Trace identification of cysteine enantiomers based on an electrochemical sensor assembled from CuxS@SOD zeolite.

The nonchiral sensor concept based on a sodalite (SOD) zeolite loaded CuxS (CuxS@SOD) catalyst is proposed as a sensing platform for chiral cysteine (Cys) determination. Chiral Cys is analyzed by the difference of binding capacity between CuxS catalysts. The observed current in amperometric i-t curve (A i-t C) is always positive for the L-cysteine (L-Cys), while it is negative for the D-cysteine (D-Cys). Under differential pulse voltammetry (DPV) method, the characteristic current peak for the CuxS@SOD moves to right (positive potential position) with the addition of L-Cys while it moves to left (negative potential direction) with the addition of D-Cys, respectively. Cyclic voltammetry (CV) is consistent with DPV and discusses the diffusion control mechanism. In this work, the ultra-trace determination of cysteine enantiomers reaches the limit of detection (LOD) of 0.70 fM and 0.60 fM by the highly efficient CuxS catalyst restrained in the nanosized SOD zeolite cages of the opening window pores, respectively. The sensor opens up a novel potential prospect for achiral composite in the field of chiral recognition through electrochemical methods with extra-low concentration.

Coral-like, self-assembled, and spatially bounded Ag nano-particles on franzinite zeolite composite sensor toward accurate, synergetic, and ultra-trace sulfadiazine detection.

A coral-like Ag@FRA zeolite nanocomposite sensor reveals high sensitivity toward sulfadiazine (SDZ) in a dual detection of fluorescence and electrochemistry. The sensor has been as-synthesized in the hydrothermal condition through a one-pot self-assembly process in which the high crystalline Ag nanoparticles (NPs) are closely arranged and stacked on the nanosized surface cage window of the FRA (Franzinite) zeolite. Strong ultrasound can drive the coral-like composite release Ag nanoparticles whose distribution range mainly from 10 to 12 nm lead to the purple fluorescence in an emission spectrum. In sea water, the fluorescence increases linearly in the SDZ concentration range of 5 × 10-18-5 × 10-10 M. Furthermore, the LOD (limit of detection) reaches 1.4 × 10-22 M by the spatial confinement effect of the coral-liked FRA cage structure in CV (cyclic voltammetry) method at the characteristic potential peak position of 0.1 V vs. SCE. The theoretical calculation also confirms that the FRA cage structure matches well with the SDZ molecules. Further studies indicate the generation of a novel stable composite sensor with high specificity, good recovery and repeatability, which depends on the induction of silver ions upon the artificial synthesis of FRA.

Highly dispersed Cu and Ni nano cluster sensor for ultrasensitive electrochemical detection of antiviral drug lamivudine.

The accurate and rapid detection for the nucleoside reverse transcriptase inhibitor lamivudine (LAM, 3TC) in cellular systems is always a challenge in the clinic application. Here, a sensitive Cu and Ni nano cluster sensor for LAM is generated under hydrothermal conditions.The Cu and Ni atoms are highly dispersed and aggregated in the nanosized opening pore windows of the synthesized LTA zeolite, through the diatomic synergistic contribution of Cu and Ni and the enrichment of zeolitic channel pores. Using differential pulse voltammetry (DPV), the detection limit (LOD) of LAM at the potential (- 0.15 V) can reach 0.001 pM and the linear range is 0.002 pM-0.002 µM. Since the nano cluster is separated and restricted by the nanosized windows of the zeolite framework, the sensor provides high stability, good recovery (92.5-109%) and RSD (0.8-3.2%) in the analysis of tap water, RPMI 1640 medium, and rabbit serum. The Cu/Ni/LTA zeolite-modified glassy carbon electrode (Cu/Ni/LTA/GCE) exhibits excellent catalytic performance for LAM with high selectivity over potentially interfering agents. A sensitive Cu and Ni nano cluster sensor for LAM is generated in the hydrothermal condition that the Cu and Ni atoms are highly dispersed and aggregated in the nanosized opening pore windows of the as-synthesized LTA zeolite. Through the diatomic synergistic contribution of Cu and Ni and the enrichment of zeolitic channel pores, the observed limit of detection (LOD) can reach 0.001 pM under differential pulse voltammetry (DPV) method with a wide linear relationship to 0.002 µM.

Application of LTA zeolite-modified electrode for sensitive detection of retinoic acid in tap water.

An electrochemical method based on a Linde Type-A zeolite-modified glass carbon electrode (LTA/GCE) was introduced for the determination of retinoic acid (RA). LTA zeolite could be synthesized through a hydrothermal method and served as a commercial electrochemical sensor with high stability and sensitivity in electrochemical progress. The as-synthesized product was characterized by scanning electron microscopy (SEM), differential thermal analysis (DTA), X-ray powder diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). Under optimal conditions, a detection limit of 0.8 µM was obtained for RA with a linear range of 0.8-20.1 µM. This electrochemical method for determining RA was simpler and cheaper than previously reported methods. Furthermore, the modified electrode could be applied to the detection of RA in tap water, achieving a linear range of 1.4-15.0 µM with a detection limit of 1.4 µM and good recovery. The modified electrode designed by this method provided good selectivity, stability, and reproducibility for RA determination and reliable application for the analysis of RA in environmental water.

