNPs in TiNM To use the POD-like activity of PBNPs in sensitive detection of telomerase, TMB, one of the well-studied substrates for evaluating POD activity, was used in our design telomerase Color 1 cell
    5071 165 VONP-LPs Above results confirmed the ultra sensitivity and excellent specificity of the VONP-LPs based dual-modality biosensor proving applicability of developed sensor for real samples (Fig. 5b). To confirm the practicability real clinical samples are examined. Different types of clinical NoV (GII. 2, GII. 3, GII.4) from human feces of infected patients are detected using the developed dual-modality sensor NoV-LPs and clinical samples Color 100-107 copies/ml 72 copies/ml
    5072 165 VONP-LPs To determine the linear range and sensitivity of the developed dualmodality sensor, different concentrations of NoV-LPs are examined. Anti-NoV antibody-conjugated VONP-LPs, MNPs and aliquot of NoV-LPs with various concentrations are mixed. VONP-LPs and the MNPs are bound with NoV-LPs through the specific interaction with antibody on their surface and a nanoconjugate of VONP-LPs, NoV-LPs and MNPs is formed. NoV-LPs Color 10-108 fg/ml 4.1 fg/ml
    5073 166 CB-CQDs The detection of biothiols was performed as follows: in a series of colorimetric tubes, 0.5 mL of TMB (20 mM), 0.5 mL of H2O2 (25 mM), and 0.1 mL of CB-CQDs were fully mixed in 3.8 mL of HAc-NaAc buffer at pH4.5. Then, various concentrations of biothiols standard solution (0.1 mL) were added into the above mixture. After they were well mixed and incubated at 40 °C for 25 min, the absorption spectra were recorded on a Unico 4802 ultraviolet-visible spectrophotometer at room temperature. The calibration curves for biothiols were established according to the decrease of absorbance defined as ΔA=A0﹣A, where A0 and A denote the absorbance at 652 nm without and with analyte, individually. cysteine Color 0.5-20 μM 0.4 μM 95.9±2.7 105.7±2.0; 109.3±1.1; 99.7±4.3; 91.5±1.0; 98.2±2.3
    5074 166 CB-CQDs The detection of biothiols was performed as follows: in a series of colorimetric tubes, 0.5 mL of TMB (20 mM), 0.5 mL of H2O2 (25 mM), and 0.1 mL of CB-CQDs were fully mixed in 3.8 mL of HAc-NaAc buffer at pH4.5. Then, various concentrations of biothiols standard solution (0.1 mL) were added into the above mixture. After they were well mixed and incubated at 40 °C for 25 min, the absorption spectra were recorded on a Unico 4802 ultraviolet-visible spectrophotometer at room temperature. The calibration curves for biothiols were established according to the decrease of absorbance defined as ΔA=A0﹣A, where A0 and A denote the absorbance at 652 nm without and with analyte, individually. cysteine Color 0.5-20 μM 0.4 μM 95.9±2.7
    5075 167 UsAuNPs/MOFs H2O2 is widely used in the treatment of bacterial infections. However, compared with H2O2, hydroxyl radicals are much more reactive and can cause more serious oxidative damages to bacteria.[37] Given the excellent POD-like activity of the prepared UsAuNPs/MOFs, the in vitro antimicrobial activities against Staphylococcus aureus and Escherichia coli were evaluated in the presence of H2O2.
    5078 168 MIL-101(Fe) According to the enzyme cascade amplification strategy, the MIL-101(Fe) nanozyme in conjunction with AChE and ChOx provided a novel label-free fluorescent assay for detection of choline and ACh with high selectivity and sensitivity. Given this, this proposed sensing strategy was successfully utilized to detect the choline in milk and ACh in human plasma with desirable results choline Fluor 0.05-10 μM 20 nM
    5076 168 MIL-101(Fe) According to the enzyme cascade amplification strategy, the MIL-101(Fe) nanozyme in conjunction with AChE and ChOx provided a novel label-free fluorescent assay for detection of choline and ACh with high selectivity and sensitivity. Given this, this proposed sensing strategy was successfully utilized to detect the choline in milk and ACh in human plasma with desirable results H2O2 Fluor 0.1-130 μM 1.1 nM
    5077 168 MIL-101(Fe) According to the enzyme cascade amplification strategy, the MIL-101(Fe) nanozyme in conjunction with AChE and ChOx provided a novel label-free fluorescent assay for detection of choline and ACh with high selectivity and sensitivity. Given this, this proposed sensing strategy was successfully utilized to detect the choline in milk and ACh in human plasma with desirable results Ach Fluor 0.1-100 μM 8.9 nM
    5079 169 FeTPP assemblies within AuTTMA monolayer The catalytic properties of the nanozymes were studied in PBS buffer through the activation of a nonfluorescent resorufin-based profluorophore (pro-Res, Figure 1B), wherereduction of theazide resultsinfragmentation and release of the fluorescent resorufin molecule
    5080 171 HS-PtNPs These obvious advantages prompted us to explore the practical use of HS-PtNPs. The pyridine ring of isoniazid has strong reductive hydrazyl substitution, which can compete with TMB for the catalytic site of HS-PtNPs (Scheme 1). The introduction of isoniazid in HS-PtNPs-catalyzed oxidation process of TMB results in a lower efficiency and colorless reaction in TMB oxidation. isoniazid Color 2.5-250 μM 1.7 μM 95%-103%
    5081 172 Fe3O4@PDA@BSA-Bi2S3 a Fe3O4@PDA@BSA-Bi2S3 composite theranostic agent was successfully prepared for synergistic tumor PTT and CDT, in which the BSA coating endows the NPs with colloidal stability and both in vitro and in vivo biocompatibility.
    5082 173 MoO3 NPs Acid phosphatase (ACP) catalyzes the hydrolysis of the ascorbic acid 2-phosphate (AAP) substrate to produce ascorbic acid (AA). AAwas found to fade the coloration process of the MoO3 NP-mediated ABTS oxidation. By combining the oxidase-mimicking property of the MoO3 NPs and the ACP-catalyzed hydrolysis ofAAP, a novel and simple colorimetric method for detecting ACP was established Acid phosphatase (ACP) Color 0.09-7.3 U/L 0.011 U/L 92-107.6%
    5083 174 IrRu-GOx@PEG NPs Iridium/ruthenium nanozyme reactors with cascade catalytic ability for synergistic oxidation therapy and starvation therapy in the treatment of breast cancer
    5084 175 Fe3O4/CoFe-LDH A sensitively and selectively visual sensor for the determination of ascorbic acid (AA) was successfully constructed based on the reduction effect of AA with enediol group on the formed oxidation of TMB Ascorbic acid (AA) Color 0.5-10 μM 0.2 μM 98.3%-101.3%
    5086 178 Au 1 Pd 5 A colorimetric test is developed for quantitative determination of acid phosphatase. Acid phosphatase (ACP) Color 1-14 U/L 0.53 U/L 102% 103% 99% To validate the application of this method in human serum, spiked-recovery experiments were carried out with different concentration of ACP. To fit the linear range of the established calibration plot, commercial human serum was appropriately diluted before addition of ACP. The recovery rates are 102 % for 4 U/L, 103 % for 8 U/L and 99 % for 12 U/L ACP (listed in Table 1). The good recovery results guarantee the reliability of this method for estimating ACP activity in biological fluid.
    5085 178 Au 1 Pd 5 A colorimetric test is developed for quantitative determination of acid phosphatase. Acid phosphatase (ACP) Color 1-14 U/L 0.53 U/L 102% 103% 99%
    5088 179 Pt@PMOF (Fe) afford ORR in PBS
    5090 179 Pt@PMOF (Fe) H2O2 sensor without adding redox mediators When applied in electrocatalysis, due to the synergy between PMOF(Fe) and Pt NPs, the Pt@PMOF(Fe) modified electrode offers high activities toward to the reduction of H2O2, which could be used for H2O2 sensor without adding redox mediators.
    5087 179 Pt@PMOF (Fe) H2O2 sensor without adding redox mediators
    5089 179 Pt@PMOF (Fe) afford ORR in PBS Furthermore, the Pt NPs with porphyrin in PMOF(Fe) could afford ORR in PBS, which has the potential for fuel cells and biofuel cells, especially in cancer diagnosis.
    5096 181 hemin@CD a colorimetric and fluorescent dual-channel sensor for H2O2, glucose and xanthine was developed, and the results are satisfied in the application of real samples H2O2 Color 0.17–133 μM 0.11 μM
    5093 181 hemin@CD a colorimetric and fluorescent dual-channel sensor for H2O2, glucose and xanthine was developed, and the results are satisfied in the application of real samples xanthine Color 0.17–33 μM 0.15 μM 93.4-102.4%
    5094 181 hemin@CD a colorimetric and fluorescent dual-channel sensor for H2O2, glucose and xanthine was developed, and the results are satisfied in the application of real samples H2O2 Fluor 0.17–133 μM 0.15 μM
    5095 181 hemin@CD a colorimetric and fluorescent dual-channel sensor for H2O2, glucose and xanthine was developed, and the results are satisfied in the application of real samples glucose Color 0.17–133 μM 0.15 μM 92.2%~105.6%
    5091 181 hemin@CD a colorimetric and fluorescent dual-channel sensor for H2O2, glucose and xanthine was developed, and the results are satisfied in the application of real samples glucose Fluor 0.17–133 μM 0.15 μM 92.2%~105.6%
    5092 181 hemin@CD a colorimetric and fluorescent dual-channel sensor for H2O2, glucose and xanthine was developed, and the results are satisfied in the application of real samples xanthine Fluor 0.17–33 μM 0.12 μM 98.8-103.6%
    5097 182 T-BiO2–x NSs overcome the hypoxia-induced radioresistance as well as increase the efficacy of RT
    5098 183 GCE/MWCNTs-Av/RuNPs highly sensitive quantification of H2O2. H2O2 E-chem 0.5—1750 μM 65 Nm
    5099 183 GCE/MWCNTs-Av/RuNPs/biot-Gox a highly sensitive pseudo-bienzymatic glucose biosensor. glucose E-chem 20—1230 μM 3.3 μM
    5100 184 DNA/GO–PtNPs detection of nucleic acids MicroRNA Color 0.05-10 nM 21.7 pM
    5101 184 DNA/GO–PtNPs detection of nucleic acids KRAS Gene Color 0.025-5 nM 14.6 pM
    5102 186 mGPB a multi-enzyme system (mGPB) with self-sufficient H2O2 supply and photoselective multienzyme-like activities was developed for enhanced tumor catalytic therapy
    5103 189 CC-PdNPs detection of iodine ions iodine ions Color 0-6.25 Nm 0.19 nM 95.52-102.8%
    5104 190 MNET remodel the microenvironment of a stroke by self-adapted oxygen regulating and free radical scavenging
    5105 193 Cu-hNFs antibacterial
    5106 194 aptamer-AuNPs determination of CRP in blood C-reactive protein (CRP) Color 0.1-200 ng/mL 8 pg/mL 94.54%–98.03%
    5108 198 TPyP-CuS ascorbic acid (AA) Ascorbic acid (AA) Color 1-30 μM 0.419 μM
    5107 198 TPyP-CuS detect H2O2 H2O2 Color 1.0-8.0 mM 121.8 μM
    5109 199 M/H-D Enhanced Tumor Penetration and Radiotherapy Sensitization
    5110 200 GeO2 Colorimetric Assay of OPs paraoxon Color 0.1-50 pM 14 fM Typically, 100 µL of different concentrations of paraoxon (0, 0.1, 2, 5, 10, 15, 30, 50, 70, 100 pm) were mixed with 20 µL of PB solutions (0.1 m, pH 8.0) containing AChE (10 µg mL−1). After the incubation for 20 min at 37 °C, 20 µL of ATCh solution (10 mm) and 20 µL of GeO2 nanozymes solution (1 mg mL−1) were added into the above mixture respectively for another 20 min incubation. The residual GeO2 nanozymes was collected by centrifugation, and added into 200 µL of acetate buffer (pH 4.0, 0.1 m) containing TMB (0.6 mm) and H2O2 (1.2 mm). Finally, the absorbance of the above reaction was measured after 30 min. Each experiment was repeated three times. The LOD was calculated by the equation LOD = (3σ/s), where σ is the standard deviation of blank signals and s is the slope of the calibration curve.
