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[Display omitted] • A novel filter paper patterning method based on parylene C. • A paper-based colorimetric sensor for detection of Al (III) using a smartphone platform. • The detection range of the sensor for Al (III) detection is 0.05 to 10 mg/mL. The detection limit is 0.05 mg/mL. • The assembled paper-based smartphone sensor platform has the potential to detect other biochemical molecules. The paper-based analytical platforms have been applied in biochemical detection and environmental monitoring due to their low cost and easy operation. Despite their advantages, the complexity of fabrication has limited their further application. Here, a simple and innovative approach using parylene C, a material commonly used in semiconductors, is reported to fabricate paper-based chips and construct a point-of-care testing (POCT) platform through smartphones. Parylene C is deposited on the filter paper through a polydimethylsiloxane (PDMS) clamp and forms a hydrophobic barrier. A three-channel paper-based chip was utilized to detect aluminum (Al) ions on a smartphone platform by the chromogenic method. The color change after Al3+ detection is represented with △E which was photographed and calculated by app on smartphone. The detection limit is 0.05 mg/L and the detection range is from 0.05 mg/L to 10 mg/L which indicates the application potential in the field of biochemical detection. This new paper-based sensing method and smartphone-based portable detection platform are simple, low-cost, fast, and highly sensitive, and provides a potential application for on-site, visual detection of ions and even other substances. [ABSTRACT FROM AUTHOR]

In recent years, paper-based Surface-enhanced Raman spectroscopy (SERS) substrates have received extensive attention in the field of rapid analysis. However, obtaining quantitative SERS results is still challenging because of the inferior uniformity originating from the irregular morphology of the filter paper. In this work, a novel paper-fluidic SERS sensor was developed and its in-depth applications in the real-word quantitative analysis of contaminants in complex matrices were demonstrated. In particular, the Au@Ag core-shell nanospheres were labeled with an internal standard molecule to successfully normalize the fluctuation of the SERS signal caused by the microstructure of the filter paper, which could significantly improve the detection accuracy and accomplish the SERS quantitative analysis. In addition, a facile and robust strategy for the fabrication of a paper-based SERS sensor, which uses a dropper and mask to transfer the nanoparticle monolayers, was developed. This convenient and flexible approach effectively achieved a precise patterned assembly of nanoparticles on the filter paper. Furthermore, the paper-fluidic SERS sensor was fabricated by cutting and packaging for two detection modes, i.e., lateral-flow and vertical-flow, which generates the functionalization of the paper-based SERS substrate. Both detection modes integrated sample pretreatment and sample enrichment with SERS detection were applied to accurately detect the pesticide thiram in a complex sample of orange juice with pulp. In summary, this paper-fluidic SERS sensor with a simple preparation process and integrated functions is an ideal candidate for real sample analysis without pretreatment. Image 1 • Internal standard method was used to improve the uniformity of paper-based sensor and complete SERS quantitative analysis. • A facile strategy was developed with aid of dropper and mask to achieve precise assembly of nanoparticles on filter paper. • Lateral-flow and vertical-flow detection modes were applied to accurately measure the pesticide in orange juice with pulp. [ABSTRACT FROM AUTHOR]

[Display omitted] • Fabrication of functionalized polymer nanoparticles via emulsion copolymerization. • Generation of oxazolidine-based polymer nanoparticles (OX-PNPs) through doping. • Optical detection of cyanide by OX-PNPs in deionized water and human blood plasma. • Optical pH sensing based on the absorption or emission spectra of OX-PNPs. • Drawing intelligent fluorescent artworks using acidochromic properties of OX-PNPs. Stimuli-responsive materials play a crucial role in developing sensor technology for rapid colorimetric and fluorometric detection applications. Their ability to undergo changes in response to external stimuli makes them suitable for creating naked-eye sensors, enabling rapid detection of hazardous ions. In this study, our main objective was to synthesize oxazolidine-based polymer nanoparticles (OX-PNPs) that exhibit dual colorimetric and fluorometric responses. These OX-PNPs were developed as sensors specifically for the detection of the cyanide ion (CN–) in solution and human blood plasma. We prepared stable emulsions of polymer nanoparticles by copolymerizing methyl methacrylate and different amounts of acrylamide through emulsion polymerization. The addition of synthesized oxazolidine to the latex samples resulted in the formation of OX-PNPs. After addition of OX-PNPs 1–7 to a solution of CN– in deionized (DI) water, instant chromogenic changes from orange to pink, accompanied by spectral shifts in the UV–Vis and increase in emission intensity spectra was observed. Notably, the detected concentration limit of OX-PNPs for CN– was found to be within the range of 3.67 × 10-9 to 1.66 × 10-8 M, surpassing the recommended guideline value for CN– in drinking water established by the World Health Organization (WHO). Furthermore, we successfully developed paper-based test strips using OX-PNPs for the colorimetric and fluorometric detection of CN– in solution. These paper test strips exhibited rapid and distinct color changes from the original orange to pink upon exposure to CN–. By employing Job's plot method, we confirmed a 1:1 stoichiometry complex formation between OX-PNPs and CN– anions. Additionally, OX-PNPs demonstrated pH-responsive behavior, displaying observable color changes in different pH solutions and on the prepared paper-based sensors across a pH range of 1–14. The pH-sensing ability of OX-PNP 7 paper strips was investigated by FESEM. These unique colorimetric and fluorometric properties make OX-PNPs ideal for applications in ionochromic and acidochromic paper-based sensors, offering immediate and reliable responses. Through this work, for the first time we present a novel application of intelligent pigments, namely oxazolidine-based polymer nanoparticles, for both intelligent artwork creation using a single pigment and as a cyanide detector in human blood plasma. These OX-PNPs hold potential for forensic medicine analysis, providing an effective means of examining cyanide-induced deaths. [ABSTRACT FROM AUTHOR]

This paper presents the development and optimization of a cost-effective paper electrochemical sensor for the detection of TNT using Fe 3 O 4 –Au core-shell nanoparticles modified with cysteamine (Fe 3 O 4 @Au/CA). The sensor was constructed by modifying a graphite paste with the aforementioned nanoparticles, which facilitated the formation of a Meisenheimer complex between cysteamine and TNT as an electron donor and an electron acceptor, respectively. The central composite design was employed to optimize four key parameters pH, modifier percentage, contact time, and buffer type to enhance the performance of the sensor. The detection limit was found to be 0.5 nM of TNT, while the linear range of the electrode response spanned from 0.002 μM to 10 μM. The simplicity and low cost of the sensor make it highly attractive for practical applications, particularly in scenarios where rapid and on-site TNT detection is required. [Display omitted] • Fabrication of a paper-based TNT sensor based on the Meisenheimer complexation. • Synergistic effect of Fe 3 O 4 @Au NPs improves the sensor's electrochemical properties. • The RSM-CCD optimization approach was used for the statistical optimization. • The detection limit of the sensor was 0.5 nM in the linear range of 0.002–10 μM. • The developed sensor can detect TNT in aqueous and soil samples, without extraction. [ABSTRACT FROM AUTHOR]