Investigation of bacteria and detergent residues on undergraduate students' dinner plates in dormitories during university lockdown.

The COVID-19 outbreak has disrupted undergraduate students' experiments since their access to the laboratory is limited. To address this problem, the bacteria and detergent residues on undergraduate students' dinner plates were investigated by the students in the dormitories. Five different types of dinner plates from 50 students were collected, which were cleaned with detergent and water in the same way and naturally dried. Then, Escherichia coli (E. coli) test papers and sodium dodecyl sulfonate test kits were used to understand the bacteria and detergent residuals. Commonly available equipment such as a yogurt maker was used for bacterial culture; detergent analyses were performed using centrifugation tubes. Effective sterilization methods and safety protection were achieved by dormitory available methods. According to the investigated results, the students found the differences in bacteria and detergent residuals between different dinner plates and made suitable choices for the future.

Highly dispersed redox antimony oxide pairs for accurate detection and electrochemistry-controlled recovery toward an antibiotic drug: Sulfadiazine.

BACKGROUND: Sulfadiazine (SDZ) is a broad-spectrum antibiotic widely used in aquaculture and animal husbandry and it is easy to remain in the water system to damage the human body. Therefore, detection and removal of sulfadiazine in water systems become critical. Nowadays, catalysts and visible light are used to degrade sulfadiazine into smaller molecules containing N and S to reduce toxicity. However, these small molecules are easily released into water and the atmosphere to be the acid rain. Therefore, it is urgent to design a sensor with the ability to detect and remove SDZ at the same time. (96) RESULTS: We designed a novel composite catalyst sensor (Sb6O13@LTA GCE) with the ability to simultaneously monitor and remove sulfadiazine. The catalyst is generated by introducing SbCl5 into the reactive gel of LTA (Linde Type A) structure zeolite. In the hydrothermal reaction, the corrosive SbCl5 is transferred into nanosized Sb6O13 nanoparticle which is highly dispersed in the opening nano-scaled windows of the zeolite through redox and self-assembled progress. In the selected electrochemical overpotential range, the Sb6O13@LTA composited modified electrode could complete adsorption and desorption of SDZ through the electron transfer from Sb3+ to Sb5+. As the catalyst is in high stability, the only loss in the whole process of recovering SDZ is a small amount of electric energy. The extra-low detection limit and the removal efficiency of Sb6O13@LTA GCE have been achieved 4.0 pM and 19.3 mg/20 mg (136) SIGNIFICANCE: The prepared novel sensor has low detection limit, high removal efficiency and high selectivity for sulfadiazine. The Sb6O13@LTA GCE sensor, which is low-cost and has a simple preparation method, exhibits good reproducibility in both seawater and cell fluid. This provides the possibility for wide application in detecting and removing SDZ in water system. (53).

A biomimetic zeolite-based nanoenzyme contributes to neuroprotection in the neurovascular unit after ischaemic stroke via efficient removal of zinc and ROS.

Zeolite-based nanomaterials have a large number of applications in the field of medicine due to their high porosity, biocompatibility and biological stability. In this study, we designed cerium (Ce)-doped Linde Type A (LTA) zeolite-based nanomaterials (Ce/Zeo-NMs) as a multifunctional mesoporous nanoenzyme to reduce dysfunction of the neurovascular unit (NVU) and attenuate cerebral ischaemia-reperfusion (I/R) injury. Owing to its unique adsorption capacity and mimetic catalytic activities, Ce@Zeo-NMs adsorbed excess zinc ions and exhibited scavenging activity against reactive oxygen species (ROS) induced by acute I/R, thus reshaping the oxidative and zinc microenvironment in the ischaemic brain. In vivo results demonstrated that Ce@Zeo-NMs significantly reduced ischaemic damage to the NVU by decreasing the infarct area, protecting against breakdown of the blood-brain barrier (BBB) via inhibiting the degradation of tight junction proteins (TJPs) and inhibiting activation of microglia and astrocytes in a rat model of middle cerebral artery occlusion-reperfusion (MCAO/R). Taken together, these findings indicated that Ce@Zeo-NMs may serve as a promising dual-targeting therapeutic agent for alleviating cerebral I/R injury. STATEMENT OF SIGNIFICANCE: Cerium (Ce)-doped Linde Type A zeolite-based nanomaterials (Ce/Zeo-NMs) as a multifunctional mesoporous nanoenzyme were designed for inducing neuroprotection after ischaemic stroke by reducing dysfunction of the neurovascular unit (NVU). Ce@Zeo-NMs had the ability to adsorb excessive Zn2+ and showed mimetic enzymatic activities. As a result, Ce@Zeo-NMs protected against cerebral ischaemia and reduced the damage of NVU by improving the integrity of blood brain barrier (BBB) and inhibiting activation of microglia and astrocytes in a rat model of middle cerebral artery occlusion-reperfusion (MCAO/R). These findings indicated that Ce@Zeo-NMs may serve as a therapeutic strategy for neuroprotection and functional recovery upon ischaemic stroke onset.

