ABSTRACT
The effective applications of electrochemiluminescence (ECL) across various fields necessitate ongoing research into novel luminophores and ECL strategies. In this study, self-luminous flower-like nanocomposites (Eu-tcbpe-MOF) were prepared by coordination self-assembly using the aggregation-induced emission material 1,1,2,2-tetrakis(4-carboxyphenyl)ethylene (H4TCBPE) and Eu(III) ions as the precursors. Compared with the monomers and aggregates of H4TCBPE, Eu-tcbpe-MOF exhibits stronger ECL emission. Such enhanced electrochemiluminescence is due to coordination as the coordination-triggered electrochemiluminescence (CT-ECL) enhancement effect. In this study, a cubic-structured nanocomposite (Co9S8@Au@MoS2) was used as an efficient quencher, and a more sensitive ECL detection platform was achieved by two quenching mechanisms: resonance energy transfer and competitive consumption of coreactants. N,N-Diethylethanolamine (DBAE) was used as a coreactant, and DBAE has a faster electron transfer rate and stronger energy supply efficiency than the traditional anodoluminescent coreactant tripropylamine, which effectively improves the ECL signal intensity of Eu-tcbpe-MOF. Hence, a sandwich-type ECL immunosensor was prepared by employing a dual-quenching mechanism, utilizing Eu-tcbpe-MOF as the detection probe and Co9S8@Au@MoS2 as the quencher, achieving precise detection of carcinoembryonic antigen from 0.1 pg·mL-1 to 100 ng·mL-1 with a detection limit of 35.1 fg·mL-1.
ABSTRACT
The electrocatalytic nitrate reduction reaction (NO3 - RR) enables the reduction of nitrate to ammonium ions under ambient conditions. It was considered as an alternative reaction for the production of ammonia (NH3 ) in recent years. In this paper, we report that the Fe doping CoS2 nanoarrays can effectively catalyze the formation of NH3 from nitrate (NO3 - ) under ambient conditions. This is mainly due to the increase of the NO3 - reaction active site by Fe doping and the porous nanostructure of the catalyst, which greatly improves the catalytic activity. Specifically, at -0.9â V vs. RHE, the NH3 yield rate (RNH3 ) of Fe-CoS2 /CC is 17.8×10-2 â mmol h-1 cm-2 with Faraday Efficiency (FE) of 88.93 %. Besides, such catalyst shows good durability and catalytic stability, which provides the possibility for the future application of electrocatalytic NH3 production.
ABSTRACT
Lung cancer is a high-mortality cancer related to the concentration of neuron-specific enolase (NSE). In this work, a sandwich-type photoelectrochemical (PEC) immunosensor was constructed for ultrasensitive detection of NSE, which is based on iron trioxide/indium zinc cadmium sulfide (Fe2O3/Cd-ZnIn2.2Sy) as a sensing platform and Ag-modified polyaniline (Ag@PANI) as a signal amplification label. The 1D Fe2O3 porous nanorods with a large specific surface area were synthesized by calcination of Fe-MIL-88A and etching of NaOH. To improve the photocurrent response, the 3D architecture Cd-ZnIn2.2Sy was combined with the 1D Fe2O3 porous nanorods to form a 1D Fe2O3/3D Cd-ZnIn2.2Sy heterostructure. Specifically, the Fe2O3/Cd-ZnIn2.2Sy heterostructure with a good energy level matching (the two can form a stepped energy level matching, which accelerates the transfer rate of electrons) can improve the separation efficiency of electron-hole pairs (e-/h+) under visible light irradiation, which enhances the photocurrent response. Ag@PANI has a strong electron transport capability and can be used as a secondary antibody marker for the signal amplification of the immunosensor. The sensor exhibits a good linear detection range of 100 fg/mL to 100 ng/mL with a low detection limit of 33.5 fg/mL. Moreover, the constructed sandwich-type PEC immunosensor shows good performance and possesses excellent specificity, selectivity, and stability over a period of 4 weeks for NSE detection. With these excellent properties, the immunosensor can be extended to analyze and diagnose other disease biomarkers.
