LAMP-visualized photofuel cell self-powered dual-mode sensing platform for detection of transmissible gastroenteritis virus.

The detection of transmissible gastroenteritis virus (TGEV) is of great significance to reduce the loss of pig industry. A LAMP-visualization/PFC self-powered dual-mode output sensor platform was constructed to detect TGEV by combining a simple and intuitive photoelectrochromic material with a highly sensitive PFC self-powered sensing platform without external power supply. The PFC sensing substrate was constructed using CdS nanoparticles modified ZnO NRs (CdS/ZnO NRs) as the photoanode, which exhibited high photoactivity, and Prussian blue (PB) as the cathode. After LAMP reaction on the optical anode, visual signals caused by PB discolorimetry can be detected semi-quantitatively, or PFC power density electrical signals collected by electrochemical workstation can be used. The output power density value is logarithm of TGEV concentration. The linear relationship was good within the detection range of 0.075 fg/µL-7.5 ng/µL, with a detection limit of 0.025 fg/µL (S/N = 3). This multi-signal output sensing platform provides more choices for quantifying TGEV detection results, and the two methods can be mutually verified, which meets the needs of different scenarios and improves the reliability of detection. It has a good effect in the actual sample detection, without the use of expensive and complex instruments, and has a broad application prospect.

Highly selective detection and removal of mercury ions in the aquatic environment based on magnetic ZIF-71 multifunctional composites with sufficient chlorine functional groups.

The development of both detection and removal technologies for heavy metal ions is of great importance. Most of the existing adsorbents that contain oxygen, nitrogen or sulfur functional groups can remove heavy metals, but achieving both selective detection and removal of a single metal ion is difficult because they bind to a wide range of heavy metal ions. Herein, we selected zeolite imidazolium hydrochloride framework-71 (ZIF-71) with sufficient chlorine functional groups to fabricate magnetic ZIF-71 multifunctional composites (M-ZIF-71). M-ZIF-71 had a large specific surface area, excellent water stability, and good magnetic properties, which made M-ZIF-71 conducive to the separation and recovery of adsorbents and the assembly of electrodes. M-ZIF-71 exhibited high selectivity, wide linear range (1-500 µg/L), and low detection limit (0.32 µg/L) for electrochemical detection of mercury ions (Hg2+). Meanwhile, M-ZIF-71 demonstrated rapid Hg2+ adsorption with a high capacity of 571.2 mg/g and excellent recyclability. The high selectivity for Hg2+ was attributed to the powerful affinity of highly electronegative chlorine and Hg2+. Moreover, XPS spectra demonstrated the interaction between chlorine and Hg2+. This work provides a new inspiration for applications in the targeted monitoring and removal of heavy metal pollution.

Photochromic visual sensing chip for isothermal amplification detection of porcine transmissible gastroenteritis virus.

The outbreak of transmissible gastroenteritis virus (TGEV) will cause huge economic losses to the whole pig industry. Hence, there is urgent need to develop a rapid and ultrasensitive method for detection of TGEV. As a nucleic acid detection technique, loop-mediated isothermal amplification (LAMP) can achieve quantitative detection of targeted nucleic acids with high sensitivity and selectivity. Nevertheless, the signal outputs of LAMP method must be acquired by complicated instruments. In this work, we firstly developed a LAMP photochromic sensing chip for porcine TGEV detection by combination of the photochromic sensing chip and nucleic acid amplification. The detection signal was based on color change of electrochromic material rather than electrical signal, and thus the detection signal can be obtained by visualization without relying on complicated instrument. The entire test was performed with small fluorinated indium tin oxide electrodes modified with zinc oxide (ZnO) (a photocatalytic material) and Prussian blue (PB) (an electrochromic material). When photoinduced electrons produced by ZnO were injected into PB under light, the PB was reduced to Prussian white. The higher the concentration of TGEV, the more double-stranded DNA was produced after amplification. The amplified product produced greater impedance, and fewer electron was transferred, which affect the corresponding color change of PB. The sensing chip also showed highly sensitive response to TGEV, with the minimum limit of detection was determined to be 2.5 fg/µL. The sensing chip developed herein will provide a new avenue for DNA amplification detection by visualization.

Ultra-sensitive photoelectrochemical biosensor for determination of African swine fever virus based on surface plasmon resonance.