The enormous demand for self-powered sensors in industry 4.0 has drawn a lot of research interest in these vital devices that do not need external power sources. This study presents the development of a self-powered paper-based humidity sensor that uses copper and aluminium as electrodes and a composite of MgCl 2 and carbon nanotubes (CNTs) as sensing material. The results demonstrate a significant improvement in humidity sensing performance as a result of the addition of CNTs and MgCl 2. In particular, the self-powered paper-based humidity sensor with MgCl 2 /CNTs composites has impressive repeatability, broad detection ranging from 11 % to 97 % relative humidity, and quick response and recovery times of 10 and 46 s, respectively. Furthermore, the self-powered paper-based humidity sensor can generate a maximum voltage of 1.07 V and a maximum power of approximately 1.984 µW. Furthermore, connecting the paper-based humidity sensors in series increases their voltage output, making them useful for charging capacitors and lighting up to six LEDs. This endeavour offers a straightforward, cost-effective, and highly responsive self-powered paper-based humidity sensor that is ideal for high-performance applications in humidity sensing within power generation fields. [Display omitted] • This study proposed a paper-based humidity sensor with MgCl 2 /CNTs composites. • The developed sensor has quick response and recovery times of 10 and 46 s. • The sensor exhibited impressive repeatability and a broad detection ranging of 11–97 % RH. • The sensor can generate a maximum voltage of 1.07 V and a maximum power of 1.984 µW. [ABSTRACT FROM AUTHOR]

The development of an advanced analytical platform with regard to SARS-CoV-2 is crucial for public health. Herein, we present a machine learning platform based on paper-assisted ratiometric fluorescent sensors for highly sensitive detection of the SARS-CoV-2 RdRp gene. The assay involves target-induced rolling circle amplification to generate magnetic DNAzyme, which is then detectable using the paper-assisted ratiometric fluorescent sensor. This sensor detects the SARS-CoV-2 RdRp gene with a visible-fluorescence color response. Moreover, leveraging different fluorescence responses, the ResNet algorithm of machine learning assists in accurately identifying fluorescence images and differentiating the concentration of the SARS-CoV-2 RdRp gene with over 99% recognition accuracy. The machine learning platform exhibits exceptional sensitivity and color responsiveness, achieving a limit of detection of 30 fM for the SARS-CoV-2 RdRp gene. The integration of intelligent artificial vision with the paper-assisted ratiometric fluorescent sensor presents a novel approach for the on-site detection of COVID-19 and holds potential for broader use in disease diagnostics in the future. [ABSTRACT FROM AUTHOR]

The large use and emission of p -nitrophenol (p-NP) seriously pollute the environment and endanger human health. In this work, a hydrazone-linked fluorescent covalent organic framework (BATHz-COF) was simply synthesized at room temperature and covalently linked N-acetyl-L-cysteine (NALC) via the "thiol-ene" click reaction, where carboxyl groups were introduced to improve dispersion and fluorescence intensity. As a rapid, good selectivity and reusability fluorescence sensor, the obtained COF-NALC has been used for quantitative analysis of p-NP predicated on the internal filtering effect (IFE). Under optimal conditions, COF-NALC enabled quantitative detection of p-NP with a linear range of 5–50 μM and the detection limit was 1.46 μM. The application of COF-NALC to the detection of p-NP in river water samples was successful, and the satisfactory recoveries were 98.0%–109.3%. Furthermore, the fluorescent COF paper chips constructed by in situ growth were combined with a smartphone to build a visual platform for the quick and real-time detection of p-NP, providing an excellent illustration for the development of intelligent fluorescence sensing in environmental analysis. [Display omitted] • Covalent Organic Frameworks are modified with N-acetyl- l -cysteine to improve dispersion and fluorescence performance. • The obtained hydrophilic framework is highly selective for the detection of p -nitrophenol. • Paper-based sensors with in-situ immobilization of frameworks are prepared for visual analysis of p -nitrophenol. [ABSTRACT FROM AUTHOR]

Given the illegal formaldehyde (FA) contamination in seafood/aqueous products, the instrument-free, chemical-free, low-cost sensor that enables on-site FA detection is of great interest. We have developed a paper-based analytical device (PAD) sensor to detect FA on-site for easy operation by integrating FA-responsive dye decoloration reaction on filter paper and timing decoloration time for quantitative signal interpretation. This innovative dry chemical PAD sensor can be easily prepared. The on-site FA detection is performed by dropping a drop of the sample into the sensor sampling zone and timing the decoloration time, respectively. The difference in decoloration time between a fictitious blank (5.0 μM) and an FA standard is proportional to the FA concentration in the range of 10–700 μM with a detection limit of 5.6 μM. The utility and effectiveness of this PAD sensor has been verified by applying it to seafood, paper cups, and water samples with the supports of official method validation. • A timing decoloration strategy for quantitative analysis was developed. • A paper-based formaldehyde sensor was fabricated with no laboratory infrastructure. • On-site, dry chemical and user-friendly formaldehyde detection in foods is achieved. • The proposed high-performance sensor is much cheaper than alternative methods. [ABSTRACT FROM AUTHOR]

The utility of strikingly simple and cheap optoelectronic detectors operating according to a Paired-Emitter-Detector-Diode (PEDD) principle for microfluidic paper-based analytical devices (μPAD) has been experimentally confirmed. The prototypes of these compact detectors have been made of only two customary light emitting diodes without any additional optical parts like lens, filters, fibers etc. Moreover, for their operation economic and portable equipment is required (low-power circuit and ordinary voltmeter). Photometric and fluorometric PEDDs for paper devices are developed. In both cases the possibility of their applicability in transmittance and reflectance modes of measurements are presented. In these investigations as model analytes some coloured and fluorescence substances have been handled, but the utility of several developed systems for real chemical analysis has also been demonstrated. The results of photometric determination of hemoglobin in human blood, as well as fluorometric determination of quinine in tonics and calcium ions in mineral waters using various PEDD-μPAD systems have been shown. [ABSTRACT FROM AUTHOR]