Subject(s)
Biosensing Techniques , Electrochemical Techniques , Limit of Detection , Cadmium , Immunoassay , Phosphopyruvate HydrataseABSTRACT
In this work, an antigen-down photoelectrochemical (PEC) immunosensor based on a signal polarity switching strategy for the detection of cytokeratin 19 fragment 21-1 (CYFRA21-1) was proposed. 3,4,9,10-Perylene tetracarboxylic acid (PTCA) is a conjugated organic dye containing five benzene nuclei, which has excellent film-forming and optical properties. PTCA sensitized by SnS2 can further improve the basal signal and the stability of the PEC immunosensor. Moreover, avidin-functionalized CuInS2 as a signal probe can convert the basal anodic photocurrent to a cathodic photocurrent. Therefore, the PEC sensor realized the photocurrent polarity conversion before and after labeling. With avidin-functionalized CuInS2, the polarity of the photocurrent was changed once CYFRA21-1 was detected. Therefore, the PEC immunosensor owns high sensitivity. The linear range of the immunosensor for the detection of CYFRA21-1 is 0.00001-500 ng·mL-1, and the detection limit is 3.5 fg·mL-1. The PEC immunosensor has good stability, high selectivity, and good repeatability. This work may provide a new way for the detection of CYFRA21-1 and other proteins.
Subject(s)
Biosensing Techniques , Antigens, Neoplasm , Avidin , Electrochemical Techniques , Immunoassay , Keratin-19 , Limit of DetectionABSTRACT
The design and construction of active centres are key to exploring advanced electrocatalysts for oxygen evolution reaction (OER). In this work, we demonstrate thein situconstruction of point defects on CrOOH by Ni doping (Ni-CrOOH/NF). Compared with pure CrOOH/NF, Ni-CrOOH/NF showed enhanced OER activity. The effect of the amount of Ni introduced on the OER performance was investigated. Ni0.2-CrOOH/NF, the best introduction of Ni, uses a low overpotential of 253 mV to achieve a current density of 10 mA cm-2with a high turnover frequency of 0.27 s-1in 1.0 M NaOH. In addition, the electrocatalytic performance of Ni0.2-CrOOH/NF showed little deterioration after 1000-cycle cyclic voltammetry scanning. In the potentiostatic test, activity was stable for at least 20 h.
ABSTRACT
BACKGROUND: Long-term high fat (HF) diet intake can cause neuroinflammation and cognitive decline through the gut-brain axis. (1, 3)/(1, 6)-ß-glucan, an edible polysaccharide isolated from medical mushroom, Lentinula edodes (L. edodes), has the potential to remodel gut microbiota. However, the effects of L. edodes derived ß-glucan against HF diet-induced neuroinflammation and cognitive decline remain unknown. This study aimed to evaluate the neuroprotective effect and mechanism of dietary L edodes ß-glucan supplementation against the obesity-associated cognitive decline in mice fed by a HF diet. METHODS: C57BL/6J male mice were fed with either a lab chow (LC), HF or HF with L. edodes ß-glucan supplementation diets for 7 days (short-term) or 15 weeks (long-term). Cognitive behavior was examined; blood, cecum content, colon and brain were collected to evaluate metabolic parameters, endotoxin, gut microbiota, colon, and brain pathology. RESULTS: We reported that short-term and long-term L. edodes ß-glucan supplementation prevented the gut microbial composition shift induced by the HF diet. Long-term L. edodes ß-glucan supplementation prevented the HF diet-induced recognition memory impairment assessed by behavioral tests (the temporal order memory, novel object recognition and Y-maze tests). In the prefrontal cortex and hippocampus, the ß-glucan supplementation ameliorated the alteration of synaptic ultrastructure, neuroinflammation and brain-derived neurotrophic factor (BDNF) deficits induced by HF diet. Furthermore, the ß-glucan supplementation increased the mucosal thickness, upregulated the expression of tight junction protein occludin, decreased the plasma LPS level, and inhibited the proinflammatory macrophage accumulation in the colon of mice fed by HF diet. CONCLUSIONS: This study revealed that L. edodes ß-glucan prevents cognitive impairments induced by the HF diet, which may occur via colon-brain axis improvement. The finding suggested that dietary L. edodes ß-glucan supplementation may be an effective nutritional strategy to prevent obesity-associated cognitive decline.
