On-site Analysis Research Articles

Programming of a Portable Digital Monitoring System-Integrated DNA Aptamer Reversely Regulated Oxidase-Like Nanozyme for Real-Time Dynamic Analysis of Atmospheric Perfluorooctanoic Acid.

Timely and efficient analysis of the fluorinated per- and polyfluoroalkyl substances (PFAS) in an atmospheric environment is critical to environmental pollution traceability, early warnings, and governance. Here, a portable, reliable, and intelligent digital monitoring device for onsite real-time dynamic analysis of atmospheric perfluorooctanoic acid (PFOA) is proposed. The sensing mechanism is attributed to the oxidase-like activity of PtCoNPs@g-C3N4 that is reversely regulated by the surface modification of a PFOA-recognizable DNA aptamer, engineering a PFOA-activated oxidase-like activity of nanozyme (Apt-PtCoNPs@g-C3N4) to combine the nonfluorescence o-phenylenediamine (OPD) as the dual-modality response system. The present PFOA interacts with its DNA aptamer and dissociates from the surface of Apt-PtCoNPs@g-C3N4, restoring the oxidase-like activity of PtCoNPs@g-C3N4 to oxidize OPD into yellow fluorescence 2,3-diphenylaniline (DAP), thereby observing a PFOA-triggered colorimetric as well as fluorescence dual-modality change. Then, a hydrogel kit-programmed Apt-PtCoNPs@g-C3N4 + OPD system is used as the sensitive element to incorporate into this homemade portable device, automatically gathering and processing the PFOA-triggered hydrogel colorimetric and fluorescence image gray values by our self-weaving software, ultimately realizing the onsite real-time dynamic analysis of atmospheric PFOA surrounding a fluorochemical production plant. This work provides a direction and theoretical foundation for designing portable onsite screening devices that cater to other atmospheric contaminants detection requirements.

A rapid on-site loop-mediated isothermal amplification technology as an early warning system for the detection of Shiga toxin-producing Escherichia coli in water.

Shiga toxin-producing Escherichia coli (STEC) is an important waterborne pathogen capable of causing serious gastrointestinal infections with potentially fatal complications, including haemolytic-uremic syndrome. All STEC serogroups harbour genes that encode at least one Shiga toxin (stx1 and/or stx2), which constitute the primary virulence factors of STEC. Loop-mediated isothermal amplification (LAMP) enables rapid real-time pathogen detection with a high degree of specificity and sensitivity. The aim of this study was to develop and validate an on-site portable diagnostics workstation employing LAMP technology to permit rapid real-time STEC detection in environmental water samples. Water samples (n=28) were collected from groundwater wells (n=13), rivers (n=12), a turlough (n=2) and an agricultural drain (n=1) from the Corrib catchment in Galway. Water samples (100 ml) were passed through a 0.22 µm filter, and buffer was added to elute captured cells. Following filtration, eluates were tested directly using LAMP assays targeting stx1, stx2 and E. coli phoA genes. The portable diagnostics workstation was used in field studies to demonstrate the on-site testing capabilities of the instrument. Real-time PCR assays targeting stx1 and stx2 genes were used to confirm the results. The limit of detection for stx1, stx2 and phoA LAMP assays were 2, 2 and 6 copies, respectively. Overall, stx1, stx2 and phoA genes were detected by LAMP in 15/28 (53.6 %), 9/28 (32.2 %) and 24/28 (85.7 %) samples, respectively. For confirmation, the LAMP results for stx1 and stx2 correlated perfectly (100 %) with those obtained using PCR. The portable diagnostics workstation exhibited high sensitivity throughout the on-site operation, and the average time from sample collection to final result was 40 min. We describe a simple, transferable and efficient diagnostic technology for on-site molecular analysis of various water sources. This method allows on-site testing of drinking water, enabling evidence-based decision-making by public health and water management authorities.

A smartphone-based approach for comprehensive soil microbiome profiling.