Developing simple, inexpensive, fast, sensitive, and specific probes for antibiotic-resistant bacteria is crucial for the management of urinary tract infections (UTIs). We here propose a paper-based sensor for the rapid detection of β -lactamase-producing bacteria in the urine samples of UTI patients. By conjugating a strongly electronegative group –N+(CH 3) 3 with the core structures of cephalosporin and carbapenem antibiotics, two visual probes were achieved to respectively target the extended-spectrum/AmpC β -lactamases (ESBL/AmpC) and carbapenemase, the two most prevalent factors causing antibiotic resistance. By integrating these probes into a portable paper sensor, we confirmed 10 and 8 cases out of 30 clinical urine samples as ESBL/AmpC- and carbapenemase-positive, respectively, demonstrating 100% clinical sensitivity and specificity. This paper sensor can be easily conducted on-site, without resorting to bacterial culture, providing a solution to the challenge of rapid detection of β -lactamase-producing bacteria, particularly in resource-limited settings. [ABSTRACT FROM AUTHOR]

Accurate shelf-life estimation of food products has the potential to improve the safety, reliability, and sustainability of food supply chains. Here, a scalable system for accurately indicating the freshness-related information of salmon for consumers was developed and characterized. The system comprises two parts, an optically changeable colorimetric sensor by dye incorporated with sol-gel functionalized paper sensor and a deep convolutional neural network (DCNN)-based freshness estimation system based on images. The paper sensor was produced based on paper and immersed, coated, or printed with (3-aminopropyl) triethoxysilane (APTMS) and tetraethyl orthosilicate (TEOS) sol-gel particles and indicators (e.g., pH indicator, ammonia gas indicator, oxidation indicator, and other volatile organic compounds indicators). After being augmented by machine learning, the limit of detection reaches as low as 17.1 ppm for ammonia detection and the accuracy achieved up to 99.2% for salmon freshness estimation, which satisfied the application in food supply chains. The system balanced the trade-off between detection sensitivity, stability, and cost with the ability for scalable batch production. [ABSTRACT FROM AUTHOR]

The long-term and excessive use of glyphosate (GLY) in diverse matrices has caused serious hazard to the human and environment. However, the ultrasensitive detection of GLY still remains challenging. In this study, the smartphone-assisted dual-signal mode ratiometric fluorescent and paper sensors based on the red-emissive gold nanoclusters (R-AuNCs) and blue-emissive carbon dots (B-CDs) were ingeniously designed accurate and sensitive detection of GLY. Upon the presence of GLY, it would quench the fluorescence of B-CDs through dynamic quenching effect, and strengthen the fluorescence response of R-AuNCs due to aggregation-induced enhancement effect. Through calculating the GLY-induced fluorescence intensity ratio of B-CDs to R-AuNCs by using a fluorescence spectrophotometer, low to 0.218 μg/mL of GLY could be detected in lab in a wide concentration range of 0.3–12 μg/mL with high recovery of 94.7–103.1% in the spiked malt samples. The smartphone-assisted ratiometric fluorescent sensor achieved in the 96-well plate could monitor 0–11 μg/mL of GLY with satisfactory recovery of 94.1–107.0% in real edible malt matrices for high-throughput analysis. In addition, a portable smartphone-assisted ratiometric paper sensor established through directly depositing the combined B-CDs/R-AuNCs probes on the test strip could realize on-site measurement of 2–8 μg/mL of GLY with good linear relationship. This study provides new insights into developing the dual-signal ratiometric sensing platforms for the in-lab sensitive detection, high-throughput analysis, and on-site portable measurement of more trace contaminants in foods, clinical and environmental samples. [Display omitted] • A two swords combination sensing strategy was proposed for the first time for glyphosate detection. • Smartphone-assisted dual-signal mode ratiometric fluorescent and paper sensors were constructed. • Blue-CDs and red-AuNCs were mixed to fabricate the dual-signal ratiometric fluorescent probes. • Smartphone-assisted ratiometric fluorescent sensor in the 96-well plate could achieve high-throughput analysis. • Smartphone-assisted ratiometric paper sensor could realize on-site measurement 2–8 μg/mL of glyphosate. [ABSTRACT FROM AUTHOR]

• A hydrophobic TENG based on sisal cellulose paper(SCP) was constructed to collect raindrop energy. • Both physical and chemical hydrophobic modification can effectively improve the SCP's dielectric constant. • The hydrophobic SCP-TENG modified by the chemical method is more suitable than the physical method for collecting raindrop energy. • The output electrical signal of SCP-TENG and the raindrop velocity have linear relationship. • The hydrophobic SCP-TENG can be used as raindrop-based sensors. Hydrophobic Sisal cellulose paper (SCP) was obtained by surface modification of SCP via physical adsorbing polymer and chemical grafting monomer, respectively. The influence of surface modification conditioning on the hydrophobicity, dielectric constant and dipole moment of the SCP was investigated. The results showed that the hydrophobicity and dielectric constant of the modified SCP increased with the concentration and amount of the modifiers. The output electrical performance of the TENGs assembled by the two types of hydrophobic SCP for rain energy collection was compared. The output electrical performance of the chemically modified hydrophobic SCP-TENG is higher than that of the physical modified. The maximum power density of the former reaches 8.2 mW/m2. Furthermore, based on the linear relationship between the output performance (output voltage intensity and output current intensity) of hydrophobic SCP-TENG and the droplet velocity, a raindrop-based sensor based on hydrophobic SCP-TENG was successfully constructed and estimated. [ABSTRACT FROM AUTHOR]

The remarkable features of a carbon fiber paper sensor (CP) were employed for detection of the estrogenic hormone 17α-ethinylestradiol (EE2), considered a contaminant of emerging concern due to its potential ecotoxicity and widespread in the aquatic ecosystems. In this work, an unpreceded CP pre-treatment study was conducted with the (Il)-hexacyanoferrate(III) ion pair, however a bare sensor without pre-treatment revealed higher efficiency on the oxidation of EE2 compared to a chemical and electrochemical pre-treated CP and a gold nanoparticles modified CP, being thus selected for EE2 determinations. The analytical conditions were thoroughly optimized in terms of electrolyte pH (pH 7), differential pulse voltammetry parameters (modulation time 0.003 s, amplitude 0.09 V, interval time 0.1 s and step potential 0.01 V), and analyte preconcentration potential (0.4 V) and time (180 s). The hormone can be determined by the CP in a wide linear range from 0.1 to 1000 nM, achieving a detection limit of 0.14 ± 0.005 nM and an outstanding sensitivity of 1636 ± 232 μA μM−1 cm−2 in the lowest linear zone (0.1–1 nM). The sensor was validated in river water and fish reaching good recoveries (91.2 ± 4.6 to 109.0 ± 7.1%), reproducibility and repeatability. Moreover, the sensor showed high selectivity to EE2 in the presence of several potential interfering compounds and frequently prescribed drugs, though it could not discriminate the similar hormone, 17β-estradiol, being the total concentration obtained in this case. CP-based sensors emerge as efficient electroanalytical tools, suggesting that modification of the surface may not always be beneficial in terms of sensitivity. [Display omitted] • A simple and effective carbon paper sensor was used for 17α-ethinylestradiol sensing. • The best analytical signal was obtained with an untreated and unmodified carbon paper. • The optimized sensor achieved high sensitivity (1636 μA μM−1 cm−2) and LOD of 0.14 nM. • Application in complex samples of fish resulted in recoveries from 102 to 109%. • Carbon paper sensors can be become valuable tools in the electroanalytical field. [ABSTRACT FROM AUTHOR]