    5111 200 GeO2 Colorimetric Assay of OPs paraoxon Color 0.1-50 pM 14 fM
    5112 201 honeycomb MnO2 enhancing photodynamic therapy and MRI effect: An intelligent nanoplatform to conquer tumor hypoxia for enhanced phototherapy
    5113 202 2.6Pt/EMT Detection of H2O2 and glucose glucose Color 0.09-0.27 mM 13.2 μM
    5114 202 2.6Pt/EMT Detection of H2O2 and glucose H2O2 Color 2.9-29.4 μM 1.1 μM
    5116 203 paper-based sensor MiRNA Detection. miRNA-141 E-chem 0.002-170 pM 0.6 fM 97.0–110.0% the recoveries and RSD were in the range of 97.0–110.0 and 1.31–13.64%, suggesting a gratifying analysis capability of the proposed sensor for miRNA-141 in complex clinical samples.
    5115 203 paper-based sensor MiRNA Detection. miRNA-141 E-chem 0.002-170 pM 0.6 fM 97.0–110.0%
    5118 205 Rosette-GCN glucose was reliably determined glucose Color 5.0-275.0 μM 1.2 μM 99.3–104.1%
    5117 205 Rosette-GCN glucose was reliably determined glucose Color 5.0-275.0 μM 1.2 μM 99.3–104.1% These results prove that rosette-GCN-based systems may serve as potent analytical platforms for the diagnosis of high glucose levels in clinical settings.
    5120 206 Au-nanozyme selective and sensitive detection of mercury(II) Hg2+ Color 0.14–7.35 mg L−1 20 µg L−1
    5119 206 Au-nanozyme selective and sensitive detection of mercury(II) Hg2+ Color 0.14–7.35 mg L−1 20 µg L−1 The method is appropriate for the analysis of Hg2+ in water samples.
    5122 209 BSA-RuO2NPs monitoring in situ H2O2 secretion from living MCF-7 cells. H2O2 Color 2-800 μM 1.8 μM
    5121 209 BSA-RuO2NPs monitoring in situ H2O2 secretion from living MCF-7 cells. H2O2 E-chem 0.4-3850 μM 0.18 μM
    5123 212 MoOx QDs efficient colorimetric quantitative detection of H2O2 based on microfluidic paper-based device. H2O2 Color 1-20 μM 0.175 μM 91.5–107.04 % this biosensing device was successfully applied for visual detection of H2O2 released from PC12 cells with the advantages of low cost, rapid response and portability
    5124 212 MoOx QDs efficient colorimetric quantitative detection of H2O2 based on microfluidic paper-based device. H2O2 Color 1-20 μM 0.175 μM 91.5–107.04 %
    5126 213 2D Cu-TCPP(Fe) sulfonamide detection SAs E-chem 1.186-28.051 ng/mL 0.395 ng/mL 64–118% The accuracy and precision of the established sensor were estimated using a spike-recovery measurement based on water samples from various sources (pure water, pond water, tap water, river water) fortified with a variety of concentrations of SMM.
    5125 213 2D Cu-TCPP(Fe) sulfonamide detection SAs E-chem 1.186-28.051 ng/mL 0.395 ng/mL 64–118%
    5127 214 PTCA-ZnFe2O4 detection of ascorbic acid (AA) AA Color 1-10 μM 0.834 μM
    5128 215 hydrogel combating bacteria and accelerating wound healing
    5129 217 IrO2/GO detection of AA Ascorbic acid (AA) Color 5-70 Nm 324 nM The corresponding absorbance exhibited good linearity to the concentration of AA in the range of 5–70 μM with a coefficient of determination (R2) equal to 0.9931
    5130 217 IrO2/GO detection of AA Ascorbic acid (AA) Color 5-70 Nm 324 nM
    5131 220 MoS2@CGTC NCR MoS2@CGTC NCR achieves glucose-responsive TME self-modulation for enhanced cascaded chemo-catalytic therapy of tumors. MoS2@CGTC NCR achieves glucose-responsive TME self-modulation for enhanced cascaded chemo-catalytic therapy of tumors.
    5132 220 MoS2@CGTC NCR MoS2@CGTC NCR achieves glucose-responsive TME self-modulation for enhanced cascaded chemo-catalytic therapy of tumors.
    5133 221 VB2-IONzymes mouth ulcer healing
    5134 222 Hg2+/heparin–OsNPs detection of heparinase in human serum samples heparinase Color 20-1000 μg L-1 15 μg L-1
    5135 223 laccase@MMOFs industrial dye degradation
    5136 224 oxidized UiO-66(Ce/Zr) sensitive determination of Pi phosphate ion Color 20-666.7 μM 6.7 μM
    5137 224 oxidized UiO-66(Ce/Zr) sensitive determination of Pi phosphate ion Color 20-666.7 μM 6.7 μM ABTS channel colorimetric
    5138 224 oxidized UiO-66(Ce/Zr) sensitive determination of Pi phosphate ion Color 3.3-666.7 μM 1.1 μM Dual-channel ratiometric colorimetric
    5139 226 Pt NPs sensitive and rapid detection of carcinoembryonic antigen (CEA), pressure-based point-of-care (POC) testing strategy carcinoembryonic antigen (CEA) Unsure 0.2-60 ng/mL 0.13 ng/mL
    5140 227 Fe SSN detection of glucose through a multienzyme biocatalytic cascade platform glucose Color 10-100 mM 8.2 μM
    5141 229 lipase immobilized on Fe3O4/SiO2/Gr NC This material can not belong to nanozyme. It is synthesized by immobolize the natural lipase on the nanomaterials framework.
    5142 230 HP-HIONs@PDA-PEG tumor therapy via modulating reactive oxygen species and heat shock proteins
    5143 231 HKUST-1 Synergic Cancer Therapy
    5144 232 AuPtRu biothiol detection Biothiol
    5145 234 CdCo2O4 colorimetric detection of glucose glucose Color 0.5-100 μM 0.13 μM
    5146 235 GOx&PVI-Hemin@ZIF-8 enhanced cascade catalysis to detect glucose glucose Color 0-200 μM 0.4 μM
    5147 257 TiO2/C-QDs GSH detection GSH Color 0.5-25 μM 0.2 μM
    5148 257 TiO2/C-QDs GSH detection GSH Color 0.5-25 μM 0.2 μM taking human serum as an example, the possibility of applying GSH colorimetry to actual biological samples wasexamined by standard addition methods.
    5149 258 RBIR for single-wavelength laser activated photothermal-photodynamic synergistic treatment against hypoxic tumors
    5150 259 Pd4 Pd6 ROS scavenging effects of PdNPs in a cellular model of oxidative stress-related disease
    5151 260 GSH@PtNPs Cu2+ detection Cu2+ Color 50-800 nM 7 nM Cu2+ ions in real human serum samples were detected
    5152 260 GSH@PtNPs Cu2+ detection Cu2+ Color 25-300 nM 6.8 nM
    5153 261 Co–Fe@hemin Nanozyme chemiluminescence paper test for rapid and sensitive detection of SARS-CoV-2 antigen CL 0.2-100 ng/mL 0.1 ng/mL
    5154 264 CeO2 microspheres colorimetric determination of phos-phoprotein concentration β-casein Color 0-600 μg/mL
    5156 266 FeBNC AChE activity and its inhibitor organophosphorus pesticides(OPs) detection paraoxon-ethyl Color 8-1000 ng/mL 2.19 ng/mL
    5155 266 FeBNC AChE activity and its inhibitor organophosphorus pesticides(OPs) detection acetylcholinesterase (AChE) Color 0.8-80 mU/mL 0.8 mU/mL
    5157 267 CeNZs drug-induced liver injury therapy
    5158 268 Fe3O4@Au MBs aptasensor for detection of aflatoxin B1 Aflatoxin B1 Color 5-200 ng/mL 35 pg/mL
    5159 269 CMS NPs in vitro and in vivo treatment of MDR Bacterial Infections
    5160 270 CexZr1-xO2 photometric determination of phosphate ion phosphate ion Color 0.33-266.7 μM 0.09 μM
    5161 271 Co3O4 nanoflowers detection of acid phosphatase Acid phosphatase (ACP) Color 0.1-25 U/L 0.062 U/L it is capable of detecting ACP in serum samples
    5162 271 Co3O4 nanoflowers detection of acid phosphatase Acid phosphatase (ACP) Color 0.1-25 U/L 0.062 U/L
    5163 272 ICG-PtMGs@HGd Persistent Regulation of Tumor Hypoxia Microenvironment via a Bioinspired Pt-Based Oxygen Nanogenerator for Multimodal Imaging-Guided Synergistic Phototherapy
    5164 273 PtGs Synergistic oxygen-inductive starvation/electrodynamic tumor therapy
    5165 274 Prussian Blue H2O2 sensor
    5166 275 GO-CTAB-AuNP-hemin nanozymes Colorimetric apta-biosensing of amphetamin and methamphetamin methamphetamin 0.5–100 μM 154 nM
    5167 275 GO-CTAB-AuNP-hemin nanozymes Colorimetric apta-biosensing of amphetamin and methamphetamin methamphetamin 0.5–100 μM 154 nM MAMP detection in mixed drug samples was investigated
    5168 275 GO-CTAB-AuNP-hemin nanozymes Quantitative detection of amphetamin and methamphetamin amphetamin 0.5–100 μM 185 nM detection and quantitation of AMP in a seized drug sample were performed
    5169 275 GO-CTAB-AuNP-hemin nanozymes Quantitative detection of amphetamin and methamphetamin amphetamin 0.5–100 μM 185 nM
    5170 276 HRP@MOFs composite biomacromolecule embedding with excellent bioactivity
    5171 277 HIONCs-GOD synergistic chemodynamic−hyperthermia therapy H2O2
    5172 278 AuNP study under non-equilibrium conditions
    5173 280 MoS2 NSs biosensing
    5174 281 MIL@GOx-MIL NRs anti-bacteria
    5175 282 Fe-SAs/NC biosensing acetylcholinesterase (AChE) fluorescence 2-70 U/L 0.56 U/L
    5176 284 LCDs biocatalysis
    5177 285 Fe3O4 anticancer
    5178 287 BM-20 nanosheets H2O2 detection H2O2 Color 1-1000 μM 0.4 μM
    5179 288 MGCN-chitin-AcOH glucose detection glucose Color 5-1000 μM 0.055 μM
    5180 289 WS2 Pb detection Pb Color 5-80 μg/L 4 μg/L
    5181 291 CuCo2O4 nanorods ascorbic acid detection Ascorbic acid (AA) Color 0-50 μM 1.94 μM
    5182 292 RuTeNRs cancer treatment
    5183 293 FeNZ water treatment
    5184 294 Hf18 proteases mimic
    5185 295 GO/Au diagnosis PBP2a Color 20-300 nM
    5186 296 GO-CeM (ex-situ) Sulfide (S2-) ion detection S2- Color 20-200 μM 11.70 μM
    5187 296 GO-CeM (ex-situ) Tin (Sn2+) ion detection Sn2+ Color 10-80 μM 5.58 μM
    5188 298 Cu‐ATP, Cu‐ADP, Cu‐AMP a chemical sensor array based on nanozymes was developed to discriminate between different metal ions and teas 12 metal ions including Sn2+, Fe3+, Cu2+, Ag+, Pb2+, Mg2+, Mn2+, Ca2+, Al3+, Cr2+, Ni+, Ba2+ Color 0.01 μM
    5189 300 A-III and B-IV A-III and B-IV coatings clearly restricted and promoted the spreading of adherent RAW264.7 macrophages, respectively.