The soil microbiome is crucial for nutrient cycling, health, and plant growth. This study presents a smartphone-based approach as a low-cost and portable alternative to traditional methods for classifying bacterial species and characterizing microbial communities in soil samples. By harnessing bacterial autofluorescence detection and machine learning algorithms, the platform achieved an average accuracy of 88% in distinguishing common soil-related bacterial species despite the lack of biomarkers, nucleic acid amplification, or gene sequencing. Furthermore, it successfully identified dominant species within various bacterial mixtures with an accuracy of 76% and three-level soil health identification at an accuracy of 80%-82%, providing insights into microbial community dynamics. The influence of other soil conditions (pH and moisture) was relatively minor, showcasing the platform's robustness. Various field soil samples were also tested with this platform at 80% accuracy compared with the laboratory analyses, demonstrating the practicality and usability of this approach for on-site soil analysis. This study highlights the potential of the smartphone-based system as a valuable tool for soil assessment, microbial monitoring, and environmental management.

An evaluation of a new rapid qPCR test for the detection of 2019-novel coronavirus nucleocapsid (N1) gene in wastewater in Roanoke and Salem VA sewersheds.

The COVID-19 pandemic initiated public interest in wastewater-based epidemiology (WBE). Public and private entities responded to the need to produce timely and accurate data. LuminUltra and Hach partnered to provide a rapid, field-based quantitative polymerase chain reaction (qPCR) test for detecting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in wastewater. This study evaluates the Hach GeneCount SARS-CoV-2 Wastewater RT-qPCR Assay Kit and LuminUltra GeneCount® Q-16 RT-PCR instrument. The Hach LuminUltra methods were compared to the Promega Wizard® Enviro Total Nucleic Acid kit and Bio-Rad CFX Opus 96 Real-time PCR Detection System. Over a 12-week period, wastewater samples were collected weekly from seven locations in the Roanoke/Salem, VA sewersheds. Concentration and extraction of the viral RNA were followed by qPCR analysis. The target gene for detection was the nucleocapsid gene (N1) of the SARS-CoV-2 virus. Costs, ease of use, time to produce results, sample preparation, and data comparisons were considered. The comparison determined that the Hach LuminUltra method and instrument were more affordable, consumed less time, and required less technical expertise. While the new method was specific, it had low sensitivity. This evaluation suggests the Hach LuminUltra method should be reserved for limited situations requiring onsite field analysis where data accuracy is not essential.

A novel colorimetric sensor through peroxymonosulfate activated by CoFe@CN nanozymes for on-site resorcinol detection

The presence of resorcinol (RS) in water contaminated with pollutants may engender environmental and ecosystem risks. In this study, we developed rapid and efficient colorimetric methods for the on-site quantitative determination of RS. Specifically, a synthetic nanozyme composed of nitrogen-doped carbon-coated cobalt-iron (CoFe@CN) was utilized to initiate the oxidation reaction of 3,3′,5,5′-tetramethylbenzidine (TMB) with the activator of peroxymonosulfate (PMS). Compared to the activator of hydrogen peroxide (H2O2), PMS demonstrated a sixfold enhancement in catalytic efficacy, markedly elevating the detection performance. Density Functional Theory calculations indicate that RS can serve as a reducing agent for oxTMB, confirming the theoretical feasibility of this process. A linear relationship between inhibition rate (IR %) of RS concentration and absorbance was established and the colorimetric analysis revealed a linear relationship between RS concentration and gray scale values over the range of 0–45 μM, with a detection limit of 3.39 μM. Furthermore, smartphone-based analysis of color images allows for on-site quantitative analysis of RS concentration, leveraging portability and real-time detection capabilities. This study provides pioneering analytical support for on-site water quality monitoring within the ecological environment.