• A novel bimetallic nanozyme (COF Fe/CoP-Ph) displayed excellent triple-enzyme mimetic activities. • The multiple enzyme-driven cascade catalysis strategy was proposed. • The colorimetric determination of malathion was achieved without the addition exogenous H 2 O 2. • A smartphone POCT analysis platform with integrated paper chip sensors was developed. Enzyme-induced biological cascade catalysis can achieve selective and efficient transformations of substrates in vivo. Thus, the biomimetic cascade systems have attracted much attention in biological detection on account of their ingenious strategies for signal conduction and amplification. In this study, a porphyrin-based covalent organic framework (COF Fe/CoP-Ph) with bimetal-nitrogen-coordinate centers (M − N 4) were constructed via Schiff base reaction. The synergistic effect of the highly exposed M − N 4 bimetallic active sites and the unique topology overcame the self-limitation of nanozyme, resulting in a significant enhancement of the triple-enzyme mimetic activities of COF Fe/CoP-Ph , namely oxidase (OXD)-, peroxidase (POD)-, and catalase (CAT)-like activities. Simultaneously, a multiple enzyme-driven cascade catalysis strategy for signal amplification was proposed utilizing the OXD- and POD-like mimetic mechanisms of COF Fe/CoP-Ph , enabling the colorimetric determination of malathion without the addition exogenous H 2 O 2. The established colorimetric sensor exhibited an exceptional linear relationship within the range of 1–18 μM and a low detection limit of 11 nM. Subsequently, a portable smartphone platform was developed by integrating paper chip, facilitating successful malathion point-of-care testing (POCT) in real samples. This work not only creates a bimetallic COF nanozyme and establishes an efficient cascade amplification strategy, but also introduces a novel design approach for development of a low-cost and user-friendly POCT method. [ABSTRACT FROM AUTHOR]

Prussian blue analogues (PBAs) are promising materials due to their rich active sites and straightforward synthesis. However, their limited conductivity and electron transfer inefficiency hinder practical applications. This study utilizes a simple one-pot synthesis approach to produce a tungsten-disulfide (WS 2) and iron-cobalt Prussian blue analogue composite (WS 2 -PBA), enhancing conductivity and electron transfer rate performance. Through the inclusion of sodium citrate into the solution, the S-edge site concentration of WS 2 increases. This augmentation introduces additional active sites and defects into the catalyst, enhancing its catalytic activity. The effectiveness of the WS 2 -PBA 3D-Origami paper device for lactate detection in sweat is also evaluated for biomedical applications. The device demonstrated a robust relationship between the lactate concentration and current intensity (R2 = 0.997), with a detection limit of 1.83 mM. Additionally, this platform has successfully detected lactate in clinical sweat, correlating with the high-performance liquid chromatography test results, suggesting promising prospects for clinical diagnosis. In the future, the excellent catalytic and R ct performance of the WS 2 -PBA will enable its use in biomedical applications. [ABSTRACT FROM AUTHOR]

• A distance-based paper sensor for the detection of DNase I is developed. • The quantitative detection of DNase I is achieved by measuring the watermark on the indicator paper. • This method exhibits the advantages of the aptamer-mediated enzyme cascade reaction, low-cost, and label-free detection. DNase I is proven to be an early predictive molecule for a variety of diseases, which is important for early diagnosis and clinical detection of diseases. Herein, we demonstrate a distance-based paper sensor to detect DNase I via an enzymatic cascade reaction mediated by the thrombin aptamer. In the presence of DNase I, the thrombin is able to clot the plasma normally because the aptamer chain is hydrolyzed by DNase I and cannot bind thrombin properly to inhibit thrombin activity. The concentration of DNase I is negatively correlated with the volume of mobile phase in sample solution, and it can be quantified by measuring the flow distance of water on the pH indicator strip. The distance-based paper sensor has good specificity, and the detection limit is 2 × 10−2 U/mL. In addition, it can be used for DNase I analysis in human serum samples to show its efficacy in the early diagnosis of diseases associated with DNase I activity. Overall, we developed a simple, fast and low-cost DNase I detection method, which has great commercial potential. [ABSTRACT FROM AUTHOR]

Flexible paper-based conducting molecularly imprinted polymer as electrochemically assisted solid phase microextraction and selective for determination of naproxen. [Display omitted] • Electrochemically prepared paper-based conducting molecularly imprinted polymer film. • Flexible paper-based film applied in naproxen selective sorbent and sensor devices. • Fabricated analytical devices were used for drug determination in human serum sample. • These devices have potential to be used in lab on a chip system and wearable sensors. An electrochemical method is presented for the preparation of paper-based conductive molecular imprinted polymer (CMIP) film as a recognition element of a sensor and a selective absorber in separation methods. The paper became conductive by chemically incorporating polypyrrole (PPy) doped with anion dopant. The effects of the anion dopant and oxidant type on the conductivity of the modified paper were studied. Afterward, a CMIP film based on PPy and an anionic drug as a template was electrochemically synthesized on conductive paper surface, which was then utilized as a selective sorbent for electrochemically assisted solid phase microextraction (EC-SPME) and a recognition element in fabricating flexible drug-selective sensor. Factors affecting the performance of the paper-based EC-SPME device were studied in naproxen (NAP) analysis. All quantitative analytical parameters in the EC-SPME device were obtained by UV–vis absorption spectroscopy. Under the optimal conditions, linearity was achieved within the range of 2.0 × 10−7–2.0 × 10−5 mol/L with determination coefficient (R2 = 0.99) and the limit of detection (LOD) was 0.6 × 10−7mol/L. Moreover, a fabricated paper-based NAP-selective sensor, showed Nernstian response slopes of −61.6 ± 0.5 mV decade−1 over the linear range of 4.0 × 10−7–1.0 × 10−2 mol/L and LOD was 2.0 × 10−7 mol/L. The applicability and efficiency of the paper-based analytical devices were investigated for NAP determination as a model drug in human serum samples. The recoveries were obtained in the range of 90.0–103.0 %. Accordingly, paper-based CMIPs were found to be a novel fabrication method for efficient, selective, flexible and cost-effective material for analytical devices. [ABSTRACT FROM AUTHOR]