Subject(s)
Cognitive Dysfunction , Shiitake Mushrooms , beta-Glucans , Animals , Brain , Cognitive Dysfunction/drug therapy , Cognitive Dysfunction/etiology , Cognitive Dysfunction/prevention & control , Colon , Diet, High-Fat/adverse effects , Male , Mice , Mice, Inbred C57BL , Mice, Obese , beta-Glucans/pharmacologyABSTRACT
Ammonia synthesis, one of the most challenging chemical synthesis processes, plays a vital role in the development of human industry and agriculture. Compared with the industrial Harber-Bosch ammonia process with huge energy input and high CO2 emissions, the search for a resource-saving, environmentally-friendly ammonia synthesis alternative is extremely urgent. Electrocatalytic nitrogen reduction appears to be a good candidate. In this communication, we report the development of ruthenium nanoparticles as a highly efficient and durable nitrogen reduction reaction (NRR) electrocatalyst in acidic electrolyte under ambient conditions. Such electrochemical NRR catalyst exhibits a large NH3 formation rate (24.88 µg h-1 mg-1 cat.) with Faradaic efficiency (0.35%) at -0.15 V versus reversible hydrogen electrode, outperforming many reported NRR electrocatalysts. Note that it exhibits high durability and stability during the entire electrochemical NRR process.
ABSTRACT
OBJECTIVE: The aim of this study was to assess the esthetic and clinical outcomes of immediate implantation using the conventional flap-less approach and the socket-shield technique (SST). METHODS: This study included 30 adult patients who underwent anterior teeth replacement and fulfilled the pre-defined criteria. Patients were randomly allocated to the SST (n = 15) and conventional flap-less (control, n = 15) groups. The esthetic outcomes were evaluated by assessing the degree of soft-tissue recession and the pink esthetic scores (PESs). Clinical parameters, including the modified plaque index, modified sulcus bleeding index (mSBI), probing depth (PD), and implant stability quotient (ISQ), were assessed. The buccal plate width (BPW) and height (BPH) were also measured. RESULTS: Implantation was clinically successful for all subjects in both groups. With a similar baseline, the SST group exhibited less reduction in the midfacial mucosal margins and the height of the mesial and distal papillae as well as higher BPW and BPH values compared with the control group (p < .001). The ISQ values were 76.01 ± 1.31 for the SST group and 75.56 ± 1.07 for the control group (p > .05), suggesting sufficient initial stability in both groups. At the 24-month follow-up, SST group patients had statistically significant lower values of PD, mSBI, and mPLI compared with the control group. There were no significant differences in the overall and individual PES values for both groups. CONCLUSION: SST may improve functional and esthetic outcomes by maintaining alveolar bone volume and peri-implant tissues. SST seems to be a promising treatment approach for implants in the esthetic zone.
Subject(s)
Dental Implants, Single-Tooth , Immediate Dental Implant Loading , Adult , Dental Implantation, Endosseous , Dental Plaque Index , Esthetics, Dental , Humans , Maxilla , Treatment OutcomeABSTRACT
The production of ammonia (NH3) in the industrial scale basically relies on the traditional technology of Haber-Bosch, which is operated under harsh conditions with high energy consumption and a huge number of greenhouse gas emissions. Electrochemical N2 reduction reaction (NRR) is a promising route for artificial N2-to-NH3 fixation with less energy consumption. However, an effective electrocatalyst, as a prerequisite of the NRR, is of significance. Here, we report that a spinel LiMn2O4 nanofiber acts as a noble-metal-free electrocatalyst for NH3 synthesis with excellent performance under ambient conditions. The electrocatalyst, which was tested in 0.1 M HCl, has an excellent Faradaic efficiency of 7.44% and a NH3 yield of 15.83 µg h-1 mgcat.-1 at -0.50 V versus reversible hydrogen electrode. Moreover, it also possesses excellent electrochemical and structure stability.
ABSTRACT
OBJECTIVES: To investigate the therapeutic effect of gelatin microspheres containing different concentrations of calcitonin gene-related peptide (CGRP) or substance P on repairing bone defects in a rabbit osteoporosis model. RESULTS: Gelatin microspheres containing different concentrations of CGRP or substance P promoted osteogenesis after 3 months in a rabbit osteoporotic bone defective model. From micro-computed tomography imaging results, 10 nM CGRP was optimal for increasing the trabecular number and decreasing the trabecular bone separation degree; similar effects were observed with the microspheres containing 1 µM substance P. Histological analysis showed that the gelatin microspheres containing CGRP or substance P, regardless of the concentration, effectively promoted osteogenesis, and the highest effect was achieved in the groups containing 1 µM CGRP or 1 µM substance P. CONCLUSIONS: Gelatin microspheres containing CGRP or substance P effectively promoted osteogenesis in a rabbit osteoporotic bone defect model dose-dependently, though their effects in repairing human alveolar ridge defects still need further investigation.