Highly fluorescent CdTe/ZnSe quantum dot-based “turn-off” sensor for the on-site rapid detection of Lead ions in aqueous medium

Lead (Pb) is a heavy metal known for its adverse effects on both human health and the environment. In recent years, the industrial utilization of Pb2+ has surged, underscoring the imperative need for efficient measurement methods. In this study, a rapid and simple photochemical method was used to synthesize thioglycolic acid (TGA)-stabilized CdTe/ZnSe core-shell quantum dots (QDs). These CdTe/ZnSe QDs emit vibrant green fluorescence and exhibit remarkable quenching in the presence of Pb2+ ions. This property enables the development of an on-site on/off sensor without the necessity of additional modifications. The proposed sensor possesses an outstanding sensitivity to Pb2+, with a detection limit and linear range of 31.8 nM and 50 nM–10 µM, respectively. Importantly, the selectivity of this fluorescence-based sensor was validated by analyzing various positively and negatively charged ions. Furthermore, the developed sensor showed reliable performance against real river, agricultural, and tap water, as confirmed by Inductively Coupled Plasma (ICP) analysis. Additionally, CdTe/ZnSe QDs immobilized on glass slides were successfully employed for on-site water sample analysis, providing a versatile solution for environmental monitoring.

A new strategy for volatile organics detection – Molecularly imprinted polymers-enabled headspace extracting and electrochemical sensing

The widely accepted method for detecting trace odor compounds such as 2-methylisoborneol (2-MIB) requires high-cost solid-phase microextraction coupled with gas chromatography-tandem mass spectrometry (SPME-GC/MS). As for now, cases that directly used SPME-GC/MS in the field are unseen, and most detection activities are still carried out in rigorous laboratory conditions. However, lengthy logistics and storage issues can compromise sample conditions, underscoring the significance of on-site detection methods. Here, we reported molecularly imprinted polymers-enabled headspace extracting and electrochemical sensing (MHEES) with the core feature of using the same piece of MIP for both headspace extracting and electrochemical sensing, allowing rapid on-site detection of trace 2-MIB in natural water bodies with a total cost of less than $2.10 per test. MHEES demonstrated exceptional sensitivity during extensively repeated laboratory experiments, achieving a detection limit of 3.7 ng∙L−1 and a standard deviation of 4.58 %. The practicality of MHEES was confirmed by conducting two rounds of on-site analyses on different reservoirs with fluctuating seasonal concentrations of 2-MIB. The developing flow of MHEES, from molecules docking to on-site application, was rigorous and could be cross-referenced to related research. The proposed MHEES design can potentially revolutionize the field of analytical chemistry by providing a versatile and affordable platform for on-site volatile compounds detection. It can readily adapt to various organic compounds and effectively address real-world challenges such as monitoring emerging pollutants, tracing disease biomarkers in body fluids, inspecting food safety, identifying chemical reaction intermediates, and supporting healthcare applications.

Entertainment type robots based on machine learning and game teaching mode applied in dance action planning of art teaching

We studied the use of machine learning models for training dance action models, collected dance action data, annotated and classified it, and established a training set for dance action models. We trained the training set to learn the feature representation and pattern recognition capabilities of dance actions. Through training and tuning the model, a model that can accurately recognize and generate dance movements was obtained. Evaluate the similarity between two dance movements and select the appropriate dance movements to form a smooth dance sequence. A planning algorithm was designed based on the kinematic and dynamic characteristics of robots to generate dance action paths suitable for the robot’s body conditions. Considering factors such as joint limitations, body stability, and smooth movement of the robot, generate a reasonable dance motion path while ensuring safety. Through on-site testing and data analysis of the system, it has been verified that it can effectively generate diverse and expressive dance movements, bringing a unique viewing experience to entertainment venues.

Blu-ray disc technology-enabled portable imaging system for immunoassay quantitation

In this work, we have developed a portable laser scanning imaging system derived from Blu-ray disc technology for high-throughput biochip and sensor array characterization. This portable imaging system was constructed by adapting a standard Blu-ray drive to perform the scanning or imaging of an entire disc or interested regions. In addition, we have compiled a complete operating software program to process the raw data, generate the assay image, and perform quantitative analysis. Furthermore, the developed BD-LSI system was successfully applied to the quantitative detection of Anti-Müllerian hormone (AMH), which is an important biomarker of reproductive potential, in standard physiological buffers and serum samples. The achieved detection limit is as low as 18 pg/mL with a dynamic range of up to 25 ng/mL, which meets the needs of clinical diagnosis. As validated by comparing with the Clinical Laboratory Improvement Amendments (CLIA) data on the same set of samples, the consistent results confirm that this BD-LSI system holds promise for multiplex on-site quantitative analysis at community clinics and even at home settings for self-monitoring of individual health.