    5191 301 His-GQD/hemin detecting blood glucose glucose Color 2.5-200 μM
    5190 301 His-GQD/hemin detecting H2O2 H2O2 Color 5-240 μM
    5193 302 MoS2-MIL-101(Fe) detecting glucose glucose Color 0.01-15 μM 0.01 μM
    5192 302 MoS2-MIL-101(Fe) On the basis, a sensitive method for H2O2 detection was proposed with a linear range of 0.01−20 μmol/L and a detection limit of 10 nmol/L. Considering H2O2 as product in the reaction of glucose catalyzed by glucose oxidase, a sensitive and selective method for glucose detection was proposed. The method can be used in blood glucose detection with good accuracy. H2O2 Color 0.01−20 μM 10 nM
    5195 303 Quercetin@ZIF-90 (QZ) a novel “Off-On” colorimetric method for ATP sensing was established ATP Color 2-80 μM MNs-QZ
    5194 303 Quercetin@ZIF-90 (QZ) a novel “Off-On” colorimetric method for ATP sensing was established ATP Color 2-80 μM
    5196 304 Mn3O4 NPs detection of heavy metals Hg(II) Color 10-200 μg/L 3.8 μg/L
    5197 304 Mn3O4 NPs detection of heavy metals Cd(II) Color 5-100 μg/L 2.4 μg/L
    5198 305 Cu-NC sensing of AA AA Color 5-15 μM 5.4 μM
    5199 309 GDYO Detection of H2O2 and Glucose H2O2 Color
    5200 309 GDYO Detection of H2O2 and Glucose Glucose Color
    5201 310 AuBP@Pt and AuPd-PDA Detection of APOE4 APOE4 E-chem 0.05-2000 ng mL -1 15.4 pg mL -1 In conclusion, an ultrasensitive electrochemical immunosensor based on AuBP@Pt nanostructures and AuPd-PDA nanozyme was developed for the detection of APOE4.
    5202 310 AuBP@Pt and AuPd-PDA Detection of APOE4 APOE4 E-chem 0.05-2000 ng mL -1 15.4 pg mL -1
    5203 311 organic nanozymes prevent oxidative damage for TBI therapy to reduce the ROS level in damaged brain tissues
    5204 312 PtRu NPs detection of Fe2+ and protection of Monascus pigments Fe2+ Color 0.2-6.0 mM 0.05 μM
    5205 313 Fe-Loaded MOF-545(Fe) Dye Degradation Dyes and the Removal of Dyes from Wastewater Color
    5206 314 Fe-MOF PSA detection PSA Color 0-60 μM 0.051 μM
    5207 316 Fe-MIL-88B we constructed an indirect competitive MOFLISA for high throughput determination of AFB1 in grain drinks AFB1 Color 0.01 to 20 ng·mL−1. 0.009 ng·mL−1 87–98% (Nestle peanut milk) 86–99%(Silk soy milk)
    5208 317 2D MnO2 nanoflakes detect microRNA Let-7a E-chem 0.4 to 100 nM 250 pM 105.4%, 96.3%, and 102.1%
    5209 318 Fe3O4@TAn nanoflowers (NFs) In vitro experiments verify that the Fe3O4@TAn NFs demon multiple reactive oxygen and nitrogen species
    5210 320 Au-BNNs and Ag-BNNs nanohybrids Our results present new elements regarding BNNs-based nanohybrids which may help expand their applications in various fields such as catalyst, antimicrobial, biomedical, biosensor, and fillers in polymer matrix.
    5211 321 PdNPs/GDY Our findings demonstrate that the rational design of a nano
    5212 322 PDI-CeCoO3 Based on this, a colorimetric assay for GSH biosensing has been developed. GSH Color 1-10 M 0.658 μM
    5213 323 MnFe2O4/g-C3N4 H2O2 Color 50-100000 nM 20.5 nM
    5214 323 MnFe2O4/g-C3N4 An extremely sensitive colorimetric glucose sensor was fabricated using a novel hybrid nanostructure comprised of manganese ferrite oxide– graphitic carbon nitride (MnFe2O4/g-C3N4). Glucose Color 100nM-0.1mM/0.1mM-10mM 17.3nM/1.13μM 90.0-105.9%
    5216 324 Cu NCs detection of GSH GSH Color 1-150 μM 0.89 μM
    5215 324 Cu NCs detection of AA DFQ Fluor 0.5-30 μM 0.144 μM
    5217 324 Cu NCs detection of H2O2 H2O2 Color 0.01-1 mM 5.6 μM
    5218 325 CoOOH NFs Cobalt oxyhydroxide nanoflakes (CoOOH NFs), a typical two-dimensional (2D) nanomaterials, were found to induce chemiluminescence (CL) of luminol since the oxidase-like activity of CoOOH NFs enables the dissolved oxygen to generate various radicals (%OH, O2%−and 1O2) even if without the addition of oxidants such as hy GSH Color 10-1000 nM 6.4 nM
    5219 326 SiO2@MPGs Imaging
    5220 327 Co4S3/Co3O4 nanotubes Antibacteria
    5221 328 Pc(OH)8/CoSn(OH)6 Detection of H2O2 and Cholesterol Cholesterol Color 0.1-1.0 mM 0.0109 mM
    5222 328 Pc(OH)8/CoSn(OH)6 Detection of H2O2 and Cholesterol H2O2 Color 0.4-0.8 mM 0.0914 mM
    5223 329 Mn3O4-PEG@C&A Cancer Therapy
    5225 331 Fe-MOFs Detection of H2O2 and Glucose glucose Color 0-50 μM 0.6 μM
    5224 331 Fe-MOFs Detection of H2O2 and Glucose H2O2 Color 0-100 μM 1.2 μM
    5226 333 Fe3O4@Au@MIL-100(Fe) Dye degradation
    5230 334 Au/MOFs(Fe, Mn)/CNTs Detection of H2O2, glucose and sulfadimethoxine sulfadimethoxine Color 0.54-41.58 μg/L 0.35 μg/L doutable
    5229 334 Au/MOFs(Fe, Mn)/CNTs Detection of H2O2, glucose and sulfadimethoxine H2O2 Color 0.34-53.05 nM 0.18 nM
    5231 334 Au/MOFs(Fe, Mn)/CNTs Detection of H2O2, glucose and sulfadimethoxine sulfadimethoxine Color 0.54-41.58 μg/L 0.35 μg/L
    5227 334 Au/MOFs(Fe, Mn)/CNTs Detection of H2O2, glucose and sulfadimethoxine glucose Color 0.005-0.3 μM 0.002 μM doutable
    5228 334 Au/MOFs(Fe, Mn)/CNTs Detection of H2O2, glucose and sulfadimethoxine H2O2 Color 0.34-53.05 nM 0.18 nM doutable
    5232 334 Au/MOFs(Fe, Mn)/CNTs Detection of H2O2, glucose and sulfadimethoxine glucose Color 0.005-0.3 μM 0.002 μM
    5233 335 nanoceria Detection of Al3+ Al3+ CL 30-3500 nM 10 nM
    5236 336 OEG-AuNPs Detection of Hg2+ Hg2+ in bottled water 10-40 ppb 2 ppb
    5234 336 OEG-AuNPs Detection of Hg2+ Hg2+ in saline solution 20-120 ppb 13 ppb
    5235 336 OEG-AuNPs Detection of Hg2+ Hg2+ in seawater 20-100 ppb 10 ppb
    5237 336 OEG-AuNPs Detection of Hg2+ Hg2+ in Tap water 10-40 ppb 2 ppb
    5238 336 OEG-AuNPs Detection of Hg2+ Hg2+ in dH2O Color 10-60 ppb 0.9 ppb
    5239 337 N-QG Detection of H2O2 in milk H2O2 Color 2-1500 μM 0.75 μM
    5240 337 N-QG Detection of H2O2 H2O2 Color 1-2000 μM 0.38 μM
    5241 338 Pt@Au Detection of Zika virus Zika virus Color 1-1000 pg/mL
    5244 339 AuNSs@CTAB human chorionic gonadotropin detection human chorionic gonadotropin Color 7.8-10000 mIU/mL 7.8 mIU/mL
    5242 339 AuNRs@CTAB human chorionic gonadotropin detection human chorionic gonadotropin Color mIU/mL 15.6 mIU/mL
    5243 339 AuNCs@CTAB human chorionic gonadotropin detection human chorionic gonadotropin Color mIU/mL 31.2 mIU/mL
    5245 340 AuNPs Escherichia coli detection Escherichia coli Color 10-10E9 CFU/mL 10 CFU/mL
    5246 341 Ce:MoS2 analyses H2O2 Color 1-50 μM 0.47 μM
    5247 342 HMPWCs relieving oxidative stress, inhibiting Tau neuropathology, and counteracting neuroinflammation, which could be used to treat Tau-related AD-like neurodegeneration.
    5248 343 rGO/PEI/Au nanohybrids addition of a trace amount of Cr6+, rGO/PEI/Au nanohybrids can effectively catalyze TMB–H2O2 in ultrapure water; thus, a visual chemosensor and electronic spectrum quantitative analysis method for Cr6+ based on chromium-stimulated peroxidase mimetic activity of rGO/PEI/Au nanohybrids were established H2O2 Color
    5249 344 Fe/N-HCN our study provided evidence that the prominent multienzyme activities of Fe/N-HCNs could be used as an anti-inflammatory alternative for both infectious and noninfectious inflammation.
    5250 345 MIL-100 (Fe) The aptasensor showed a wide linear range of 1.0 × 10−10 g L−1 to 3.0 × 10−5 g L−1 and a low detection limit of 7.7 × 10−11 g L−1. The aptasensor also showed excellent selectivity and sensitivity. The novel sensing platform could provide a potential alternative method for AFP detection in simple samples. CL 1E-10-3E−5 g/L 7.7 × 10−11 g/L
    5251 346 Zr-MOFs new angle for the design of future MOF catalysts
    5252 348 CMC The anti-tumor mechanism of this system includes two aspects: (i) the generated oxygen can improve the hypoxic state of the tumor microenvironment and enhance the radiotherapy sensitivity and (ii) CPT can induce cell cycle arrest in the S-phase at a low dose, which further increases the radio-sensitivity of tumor cells and augmented radiation-induced tumor damage.
    5253 349 IONzymes/ISNzymes reduces the bacteria number
    5254 350 AuNP@Fe-TCPP-MOF highly sensitive and selective detection of Hg2+ ions
    5255 351 OCN improved peroxidase-like activity
    5256 353 Au@Pt-nanoparticles on-site and quantitative detection of Escherichia coli O157:H7
    5258 356 MoS2/rGO VHS excellent antibacterial effect in situ
    5257 356 MoS2/rGO VHS excellent antibacterial effect in situ not only develops a new protocol to construct efficient nanozymes with capturing ability, as alternative antibiotics, but also provides new insight into the smart biomaterials design by defecting chemistry, integrating nanotopology, and catalytic performance
    5259 357 PtNFs the quantitative detection of DHEA in human urine DHEA Color 2.1- 118.1 ng mL−1 1.3 ng mL−1 The IC50 value is 15.7 ng mL−1, LOD is 1.3 ng mL−1, and the linear range is 2.1 ~ 118.1 ng mL−1,
    5260 357 PtNFs the quantitative detection of DHEA in human urine DHEA Color 2.1- 118.1 ng mL−1 1.3 ng mL−1
    5261 358 50Co/CuS-MMT detection of H2O2 residue in contact lens solution H2O2 Color 10-100 μM 2.2 μM
    5262 358 50Co/CuS-MMT detection of H2O2 residue in contact lens solution H2O2 Color 10-100 μM 2.2 μM Fig. 6B displays that the absorbance at 652 nm was linearly correlated with H2O2 concentration from 10 to 100 μM and the limit of detection (LOD) was calculated to be 2.2 μM (LOD = 3 s/k, where s, k are the relative standard deviation of eight parallel controlled measurements and the slope of the linear calibration plots, respectively. In this formula, s = 0.000157, k = 2.14 × 10−4, and therefore, LOD =2.2 μM).
    5263 361 CoO@AuPt initiate intracellular hemodynamic reactions in response to TME clues
    5264 362 Aptamer-gold nanozyme to develop an Aptamer-nanozyme lateral flow assay (ALFA) CA125 in human serum CL 7.5-200 U/mL 5.21 U/mL
    5266 363 SNC TAC biosensor AA SERS 0.1-5 mM 0.08 mM the absorbance value.Under the optimal condition, the absorbance of ox-TMB decreases with the increase in AA concentration (Figure 4c).
    5265 363 SNC TAC biosensor AA SERS 0.1-5 mM 0.08 mM
    5270 364 Fe, N-CDs the H2O2 and xanthine determination in human serum and the urine H2O2 Color 0–100 μM 0.047 μM The detection limits of H2O2 and xanthine were 0.047 μM and 0.02 μM for ratiometric fluorometric and 0.05 μM and 0.023 μM for colorimetric, respectively.