Subject(s)
Bone and Bones/pathology , Calcitonin Gene-Related Peptide/therapeutic use , Gelatin/chemistry , Microspheres , Osteoporosis/drug therapy , Substance P/therapeutic use , Wound Healing , Animals , Bone Regeneration/drug effects , Bone and Bones/diagnostic imaging , Bone and Bones/drug effects , Calcitonin Gene-Related Peptide/pharmacology , Delayed-Action Preparations , Disease Models, Animal , Female , Microscopy, Electron, Scanning , Osteoporosis/diagnostic imaging , Osteoporosis/pathology , Ovariectomy , Rabbits , Staining and Labeling , Substance P/pharmacology , Wound Healing/drug effects , X-Ray MicrotomographyABSTRACT
The construction of assays is capable of accurately detecting cytokeratin-19 (CYFRA 21-1), which is critical for the rapid diagnosis of nonsmall cell lung cancer. In this work, a novel electrochemiluminescence (ECL) immunosensor based on the co-reaction promotion of luminol@Au@Ni-Co nanocages (NCs) as ECL probe by Ti3C2Tx MXene@TiO2-MoS2 hybrids as co-reaction accelerator was proposed to detect CYFRA 21-1. Ni-Co NCs, as a derivative of Prussian blue analogs, can be loaded with large quantities of Au NPs, luminol, and CYFRA 21-1 secondary antibodies due to their high specific surface area. To further improve the sensitivity of the developed ECL immunosensor, Ti3C2Tx MXene@TiO2-MoS2 hybrids were prepared by in situ growth of TiO2 nanosheets on highly conductive Ti3C2Tx MXene, and MoS2 was homogeneously grown on Ti3C2Tx MXene@TiO2 surfaces by the hydrothermal method. Ti3C2Tx MXene@TiO2-MoS2 hybrids possess excellent catalytic performance on the electro-redox of H2O2 generating more O2·- and obtaining optimal ECL intensity of the luminol/H2O2 system. Under the appropriate experimental conditions, the quantitative detection range of CYFRA 21-1 was from 0.1 pg mL-1 to 100 ng mL-1, and the limit of detection (LOD) was 0.046 pg mL-1. The present sensor has a lower LOD with a wider linear range, which provides a new analytical assay for the early diagnosis of small-cell-type lung cancer labels.
Subject(s)
Antigens, Neoplasm , Biosensing Techniques , Disulfides , Electrochemical Techniques , Gold , Keratin-19 , Luminescent Measurements , Luminol , Molybdenum , Titanium , Keratin-19/blood , Keratin-19/immunology , Titanium/chemistry , Luminol/chemistry , Molybdenum/chemistry , Gold/chemistry , Antigens, Neoplasm/immunology , Electrochemical Techniques/methods , Humans , Biosensing Techniques/methods , Luminescent Measurements/methods , Immunoassay/methods , Disulfides/chemistry , Limit of Detection , Nickel/chemistry , Cobalt/chemistry , Metal Nanoparticles/chemistry , Antibodies, Immobilized/immunology , Antibodies, Immobilized/chemistryABSTRACT
The electrochemical nitrate reduction reaction (NO3-RR) is a novel green method for ammonia synthesis. However, the lack of sufficient catalysts has hindered the development of the NO3-RR. This research develops a transformation of porous CoP@N-C/CC into porous phosphorus-rich CoP4@N-C/CC through high-temperature calcination. Due to its unique phosphating-rich structure, CoP4@N-C/CC exhibits an excellent Faraday efficiency (FE: 92.3%) and NH3 yield (610.2 µmol h-1 cm-2). Such a catalyst with more P-P bonds can provide more active sites, effectively enhancing the adsorption and reaction processes of reactant molecules. In addition, the catalyst has good durability and catalytic stability, which provides a possibility for the future application of electrocatalytic ammonia production.
