| 4980 |
54 |
GOx@MOF-545(Fe) |
|
glucose |
Color |
0.5–100 |
μM |
0.28000000000000003 |
μM |
|
|
| 4995 |
82 |
PNCNzyme |
Activating IAA to produce abundant ROS and triggering tumor cell apo-ptosis |
|
|
|
|
|
|
|
|
| 4998 |
90 |
heteroatom-doped graphene |
Constructingnanozymesensorarrayfordetectingpesticides |
|
|
|
|
|
|
|
|
| 5029 |
128 |
BNS-CDs |
|
H2O2 |
Color |
3-30 |
μM |
0.8 |
μM |
92.7-108.3% |
Smartphone colorimetric determination |
| 5043 |
142 |
CDs |
conformational transition of pDNA |
|
|
|
|
|
|
|
|
| 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 |
|
| 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. |
| 5118 |
205 |
Rosette-GCN |
glucose was reliably determined |
glucose |
Color |
5.0-275.0 |
μM |
1.2 |
μM |
99.3–104.1% |
|
| 5199 |
309 |
GDYO |
Detection of H2O2 and Glucose |
H2O2 |
Color |
|
|
|
|
|
|
| 5200 |
309 |
GDYO |
Detection of H2O2 and Glucose |
Glucose |
Color |
|
|
|
|
|
|
| 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 |
|
|
| 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. |
|
|
|
|
|
|
|
|
| 5265 |
363 |
SNC |
TAC biosensor |
AA |
SERS |
0.1-5 |
mM |
0.08 |
mM |
|
|
| 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). |
| 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 |
|
|
| 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. |
| 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 |
|
|
| 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 |
|
|
| 5289 |
379 |
EPC-900 |
luorometric sensing of glucose |
glucose |
Color |
0.05–10 |
mM |
30 |
μM |
|
|
| 5420 |
474 |
Ce/Pr-CQDs |
readily internalized into cytoplasm, decreasing the level of reactive oxygen species (ROS). |
|
|
|
|
|
|
|
|
| 5450 |
506 |
Fe–N4 pero-nanozysome |
Hyperuricemia and Ischemic Stroke |
|
|
|
|
|
|
|
|
| 5489 |
545 |
NSP-CQDs |
NSP-CQDs was further utilized for antibacterial assays |
|
|
|
|
|
|
|
|
| 5509 |
571 |
N/Cl-CDs |
Detection of H2O2 |
H2O2 |
fluorescence |
1-30 |
μM |
0.27 |
μM |
|
|
| 5520 |
581 |
Fe–N–C |
detection of uracil DNA glycosylase |
uracil DNA glycosylase |
electrochemical |
0.0005-1 |
U/mL |
74 |
μU/mL |
|
|
| 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 |
|
|
| 5595 |
665 |
GO-UO22+ NPs |
detection of uranyl ions |
TMB |
Color |
5.9-943 |
μM |
4.7 |
μM |
96.82-98.31% |
|
| 5599 |
669 |
GNR |
detection of dopamine |
DA |
Color |
0.1–1, 2.5–50 |
μM |
0.035 |
μM |
90-110% |
|
| 5605 |
675 |
AIronNPs |
wound disinfection and healing |
|
|
|
|
|
|
|
|
| 5608 |
678 |
g-C3N4 |
analyzing biological fluids. |
|
Fluor |
|
|
1 |
μM |
|
|
| 5653 |
731 |
CD |
inhibiting neuronal death |
|
|
|
|
|
|
|
|
| 5659 |
736 |
CQDs |
determination of ascorbic acid |
AA |
Color |
1.0-105 |
μM |
0.14 |
μM |
94.3–110.0% |
|
| 5727 |
800 |
CDs |
Reducing Oxidative Damage of Plants |
|
|
|
|
|
|
|
|
| 5799 |
872 |
OAC |
This study indicates the direct participation of the intrinsic radical in the catalytic turnover of a highly active SOD-like nanozyme. |
|
|
|
|
|
|
|
|
| 5800 |
873 |
H-GNs |
It was supposed to be applied for Tg determination in serum to evaluate persistent or recurrent differentiated thyroid carcinoma. |
Thyroglobulin (Tg) |
|
0.7-100 |
ng/mL |
0.1 |
ng/mL |
|
|
| 5813 |
887 |
PEI-600-Fe C-dots |
for Enhanced Synergistic Cancer Starving−Catalytic Therapy |
|
|
|
|
|
|
|
|
| 5827 |
913 |
Cu-HCSs |
Photolysis of methicillin-resistant Staphylococcus aureus |
Staphylococcus aureus |
|
|
|
|
|
|
|
| 5866 |
963 |
N@GQDs |
Selective detection of dopamine |
Dopamine (DA) |
Color |
0.12–7.5 |
mM |
0.04 |
μ M |
|
|
| 5877 |
974 |
GQD |
Cancer treatment |
TMB |
Color |
|
|
|
|
|
|
| 5969 |
1060 |
LSG |
intelligent evaluation of fish freshness |
XT |
E-chem |
0.3-179.9 |
μM |
0.26 |
μM |
|
|
| 5970 |
1060 |
LSG |
intelligent evaluation of fish freshness |
HX |
E-chem |
0.3-159.9 |
μM |
0.18 |
μM |
|
|
| 6030 |
1126 |
g-CNQDs |
fluoride ions detection |
fluoride ions detection |
Color |
10-120 |
μM |
4.06 |
μM |
|
|
| 6056 |
1162 |
(Fe,Co) codoped-CDs |
rapid detection of putrescine (Put) and cadaverine (Cad) |
Put and Cad |
Color |
0.25-10 |
mg kg−1 |
0.06 |
mg kg−1 |
98.2%–115.7% |
|
| 6095 |
1214 |
Cu2+-HCNSs-COOH |
a colorimetric sensing platform by detecting the absorbance of the 3,3′,5,5′-tetramethylbenzidine-H2O2 system at 652 nm for
quantifying H2O2, which holds good linear relationship between 1 and 150 μM and has a detection limit of 0.61 μM. |
H2O2 |
|
1-150 |
μM |
0.61 |
μM |
|
|
| 6096 |
1216 |
g-C3N4 + Fe(III)+ Cu(II) |
the whole system and its sensitivity for glucose detection. Moreover,
TMB adsorbtion on a solid catalyst can pave the way to the development
of glucose sensoring applications based on, for instance, cellulose or
polymeric strips |
glucose |
|
0.001-0.00001 |
μM |
0.22 |
μM |
|
Colorimetric (UV–Vis diffuse
reflectance of solids) |
| 6115 |
1243 |
carbon polymer hollow spheres (CPHSs) |
Detection of H2O2 |
H2O2 |
Color |
50-500 |
μM |
10 |
μM |
|
|
| 6145 |
1284 |
CQDs |
quantitative detection of H2O2 |
H2O2 |
Colorimetric |
5.00–60.0 |
μM |
0.86 |
μM |
|
|
| 6174 |
1325 |
GOQD-MPS |
degradation of organic dyes |
|
|
|
|
|
|
|
|
| 6213 |
1360 |
nC60 |
water treatment |
|
|
|
|
|
|
|
|
| 6230 |
1376 |
Gd@C82 |
Superoxide Scavengers |
|
|
|
|
|
|
|
|
| 6250 |
1399 |
CeCDs |
degradation of organophosphorus pesticide chlorpyrifos |
chlorpyrifos |
Unsure |
|
|
|
|
|
|
| 6269 |
1419 |
Graphene |
For the determination of anti-oxidant activity of drugs |
|
|
|
|
|
|
|
|