Technology in Forensic Sciences: Innovation and Precision

The advancement of technology and its developments have provided the forensic sciences with many cutting-edge tools, devices, and applications, allowing forensics a better and more accurate understanding of the crime scene, a better and optimal acquisition of data and information, and faster processing, allowing more reliable conclusions to be obtained and substantially improving the scientific investigation of crime. This article describes the technological advances, their impacts, and the challenges faced by forensic specialists in using and implementing these technologies as tools to strengthen their field and laboratory investigations. The systematic review of the scientific literature used the PRISMA® methodology, analyzing documents from databases such as SCOPUS, Web of Science, Taylor & Francis, PubMed, and ProQuest. Studies were selected using a Cohen Kappa coefficient of 0.463. In total, 63 reference articles were selected. The impact of technology on investigations by forensic science experts presents great benefits, such as a greater possibility of digitizing the crime scene, allowing remote analysis through extended reality technologies, improvements in the accuracy and identification of biometric characteristics, portable equipment for on-site analysis, and Internet of things devices that use artificial intelligence and machine learning techniques. These alternatives improve forensic investigations without diminishing the investigator’s prominence and responsibility in the resolution of cases.

Microsyringe-assisted visual volume detection based on phase separation: the case of chymosin milk-clotting activity study.

The constantly diverse demand scenarios for rapid on-site analysis have put forward high requirements for developing low-cost and user-friendly visual detection methods. Therefore, developing a visual detection method with simple operation and intuitive results has important practical value in the field of analysis and detection, but it is also challenging. In this work, we propose a microsyringe-assisted visual volume detection method based on phase separation, and apply it to analyze the milk-clotting activity of chymosin. Chymosin can cause phase separation of milk with whey in the mobile phase and curd in the gel state. The network structures of casein in curd can trap water molecules, resulting in separation of whey from curd gradually. Therefore, the analysis of chymosin milk-clotting activity can be realized according to the volume of whey measured using a portable microsyringe. This method shows a good linear correlation when the concentration of chymosin ranges from 1.02 U L-1 to 1020 U L-1 and the limit of detection of this method for chymosin is calculated to be 0.03 U mL-1. This work successfully realizes the visual analysis of chymosin milk-clotting activity based on the enzyme-triggered phase separation. It also shows great promise to be applied in other phase separation-based detection systems with the advantages of high accuracy, great portability and user-friendliness.

Rapid differentiation of cystic fibrosis-related bacteria via reagentless atmospheric pressure photoionisation mass spectrometry

Breath analysis is an area of significant interest in medical research as it allows for non-invasive sampling with exceptional potential for disease monitoring and diagnosis. Volatile organic compounds (VOCs) found in breath can offer critical insight into a person’s lifestyle and/or disease/health state. To this end, the development of a rapid, sensitive, cost-effective and potentially portable method for the detection of key compounds in breath would mark a significant advancement. Herein, we have designed, built and tested a novel reagent-less atmospheric pressure photoionisation (APPI) source, coupled with mass spectrometry (MS), utilising a bespoke bias electrode within a custom 3D printed sampling chamber for direct analysis of VOCs. Optimal APPI-MS conditions were identified, including bias voltage, cone voltage and vaporisation temperature. Calibration curves were produced for ethanol, acetone, 2-butanone, ethyl acetate and eucalyptol, yielding R2 > 0.99 and limits of detection < 10 pg. As a pre-clinical proof of concept, this method was applied to bacterial headspace samples of Escherichia coli (EC), Pseudomonas aeruginosa (PSA) and Staphylococcus aureus (SA) collected in 1 L Tedlar bags. In particular, PSA and SA are commonly associated with lung infection in cystic fibrosis patients. The headspace samples were classified using principal component analysis with 86.9% of the total variance across the first three components and yielding 100% classification in a blind-sample study. All experiments conducted with the novel APPI arrangement were carried out directly in real-time with low-resolution MS, which opens up exciting possibilities in the future for on-site (e.g., in the clinic) analysis with a portable system.