ABSTRACT
BACKGROUND: Photoelectrochemical (PEC) sensors have attracted much attention due to their low cost, simple instrumentation and high sensitivity. However, conventional PEC sensors require layer-by-layer modification of the photoelectrode surface, which has the disadvantages of being time-consuming and unstable. In addition, complex interfering substances in real samples may lead to false-positive or false-negative detection results. It was thought that the above drawbacks could be eliminated by the construction of a polarity inversion PEC sensor. In this work, a magnetically separated PEC sensor was constructed for the detection of Carcinoembryonic antigen (CEA). RESULTS: During the experiment, the construction of the sensor was used for sensitive detection of CEA. In the experimental process, Fe3O4@SiO2@CdS, a semiconductor material with magnetic properties, was chosen as the substrate material, and ZnO/CuO was used as the marker on the DNA2 molecule, and a split magnetic separation PEC sensor was constructed, which was used to realize the sensitive detection of CEA. Eventually, the detection range of the sensor for CEA detection is 1-10000 pg/mL, with the detection limit of 0.34 pg/mL. Additionally, the PEC sensor has the advantages of high speed, high efficiency, high sensitivity, good specificity, and high stability. The sensing platform constructed in this work can also be extended to detect other targets, which provides a new idea for PEC sensing platforms. SIGNIFICANCE: In this experiment, we developed a split PEC immunosensor based on magneto-optic nanostructure and photocurrent polarity switching strategy. Specifically, the proposed magnetic nanostructure Fe3O4@SiO2@CdS-DNA1 exhibits good paramagnetism and dispersion ability. By magnetic separation process, the PEC signals of opposite polarity can be obtained.
ABSTRACT
The incidence of esophageal cancer is positively associated with fumonisin contamination. It is necessary to develop methods for the rapid detection of fumonisins. In this work, a self-powered photoelectrochemical aptamer sensor based on ZnIn2S4/WO3 photoanode and Au@W-Co3O4 photocathode is proposed for the sensitive detection of fumonisin B1 (FB1). Among them, under visible light irradiation, the Z-type heterostructure of ZnIn2S4/WO3 acts as a photoanode to improve the electron transfer rate, which contributes to the enhancement of the photocathode signal and lays the foundation for a wider detection range. The Au@W-Co3O4 photocathode as a sensing interface reduces the probability of false positives (comparison of anode sensing platforms). The PEC sensor has a good working performance in the detection range (10 pg/mL-1000 ng/mL) with a detection limit of 2.7 pg/mL (S/N = 3). In addition, the sensor offers good selectivity, stability and excellent recoveries in real sample analysis. This work is expected to play a role in the field of analyzing environmental toxins.
Subject(s)
Aptamers, Nucleotide , Biosensing Techniques , Electrochemical Techniques , Fumonisins , Limit of Detection , Fumonisins/analysis , Fumonisins/chemistry , Aptamers, Nucleotide/chemistry , Tungsten/chemistry , Electrodes , Oxides/chemistry , Gold/chemistry , Humans , Light , Zinc/chemistryABSTRACT
The improvement of electrochemiluminescence (ECL) performance relies on the electron transfer efficiency between luminophore and coreactant. An ultrasensitive ECL micro-reactor with confinement-enhanced performance was prepared by using the covalent organic framework-LZU1-functionalized metal-organic framework (MOF@COF-LZU1) as a platform to assemble enormous N,N-dibutyl-2-hydroxyethylamine (DBAE) and tris(4,4'-dicarboxylic acid-2,2'-bipyridyl) ruthenium(II) [Ru(dcbpy)32+] into its pore channels. Compared to individual substances of γ-CD-MOF and COF-LZU1, the synergistic effects can conduce to the enhancement of the intensity, durability and sensitivity of the micro-reactor. Besides, COF-LZU1 can provide a mild environment to accommodate a certain amount of DBAE by concentrating them from the aqueous solution into its hydrophobic cavities and boost the oxidation efficiency of DBAE to generate more DBAEâ+ and profited the survival of DBAEâ, leading to an improved reaction efficiency with the Ru(dcbpy)32+ intermediate. Thanks to the confinement-enhanced strategy, engineered as high-functioning luminescent materials, Ru@γ-CD-MOF@COF-LZU1 micro-reactors decorated with Au NPs can facilitate electron transfer and capture primary antibodies (Ab1). Moreover, Au-Pd-Pt noble metal aerogels (NMAs) functionalized MoS2 NFs (Au-Pd-Pt NMAs@MoS2 NFs) were chosen as base material due to its large specific surface areas, high porosity, and excellent electrical conductivity. Based on above merits, the sensor demonstrated a sensitive response to CYFRA 21-1 detection in a linear concentration gradient from 10 fg/mL to 50 ng/mL with a detection limit of 0.0055 pg/mL (S/N = 3). The COF-LZU1 decorated ECL micro-reactors were constructed based on the signal amplification strategies to realize accurate CYFRA 21-1 detection.