    5267 364 Fe, N-CDs the H2O3 and xanthine determination in human serum and the urine xanthine Color 0-70 μM 0.02 μM The detection limits of H2O2 and xanthine were 0.047 μM and 0.02 μM for ratiometric fluorometric and 0.05 μM and 0.024 μM for colorimetric, respectively.
    5268 364 Fe, N-CDs the H2O3 and xanthine determination in human serum and the urine xanthine Color 0-70 μM 0.02 μM
    5269 364 Fe, N-CDs the H2O2 and xanthine determination in human serum and the urine H2O2 Color 0–100 μM 0.047 μM
    5271 366 Pd−Ir core-shell nanoparticles This work not only demonstrates the size effect, but also provides an effective strategy to enhance the performance of nanozymes in certain applications. 10- 2000 pg/mL 8.2, 4.6, and 3.7 pg/mL
    5272 366 Pd−Ir core-shell nanoparticles This work not only demonstrates the size effect, but also provides an effective strategy to enhance the performance of nanozymes in certain applications. 10- 2000 pg/mL 8.2, 4.6, and 3.7 pg/mL the limit of detection (LOD, which was defined by the 3SD method33) for the ELISAs were lowered from 9.3, to 8.2, 4.6, and 3.7 pg/mL when the size of Pd−Ir NPs was reduced from 13.0 to 9.8, 5.9, and 3.3 nm, respectively.
    5273 367 FeS2 NSs Simultaneously, the FeS2 NSs were applied to rapidly detect H2O2 concentrations in actual samples, such as lens solution, beer and disinfectant (all bought from supermarkets). H2O2 Color 0.02–4.00 μM 0.00760 μM
    5274 370 Cu3V2O7(OH)2·2H2O detection of glutathione glutathione Color 0.08 μM 93-109%
    5275 371 Mn3O4@Au-dsDNA/DOX synergistic antitumor immunotherapy
    5277 372 Cu2(OH)3NO3 detect biothiols in human blood serum On the basis of the oxidase-like catalytic of Cu2(OH)3NO3 nanosheets, a simple, quick, sensitive, and selective colorimetric assay was developed to determine biothiols. More interestingly, this technique was successfully applied to detect biothiols in human blood serum, suggesting it has a hopeful prospect for diagnostic in the relevant application.
    5276 372 Cu2(OH)3NO3 detect biothiols in human blood serum
    5278 374 AL-PB-600 a promising agent in antioxidant therapies
    5280 375 ZnO NO-releasing biomaterials and devices NO E-chem 1 × 10−9 M
    5279 375 ZnO NO-releasing biomaterials and devices NO E-chem 1 × 10−9 M In detail, the probe was suspended in a glass vial filled with 10 mL 0.1 M H2SO4/0.1 M KI solution. Incremental volumes of 25 × 10−6 m KNO2 solution were added to the glass vial after a stable current baseline was observed. NO concentration was determined based on the amount of KNO2 added as the conversion of KNO2 to NO was stoichiometrically 1:1. To assess the capability of ZnO particles to catalyze GSNO to generate NO, the NO probe was placed in a glass vial containing 3.95 mL ZnO particles (0.1–0.4 g L−1) in PBS. Fifty microliters of GSNO solutions (5× 10−6–100 × 10−6 m) was added to the glass vial when a stable baseline was reached. Changes in current response were recorded over time using LabScribe2 software. All NO measurements were carried out in dark at 37 °C on a hot plate with constant stirring.
    5281 376 ND nanozymes multifunctional antibacterial agents
    5282 377 A-PCM self-energy biomimetic sensing platform DPV responses E-chem 0.3–100 μM 8.4 nM This will provide experimental support for self-energy biomimetic sensing platform based on PCM integrated with a supercapacitor self-energy system and oxidase-like sensing system in the near future.
    5283 377 A-PCM self-energy biomimetic sensing platform DPV responses E-chem 0.3–100 μM 8.4 nM
    5284 378 rGO/CM (6 h) (2:1) glucose sensing activity Color 1–10 μM 0.15 μM
    5286 378 rGO/CM (6 h) (2:1) glucose sensing activity Color 1–10 μM 0.15 μM Fig. 5d shows the HR-TEM images of rGO/CM (48 h) nanocomposites where large size (∼500 nm) polyhedrons are attached with rGO sheet.
    5285 378 rGO/CM (6 h) (2:1) glucose sensing activity glucose Color 1–50 μM 0.43 μM
    5289 379 EPC-900 luorometric sensing of glucose glucose Color 0.05–10 mM 30 μM
    5287 379 EPC-900 Colorimetric detection of ACP Acid phosphatase (ACP) Color 0.5-15 U/L 0.1 U/L The ΔA652nm value increased linearly with the increasing ACP activity from 0.5 to 15  U L−1.
    5288 379 EPC-900 Colorimetric detection of ACP Acid phosphatase (ACP) Color 0.5-15 U/L 0.1 U/L
    5290 381 PdCu TPs/PG sensitive detection of HBe Ag HBe Ag Color from 60 fg·mL−1 to 100 ng·mL−1 20 fg·mL−1
    5291 382 MnO2-Silk film may have significant implications on understanding the interaction of other metal oxides with various biomaterials.
    5292 383 AuNPs@Ag detect the viral HEV containing in fecal samples collected from HEV-infected monkey HEV-LPs Color 8.75 × 10−8– 10−11 g mL−1 4.3 × 10−12 g mL−1
    5293 385 Au@Pt nanoparticles a signal amplification strategy a widespread and dangerous phytopathogenic bacteria species (Clavibacter michiganensis)
    5294 386 PEI-AgNCs With the above understanding, the PEI-AgNC-catalyzed TMB + Cr6+ chromogenic reaction is able to be employed to detect toxic Cr6+ photometrically. Cr3+ Color 5~100 μM 3.7 μM
    5297 387 Ag@Ag2WO4 NRs H2O2 and glucose sensing H2O2 Color 62.34~2400 μM 6.25 μM Since Glucose oxidase could be denatured at pH 3.0 acetate buffer solution, glucose detection was realized by the following procedure: 200 μL of glucose with different concentrations in 0.01 M acetate buffer solution (pH 5.0) was prepared with 50 μL of 10 mg mL-1 GOx and incubated at 37 °C for 30 min. This solution was then added to a mixture of 50 μL of 10 mM TMB, 100 μL of 0.5 mg mL-1 Ag2WO4 NRs and 200 μL of 0.1 M acetate buffer (pH 5.0). The mixed solution was incubated at room temperature for 30 min, and used for absorbance measurement at 652 nm.
    5295 387 Ag@Ag2WO4 NRs H2O2 and glucose sensing glucose Color 27.7~300 μM 2.6 μM
    5296 387 Ag@Ag2WO4 NRs H2O2 and glucose sensing H2O2 Color 62.34~2400 μM 6.25 μM
    5298 388 COF-300-AR The practical application of COF-300-AR oxidase mimic for colorimetric detection of glutathione (GSH) was examined GSH Color 1~15 μM 1.0 μM
    5299 389 Au@PtNP Although these methods demonstrated advantages such as low cost and high selectiveness, the sensitivity needed to be improved further. In this work, we combined this Pb2+-S2O3 2−-based metal leaching with Au@PtNP nanozyme together to fabricate a new colorimetric determination of Pb2+. pb2+ Color 20~800 nM 3.0 nM
    5300 390 Nanozymes with hard coronas (Corona-NZ) We observed that the structure of the AuNP ligands dictates the formation of protein coronas and selectively controls catalytic activity of nanozymes. A hard “irreversible” corona (without TEG) deactivated nanozymes through aggregation and steric blocking, while a soft “reversible” corona (with TEG) partially reduced the catalytic activity. The catalytic activity of both soft and hard nanozymes was restored after proteolytic degradation of the protein corona through endogenous proteases present in the endosome and lysosome. Hence, a selective intracellular activation system (without TEG) and an always-on system (with TEG) are obtained by engineering the monolayer of ligands on nanoparticles. This study provides a direct and versatile approach for specific activation of bioorthogonal catalysts through tuning the formation of the protein corona on nanozymes. This approach has the potential to reduce the off-target effect and extend on-demand generation of imaging agents and localized therapeutics. The generality of this system is suitable for in vivo applications, which are currently under investigations in our group.
    5301 391 CuS HNSs. a portable and cost-effective Hg2+ nanosensor has been developed based on a desorption-free enrichmentdetection integration strategy. The core of the nanosensor is the employment of CuS HNSs, which play three roles including recognition unit for Hg2+ sensing, enrichment carrier for Hg2+ preconcentration, and mimetic peroxidase for signal amplification and readout. The customizable enrichmentdetection integration strategy gives the nanosensor a high selectivity, a wide detection range (50 ppt to 400 ppb), and a high sensitivity with a minimum detectable Hg2+ concentration of 50 ppt. In addition, the as-developed nanosensor is feasible for analysis of Hg2+ in real-world environmental and food samples with moderate accuracy (deviation <10%) and reproducibility (recovery ∼82%). Hg2+ Color 0.05 ppb 82
    5302 392 2D TCPP(Fe)-BDMAEE The 2D supramolecular nanosheets possess distinctive features such as large area and excellent dispersibility, offering promising opportunity for catalytic and sensing applications. As a proof-of-concept application, the obtained 2D TCPP(Fe)-BDMAEE displays intrinsic peroxidase-like catalytic activity. H2O2 Color 20-100 μM 3.94 μM
    5303 393 C‑dots/Mn3O4 nanocomposite Fe2+ Color 0.03-0.83 μM 0.03 μM
    5305 394 Fe3O4@Cu/C To evaluate the peroxidase catalytic performance of Fe3O4@Cu/C and Fe3O4@CuO composites, catalytic experiments were performed toward the oxidative degradation of model organic dyes (MB)
    5304 394 Fe3O4@CuO To evaluate the peroxidase catalytic performance of Fe3O4@Cu/C and Fe3O4@CuO composites, catalytic experiments were performed toward the oxidative degradation of model organic dyes (MB)
    5306 395 Gold-Mesoporous Silica Heteronanostructures Au NPs supported onto mesoporous silica supports via electrostatic attraction represents a feasible and straightforward strategy to fabricate glucose-oxidase enzyme-like inorganic platforms able to deliver a successful performance under mild reaction conditions (neutral pH and temperature).
    5307 396 Certain engineered nanoparticles we present high-throughput screening assay using mesophyll protoplasts as model for studying the interaction between NPs and plants
    5308 397 PtNi nanocubes Herein, based on PtNi NCs-catalyzed TSA strategy, an enzyme-free and ultrasensitive ECL cytosensor for the detection of HepG2 cells (as a model) was constructed. tyramine-luminol Fluor 10~100000 cells/ml 3 cells/ml
    5309 398 FePPOPBFPB By utilizing its superior peroxidase activity, rapid and visible detection ofS. aureus based on FePPOPBFPB was first established with acceptable specificity, sensitivity, and stability. S. aureus Color 100-107 CFU/ml 24 CFU/ml
    5310 399 GO−Fe(III) Selective Photoreduction of Highly Toxic Pollutants
    5311 400 MS@MnO2 hybrid In situ fabrication of MS@MnO2 hybrid as nanozymes for enhancing ROS-mediated breast cancer therap
    5312 405 Ag3PO4 NPs chlorpyrifos Color 9.97 ppm 119.6738-179.3717
    5313 407 Au NPs Hg2+ surface plasmon resonance 1-2000 pM 0.46 pM
    5314 410 Au@HMPB Detection protein biomarker sCD25 E-chem 10pg/ml-10ng/ml 3 pg/mL 96.2-98.3
    5315 413 MoS2-QDs-AgNPs visual determination of cysteine cysteine Color 1-100 μM 824 nM 90-109
    5316 414 PBA NCs Online Visible Light Absorption H2S Color 0.1-20 μM 33 nM
    5317 417 Fe3O4@MoS2-Ag nanozyme antibacterial
    5318 419 core–shell Mn/Fe PBA@Mn/Fe PBA Colorimetric analysis Cys Cys Color 1-25 μM 0.36 μM
    5320 419 core–shell Mn/Fe PBA@Mn/Fe PBA Colorimetric analysis of H2O2 H2O2 Color 1-300 μM 0.05 μM
    5319 419 core–shell Mn/Fe PBA@Mn/Fe PBA Colorimetric analysis Hg2+ Hg2+ Color 0.1-15 μM 0.02 μM
    5321 420 ZnCo2O4 Colorimetric assay of pyrophosphatase (PPase) ppase Color 0.01-1 U/mL 0.004 U/mL
    5322 420 ZnCo2O4 Colorimetric assay of Pyrophosphate (PPi) ppi Color 0.05-1 mM 0.01 mM
    5324 421 Por-NiCo2S4 detect H2O2 and cholesterol with a very low detection limit H2O2 Color 0.02-1.0 mM 10.06 μM
    5323 421 Por-NiCo2S4 Determination of cholesterol in human serum cholesterol Color 0.1-9 mM 19.36 μM
    5326 422 BSA-PtNP@MnCo2O4 biosensing of glutathione GSH Color 1-10 μM 0.42 μM
    5325 422 BSA-PtNP@MnCo2O4 Determination of glucose glucose Color 10-120 μM 8.1 μM
    5328 423 Lyz-AuNPs antibacterial
    5327 423 Lyz-AuNPs antibacterial We realise an antibacterial nanomaterial based on the self-limited assembly of patchy plasmonic colloids, obtained by adsorption of lysozyme to gold nanoparticles.