An instrument-free, user-friendly, and cost-effective PAD colorimetric sensor that can quantitative detection of H 2 O 2 has been realized by using bimetallic nickel–cobalt selenides as highly active peroxidase mimic and smartphone integrated with dark cavity as detector. Integrated with an ANN model and a self-compiled easy-to-use smartphone APP, the intelligent and on-site detection of H 2 O 2 was constructed, which exhibited an ultra-wide dynamic range. [Display omitted] • An effective paper-based colorimetric sensor was prepared based on nanozyme. • The optimized Ni 0.75 Co 0.25 Se exhibited excellent peoxidase-mimetic activities. • The on-site detection of H 2 O 2 was constructed by a self-compiled smartphone APP. • The machine learning-assisted sensor can detect H 2 O 2 over a wide dynamic range. Paper-based analytical devices (PADs) integrated with smartphones have shown great potential in various fields, but they also face challenges such as single signal reading, complex data processing and significant environmental impacting. In this study, a colorimetric PAD platform has been proposed using bimetallic nickel–cobalt selenides as highly active peroxidase mimic, smartphone with 3D-printing dark-cavity as a portable detector and an artificial neural network (ANN) model as multi-signal processing tool. Notably, the optimized nickel–cobalt selenides (Ni 0.75 Co 0.25 Se with Ni to Co ratio of 3/1) exhibit excellent peoxidase-mimetic activities and are capable of catalyzing the oxidation of four chromogenic reagents in the presence of H 2 O 2. Using a smartphone with image capture function as a friendly signal readout tool, the Ni 0.75 Co 0.25 Se based four channel colorimetric sensing paper is used for multi-signal quantitative analysis of H 2 O 2 by determining the Grey, red (R), green (G) and blue (B) channel values of the captured pictures. An intelligent on-site detection method for H 2 O 2 has been constructed by combining an ANN model and a self-programmed easy-to-use smartphone APP with a dynamic range of 5 μM to 2 M. Noteworthy, machine learning-assisted smartphone sensing devices based on nanozyme and 3D printing technology provide new insights and universal strategies for visual ultrasensitive detection in a variety of fields, including environments monitoring, biomedical diagnosis and safety screening. [ABSTRACT FROM AUTHOR]

Polygalacturonase (PG) activity in plants can serve as an important index for plant disease. However, the conventional method to detect PG activity is a complex process and requires a skilled technician and expensive analytical equipment. In this study, a paper-based colorimetric sensor was developed based on the principle of the ruthenium red (RR) dye method for easy and simple measurement of PG activity. The proposed paper-based sensor has a three-layer structure for detection of PG activity in samples. The sensor sensitivity was enhanced by optimizing the pH of the sodium acetate buffer used in polygalacturonic acid (PGA)-RR complex formation and the reaction temperature for PG and the PGA-RR complex. Further, for quantitative analysis of PG activity, Delta RGB analysis was conducted to detect color changes in the sensing window of the sensor. Results presented that the linear measurement range of the paper sensor was 0.02–0.1 unit with the limit of detection of 0.02 unit, which showed a similar detection range, but a lower detection limit, compared to the spectrophotometry. Furthermore, PG activity based on culture condition was measured using samples from Sclerotium cepivorum to verify the potential application of the developed paper-based sensor in the field. The measured activity showed no statistically significant difference from the values obtained from the spectrophotometry at 95% confidence level. Therefore, the paper-based colorimetric sensor can be used to predict plant diseases in Allium crops during the stage of pathogen invasion, potentially contributing to the improvement of crop production. Image 1 • A paper-based colorimetric sensor for detecting PG activity is developed. • The linear measurement range of the paper sensor is 0.02–0.1 unit with the LOD of 0.02 unit. • The measured PG activity of the paper sensor using S. cepivorum samples is similar to that of the spectrophotometry. • The paper sensor has potential for the early detection of plant disease. [ABSTRACT FROM AUTHOR]

An ultra-sensitive paper-based molecularly imprinted sensor for detection of H5N1 was described. The results can not only be detected quantitatively by fluorescence, but also can be directly read with naked eyes under visible light or ultraviolet light within 10 min. With naked eye detection, its sensitivity is obviously better than that of commercial kits. In particular, the cost of the sensor is cheap (Original size: RMB 1.53 Yuan each; Smaller size: RMB 0.08 Yuan each), which is beneficial to application. [Display omitted] • Paper-based molecularly imprinted sensor; • Ultra-sensitive detection of H5N1 (LOD, 0.58 fM); • Rapid visual detection of influenza H5N1 within 10 min; • More intuitive and sensitive results than commercially available kit; • Low cost (Original size, 1.53 yuan/piece; Smaller size, 0.08 yuan/piece). The rapid detection of pathogens is important to the control of epidemics. Here, a paper-based molecularly imprinted sensor has been developed for the visual detection of influenza H5N1 virus. Firstly, the paper-based molecularly imprinted was prepared by a sol–gel reaction. Then, H5N1 ∼ Apt was covalently bound to the surface of the ZIF-8-NH 2 coated with rhodamine B (RhB) through an amide bond, to produce the fluorescent and colorimetric probe ZIF-8-NH 2 @RhB ∼ Apt. When H5N1 and ZIF-8-NH 2 @RhB ∼ Apt are added to the paper-based MIPs, the H5N1 will be combined with MIPs through the synergistic effects of shape and size compatibility and interaction with the functional groups of the monomers, and ZIF-8-NH 2 @RhB ∼ Apt will bind to H5N1 through its aptamers to form a sandwich structure. The sensor has ultra-high sensitivity and the detection limit is 0.58 fmol/L by using fluorescence spectroscopy. A semi-quantitative signal can also be observed with the naked eye within 10 min. A comparative study showed that direct visual detection was highly reliable, and the sensitivity was better than that achieved with a commercially available kit. Importantly, the paper-based sensor is low in produce cost (Original size: RMB 1.53 Yuan each; Smaller size: RMB 0.08 Yuan each) and is easy to cut, store and carry. This sensor is expected to allow self-service, visual, high-throughput, and real-time virus detection, which is of great significance for epidemic prevention and control. [ABSTRACT FROM AUTHOR]