ABSTRACT
Lead ions (Pb2+) are heavy metal ions that are harmful to living organisms and ecosystems. It is important to realize sensitive detection of Pb2+ in the environment. In this study, a signal enhancement photoelectrochemical (PEC) sensor with high sensitivity was constructed for the detection of Pb2+. Firstly, to obtain excellent electron transfer performance, sulfur defect-engineered Bi2S3-x/In2S3-y mediated signal enhancement formed by Bi2S3 and In2S3 with well-matched structure in terms of energy level as the substrate materials. In this case, the introduction of sulfur vacancies further affects the electronic structure of the material, which significantly improves the electrical conductivity and effectively increases the electron transfer rate. In addition, the as-synthesized Cu@Cu2O nanosphere is chosen as the marker to accelerate the electron transfer through the surface plasmon resonance effect of Cu. The constructed sensor was able to detect Pb2+ in the range of 1 ng mL-1-100 µg mL-1 with a limit of detection of 19.2 pg mL-1. The sensor exhibits good reproducibility, specificity, and stability, indicating such PEC sensor can achieve the sensitive detection of Pb2+ in the environment. This work paves a new way for the construction of PEC sensors and the specific PEC detection of Pb2+ in environmental waters.
ABSTRACT
The establishment of rapid target analysis methods for cytokeratin fragment antigen 21-1 (CYFRA 21-1) is urgently needed. [Ir(pbi)2(acac)] (pbi = 2-(4-bromophenyl)-1-hydrogen -benzimidazole, acac = acetylacetonate) as traditional electrochemiluminescence (ECL) luminophores has been confined due to its non-negligible dark toxicity and poor water solubility leading to poor biocompatibility and electrical conductivity as an organic molecule. Hence, to overcome this limitation, [Ir(pbi)2(acac)] can be effectively loaded on the polyvinyl alcohol hydrogel modified Ti3C2Tx MXene surface (Ir@Ti3C2Tx-PVA) as sensing platform which can emit high ECL signals. Then, a quenching strategy was proposed to fabricate an ECL sandwich immunosensor using H2O2 as quencher molecules which can generated by Pd@Au0.85Pd0.15. Especially, the generation of O2 to H2O2 can be achieved through a two-electron (2e-) reaction pathway by Pd@Au0.85Pd0.15, to overcome the restriction that the H2O2 was virtually impossible to label or immobilize on the non-enzyme nanomaterials. The proposed ECL assay achieves a response to CYFRA 21-1 within the range of 0.1 pg/mL-100 ng/mL, with a detection limit of 8.9 fg/mL (S/N = 3). This work provided a feasible tactic to seek superior-performance ECL luminophore and quencher consequently set up a novel means to makeup ultrasensitive ECL biosensor, which extended the utilization potential of Ir(pbi)2(acac) in ECL assays.
Subject(s)
Biosensing Techniques , Electrochemical Techniques , Gold , Hydrogen Peroxide , Keratin-19 , Luminescent Measurements , Palladium , Polyvinyl Alcohol , Hydrogen Peroxide/chemistry , Hydrogen Peroxide/analysis , Electrochemical Techniques/methods , Palladium/chemistry , Catalysis , Biosensing Techniques/methods , Polyvinyl Alcohol/chemistry , Gold/chemistry , Humans , Luminescent Measurements/methods , Keratin-19/analysis , Immunoassay/methods , Antigens, Neoplasm/analysis , Antigens, Neoplasm/immunology , Titanium/chemistry , Limit of Detection , Iridium/chemistry , Metal Nanoparticles/chemistryABSTRACT
Mercury ion (Hg2+) poses a serious threat to human health due to its high toxicity. In this study, a smartphone-based photoelectrochemical sensor based on oxygen vacancies (OVs) driven signal enhancement for mercury ion detection was designed. BiVO4-x/Bi2S3/AuNPs were combined with T-Hg2+-T recognition mode to construct a multi-sandwich photoelectrochemical sensor. On the one hand, the OVs can increase the adsorption of light by the materials and enhance the photocurrent response as well as the superconductivity of Au NPs to accelerate the charge transfer at the electrode interface. On the other hand, the multi-sandwich structure was exploited to increase the binding site of Hg2+, as well as the T-Hg2+-T structure for sensitive recognition of Hg2+ and signal amplification. The sensor showed good linearity for Hg2+ concentration in the range of 0.1 nM-1.0 µM with a detection limit of 4.8 pM (S/N = 3). Eventually the smartphone-based real-time detection sensor is expected to contribute to the future analysis of heavy metal ions.