    5329 424 m-SAP/cDNA detection of aflatoxin B1 (AFB1) Aflatoxin B1 Color 0.01-1000 ng/ml 5 pg/ml 0.042000000000000003
    5330 425 AgBiS2 Multimodal Tumor Therapy
    5332 427 BMH Hydrogel simultaneous melanoma therapy and multidrug-resistant bacteria-infected wound healing we developed an injectable redox and light responsive bio-inspired MnO2 hybrid (BMH) hydrogel for effective melanoma photothermo-chemotherapy and MDR bacteria infected-wound healing.
    5331 427 BMH Hydrogel simultaneous melanoma therapy and multidrug-resistant bacteria-infected wound healing
    5334 428 Au–MoS2 nanocomposites detection of cadmium cadmium Color 1-500 ng/ml 0.7 ng/ml The developed method was successfully applied for the analysis of cadmium ions in white wine samples.
    5333 428 Au–MoS2 nanocomposites detection of cadmium cadmium Color 1-500 ng/ml 0.7 ng/ml
    5335 429 ZIF@GOx/GQDs tumor therapy enhanced penetration and deep catalytic therapy
    5336 429 ZIF@GOx/GQDs tumor therapy
    5337 430 Pt@MnO2 sensitive Salmonella biosensor Salmonella Color 15-150000 CFU/mL 13 CFU/mL
    5338 430 Pt@MnO2 sensitive Salmonella biosensor Salmonella Color 15-150000 CFU/mL 13 CFU/mL Then, the detection antibodies (DAbs) modified Pt@MnO2 NFs were used for labelling magnetic bacteria to form MNB-CAb-Salmonella-DAb-Pt@MnO2 NF complexes (nanoflower bacteria). After nanoflower bacteria were resuspended with H2O2 in a sealed centrifuge tube, H2O2 was catalyzed by Pt@MnO2 NFs to produce O2, resulting in the increase on pressure.
    5340 431 NC Stem cell and tissue regeneration analysis Cerium oxide nanoparticles (nanoceria) show radioprotective effects on stem cells and in tissue regeneration in planarians.
    5339 431 NC Stem cell and tissue regeneration analysis
    5341 432 GMOF-LA Cancer Therapy
    5343 433 AuNP−TTMA protection of biorthogonal transition metal catalysts
    5342 433 AuNP−TTMA protection of biorthogonal transition metal catalysts We demonstrate here the protection of biorthogonal transition metal catalysts (TMCs) in biological environments by using self-assembled monolayers on gold nanoparticles (AuNPs).
    5344 435 MnNS:CDs non-invasive multi-modal imaging and therapy
    5345 436 MPBs detection of uric acid in whole blood UA Color 1.5-8.5 mg/dL
    5346 436 MPBs detection of uric acid in whole blood UA Color 1.5-8.5 mg/dL The mHealth LFP could achieve a wide detection range of 1.5-8.5 mg/dL UA.
    5348 437 Au NP protein detection
    5347 437 Au NP protein detection A colorimetric sensor array for protein detection is developed.
    5350 438 CS-IONzymes provides an antiviral alternative for designing nasal vaccines based on IONzyme to combat influenza infection This work provides an antiviral alternative for designing nasal vaccines based on IONzyme to combat influenza infection.
    5349 438 CS-IONzymes provides an antiviral alternative for designing nasal vaccines based on IONzyme to combat influenza infection
    5351 440 PEG-Au/FeMOF@CPT NPs Cancer Therapy Triggered by the high concentration of phosphate inside the cancer cells, Au/FeMOF@CPT NPs effectively collapse after internalization, resulting in the complete drug release and activation of the cascade catalytic reactions.
    5352 440 PEG-Au/FeMOF@CPT NPs Cancer Therapy
    5353 441 Pdots@AMP-Cu detection of dopamine Dopamine (DA) Fluor 10-400 μM 4 μM
    5354 443 Au-nanozymes and MnO2-nanozymes colorimetric method for glutathione (GSH) detection GSH Color 0.05-0.19,0.19-11.35 mg/L 0.02 mg/L
    5355 443 Au-nanozymes and MnO2-nanozymes colorimetric method for glutathione (GSH) detection GSH Color 0.05-0.19,0.19-11.35 mg/L 0.02 mg/L Using Au-nanozymes for selectivity and MnO2-nanozymes for sensitivity enchantment.
    5357 444 HA@Fe3O4@SiO2 Colorimetric determination of tumor cells tumor cell Color In the presence of HeLa cells, the visible region absorbance sharply decreased up to the cell concentration of 0.25 × 106 cells/mL, with both nanozymes (Fig. 9A). In the concentration range of 0.25–4.0 × 106 cells/mL, the visible region absorbance linearly decreased with the increasing cell concentration, with satisfactorily high correlation coefficients for both nanozymes. However, a sharper linear decrease with almost 1.6 times higher slope was observed with HA@Fe3O4@SiO2 microspheres with respect to Fe3O4@SiO2 microspheres with HeLa cells.
    5356 444 HA@Fe3O4@SiO2 Colorimetric determination of tumor cells tumor cell Color
    5358 445 FNs mitigation of potential cytotoxicity
    5359 445 FNs mitigation of potential cytotoxicity This work raises new questions about the roles of biogenic nanomaterials in the coevolution of the lithosphere and biosphere and provides a step toward understanding the feedback pathways controlling the evolution of biogenic mineral formation.
    5360 446 Au@Co-Fe NPs antibacterial
    5361 447 KD8@N-MCNs phototherapy of Alzheimer’s disease (AD)
    5362 448 PtCuCo-TAs miRNA-21 detection miRNA-21 CL 5 × 10−16 - 1 × 10-10 M 1.67 × 10−16 M 99.0–104.4% this method can effectively apply for the detection of miRNA-21 with accuracy and reliability in sample analysis.
    5363 448 PtCuCo-TAs miRNA-21 detection miRNA-21 CL 5 × 10−16 - 1 × 10-10 M 1.67 × 10−16 M 99.0–104.4%
    5364 449 CNP/CNPs Antioxidative photochemoprotector effects
    5365 450 RGD-BSA-CuCs catalytic cancer-specific DNA cleavage and operando imaging
    5367 451 PI/CdS detection of hypoxanthine hypoxanthine E-chem 0.010-10.0 mM 5.28 μM 95.5 %–105.9 %
    5366 451 PI/CdS detection of hypoxanthine hypoxanthine E-chem 0.010-10.0 mM 5.28 μM 95.5 %–105.9 % Human serum samples were diluted 20-fold with phosphate buffer solution (pH 7.4) in advance.
    5370 452 GO/AuNPs H2O2 detection H2O2 Color 3.8×10–7~5.5×10–5 M 4.2×10–8 M
    5368 452 GO/AuNPs glucose detection glucose Color 5.1×10–6~5.1×10–4 M 6.3×10–7 M 105.3%-108.3% The real human serum was used as test samples to investigate the practical application of the proposed analysis. Human serum samples were taken from Xi'a University of Science and Technology Hospital. As the normal content of human blood glucose is 3.9–6.1 mmol/L [38], before the test, the collected serum samples need to be diluted to meet the requirements of this method after centrifugation. The glucose test results are shown in Table 2. For three different test samples, the detection results from this method are not substantially different from those given by the hospital.
    5369 452 GO/AuNPs glucose detection glucose Color 5.1×10–6~5.1×10–4 M 6.3×10–7 M 105.3%-108.3%
    5372 453 Pt Colorimetric Determination of Total Antioxidant Level in Saliva TAC levels of saliva samples collected from 83 healthy volunteers, aged between 20 and 50 years, measured by the nanozyme-based assay.
    5371 453 Pt Colorimetric Determination of Total Antioxidant Level in Saliva
    5373 454 Anti-PSA-Ab Coated Au NPs Sensitive Colorimetric Detection of Prostate Specific Antigen BSA Color 0.25-2500 ng/mL 0.23 ng/mL
    5374 456 Nanocages the laccase-like activity of Nanocages was integrated with an online sensing platform for in vivo and continuous optical hydrogen sulfide monitoring in the brains of living rats hydrogen sulfide E-chem 0.1-15 μM 33 nM After testing the excellent capabilities of the OODP toward H2S monitoring, the animal model was carried out to test the ability of the constructed method.
    5375 456 Nanocages the laccase-like activity of Nanocages was integrated with an online sensing platform for in vivo and continuous optical hydrogen sulfide monitoring in the brains of living rats hydrogen sulfide E-chem 0.1-15 μM 33 nM
    5376 456 Nanocages The peroxidase- and catalase-mimicking activities were applied to eliminate reactive oxygen species in cells
    5377 457 CuS-BSA-Cu3(PO4)2 detection of H2O2 H2O2 Color 0–8 μM 22 nM 98.12-101.9% Typically, using a standard addition method, H2O2 at 20, 50, and 100 nM is spiked into contact lens care solution obtained from a pharmacy. The H2O2 content present in lens care solution is determined from an already established calibration plot, generated at 654 nm using different H2O2 concentrations under the same assay mentioned above. Percentage recovery is assessed using Eq. (8), and the results are summarized in Table 3 (n = 3).
    5378 457 CuS-BSA-Cu3(PO4)2 detection of H2O2 H2O2 Color 0–8 μM 22 nM 98.12-101.9%
    5380 458 Fe3O4@MnOx quantifying and identifying chlorophenols chlorophenols Color 10–1600 μM 0.85 μM 97.0% to 107.2% In the present study, the tap water was obtained from our research laboratory, and the river water was gained from the campus of Jiangsu University, China. Prior to test, these water samples were filtered by 0.22 μm microfiltration membranes. The detection results are listed in Table S2 (Supplementary Information).
    5379 458 Fe3O4@MnOx quantifying and identifying chlorophenols chlorophenols Color 10–1600 μM 0.85 μM 97.0% to 107.2%
    5383 459 Ag-MA selective colorimetric and efficient removal strategy for mercury (II) Hg2+ ions Color 0.50-700 nM 0.18 nM 98.15–105.1 % Hg2+ ions in wastewater samples
    5381 459 Ag-MA selective colorimetric and efficient removal strategy for mercury (II) Hg2+ ions Color 1.0-600 nM 0.33 nM
    5384 459 Ag-MA selective colorimetric and efficient removal strategy for mercury (II) Hg2+ ions Color 1.0-600 nM 0.33 nM probe Hg2+ ions in blood
    5382 459 Ag-MA selective colorimetric and efficient removal strategy for mercury (II) Hg2+ ions Color 0.10–700 nM 0.025 nM Fig. 6A illustrates the calibration detection curve for Hg2+ ions in buffer
    5385 460 CeO2–x Antibacterial
    5387 461 PdCuAu NPs detect glucose glucose Color 0.5–500 μM 25 nM
    5386 461 PdCuAu NPs detection of H2O2 H2O2 Color 0.1–300 μM 5 nM
    5388 462 CuO NPs AA sensing AA Color 1.25-112.5 μM 32 nM 92.6-110.6 %
    5389 463 ZV-Mn NPs Detection of hydrogen peroxide H2O2 Color 10–280 μM 0.20 μM
    5390 464 FePorMOF CL Imaging Assay of Glucose and AFP Glucose CL 50-1000 μM 39.2 μM
    5394 465 Pt NC/3D GF nanohybrid Detection of Catechol and Hydroquinone HQ Color 0.05–1 and 1–50 μM 10 nM 95.8-99.6% different concentrations of HQ were spiked in the systems containing CC and then analyzed with the means
    5391 465 Pt NC/3D GF nanohybrid Detection of Catechol and Hydroquinone Catechol Color 0.5-800 μM 50 nM As shown in Figure 6, after incubation with the Pt NC/3D GF nanohybrid in pH 7.0 BR buffer at 30 °C for 15 min, the absorbance of the system at 388 nm gradually increased with the increase of catechol concentration.