A series of aminoquinoline derivatives with different N -alkyl substituents were synthesized and used in the development of paper-based fluorescent sensors. In aqueous solutions, the quinoline ligands show strong green fluorescence selectively upon binding to Zn2+ that is clearly observed by naked eyes under blacklight illumination. The paper-based sensors were prepared by depositing the amidoquinoline derivatives in wax-printed channels on filter paper. Developing of Zn2+ samples, deposited below the ligand spots, with an aqueous buffer solution creates green fluorescent lines suitable for distance measurement. The ligands with a tertiary amino group showed better-defined fluorescent lines than those of ligands containing primary and secondary amino groups. The length of the fluorescent lines increases linearly with the amounts of Zn2+ in the range of 2.5–80 nmol that can be easily determined by naked-eye observation or an image processing software. The increase in hydrophobicity of the ligands results in a wider dynamic concentration range of the detection. The paper-based sensor can accurately and conveniently quantify Zn2+ in drinking water, dietary supplement, and fertilizer samples. • New series of fluorescent ligands having variable hydrophobicity were synthesized. • Paper-based sensors for of Zn2+ with distance-based quantification were developed. • Dynamic range of Zn2+ quantification increases with hydrophobicity of the ligands. • The sensor is handy for quantitative analysis of Zn in water and food supplements. [ABSTRACT FROM AUTHOR]

As a crucial biomarker for some diseases, the determination of cholesterol in human serum is of great significance for the diagnosis and prevention of these diseases. Hence, a portable cholesterol detection method is necessary for clinical and domestic applications. Here, a portable paper sensor was designed for cholesterol detection by modifying screen-printed electrode (SPE) with nanoporous gold (NPG). To achieve the reliable cholesterol detection, a synergistic strategy was proposed based on the oxidation of cholesterol by cholesterol oxidase (ChOx) and the reduction of oxidation product (H 2 O 2) by NPG. Compared to existing electrochemical sensors, the resulting paper sensor exhibited a wider linear response in a range from 50 μM to 6 mM as well as a higher sensitivity of 32.68 μA mM−1 cm−2 with a lower detection limit of 8.36 μM. Moreover, the portable paper sensor presented strong anti-interference capability and stability in the detection of cholesterol in human serum, and the data detected by the portable paper sensor were consistent with that obtained by an automatic biochemical analyzer. These unique performances confirmed that the proposed paper sensor was a sensitive, reliable, and portable cholesterol detection method, making it a good choice for cholesterol detection. [ABSTRACT FROM AUTHOR]

The widely used pesticide thiram is found in various environments and foodstuffs, posing a risk to human health and contaminating the environment. In this work, the novel SERS flexible sensor (FP/AgNWs@ZIF-8) consisting of silver nanowires and zeolite imidazole frameworks combined with filter paper was prepared for the sensitive and rapid detection of thiram on fruit peel surfaces. The effect that different coating cycles of ZIF-8 films exert on the Raman signal enhancement of the sensor was investigated. The results show that optimal Raman response to 4-Aminothiophenol (4-ATP) was demonstrated in the FP/AgNWs@ZIF-8(5) sensor, with a low LOD of 1.6 × 10−15 M due to a coating period of 5. Furthermore, a novel SERS FP/AgNWs@ZIF-8 sensor with a porous and flexible structure on low-cost and eco-friendly paper was obtained, as to be immersed in a solution of thiram or wiped on a nectarine skin surface, and the highly sensitive LODs of 1.4 × 10−12 M and 7.4 fg/cm2 were achieved, respectively. Therefore, this facile, rapid, and sensitive flexible sensor at low-cost has excellent potential for pesticide residue detection and environmental toxicity analysis. [Display omitted] • In situ zeolitic imidazolate framework (ZIF-8) growth on silver nanowires (AgNWs). • Multi-layer flexible film detects hazardous organic pesticides in peel and aqueous solutions. • Adsorbs dyes and pesticides smaller than the size of ZIF-8. • Synergistic enhancement of Raman response by AgNWs and ZIF-8. [ABSTRACT FROM AUTHOR]

[Display omitted] • EDTA etched-CdTe@CdS QDs act as both recognition element and signals probe. • EDTA etched-CdTe@CdS QDs sensor achieved a sensitive detection for Cd(II). • Chips based on EDTA etched-CdTe@CdS QDs realized the on-site and visual detection of Cd(II). • The proposed method exhibited excellent specificity, stability, and sensitivity. • The proposed method showed high recovery for Cd(II) in rice samples. EDTA-etched CdTe@CdS QDs were used as the specific recognition element and signal probe of a fluorescence sensor or paper chip for the highly sensitive detection of Cd(II) with an electronic eye device as readout. The results showed that the CdTe@CdS QDs were successfully synthesized with a typical core–shell structure. Under the optimum conditions, the EDTA-etched CdTe@CdS QDs sensor achieved the sensitive detection of Cd(II) with a detection limit of 0.092 μM and a concentration range of 0.44–6.67 μM. The paper chips based on the EDTA-etched CdTe@CdS QDs sensor had a visual cut-off value of 0.44 μM with a short detection time (<15 min). The proposed method also exhibited excellent stability, high specificity, and good recovery for Cd(II) in real rice samples. These results suggested that the EDTA-etched CdTe@CdS QDs provide a promising platform for on-site and visual detection of Cd(II) in rice samples. [ABSTRACT FROM AUTHOR]

• A simple and scalable synthesis of exfoliated graphite carbon paper. • ExGCP potential for nonenzymatic glucose sensor. • A high sensitivity of about ∼5.93 µA mM−1 cm−2. • Diffusion controlled sensing reaction in ExGCP. The continuous real-time monitoring of glucose is essential for patients suffering from diabetes. Therefore, the low-cost and flexible glucose sensor is necessary, showing enhanced sensitivity and limit of detection. We report results of studies resulting in developing a nanostructured exfoliated graphite carbon paper (ExGCP) based efficient electrode for application to a nonenzymatic glucose sensor. This glucose sensor showed ∼ sensitivity as 5.93 µA mM−1 cm−2 with a linear response in the 2–8 mM concentration range and ∼0.812 mM as the limit of detection. The diffusion-controlled sensing reaction on ExGCP reduces electron transfer resistance with increasing glucose concentration, revealing ExGCP as an efficient and flexible electrode material for glucose sensing applications. [ABSTRACT FROM AUTHOR]