Engineering the nanozyme hydrogel beads by polyvinyl alcohol/chitosan encapsulation with recyclable and sustainable catalytic activity for visual analysis of hydrogen peroxide

BackgroundHydrogen peroxide (H2O2) plays a vital role in human health and have been regarded as a crucial analyte in metabolic processes, redox transformations, foods research and medical fields. Especially, the long-time and excessive digestion of H2O2 may even cause severe diseases. Although conventional instrumental methods and nanozymes-based colorimetric methods have been developed to accomplish the quantitative analysis of H2O2, the drawbacks of instrument dependence, cost-effectiveness, short lifespan, non-portable and unsustainable detection efficacies will limit their applications in different detection scenarios. ResultsHerein, to address these challenges, we have proposed a novel strategy for nanozyme (RuO2) hydrogel preparation by the solid support from cross-linked polyvinyl alcohol (PVA) and chitosan (CS) to both inherit the dominant peroxidase-like (POD) activity and protect the RuO2 from losing efficacies. Taking advantages from the hydrogel, the encapsulated RuO2 were further prepared as the regularly spherical beads (PCRO) to exhibit the sustainable, recyclable, and robust catalysis. Moreover, the intrinsic color interferences which originated from RuO2 can be avoided by the encapsulation strategy to promote the detection accuracy. Meanwhile, the high mechanical strength of PCRO shows the high stability, reproducibility, and cyclic catalysis to achieve the recyclable detection performance and long lifetime storage (40 days), which enables the sensitively detection of H2O2 with the detection limit as lower to 15 μM and the wide detection linear range from 0.025 to 1.0 mM. SignificanceOn the basis of the unique properties, PCRO has been further adopted to construct a smartphone detection platform to realize the instrument-free and visual analysis of H2O2 in multi-types of milk and real water samples through capturing, processing, and analyzing the RGB values from the colorimetric photographs. Therefore, PCRO with the advanced detection efficacies holds the great potential in achieving the portable and on-site analysis of targets-of-interest.

A paper-based lateral flow immunochromatographic sensor for the detection of tricyclazole in rice

Tricyclazole is commonly used to prevent rice blast to meet the carbohydrate intake needs of half of the global population, and a large number of toxicological reports indicate that monitoring of tricyclazole is necessary. Here, we analyzed the structure of tricyclazole and designed different hapten derivatization strategies to prepare a high-performance monoclonal antibody (half inhibition concentration of 1.61 ng/mL), and then a lateral flow immunochromatographic sensor based on gold nanoparticles for the detection of tricyclazole in rice, with a limit of detection of 6.74 μg/kg and 13.58 μg/kg in polished and brown rice, respectively. The recoveries in rice were in the range of 84.6–107.4%, no complex pretreatment was required for comparison with LC-MS/MS, and the comparative analysis demonstrated that our method had good accuracy and precision. Therefore, the developed lateral flow immunochromatographic analysis was a reliable and rapid means for the on-site analysis of tricyclazole in rice.

Bottle-in-bottle reaction device: Portable gas pressure meter for rapid and on-site analysis of oxalate in spinach and tea beverages

A gas pressure meter-based portable/miniaturized analytical kit was established for rapid and on-site detection of oxalate. Potassium permanganate (KMnO4) and oxalate solution were mixed together in bottle-in-bottle reaction device, a simple oxidation reaction process occurred within 6 min and carbon dioxide (CO2) was generated, inducing the pressure of the sealed bottle changed, which was measured by a portable gas pressure meter. A detectable range of 0.1–6 μmol mL−1 and a detection limit of 0.064 μmol mL−1 were achieved. The proposed analytical method was further used for the analysis of several real samples (spinach, beverages and water samples), with the recoveries of 89–111%. Considering the interferences from the complicated matrix, calcium chloride (CaCl2) was served as a precipitant, oxalate (C2O42−) was precipitated with Ca2+ to form precipitation (CaC2O4), CaC2O4 was then separated from the matrix by centrifuge/filter, eliminating the interferences. It is a rapid, easy-used and interference-free analytical system/device for oxalate on-site and real time analysis.