    5392 465 Pt NC/3D GF nanohybrid Detection of Catechol and Hydroquinone HQ Color 0.05–1 and 1–50 μM 10 nM 95.8-99.6%
    5393 465 Pt NC/3D GF nanohybrid Detection of Catechol and Hydroquinone Catechol Color 0.5-800 μM 50 nM
    5396 466 4-AHA@AuNPs nanoparticles selective determination of mercury and iron in ground water Fe3+ Color 5–50 ppb 4.0 ppb
    5395 466 4-AHA@AuNPs nanoparticles selective determination of mercury and iron in ground water Hg2+ Color 5-200 ppb 2.5 ppb
    5397 468 Ag2-xCuxS NPs Colorimetric urine glucose detection glucose Color 0-30 mM 0.37 mM The obtained glucose concentrations are mostly consistent with that tested by GOD-PAP biochemical analyzer in hospital (Table S2, SI).
    5398 468 Ag2-xCuxS NPs Colorimetric urine glucose detection glucose Color 0-30 mM 0.37 mM
    5400 469 V2O5 nanobelts glucose detection glucose Color 1-1000 μM 0.33 μM
    5399 469 V2O5 nanobelts glucose detection glucose Color 1-1000 μM 0.33 μM Online Monitoring of Glucose in Living Rat Brain
    5401 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Morus Color 0-40 μM 0.47 μM
    5402 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Cichorium intybus Color 0-30 μM 0.37 μM
    5403 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Orange juice Color 0-8 μM 0.08 μM
    5404 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Trolox Color 0-35 μM 0.34 μM
    5405 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Chlorogenic acid Color 0-12 μM 0.11 μM
    5406 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Tannic acid Color 0-6 μM 0.06 μM
    5407 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Ferulic acid Color 0-12 μM 0.19 μM
    5408 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. L-cysteine Color 0-30 μM 0.37 μM
    5409 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Ascorbic acid (AA) Color 0-35 μM 0.39 μM
    5410 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Lemon juice Color 0-7 μM 0.08 μM
    5411 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Caffeic acid Color 0-20 μM 0.27 μM
    5412 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Quercetin Color 0-7.5 μM 0.11 μM
    5413 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Eucalyptus Color 0-15 μM 0.24 μM
    5414 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Thymes Color 0-35 μM 0.42 μM
    5415 470 Tα-MOF The apparent Km of Tα-MOF is measured 3.180 mM and 0.0109 µM for TMB and H2O2, respectively. In this study, the LOD values for Ferulic acid, Tannic acid, and Chlorogenic acid were 0.19, 0.06, and 0.11, respectively. The RAC value obtained for tannic acid, orange juice, and lemon juice was 4.79, 3.37, and 3.53, respectively. Ascorbic acid (AA) Color 0-35 μM 0.39 μM Relatively, the extracts lead to a discoloring tendency in the order of Lemon Juice > Orange Juice > Eucalyptus > Cichorium intybus > Thymes > Morus
    5417 471 Co2V2O7 particles H2O2 and Glucose Detection H2O2 Fluor 0.008-3.2 μM 0.002 μM
    5419 471 Co2V2O7 particles H2O2 and Glucose Detection glucose Fluor 0.1–80 μM 0.03 μM 99.02-104.93% The glucose detection system also possessed good selectivity, and when the concentration of other sugars was 10 times higher than that of glucose (Figure 5f), no significant interference with the reaction system was observed.
    5418 471 Co2V2O7 particles GSH Detection GSH Color 2.5–20 μM 0.64 μM 97.4-98.7%
    5416 471 Co2V2O7 particles H2O2 and Glucose Detection glucose Fluor 0.1–80 μM 0.03 μM 99.02-104.93%
    5420 474 Ce/Pr-CQDs readily internalized into cytoplasm, decreasing the level of reactive oxygen species (ROS).
    5421 475 Fe3O4-NPs Attenuated Salmonella Infection in Chicken Liver
    5422 477 NC@GOx NPs Starvation therapy enhanced photothermal and chemodynamic tumor therapy
    5423 478 DNA/MoS2 NSs Detection of carcinoembryonic antigen (CEA) in a sensitive manner carcinoembryonic antigen (CEA) Color 50-1000 ng/mL 50 ng/mL
    5424 479 GO/PVA/G4/H hydrogel Electrochemical detection of H2O2 H2O2 E-chem 100-100000000 nM 100 nM
    5425 483 DMSN@AuPtCo Decontaminate two kinds of wastewater and avoiding secondary pollution
    5426 484 Co3O4/MO3 Sense H2O2 and screen acetylcholinesterase activity and its inhibitor H2O2 Color 0.1-200 μM 0.08 μM
    5427 484 Co3O4/MO3 Sense H2O2 and screen acetylcholinesterase activity and its inhibitor acetylcholinesterase (AChE) Color 0.005-1.0 U/L 0.1 mU/L
    5428 485 CeO2 NCs Promise antibacterial performance
    5429 486 Mn3O4 NPs Boost endogenous antioxidant metabolites in cucumber (Cucumis sativus) plant and enhance resistance to salinity stress
    5430 487 Cu-MOPN Highly selective detection of Cys in serum cysteine Fluor 1-50 μM 93 nM
    5431 488 HRP/MB/chitosan/MoS2/GF Enhanced voltammetric determination of hydrogen peroxide H2O2 E-chem 0.1-90 μM 30 nM
    5432 489 Fe/Al-GNE pH-independent chemodynamic therapy of cancer
    5434 490 Zn-TCPP(Fe) Colorimetric detection of alkaline phosphatase Alkaline phosphatase (ALP) Color 50-200 U/L 50 U/L Three linear ranges of 2.5–20 U L−1, 5–60 U L−1, and 50–200 U L−1 could be obtained by using PPi, ATP, and ADP as inhibitors, respectively.
    5433 490 Zn-TCPP(Fe) Colorimetric detection of alkaline phosphatase Alkaline phosphatase (ALP) Color 50-200 U/L 50 U/L
    5435 492 CoPc Determination of hydrogen peroxide and glucose glucose E-chem 0.1-1 mM 63 μM
    5436 492 CoPc Determination of hydrogen peroxide and glucose H2O2 E-chem 12.3–49 000 μM 8 μM
    5437 493 molecularly imprinted film conjugated with horseradish peroxidase(HRP) Determination of Methimazole in Urine Sample methimazole Unsure 0.9 μg/L
    5438 493 molecularly imprinted film conjugated with horseradish peroxidase(HRP) Determination of Methimazole in Urine Sample methimazole Unsure 0.9 μg/L This is the first example to monitor methimazole with a direct com-petitive biomimetic enzyme-linked immunosorbent assay (BELISA) method
    5439 495 β-CD@AuNPs–MWCNTs Sensitive electrochemical analysis of target 8-hydroxy-2′-deoxyguanosine (8-OHdG) based on reversible capture/release of electronic media in a fast and green manner 8-hydroxy-2′-deoxyguanosine E-chem 0.0001-10 nM 30 fM
    5440 496 CS-MNPs Colorimetric Bacteria Detection bacteria Color 10^2-10^6 CFU/mL 10^2 CFU/mL
    5441 497 CuS NPs Antibacterial treatment
    5442 498 SPDA Colorimetric detection of pyrophosphate pyrophosphate Color 0.1-30 μM 0.06 μM
    5444 500 CNF/FeCDs Smartphone-based colorimetric detection of hydrogen peroxide and glucose glucose Color 10-70 μM 1.73 μM
    5443 500 CNF/FeCDs Smartphone-based colorimetric detection of hydrogen peroxide and glucose H2O2 Color 6-42 μM 0.93 μM
    5445 501 Cu-HCF SSNEs Tumor-Specific Amplified Cascade Enzymatic Therapy
    5446 502 M/CeO2 Detection of H2O2 and glucose H2O2 Color 10-100 μM 2 μM
    5447 502 M/CeO2 Detection of H2O2 and glucose glucose Color 0.01-1 mM 8.6 μM
    5448 504 COF-Au-MnO2 Enhanced photodynamic therapy via catalytic cascade reactions
    5449 505 PtCu NAs Prevention of pathologic α-synuclein transmission in Parkinson’s disease
    5450 506 Fe–N4 pero-nanozysome Hyperuricemia and Ischemic Stroke
    5451 507 PtCu bimetallic nanoalloys (NAs) S for prevention of pathologic -synuclein transmission in Parkinson’s disease
    5453 509 AuNPs@C.CNF Detection of glucose glucose Color 1–60 μM 0.67 μM
    5452 509 AuNPs@C.CNF Detection of H2O2 H2O2 Color 0.5–30 μM 0.30 μM
    5454 510 Mn3O4 nanoparticles (NPs) c Procedure for arsenic determination arsenic Color 5-100 μg/L 1.32 μg/L 91.74% - 112.14%
    5455 511 ZnO-Pt-gC3N4 glucose sensing glucose E-chem 0.25–110 mM 0.1 μM 100, 98.2 and 95%
    5456 512 NiCo2O4-Au composite for killing bacteria and disinfecting wound
    5457 513 FA-AgNPs for rheumatoid arthritis therapy
    5458 515 aptamers@BSA-AuNCs for colorimetric detection of Salmonella typhimurium Salmonella typhimurium Color 101-106 cfu/mL 1 cfu/mL 92.4% - 110%
    5459 517 GOx@h-CNT/Fe3O4/ZrO2 Colorimetric detection of glucose glucose Color 0–1.6 mM 6.9 μM
    5460 518 Hep-Pt NCs Colorimetric tests of H2O2 and glucose glucose Color 0.1 ∼ 2.0 mM 33 μM 98%-104.0%
    5461 520 MPBN Analysis of RAC and CLE in real samples CLE Color 0.5-12 ng/mL 0.20 ng/mL 86.96%–119.94%
    5462 520 MPBN Analysis of RAC and CLE in real samples RAC Color 0.5-6 ng/mL 0.12 ng/mL 84.01% - 119.94%
    5463 521 Fe3O4 Determination of Cr6+ Cr6+ Color 0−500 μM 0.03465 μM 92.43%-110.66%
    5464 522 MIL-88@Pt@MIL-88@sDNA exosomal miRNAs detection exosomal miRNAs E-chem 1 fM to 1 nM 2.00 fM
    5466 523 CeO2 NPs for organophosphorus pesticides (OPs )and oxytetracycline(OTC) detection using CeO2 NPs oxytetracycline(OTC) Color 100–800 nM 10.2 nM 92.9% - 104.1%
    5465 523 CeO2 NPs for organophosphorus pesticides (OPs )and oxytetracycline(OTC) detection using CeO2 NPs organophosphorus pesticides (OPs Color 50–1000 ng/mL 7.6 ng/mL 97.2%-107.0%
    5467 524 Pd@Pt-GOx/hyaluronic acid (HA for High-Efficiency Starving-Enhanced Chemodynamic Cancer Therapy
    5468 525 Gold and magnetic particles (GoldMag) for determination of cholesterol cholesterol Color 0.018–1.4 mM 7.9 μM 98.57%-106.8%
    5469 526 Pt2+@g-C3N4 for glucose detection glucose Color 13–2000 μM 10 μM
    5470 527 Fe3O4 NPs for Diabetes Care in Genetically or Diet-Induced Models
    5472 528 CuO nanorods (NRs) Application in living cell epinephrine analysis epinephrine E-chem 0.04-14 μM 0.02 μM
    5471 528 CuO nanorods (NRs) Application in living cell epinephrine analysis epinephrine Color 0.6-18 μM 0.31 μM
    5473 529 man-PB for rapid detection of Escherichia coli O157:H7 (E. coli O157:H7) Escherichia coli O157:H7 (E. coli O157:H7) Color 0-108 cfu/mL 102 cfu/mL 90% - 110%
    5474 530 HCS@Pt NPs for photodynamic and catalytic synergistic tumor therapy
    5475 531 Zn-N-C-800 peroxidase-like activity
    5476 533 Ag-CoO NP for colorimetric sensing hydrogen peroxide and o-phenylenediamine hydrogen peroxide Color 5-20 μM 3.47 μM