Lactose (LAC) is a disaccharide - major sugar, present in milk and dairy products. LAC content is an important indicator of milk quality and abnormalities in food industries, as well as in human and animal health. The present study reports the development of an innovative imprinted voltammetric sensor for sensitive detection of LAC. The sensor was constructed using electropolymerized pyrrole (Py) molecularly imprinted polymer (MIP) on graphite paper electrode (PE). The MIP film was constructed through the electrosynthesis of polypyrrole (PPy) in the presence of LAC (template molecule) on PE (PPy/PE). To optimize the detection conditions, several factors affecting the PPy/PE sensor performance were assessed by multivariate methods (Plackett–Burman design and central composite design). Under optimized conditions, the proposed analytical method was applied for LAC detection in whole and LAC-free milks, where it demonstrated high sensitivity and selectivity, with two dynamic linear ranges of concentration (1.0–10 nmol L−1 and 25–125 nmol L−1) and a detection limit of 0.88 nmol L−1. The MIP sensor showed selective molecular recognition for LAC in the presence of structurally related molecules. The proposed PPy/PE sensor exhibited good stability, as well as excellent reproducibility and repeatability. Based on the results obtained, the PPy/PE is found to be highly promising for sensitive detection of LAC. Image 1 • A disposable paper-based non-enzymatic voltammetric sensor used for lactose detection. • A novel electrosynthesized MIP modified disposable paper sensor for lactose detection. • Lactose was selectively recognized by the MIP used as synthetic receptor. • The proposed MIP paper-based sensor exhibited good reproducibility and robustness. • The MIP sensor presented excellent performance for lactose determination in milk samples. [ABSTRACT FROM AUTHOR]

In advanced missions, handling thin and soft membranes is difficult for robots. This task is composed of several sub-tasks, including turning and removing a sheet from a pile of papers on a table, folding paper, and sticking two pieces of paper together. In this study, a hand robot turns and removes a sheet from a pile of papers, and ensures that only one sheet is grasped. To perform this task, two robotic fingers compress the piled papers in the normal direction of the table with a specific force as they close. We therefore incorporated position-based force control into our system; for the force controller, we adopted stiffness control that calculates position modification proportionally to the difference between the target force and an external force measured by the tactile sensor. With this controller, the robot was able to remove a sheet from a pile of papers and ensure that only one sheet was removed. Using this discrimination, the maximum-minimum shearing forces are better classified than with normal force distribution deviation. [ABSTRACT FROM AUTHOR]

Abstract This study describes the development of paper-based devices for the determination of biothiols. The devices are inexpensive (composed of paper and silver halide particles), and the analytical protocol is easily executable with minimum technical expertise and without the need of specialized equipment; the user has to add a test sample, illuminate the device with a UV lamp, and read the color change of the sensing area using a simple imaging device (i.e., cell-phone camera) or a bare eye. The detection mechanism of the assay is based on the biothiols-mediated photoreduction of nanometer-sized silver chloride particles deposited on the surface of paper; photoreduced silver chloride particles have a grayish coloration that depends on the concentration of biothiols in the tested solution. This is the first time that the UV-mediated photoreduction of solid silver halides particles is used for analytical purposes. The performance of the devices has been tested on the detection of total biothiols content of artificial body fluids and protein–free human blood plasma samples, and the results were satisfactory in terms of sensitivity, selectivity, recoveries and reproducibility. Graphical abstract Image 1 Highlights • Paper-based devices have been developed for the determination of biothiols. • Silver halides are employed for the first time on paper devices in a heterogeneous chemical reaction. • Biothiols enhance the UV photoreduction of silver halides. • Easy-to-use devices: Add sample, illuminate with UV lamp, read the developed color. [ABSTRACT FROM AUTHOR]

We report an innovative sensor for the determination of low levels of total cholesterol (TC) in saliva. The sensor consists of an enzyme-loaded nitrocellulose (NC) paper and an impedimetric sensor based on hybrid material derived from Pt black/PEDOT:PSS (BPt/PEDOT) and Pt black/Nafion (BPt/Nafion) composite. The enzyme-loaded NC paper combined impedimetric sensor with the BPt/Nafion composite was able to detect TC values in the range of 5–4000 ng/ml with a normalized sensitivity (impedance change) of 7.5%/decade at 1 kHz and 0.99 linear correlation. In order to detect cholesterol in saliva reliably, the detection limit should be lower than the clinical level in saliva (5–46 μg/ml). The fabricated sensor had a detection limit that was sufficiently low and it had a wide detection range. In addition, the impedimetric sensor with BPt/Nafion composite exhibited more reproducible and cholesterol-selective normalized impedance changes than the sensor with the BPt, BPt/PEDOT electrode. In the human serum and saliva test, the impedance change from diluted serum and saliva concentration was compared. The impedimetric sensor exhibited relatively well matched correlation between diluted serum and standard TC. And TC concentration in saliva was at least 10 −3 less than the concentration in the serum. [ABSTRACT FROM AUTHOR]

Graphene-based nanomaterials have found significant interest in the development of embedded sensors to monitor the fracture behavior in composite structures. In this work, in-situ crack propagation and fracture behavior within a glass fiber reinforced polymer composite (GFRP) was monitored using embedded reduced graphene oxide (rGO) coated fabrics and highly conductive graphene nanoplatelet (GnP) paper. All laminates were fabricated using the resin infusion process. The piezoresistive performance of both types of laminates was evaluated using in-plane and out-of-plane mechanical tests. The effect of GnP paper thickness (50/150/240 µm) and loading rate was also evaluated using tensile and Mode-I fracture loadings. Piezoresistivity of the sensors was reduced by increasing loading rate during tensile tests. All laminates with GnP paper exhibited poor mechanical performance under tensile loading. The laminates with 50 µm GnP paper showed highest sensitivity under Mode-I loading. In comparison to pristine laminates, the interlaminar fracture toughness of laminates with 50 µm GnP paper was reduced by 70%. Furthermore, laminates with rGO coated fabrics demonstrated stable crack propagation under Mode-I loading as compared to GnP based laminates. The fractured surfaces were analyzed using scanning electron microscopy to investigate the underlying fracture mechanisms of the sensors in the composite laminates. [Display omitted] • Composites with embedded GnP paper and rGO coated fabric sensors were manufactured. • Sensor based on thin GnP paper was found more sensitive than the thick GnP sensors. • Loading rate and thickness effects on the sensing behavior were characterized. • Increasing the load rate during in-plane tensile tests decreases the sensitivity. • rGO based sensor exhibited high mechanical properties than the GnP based sensors. [ABSTRACT FROM AUTHOR]