Sensitive and specific detection of African swine fever virus (ASFV) is crucial for agricultural production and economic development due to the mortality and infectivity. In this study, a bismuth induced enhanced photoelectrochemical (PEC) biosensor based on in-situ loop mediated isothermal amplification (LAMP) was constructed using deposited bismuth nanoparticles loaded bismuth oxycarbonate (Bi/(BiO)2CO3) as photoactive material, using primers designed according to LAMP as recognition elements, and using in-situ LAMP to achieve nucleic acid amplification of target genes. As the Bi induced surface plasmon resonance (SPR) effect, enhanced light captures and effective electron hole separation, it could effectively enhance the photoelectric activity, so the prepared Bi/(BiO)2CO3 nanohybrid had higher photocurrent intensity and good stability. The constructed PEC biosensor has realized the detection of ASFV in real samples with good sensitivity, specificity and repeatability. In the range from 1.0 × 10-13 to 1.0 × 10-7 g/L, the photoelectric current decreased with the increase of the concentration of ASFV, and the detection limit was 3.0 × 10-14 g/L (about 0.048 copies/µL). Combining the advantages of LAMP with the excellent performance of PEC, it provides a simple, economical and efficient method for nucleic acid diagnosis, and also provides a new idea for biosensor detection.

Accurate and ultrasensitive detection for PEDV based on photoelectrochemical sensing coupling loop-mediated isothermal amplification.

Porcine epidemic diarrhea (PED) is a serious disease requiring a simple and accurate detection method. Accordingly, this study developed a novel, ultrasensitive photoelectrochemical (PEC) sensing platform using the loop-mediated isothermal amplification (LAMP) technique (LAMP-PEC). An amino (-NH2)-modified LAMP product is obtained by amplification of the PED virus gene with specially designed primers. The generated NH2-modified LAMP product is assembled on the surface of an electrode by forming imine linkages between aldehyde and amino groups based on the Schiff base reaction. A stable photocurrent is provided by a CdIn2S4 photoactive material, which possesses high photoelectric conversion efficiency. Amplified DNA assembled on the electrode surface increases steric hindrance and hinders electrons from moving from the electrode to electron acceptors, which decreases the photocurrent. This strategy can detect PEDV with a low detection limit of 0.3 fg µL-1 and a wide linear range of 1 × 10-3-1 × 102 pg/µL. The sensing platform has excellent specificity and sensitivity and can be used for the quantitative detection of many other pathogens with the assistance of LAMP.

A membrane/mediator-free high-power density dual-photoelectrode PFC aptasensor for lincomycin detection in milk and chicken.

Over use of lincomycin (LIN) as antibiotic in animals can lead to multiple harmful impacts to public health, thus detection of LIN at trace level in milk and chicken sample matrixes is vital. In this work, Zinc phthalocyanine nanoparticles sensitized MoS2 (ZnPc/MoS2) was firstly developed as a novel photocathode material combined with nitrogen-doped graphene-loaded TiO2 nanoparticles (TiO2/NG) as photoanode material to construct a dual-photoelectrode photofuel cell (PFC). The as-prepared membrane/mediator-free PFC achieved excellent output performance that the maximum power density (Pmax) reached 11.83 µW cm-2. Specific aptamers are adopted as LIN recognition elements, the as-proposed self-powered aptasensor for LIN exhibited a linear scope in 10-11 -10-5 mol L-1 along with a low detection limit (3S/N) of 3.33 pmol L-1. Consequently, such high-power density dual-photoelectrode PFC aptasensor may be a reassuring candidate electrochemical sensor for the detection of trace contamination in food samples.

Sensitive and stable detection of deoxynivalenol based on electrochemiluminescence aptasensor enhanced by 0D/2D homojunction effect in food analysis.

Sensitive detection for deoxynivalenol (DON) should be developed due to DON as a kind of harmful mycotoxins which can poses health risk to human health even at low concentrations. In this work, an electrochemiluminescence (ECL) DON aptasensor was proposed based on Ti3C2 dots/Ti3C2 nanosheet (TDTN). Compared with Ti3C2 dots and Ti3C2 nanosheet, the ECL intensity of TDTN was 4 times of Ti3C2 dots and 2 times of Ti3C2 nanosheet as emitters. This was attributed to homojunction effect which could provide continuity of band bonding and effectively accelerate charge transfer at the interface. Based on ECL signal changes generated by aptamer and DON fixed on the electrode surface, the ECL aptasensor showed "on-off-on" performances and detected DON specifically in milk, with detection range of 0.001-20 ng/mL and detection limit of 0.3 pg/mL (S/N = 3). Therefore, the constructed ECL aptasensor is a promising detection method for food safety analysis.

Enhanced cathodic electrochemiluminescent microcystin-LR aptasensor based on surface plasmon resonance of Bi nanoparticles.