A renewable screen-printed electrode based on magnetic NiCo@N-doped carbon nanotubes derived from Co-MOF for ractopamine detection.

A renewable electrochemical screen-printed electrode (SPE) is proposedbased on magnetic bamboo-like nitrogen-carbon (N-C) nanotubes loaded with nickel-cobalt alloy (NiCo) nanoparticles (NiCo@N-CNTs) for the determination of ractopamine (RAC). During the preparation of NiCo@N-CNTs, Co-MOF-67 (ZIF-67) was firstly synthesized, and then blended with dicyandiamide and nickel acetate, followed by a one-step pyrolysis procedure to prepare NiCo@N-doped carbon nanotubes. The surface morphology, structure, and chemical composition of NiCo@N-CNTs were characterized by SEM, TEM, XRD, XPS, and EDS. The electrocatalytic and electrochemical behavior of NiCo@N-CNTs were investigated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The results demonstrated that NiCo@N-CNTs possessed remarkable conductivity and electrocatalysis to the oxidation of ractopamine (RAC). By using screen-printed electrode (SPE), NiCo@N-CNTs, and a designed base support, a magnetic RAC sensor (NiCo@N-CNTs/SPE) was successfully constructed. It presented a detection linear range of 0.05-80μM with a detection limit of 12nM (S/N = 3). It also exhibited good sensitivity, reproducibility, and practicability in spiked real pork samples. Since the adhesion of NiCo/N-CNTs on SPE was controlled by magnet, the NiCo@N-CNTs was easily detached from theSPE surface by magnetism and thus displayed excellent renewability. This work broadened insights into portable devices for on-site and real-time analysis.

Miniaturized confocal Raman and Laser-induced breakdown spectroscopy imaging system based on micro-electro-mechanical mirror

Detection of the elemental and molecular structural distribution with high resolution and miniaturization of unknown minerals is a main bottleneck in deep space exploration and geology analysis. The aim is to enhance the accuracy of the chemical analysis of micro-samples by combining the distribution information from Raman spectroscopy and laser-induced breakdown spectroscopy (LIBS). The existing Raman-LIBS imaging methods are difficult to balance the imaging performance and system volume. There is an urgent need to develop a Raman-LIBS imaging method with miniaturization, and high imaging performance. A miniaturized Raman-LIBS imaging instrument based on the micro-electro-mechanical (MEMS) mirror has been developed to overcome these challenges. The instrument utilizes dual 2D MEMS mirror scanning technology to shorten the optical length of the system and improve the detection efficiency of hybrid spectral signals. The optical probe measures 94 mm × 66 mm, and has an axial focusing ability of approximately 40 nm, with a lateral resolution of approximately 700 nm for Raman maps and 9.5 μm for LIBS maps. As a proof experiment, 3D high-resolution Raman-LIBS hybrid spectral distribution maps of meteorite Tisserlitine 001 were obtained. The attainment of high imaging performance and miniaturization in hybrid spectral imaging is crucial for on-site chemical analysis. The proposed instrument enables in-situ spectrum and multispectral imaging with miniaturization, high spatial resolution, and high stability. The instrument is a powerful tool for composition and structural information characterization in the fields of space exploration and geological exploration.