ABSTRACT
Lead ion (Pb2+) is one of the heavy metal contaminants within the environment, which can seriously affect biological health. Thus, it is very important to detect lead ions, especially exceeding the standard concentration (100 ng/mL). In this work, we have developed a photoelectrochemical (PEC) aptamer sensor with Z-scheme Fe2O3/g-C3N4 heterojunction as a substrate material for sensitive detection of Pb2+. Specifically, Fe2O3/g-C3N4 is employed as a substrate with a powerful and stable photocurrent response. Au and DNA-1 connected to the substrate material via the Au-S bond and increased the electron conduction. Marking DNA-2 with ZnO effectively reduced the light absorption intensity resulting in a lower photocurrent response. Surprisingly, the Pb2+ PEC sensor showed good linearity in the detection range of 62 pg/mL to 1 µg/mL with a detection limit as low as 7.9 pg/mL (S/N = 3). The sensor showed stable recovery and low relative standard deviation in real sample detection. Additionally, the sensor exhibited excellent stability, selectivity, and reproducibility. The reproducibility of the electrodes was evaluated, and the accuracy of the individual electrode current values was calculated to range from 0.5% to 2.71% with an RSD of 1.74%. Such PEC sensor guarantees to supply a brand-new approach to the detection of Pb2+.
ABSTRACT
BACKGROUND: Gut homeostasis, including intestinal immunity and microbiome, is essential for cognitive function via the gut-brain axis. This axis is altered in high-fat diet (HFD)-induced cognitive impairment and is closely associated with neurodegenerative diseases. Dimethyl itaconate (DI) is an itaconate derivative and has recently attracted extensive interest due to its anti-inflammatory effect. This study investigated whether intraperitoneal administration of DI improves the gut-brain axis and prevents cognitive deficits in HF diet-fed mice. RESULTS: DI effectively attenuated HFD-induced cognitive decline in behavioral tests of object location, novel object recognition, and nesting building, concurrent with the improvement of hippocampal RNA transcription profiles of genes associated with cognition and synaptic plasticity. In agreement, DI reduced the damage of synaptic ultrastructure and deficit of proteins (BDNF, SYN, and PSD95), the microglial activation, and neuroinflammation in the HFD-fed mice. In the colon, DI significantly lowered macrophage infiltration and the expression of pro-inflammatory cytokines (TNF-α, IL-1ß, IL-6) in mice on the HF diet, while upregulating the expression of immune homeostasis-related cytokines (IL-22, IL-23) and antimicrobial peptide Reg3γ. Moreover, DI alleviated HFD-induced gut barrier impairments, including elevation of colonic mucus thickness and expression of tight junction proteins (zonula occludens-1, occludin). Notably, HFD-induced microbiome alteration was improved by DI supplementation, characterized by the increase of propionate- and butyrate-producing bacteria. Correspondingly, DI increased the levels of propionate and butyrate in the serum of HFD mice. Intriguingly, fecal microbiome transplantation from DI-treated HF mice facilitated cognitive variables compared with HF mice, including higher cognitive indexes in behavior tests and optimization of hippocampal synaptic ultrastructure. These results highlight the gut microbiota is necessary for the effects of DI in improving cognitive impairment. CONCLUSIONS: The present study provides the first evidence that DI improves cognition and brain function with significant beneficial effects via the gut-brain axis, suggesting that DI may serve as a novel drug for treating obesity-associated neurodegenerative diseases. Video Abstract.