    5477 533 Ag-CoO NP for colorimetric sensing hydrogen peroxide and o-phenylenediamine o-phenylenediamine Color 1−20 μM 0.65 μM
    5478 534 Ag@Ag2WO4 NRs for colorimetric detection of Hg2+ Hg2+ Color 0.25 - 8.0 μM 1.6 nM 95.0% -106.0%
    5479 535 Fe-Nx SANs Detection of Aβ 1-40 Aβ 1-40 Color 1-2000 pg/mL 0.88 pg/mL
    5480 536 Cu/Au/Pt TNs Detection of microcystin-LR microcystin-LR Color 4.0-10000 ng/L 3.0 ng/L
    5481 537 MoS2/C-Au600 Detection of H2O2 H2O2 Color 10-200 µmol/L 1.82 µmol/L
    5482 537 MoS2/C-Au600 MoS2/C-Au600 with peroxidase-like activity can image cancer cells in the presence of TMB and H2O2
    5483 538 iron alkoxide Detection and removal of arsenate arsenate Color 3.33-333.33 μg/L 1.57 μg/L
    5484 539 GA-NFs Detection of m‑cresol m‑cresol Color 0.05-0.5 mM
    5485 540 Fe3O4@CP Detection of GSH GSH Color 0.2-40 μM 0.05 μM
    5486 540 Fe3O4@CP Detection of H2O2 H2O2 Color 0.2-300 μM 0.11 μM
    5487 543 Au@SiO2-NH2 Gold nanorod-based nanoplatform catalyzes constant NO generation and protects from cardiovascular injury
    5488 544 CuCo2S4 NPs For combating burn infections
    5489 545 NSP-CQDs NSP-CQDs was further utilized for antibacterial assays
    5490 546 Detection of acetylcholinesterase activity Detection of acetylcholinesterase activity acetylcholinesterase (AChE) Color 0.2-50 mU/mL 0.14 mU/mL
    5491 549 β-CD@AuNPs sense PPase activity at neutral pH colorimetric and photothermal
    5492 552 MnO2 nanoparticles Colorimetric detection of TATP TATP Color 1.57-10.50 mg/L 0.34 mg/L 105
    5493 553 CoMoO4 nanobelts Colorimetric detection of H2O2 H2O2 Color 0.5-25 μM 0.27 μM
    5494 554 Pd@Au nanostructures Detection of glucose glucose Color 0.02-2 mM 9.28 μM
    5495 555 MnO2–Au antitumor
    5496 556 UiO-66 Enhances Hydrolytic Activity toward Peptide Bonds
    5497 557 Magnetic Nanoflowers this work documented MNPs PDA–Cu NFs as an efficient catalyst for catalytic reduction of organic dyes with the ability of facile recyclability. Additionally, MNPs PDA–Cu NFs were recognized as one of the nanozymes owing to peroxidase-like activity. Polydopamine and copper nanoparticles in MNPs PDA–Cu NFs have shown antimicrobial behavior toward Gram-negative bacteria (P. aeruginosa and E. coli) and Gram-positive bacteria (S. aureus).
    5498 558 Fe3O4@NH2-MIL-101(Fe) colorimetric detection of glucose glucose Color 1.7-750 μM 0.22 μM 100.5
    5499 559 Ni/Al–Fe(CN)6 LDH Determination of Cr (VI) Cr (VI) Fluor 0.067-10 μM 0.039 μM
    5500 560 Mesoporous Pd@Pt detection of atrazine atrazine Color 0.1-500 ng/mL 0.5 ng/mL 98.6-103.3
    5501 561 urchin-like Pt nanozymes monitoring of glycated albumin glycated albumin Color 10-5000 ug/mL 9.2 ug/mL 106-107
    5502 563 ficin@PCN-333(Fe) colorimetric detection of glucose glucose Color 0.5-180 μM 96 nM
    5503 565 Au–Ag@HA NPs Enhanced Cancer Therapy
    5504 566 Cerium Oxide NSs Detection of H2O2 H2O2 Electrode 20–100 mM 0.02 μM
    5505 567 Co3O4 NCs Detection of NO2 NO2 electrodes 0.3-1.5 ppm 0.3 ppm
    5506 568 Cu2O nanocubes Detection of S. aureus S. aureus Photoelectric 50-10e9 CFU mL−1 10 CFU mL−1
    5507 569 Au NPs DNA release
    5508 570 DNA-Cu/Ag NCs Detection of H2O2 H2O2 colorimetric 100-1000 μM 7.42 μM
    5509 571 N/Cl-CDs Detection of H2O2 H2O2 fluorescence 1-30 μM 0.27 μM
    5510 572 CFPN oxidation of natural organic matters
    5511 573 AgNPs@Fe3O4 Detection of cysteine cysteine colorimetric 0-20 μM 87 nM
    5512 574 Pt-HMCNs Detection of H2O2 H2O2 colorimetric 6.0-60 μM 2.81 μM
    5513 575 BP QDs Detection of cysteine cysteine colorimetric 0.1-10.0 μM 0.03 μM
    5514 575 BP QDs Detection of glutathione glutathione colorimetric 0.1-5.0 μM 0.02 μM
    5515 576 EMSN-PtNCs Detection of H2O2 H2O2 colorimetric 1-50 μM 0.87 μM
    5516 577 Zn-TCPP(Fe) superoxide scavenging
    5517 578 Co4S3 Antibacterial
    5518 579 MnO2 Detection of glutathione glutathione colorimetric 0.11-45 μM 0.1 μM
    5519 580 WO3−x QDs detection of cholesterol cholesterol colorimetric 0.01-1.0 mM 3.0 μM
    5520 581 Fe–N–C detection of uracil DNA glycosylase uracil DNA glycosylase electrochemical 0.0005-1 U/mL 74 μU/mL
    5521 582 Ag5PMo12@PPy detection of uric acid uric acid colorimetric 1-50 μM 0.47 μM
    5522 583 FA-PMo4V8 detection of sarcosine sarcosine colorimetric 0.2-500 μM 0.311 μM
    5523 584 NMPs Antibacterial
    5524 585 Fe3O4-PAA-PB-AA Fenton/ferroptosis therap ROS
    5525 587 CeO2 microcapsule assessing intracellular ROS
    5526 588 PPy@MoS2@Au detection of tannic acid tannic acid colorimetric 1.0-100 μM 0.87 μM
    5527 590 GdW10O36 nanoclusters Antibacterial
    5528 591 TACN AuNPs anticancer prodrugs
    5529 592 Au−Cu2−xS photothermal therapy and chemical dynamic therapy
    5530 594 Pt/ZnCo2O4 Detection of ascorbic acid Ascorbic acid (AA) 1-15 μM 0.456 μM
    5531 596 GOx@Pd@ZIF-8 a synergistic cancer therapeutic that blocks glucose metabolism and produces ROS
    5532 597 6-PAAC-30 alcohol and glucose detection glucose E-chem 0-40 mM 2.50 mM
    5533 597 6-PAAC-30 alcohol and glucose detection alcohol E-chem 0-6 mM 0.50 mM
    5534 598 CeO2 NPs personal glucose meter-based label-free target DNA detection DNA Color 5-100 nM
    5535 599 Pd91-GBLP NPs the colorimetric detection of glucose glucose Color 2.5-700 μM 1 μM
    5536 600 PtNPs@PCs lead ion detection lead ion E-chem 0.05-1000 nM 0.018 nM
    5537 601 AuMS the selective colorimetric detection of dopamine Dopamine (DA) Color 10-80 μM 1.28 nM
    5538 602 Fe3O4 nanoparticles enhance the yield of DMBQ in the fermentation process
    5539 603 ACP/hemin@Zn-MOF ratiometric fluorescent arsenate sensing arsenate Fluor 3.33-300 μg/L 1.05 μg/L
    5540 604 GO/AuNPs detection of Hg2+ Hg2+ Color 5.2-120 nM 0.38 nM
    5541 605 Ce-MOF sensitive detection of hydrogen peroxide and ferric ions Fe2+ Fluor 0.016-0.133 μM 0.016 μM
    5542 605 Ce-MOF sensitive detection of hydrogen peroxide and ferric ions H2O2 Fluor 200-1500 μM 10 μM
    5543 606 Pt NPs-PVP theranostic application in acute kidney injury
    5544 607 Cu-rGO Colorimetric detection of H2O2 and glucose glucose Color 10-100 μM 10 μM
    5545 607 Cu-rGO Colorimetric detection of H2O2 and glucose H2O2 Color 10-100 μM 0.1 μM
    5546 609 Mn3(PO4)2/MXene realtime sensitive sensing cell superoxide O2•− E-chem 5.75-25930 nM 1.63 nM
    5547 610 FePc/HNCSs ynergistic Catalytic Therapy and Dual Phototherapy
    5548 611 CeVO4 Regulates Mitochondrial Function and ATP Synthesis in Neuronal Cells
    5549 613 NH2-MIL-53(Fe) dual-mode detection of prostate specific antigen PSA CL 1-30 ng/mL 0.3 ng/mL
    5550 613 NH2-MIL-53(Fe) dual-mode detection of prostate specific antigen PSA Fluor 0.5-30 ng/mL 0.2 ng/mL
    5551 614 PbS NPs@RGO/NiO NSAs Function-switchable self-powered photoelectrochemical biosensor for H2O2 and glucose monitoring H2O2 0-100 mM 0.018 mM
    5552 614 PbS NPs@RGO/NiO NSAs Function-switchable self-powered photoelectrochemical biosensor for H2O2 and glucose monitoring glucose 0.1 ~ 1 × 10-7 M 5.3*10-8 M
    5553 615 Pt-Ce6 enhanced PDT/PTT tumor therapy
    5554 617 LM portable immunoassay of allergenic proteins based on A smartphone α-LA 0.12-3.46 ng/mL 0.056 ng/mL
    5555 618 MoO3−x NDs Near-Infrared Regulated Nanozymatic/Photothermal/Photodynamic Triple-Therapy for Combating Multidrug-Resistant Bacterial Infections
    5556 619 DFHHP overcoming hypoxia-induced resistance to chemotherapy and inhibiting tumor growth by inducing collaborative apoptosis and ferroptosis in solid tumors
    5557 621 Au@Pt Ag+ detection by LSPR spectroscopy Ag+ Color 0.5-1000 μM 500 nM
    5558 622 TiO2/Bi2WO6/Ag heterojunction hydrogen sulfide detection H2S 0.5-100 μM 0.06 μM
    5559 622 TiO2/Bi2WO6/Ag heterojunction hydrogen sulfide detection H2S E-chem 0.5-300 μM 0.08 μM
    5560 623 thiamine-MnO2 A thiamine-triggered fluormetric assay for acetylcholinesterase activity and inhibitor screening acetylcholinesterase (AChE) Fluor 0.02-1 mU/mL 15 μU/mL
    5561 624 AMP-Cu Efficient elimination and detection of phenolic compounds in juice phenolic compounds 0.1-100 μmol·L−1 0.033 μmol·L−1
    5562 625 Ceria NPs Acute Kidney Injury Alleviation
    5563 626 AuPd @MnO2 Detection of Tetrabromobisphenol A Tetrabromobisphenol A E-chem 0.44-46.49 ng/mL 0.10 ng/mL
    5564 627 Supramolecular Amino acids Photosensitizing Nanozyme for Combating Hypoxic Tumors
    5565 628 MIL-100 For synergetic chemo-photodynamic tumor therapy
    5566 629 DNA-Au/Pt NCs Detection of Staphylococcus aureus bacteria Color 102-108 CFU/mL 80 CFU/mL
    5567 630 POMOFs@PDDA-rGO Detection of H2O2 and Citric acid Citric acid 1–60 μM 2.07 μM
    5568 631 Fe-PorCOF Glucose sensing Glucose 0.01to 10.0 μmol·L-1 5.3 nmol·L-1
    5569 636 MWCNT@MoS2 NS's Determination of 5-Nitroguaiacol 0.1–70 μM 0.02 μM
    5570 637 Magnetite@cellulose NCs Glucose monitoring Glucose 5 mM
    5571 638 Fe3O4 For Cancer Magneto-Catalytic Theranostics
    5572 639 WS2 QDs For Antibacterial and Anti-biofilm Therapie
    5573 640 Pd12 nanocage Photocatalytic antibacterial activity
    5574 643 CuO Sensing of Alkaline phosphate Ascorbic acid (AA) Fluor 2.92×10-8 M
    5575 643 CuO Sensing of Alkaline phosphate Alkaline phosphatase (ALP) Fluor 0.058 U/L
    5576 647 MoSe2 Sening H2O2 Color 10-100 μM 4 μM
    5577 648 Au/OMCS Electrochemical Sensor Xanthine E-chem 0.10–20 μM 0.006 μM
    5579 651 FeS2/SiO2 Detection TMB Color 1-4- μM 0.16 μM
    5578 651 FeS2/SiO2 Detection H2O2 Color /L μM 0.00420 μM
    5580 653 MnO2 CO Therapy Color
    5581 654 FeS2/SiO2 Detection H2O2 Color /L μM 0.00420 μM
    5582 654 FeS2/SiO2 Detection TMB Color 1-4- μM 0.16 μM
    5583 655 Cu-Carbon dots Detection Cr Fluor 0.2-100 μM 36 nM
    5584 656 CeO2 pesticide detection. Methyl-paraoxon E-chem 0.1-100 and 0.1-10 μM/L 0.06 μM/L What's more, the oxidation peak current increased linearly with MP concentration in the ranges of 0.1–10 μmol/L and 10–100 μmol/L, with correlation coefficients (R2) higher than 0.99 for both two analytical curves (n=3, Fig. 6B).