A colorimetric/electrochemical microfluidic biosensor using target-triggered DNA hydrogels for organophosphorus detection

Organophosphorus compounds are widely distributed and highly toxic to the environment and living organisms. The current detection of organophosphorus compounds is based on a single-mode method, which makes it challenging to achieve good portability, accuracy, and sensitivity simultaneously. This study designed a multifunctional microfluidic chip to develop a dual-mode biosensor employing a DNA hydrogel as a carrier and aptamers as recognition probes for the colorimetric/electrochemical detection of malathion, an organophosphorus compound. The biosensor balanced portability and stability by combining a microfluidic chip and target-triggered DNA hydrogel-sensing technologies. Moreover, the biosensor based on target-triggered DNA hydrogel modified microfluidic developed in this study exhibited a dual-mode response to malathion, providing both colorimetric and electrochemical signals. The colorimetric mode enables rapid visualization and qualitative detection and, when combined with a smartphone, allows on-site quantitative analysis with a detection limit of 56 nM. The electrochemical mode offers a broad linear range (0.01–3000 μM) and high sensitivity (a limit of detection of 5 nM). The two modes could validate each other and improve the accuracy of detection. The colorimetric/electrochemical dual-mode biosensor based on target-triggered DNA hydrogel modified microfluidic chip offers a portable, simple, accurate, and sensitive strategy for detecting harmful environmental and food substances.

Smartphone assisted paper strip-based colorimetric sensing of phosphate and copper ions utilizing bi-ligand intercalated cobalt-MOF as a dual functional nanozyme

Monitoring phosphate and copper ions is vital for environmental and food safety due to associated health risks. To address this need, a new cobalt and bi-organic ligand based metal organic framework (BDC-Co-BIm MOF) has been developed. This MOF acts as a dual-function nanozyme, displaying peroxidase-like activity and selective detection abilities for PO43- ion. The Co(II) nodes and sp2 carbon within the framework exhibit excellent Fenton-like reaction, efficiently catalyzing the conversion of 3,3′,5,5′-tetramethylbenzidine (TMB) into oxidised TMB (oxTMB). Also, steady-state kinetic analysis indicated that BDC-Co-BIm MOF exhibited high affinity toward both TMB and H2O2. The Co(II) nodes and positive charge of the BDC-Co-BIm MOF capture PO43- ion through Co-O-P bonding and electrostatic interaction, limiting the electron transfer between BDC-Co-BIm MOF and H2O2. This reduces TMB oxidation and changes the color from blue to colorless. When ionic Cu2+ ion are added to the system, they react with PO43- ion to form a stable Cu3(PO4)2 complex. This reactivates the electron transfer process, allowing the H2O2 to decompose into •OH. As a result, TMB oxidation is restored and producing the blue color product again. Based on these principles, a colorimetric assay has been developed for the rapid and selective detection of PO43- and Cu2+ ions. A strong linear correlation has been established between their concentrations and the UV absorbance at 652 nm, with limit of detection (LOD) of PO43- and Cu2+ was 0.05 and 0.13 µM, respectively. These limits are notably lower than the thresholds established by the Environmental Protection Agency and World Health Organization (EPA & WHO) at 0.18 µM for PO43- and 30 µM for Cu2+. A Paper-based smartphone-assisted sensing of PO43- and Cu2+ ions was successfully achieved using intelligent Red, Green, and Blue (RGB) analysis. The platform showed high selectivity and performance with environmental water samples. This research presents a novel method for visually detecting PO43- and Cu2+ ions using versatile nanozyme, advancing portable on-site environmental safety analysis.

Construction of a portable copper ion detection method based on colorimetric fluorescent probe and its application in food and organisms

In the subject of food safety, identifying and measuring the active components in food is a hot topic. Food safety and biological health are all strongly correlated with the amount of copper ions (Cu2+) presented in the environment. Nevertheless, the existing Cu2+ detection technology has disadvantages such as difficult operation and inconvenient on-site analysis. Therefore, a new Cu2+ fluorescent probe RH-Cu with a fast response and low limit of detection was built in this study. It can be used to measure the quantity of Cu2+ in real food and water samples. Additionally, a relationship was established between the color RGB values and the concentration of Cu2+. A new mobile phone software (Pick RGB) was developed to realize the portable detection of Cu2+. This work offers a portable instrument for the detection of Cu2+ and provides an idea for developing portable detection techniques for other significant foods’ active constituents.