FeMo2Ox(OH)y-based mineral hydrogels as a novel POD nanozyme for sensitive and selective detection of aromatic amines contaminants via a colorimetric sensor array.

Developing convenient pathways to discriminate and identify multiple aromatic amines (AAs) remains fascinating and critical. Here, a novel three-channel colorimetric sensor array based on FeMo2Ox(OH)y-based mineral (FM) hydrogels is successfully constructed to monitor AAs in tap water. Benefiting from the substantial oxygen vacancies (VO), FM nanozymes exhibit extraordinary peroxidase (POD)-like activities with Km of 0.133 mM and Vmax of 2.518 × 10-2 mM·s-1 toward 3,3',5,5'-tetramethylbenzidine (TMB), which are much better than horseradish peroxidase and most of POD mimics. This reveals that doping Cu and Co into FM (FM-Cu and FM-Co) can change POD activity. Based on various POD activities, TMB and H2O2 are used to generate fingerprint colorimetry signals from the colorimetry sensor array. The analytes can accurately discriminate through linear discriminant analysis, with a detection limit as low as 2.12 × 10-2-0.14 µM. The sensor array can effectively identify and discriminate AA contaminants and their mixtures and has performed well in real sample tests.

A magnetic molecular imprinting-based fluorescence probe for sensitive and selective detection of 2,4-D herbicide.

A new magnetic molecular imprinting-based turn-on fluorescence probe (Fe3 O4 NPs@SiO2 @NBD@MIPs) has been synthesized via a facile sol-gel polymerization for the detection of 2,4-dichlorophenoxyacetic acid (2,4-D). Based on the photoinduced electron transfer (PET) of nitrobenzoxadiazole (NBD), 2,4-D can be recognized by enhancement of NBD fluorescence. With the presence of Fe3 O4 in the core of the probe, this sensor can also be reused many times using magnetic aggregation methods. After the addition of various concentrations of 2,4-D, the fluorescence peak at 530 nm (excitation of 468 nm) increased linearly ranging from 0.1 to 3 µM with a detection limit of 0.023 µM. This sensing system is believed to be available for detecting 2,4-D in real samples, with high recovery rates ranging from 94% to 108% for three spike levels of 2,4-D with precisions below 5%.

Catechol oxidase nanozyme based colorimetric sensors array for highly selective distinction among multiple catecholamines.

In order to effectively monitor multiple catecholamine (CA) neurotransmitters with extreme similar structures, a rapid, sensitive and selective detection strategy has become an urgent problem to be solved. In this paper, a novel colorimetric sensors array based on CuNCs protected by various ligands such as tannic acid, ascorbic acid and polymethylacrylic acid (CuNCs@TA, CuNCs@AA and CuNCs@PMAA) was constructed. All of these CuNCs could mimic catechol oxidase to selective catalyze catechol-type analogues (such as CAs) to corresponding quinones along with color changes. Furthermore, experiments and theory calculations demonstrated that Cr6+-modification on the surface of CuNCs facilitated the steady-state kinetics of enzymatic activity. Based on these CuNCs as sensing probes, this sensors array can quickly detect different CAs (such as epinephrine (EP), including dopamine (DA), norepinephrine (NE) and l-dopa) with similar structures. When those analogues were added to the CuNC-based colorimetric array sensors, different absorbance changes were produced at 485 nm. Linear discriminant analysis (LDA) showed that the tri-probe colorimetric array sensors could recognize and distinguish these analogues, and corresponding binary and ternary mixtures could be well categorized. The value of Factor 1 of an array with varied CA concentrations had a good linear correlation, and the detection limit (LOD) was as low as 10-8∼10-9 mol/L. Four CA analogues in real samples were identified by CuNCs-based colorimetric array sensors. This work provides a fast and convenient experimental basis for monitoring the complex structure CAs neurotransmitters.

NH2-MIL-101(Fe) nanozyme-based dual-modality sensor for determination of alendronate sodium and study of two-dimensional correlation spectroscopy.

We developed a dual-modality sensing platform for ratiometric fluorescence and colorimetric determination of alendronate sodium (ALDS). This platform was performed by using a NH2- MIL-101(Fe) as a peroxidase mimic. Since preferential complexing between Fe3+ (active site for peroxidase) and ALDS, the production of 2,3-diaminophenazine (DAP, oxidized product of OPD) has been inhibited in the presence of H2O2. As a result, the ratiometric fluorescence value of F556/F456 and absorbance at 450 nm exhibited significant changes, which could be used as the dual-modality sensing platform. In addition, Two-dimensional correlation spectroscopy (2D-COS) analysis on Fourier-transform infrared (FTIR), ultraviolet visible and ratiometric fluorescence spectra were applied to investigate the binding features. Synchronous and asynchronous maps of these spectra confirmed our above hypothesis, in which Fe3+-ALDS complex was the critical factor that regulated dual-modality signals. To our knowledge, the 2D-COS method was applied to study the catalytic and sensing mechanism of nanozyme as NH2- MIL-101(Fe) for the first time. This technique was helpful to understand interaction of substrates on nanozyme and develop more sensitive sensors for assaying.