A thermoreversible antibacterial zeolite-based nanoparticles loaded hydrogel promotes diabetic wound healing via detrimental factor neutralization and ROS scavenging.

BACKGROUND: As recovery time of diabetic wound injury is prolonged by the production of detrimental factors, including reactive oxygen species (ROS) and inflammatory cytokines, attenuating the oxidative stress and inflammatory reactions in the microenvironment of the diabetic wound site would be significant. EXPERIMENTAL DESIGN: In our study, we prepared thermoreversible, antibacterial zeolite-based nanoparticles loaded hydrogel to promote diabetic wound healing via the neutralization of detrimental factors such as inflammatory cytokines and ROS. RESULTS: The cerium (Ce)-doped biotype Linde type A (LTA) zeolite nanoparticles synergistically eliminated mitochondrial ROS and neutralized free inflammatory factors, thus remodeling the anti-inflammatory microenvironment of the wound and enhancing angiogenesis. Moreover, the thermoreversible hydrogel composed of Pluronic F127 and chitosan demonstrated strong haemostatic and bactericidal behavior. CONCLUSIONS: In conclusion, the obtained thermoreversible, antibacterial, zeolite-based nanoparticles loaded hydrogels represent a multi-targeted combination therapy for diabetic wound healing.

Assembly of Carbon Dots into Frameworks with Enhanced Stability and Antibacterial Activity.

Carbon dots (CDs) have been widely used as antimicrobials due to their active surface, but some CDs suffer instability. Therefore, the relative applications such as the antibacterial activity may not be reliable for long-term use. Herein, we synthesize CDs with blue fluorescence by a hydrothermal process. Thereafter, polyethylenimine was applied for the assembly of CDs into CDs-based frameworks (CDFs). The CDFs exhibited quenched fluorescence but showed more stable properties based on the scanning electron microscope and zeta potential investigations. Both CDs and CDFs show antibacterial activity toward Gram-negative Escherichia coli (E. coli) and Gram-positive Staphylococcus aureus (S. aureus), but CDFs exhibited better antibacterial performance, and S. aureus could be completely inhibited with the minimum inhibitory concentration of 30 µg/mL. This reveals CDFs magnify both the stability and antibacterial activity, which would be more promising for practical applications.

Facile nano-free electrochemiluminescence biosensor for detection of sulphamethoxazole via tris(2,2'-bipyridyl)ruthenium(II) and N-methyl pyrrolidone recognition.

The electrochemiluminescence (ECL) system based on the ruthenium complex has become a powerful tool in the field of analytical chemistry. However, the non-aqueous ECL luminescence system, which does not involve complex nano-modification, has not been widely used for the determination of analytes. In this study, N-methyl pyrrolidone was selected as the solvent, and it could also act as a co-reactant of [inline-formula removed]. Based on this, a simple ECL system without nanomaterials was established. Strong ECL was generated. Furthermore, a quenching effect between the excited state of [inline-formula removed] and sulphamethoxazole (SMZ) was observed. Based on this, a sensitive ECL sensor for detecting SMZ is constructed. A linear relationship between ECL signal quenching intensity (ΔI) and the logarithm of SMZ concentration (log C) in the concentration range of 1 × 10-7-1 × 10-5 mol/l is obtained. The limit of detection is as low as 3.33 × 10-9 mol/l. The method has been applied to the detection of SMZ in tap water samples with different concentration levels with satisfactory results, and the recovery was 95.3-102.6%.

Preparation TiO2 core-shell nanospheres and application as efficiency drug detection sensor.

In this paper, we report the facile preparation of monodisperse titanium dioxide-diltiazem/tetrachlorobismuth core-shell nanospheres (TiO2@DTMBi), in which, diltiazem (DTM)/tetrachlorobismuth (BiCl4) complexes were employed as electroactive materials. The morphology, size, formation, and structure of the obtained TiO2@DTMBi spheres were investigated by transmission electron microscopy, scanning electron microscopy, dynamic light scattering, Fourier transform infrared spectroscopy, and X-ray diffraction. The optimal condition of obtained monodisperse 40-nm TiO2@DTMBi spheres was researched. The results of using TiO2@DTMBi nanospheres as proposed drug sensor indicate a wide linear range (10(-7) to 10(-1) M) and a very low detection limit of 0.20 µg/mL.

Growing vertical ZnO nanorod arrays within graphite: efficient isolation of large size and high quality single-layer graphene.

We report a unique strategy for efficiently exfoliating large size and high quality single-layer graphene directly from graphite into DMF dispersions by growing ZnO nanorod arrays between the graphene layers in graphite.

A catalytic nanostructured cobalt oxide electrode enables positive potential operation for the cathodic electrogenerated chemiluminescence of Ru(bpy)3(2+) with dramatically enhanced intensity.

We report the first novel cathodic electrochemiluminescence of Ru(bpy)(3)(2+) at positive potential of +0.6 V (vs. Ag/AgCl) with a strong light emission clearly visible to the naked eye triggered by reactive oxygen species O(2)(-) on an in situ electrodeposited Co(3)O(4) nanostructured electrode.