Sensitive testing for Microcystins-LR (MC-LR) is needed because of its serious environmental and human health hazards. In this work, a new type of surface plasmon resonance (SPR) enhanced cathodic electrochemiluminescence (ECL) aptasensing platform was designed in which boron and nitrogen co-doped graphene quantum dots (BN-GQDs) were used as the luminary and bismuth nanoparticles (Bi NPs) were used as the SPR source. SPR effect of non-precious metal Bi NPs can induce and enhance ECL signal of BN-GQDs because the fluorescence spectrum of BN-GQDs overlaps well with the ultraviolet-visible absorption spectrum of Bi NPs. On this basis, a sensitive sensing system based on the Bi NPs and BN-GQDs was established for MC-LR detection. The results showed that the ECL sensing signal obtained was linear with the negative logarithm of the target MC-LR concentration in the range of 0.01-5000 pM, and the detection limit was 0.003 pM. In addition, the sensor had high stability and good reproducibility, which can be applied to the detection of MC-LR in actual samples. The method had good specificity and can not be disturbed by its homolog, which can be used for sensitive and reliable detection of complex samples.

Ultrasensitive photoelectrochemical aptasensor for carbendazim detection based on in-situ constructing Schottky junction via photoreducing Pd nanoparticles onto CdS microsphere.

Carbendazim (CBZ) has been widely used in agricultural production to control fruits and vegetables diseases, but it can also destroy the human endocrine system. Therefore, sensitive detection of CBZ has attracted increasing attention worldwide. In this study, Pd nanoparticles (Pd NPs) decorated on CdS microsphere (Pd NPs/CdS) was prepared by the in-situ photoreduced method, and based on the surface plasmon resonance (SPR) effect of noble metal and Schottky junction between Pd nanoparticles (Pd NPs) and CdS microsphere, the photocurrent after introducing Pd NPs is 7.7 times higher than that of bare CdS microsphere. In view of the outstanding photoelectrochemical (PEC) performance of Pd NPs/CdS and the high specificity of the aptamer, the as-fabricated PEC aptasensor for CBZ detection possesses the excellent detection performance including a broad linear ranging from 1.0 × 10-12 to 1.0 × 10-6 mol/L as a low detection limit of 3.3 × 10-13 mol/L (S/N = 3). Furthermore, the PEC aptasensor was used for determination of lettuce samples from actual agricultural products with satisfactory results.

Catalysis-induced performance enhancement of an electrochemical microcystin-LR aptasensor based on cobalt-based oxide on a B, N co-doped graphene hydrogel.

Microcystin detection is of great significance and an urgent need because of its damage to water environments and human health. In this paper, an electrochemical aptasensor was developed by combining a 3D cobalt-based oxide modified boron and nitrogen co-doped graphene hydrogel (3D BNG/Co) with a DNA aptamer for sensitive detection of microcystin (MC-LR) through differential pulse voltammetry (DPV) technology. By using 3D BNG/Co as a catalyst and [Fe(CN)6]3-/4- as a redox probe, the catalytic current signal was 3.8 times higher than that of the bare glassy carbon electrode, which can better monitor the electron conduction on the electrode surface and then improve the sensitivity. The as-fabricated electrochemical aptasensor displayed a wide detection range (0.1-1000 pmol L-1), low detection limit (0.03 pmol L-1), good sensitivity, and repeatability, which has potential applications for the protection of the ecological environment and human health.

Visible light-driven photoelectrochemical ampicillin aptasensor based on an artificial Z-scheme constructed from Ru(bpy)32+-sensitized BiOI microspheres.

Dye sensitization is an alternative strategy to improve photoelectric activity of semiconductors and, particularly, to enhance the activity towards visible light domain. Herein, an artificial Z-scheme bipyridine ruthenium (Ru(bpy)32+) sensitizing narrow-gap bismuth oxy-iodide (BiOI) microspheres was constructed by a simple electrostatic interaction strategy for the first time. The electrochemical impedance spectroscopy (EIS) and photoluminescence (PL) analysis showed that this design of such Z-scheme structure was helpful to enhance the interfacial charge transfer and improve the photoelectric conversion efficiency. In addition, due to the sensitization of Ru(bpy)32+, the band gap was narrowed from 1.8 eV of BiOI microspheres to 1.3 eV of BiOI/Ru(bpy)32+ microspheres, leading to improve the utilization of visible light. So that, the photocurrent of the resulted BiOI/Ru(bpy)32+ was 13.0 times that of pure BiOI microspheres. In view of the outstanding photoelectrochemical (PEC) performance of BiOI/Ru(bpy)32+ and the high specificity of the aptamer, the PEC aptasensor for ampicillin (AMP) merits the excellent detection performance including a broad linear ranging from 1 × 10-7 nM to 100 nM as well as a low detection limit of 3.3 × 10-8 nM (S/N = 3). This work not only provides a novel way to construct and design highly efficient photoactive materials for PEC detection, but also broadens the application of Z-scheme in the field of sensing.