    5585 657 iron oxides The activity curves and descriptors are expected to serve as a simple but robust theoretical tool for computer-aided screening and design of nanozymes, which could greatly facilitate the discovery of new nanozymes in the future.
    5586 658 AuNPs detection cysteine Color 0.5-20 μM 0.5 μM
    5587 658 AuNPs detection cysteine in biological fluids Color 0.5-50 μM 0.5 μM To this end, we tested human urine samples for different concentrations of cysteine using the system established in this paper.
    5588 659 Mn/Ni(OH)x LDHs antibacteria
    5589 660 Fe3O4/Au NPs detection of Staphylococcus aureus S. aureus Color 10 ~ 1000000 cfu/mL 10 cfu/mL
    5590 661 Fe-SAzyme detection of galactose TMB Color 50-500 μM 10 μM 104.83~105.33%
    5591 662 g-C3N4 detection of H2O2 H2O2 Fluor 90-2500 nM 73 nM
    5592 663 S-rGO detection of glucose TMB Color 1-100 μM 0.38 μM
    5593 664 NLISA-T detection of serum TMB Color 0.1-10 ng/mL 0.08 ng/mL
    5594 664 NLISA-H detection of serum HAuCl4 Color 0.1-10 ng/mL 0.05
    5595 665 GO-UO22+ NPs detection of uranyl ions TMB Color 5.9-943 μM 4.7 μM 96.82-98.31%
    5596 666 AuNCs-SF detection of H2O2 H2O2 Fluor 0.1-100 mM 0.072 mM 95.12-99.76%
    5597 667 nanoceria ROS elimination
    5598 668 D-Trp-OMe@AuNCs detection of trtracycline TMB Color 1.5-30.0 μM 0.20 μM 99.0-105.0%
    5599 669 GNR detection of dopamine DA Color 0.1–1, 2.5–50 μM 0.035 μM 90-110%
    5600 670 Fe3S4 detection of glucose glucose Color 0.5-150 μM 0.1 μM 93.7-101.4%
    5601 671 IrNPs antibacteria
    5602 672 MoS2-Lys NSs antibacteria
    5603 673 metallo-nanozymes This work highlights the minimal principle and excellent catalytic performance of stable metallo-nanozymes, opening up immense opportunities in the development of highly efficient nanozymes and catalytic prodrug conversion.
    5604 674 Fe3O4 MNPs cell disruption
    5605 675 AIronNPs wound disinfection and healing
    5606 676 PBNPs-icELISA determination of free GCA GCA Color 0.03-1.20 μg/mL 2.5 × 10−3 μg/mL
    5607 677 HyPEI-supported ZnS NC The catalyst, however, could be easily adapted to apply broadly to different protoenzymatic systems.
    5608 678 g-C3N4 analyzing biological fluids. Fluor 1 μM
    5609 679 R-MnCo2O4 construct highly sensitive biosensors. TMB Color
    5610 680 Mn3O4 enhance the biosemiconductor performance
    5611 682 Cu-Cys NLs detetion of epinephrine epinephrine Color 9–455 μM/L 2.7 μM/L 100.1-108.3%
    5612 683 BiVO4 detection of β-lactoglobulin β-lactoglobulin E-chem 0.01-1000 ng/mL 0.007 ng/mL
    5613 686 nano-MnO2 driven E2 radical polymerization and decomposition
    5614 687 CuSNPs determination of o,o-dimethyl-o-2,2-dichlorovinyl phosphate (DDVP) DDVP Fluor 0.0001 to 0.1 μg/mL 0.1 ng/mL
    5615 688 RuO2 detection of H2O2 H2O2 Color 10-600 μM
    5616 689 Fe@NCDs detection of uric acid uric acid Color 2–150 μM 0.64 μM
    5617 690 Cu2+-NMOFs detection of bacterial lipopolysaccharide (LPS) LPS E-chem 0.0015 to 750 ng/mL 6.1 × 10−4 ng/mL
    5619 691 Fe-doped g-C3N4 nanoflake detection of sarcosine (SA) SA Color 10-500 μM 8.6 μM
    5618 691 Fe-doped g-C3N4 nanoflake detection of hydrogen peroxide (H2O2) H2O2 Color 2-100 μM 1.8 μM
    5620 692 CDs enzymatic enantioselectivity
    5621 693 Au-Fe2O3 cancer assay detection T47D cancer cell line E-chem 10–100000 cells ml−1 0.4 U ml−1
    5622 694 graphene/Fe3O4-AuNP detection of Pb2+ Pb2+ Color 1–300 ng/mL 0.63 ng/mL
    5623 695 Pt detect ascorbic acid in triplicate Ascorbic acid (AA) Color 1-20 μM The limits of detection were 131 ± 15, 144 ± 14, and 152 ± 9 nM, with little difference.
    5624 696 Fe3O4@MnO2 enhance the radiosensitivity
    5625 699 MCDs-MnO2 NPs detection of food- and water-borne pathogens gram-negative bacterium and the gram-positive bacterium Color 10 to 1000000 cfu mL−1 100 cfu mL−1
    5626 700 Fe3O4 MCs facilitate the CDT
    5627 701 Hep-Pd NPs determination of Pro protamine Color 0.02 ~ 0.8 μg mL−1 0.014 μg mL−1
    5628 702 CSA-based nanoparticles detection of H2O2 H2O2 Color 5-400 μM 3.32 μM
    5629 703 GO/Ag biosensing
    5630 704 Au-hematene glucose sensor glucose E-chem 0-3.2 mM mM 0.4 mM
    5631 705 ATF detection of cancer cells cancer cells 2000 cancer cells/mL
    5632 707 AuNPs detection of Opisthorchis viverrini antigen (OvAg) in urine samples Opisthorchis viverrini antigen (OvAg) Color 23.4 ng mL-1
    5633 708 Mn-MPSA-PCC monitoring of O2 •− released from cancer cells O2 •− E-chem
    5634 709 HA-PB/ICG drug delivery
    5635 710 LaMNPs inhibition of the tumor growth
    5636 711 DhHP-6-c-ZrMOF promising catalyst for the high-efficiency degradation of phenol pollutants
    5637 712 hemin-GroEL detection of glucose glucose Fluor 0-6 mM
    5638 713 SOD-Fe0@Lapa-ZRF kill tumor cells via the multi-enzyme cascades
    5639 714 A-nanoceria an effective alternative to the current DMARDs in RA therapy
    5640 715 gCuHCF as a peroxidase mimetic in oxidase-based biosensors
    5641 717 Fe2O3/CNTs Highly Efficient Dopamine Sensing Dopamine (DA) Color 0-25 μM 0.11 μM
    5642 719 Fe-BTC H2O2 dection H2O2 Color 0.04-30 μM 36 nM
    5643 719 Fe-BTC glucose biosensing glucose Color 0.04-20 μM 39 nM
    5645 722 PtNPs@MWCNTs xylose biosensor xylose E-chem 5-400 μM 1 μM
    5644 722 PtNPs@MWCNTs NADH detection NADH 1-200 μM 0.8 μM
    5646 723 dex-MoSe2 NS detection of glucose glucose Color 0.04-0.40 mM 0.028 mM 97.2%-106.1%
    5647 725 laccase/Fe-BTC-NiFe2O4 degrade pollutants in water
    5648 726 NH2-MIL-88B(Fe)-Ag wound-healing
    5650 727 Ir NPs detection of glucose glucose Color 0.01-2 mM 5.8 μM 93.3–104%
    5649 727 Ir NPs detection of glutathione GSH Color 0.2-100 μM
    5651 728 GOx@MOF One-step cascade detection of glucose at neutral pH glucose Color 8-140 μM 2.67 μM
    5652 729 Ags-APMSNs Mumps Virus Diagnosis mumps-specific IgM antibodies Color 10-100000 ng/mL 10 ng/mL
    5653 731 CD inhibiting neuronal death
    5654 732 Mn0.98Co0.02O2 treatment of gout
    5656 733 Ti3C2 detect IR-b IR-b Color 0.5-8 ng/mL
    5655 733 paper-based sensors of His-Ti3C2 detection of glucose glucose Color 0.01-0.64 mM 0.01 mM
    5657 734 ZrO2 NPs near-infrared intracellular imaging
    5658 735 Au@Pt highly sensitive sensing of matrix metalloproteinase 2 MMP-2 E-chem 0.5–100 ng/mL 0.18 ng/mL 96.1 to 104.4%
    5659 736 CQDs determination of ascorbic acid AA Color 1.0-105 μM 0.14 μM 94.3–110.0%
    5660 737 H-MnFe(OH)x multi-therapeutics delivery and hypoxia-modulated tumor treatment
    5661 738 LIPIA as Chiral Scaffolds for Supramolecular Nanozymes
    5662 739 QG Slowed Inflammation and Increased Tissue Regeneration in Wound Hypoxia
    5663 740 SP-SPIO-IR780 and SPA-SPIO-IR780 Dual-modality Imaging Guided Nanoenzyme Catalysis Therapy and Phototherapy
    5664 741 Fe-COFs detect H2O2 and degrade RhB H2O2 Color 10-2000 μM 5.6 μM 96.27-100.70%
    5665 742 PFO/PFDBT-5 Pdots AChE detection acetylcholinesterase (AChE) Fluor 0-500 U/L 0.59 U/L
    5666 743 ADH/GOx@TM sustainable catalytic NAD+ /NADH cycling
    5667 744 Pt-GNRs cancer treatment
    5668 745 Pt/WO2.72 H2O2 detection H2O2 Color 0.005-12 mM 2.33 μM
    5669 745 Pt/WO2.72 glucose detection glucose Color 0.01-0.6 mM 5.9 μM
    5670 745 Pt/WO2.72 radical elimination
    5671 747 2D Co3O4@Rh NC colorimetric sensing of urea and p-Ap UREA Color 6-165 μM 1.1 μM 96-105.8
    5672 747 2D Co3O4@Rh NC colorimetric sensing of urea and p-Ap p-aminophenol Color 1.7-105 μM 0.68 μM 96-105.8
    5673 748