Antimicrobial stewardship practices are critical in preventing the further erosion of treatment options for bacterial infections. Yet, at the same time, determination of an infection's antimicrobial susceptibility requires multiple rounds of culture and expensive lab automation systems. In this work, we report the use of paper-based surface enhanced Raman spectroscopy (SERS) sensors and portable instrumentation to phenotypically discriminate multi-drug resistance with fewer culture steps than conventional clinical microbiology. Specifically, we demonstrate the identification of resistance to varying generations of β -lactam antibiotics by detecting the activity of particular β -lactamase enzymes in a multiplexed assay. The method utilizes molecular reporters that consist of β -lactams with SERS barcodes. Hydrolysis of the β -lactam by β -lactamase enzymes in the sample expels the barcode; the released sulfur-containing barcode is then detected via SERS. Using this approach, we demonstrate the differentiation of E. coli strains with (1) extended spectrum β -lactamase (ESBL), (2) narrow-spectrum β -lactamase, and (3) no resistance, using only a single measurement on a single sample. In addition, we experimentally validate an approach to expand the library of reporters through the simple chemical synthesis of new barcoded β -lactams. Importantly, the reported method determines the susceptibility based on phenotypic β -lactamase activity, which is aligned with current microbiology lab standards. This new method will enable the precise selection of effective β -lactam antibiotics (as opposed to defaulting to drugs of last resort) faster than current methods while using simple steps and low-cost portable instrumentation. Image 1 • We demonstrate phenotypic detection of β-lactamase activity using paper SERS sensors and portable instrumentation. • We show discrimination of β -lactamases with different degrees of resistance in a single sample on a single sensor. • We demonstrate a simple synthesis method to expand the library of SERS-based β -lactamase reporters. • We accomplish β-lactamase discrimination in significantly less time than conventional microbiology. [ABSTRACT FROM AUTHOR]

Point-of-care testing (POCT) technology is urgently required owing to the prevalence of the Internet of Things and portable electronics. In light of the attractive properties of low background and high sensitivity caused by the complete separation of excitation source and detection signal, the paper-based photoelectrochemical (PEC) sensors, featured with fast in analysis, disposable and environmental-friendly have become one of the most promising strategies in POCT. Therefore, in this review, the latest advances and principal issues in the design and fabrication of portable paper-based PEC sensors for POCT are systematically discussed. Primarily, the flexible electronic devices that can be constructed by paper and the reasons why they can be used in PEC sensors are expounded. Afterwards, the photosensitive materials involved in paper-based PEC sensor and the signal amplification strategies are emphatically introduced. Subsequently, the application of paper-based PEC sensors in medical diagnosis, environmental monitoring and food safety are further discussed. Finally, the main opportunities and challenges of paper-based PEC sensing platforms for POCT are briefly summarized. It provides a distinct perspective for researchers to construct paper-based PEC sensors with portable and cost-effective, hoping to enlighten the fast development of POCT soon after, as well as benefit human society. • The merits of functionalized paper for PEC sensor are introduced. • Photosensitive material and signal amplification strategy of paper-based PEC sensor are discussed. • The application of paper-based PEC sensor in the field of POCT is highlighted. • The limitations and challenges of paper-based PEC sensor are summarized. [ABSTRACT FROM AUTHOR]

Abstract: A novel method for the fabrication of paper-based microfluidic diagnostic devices is reported; it consists of selectively hydrophobizing paper using cellulose reactive hydrophobization agents. The hydrophilic–hydrophobic contrast of patterns so created has excellent ability to control capillary penetration of aqueous liquids in paper channels. Incorporating this idea with digital ink jet printing techniques, a new fabrication method of paper-based microfluidic devices is established. Ink jet printing can deliver biomolecules and indicator reagents with precision into the microfluidic patterns to form bio-chemical sensing zones within the device. This method thus allows the complete sensor, i.e. channel patterns and the detecting chemistries, to be fabricated only by two printing steps. This fabrication method can be scaled up and adapted to use high speed, high volume and low cost commercial printing technology. Sensors can be fabricated for specific tests, or they can be made as general devices to perform on-demand quantitative analytical tasks by incorporating the required detection chemistries for the required tasks. [Copyright &y& Elsevier]

[Display omitted] • A red-emissive carbon dots based fluorescent nanosensor was fabricated for sensing carbendazim. • R-CDs were synthesized by solvothermal method and surface charge engineering with excellent performance. • The novel nanosensor exhibited LOD of 3.5 ng/mL and range of 10–250 ng/mL for carbendazim. • Real application in Lotus seeds confirmed the excellent reliability with satisfactory recovery. • Visual paper-based sensor with smartphone was developed for rapid on-site carbendazim detection. Trace detection of carbendazim (CBZ), a worldwide used pesticide, in crops and foods is important and urgent to reduce risks to human health. Herein, newly red-emissive carbon dots (R-CDs) based fluorescent and smartphone-integrated paper sensors were developed for highly-selective, and -sensitive rapid sensing of CBZ. R-CDs were synthesized from citric acid and urea via a DMF solvothermal method, which showed excellent analytical performance due to abundant carboxyl groups on the surface and long emission wavelength to avoid autofluorescence interference of matrix. According to the red fluorescence quenching by CBZ via π-π interaction and photoinduced electron-transfer effect, the newly fluorescent nano sensor could realize CBZ sensing within 3 min with high selectivity out of the other six interfering pesticides, as well as fascinating sensitivity with an ultralow detection limit of 3.5 ng/mL. The practicable application in the spiked medicinal Lotus seeds samples exhibited satisfactory recoveries of 95.5%-108.3%. The portable paper-based sensor fabricated by depositing R-CDs on the filter paper enabled quantitative readout of test strip results assisted with a smartphone, providing a rapid on-site tool for CBZ detection in medicinal foods. This is the first report of a novel, sensitive, and portable R-CDs based sensing platform for simple, cost-effective, and rapid on-site detection of CBZ in the field of food safety with great application potential. [ABSTRACT FROM AUTHOR]

Free proline, termed proline, is a biomarker used for diagnosing drought stress in plants. A previously developed proline–ninhydrin reaction-based paper sensor could quickly and easily detect proline, but it was limited by low sensitivity. In this study, we developed an enclosed multilayer paper-based microfluidic sensor with high sensitivity for the quantitative detection of proline in plants. The multilayer paper-based sensor was manufactured using simple wax printing and origami methods, and contained an internal mixing channel to allow good mixing of the proline with ninhydrin, increasing the proline–ninhydrin reactivity and providing accurate and sensitive proline detection. By preloading ninhydrin onto the sample loading area, uniform coloration of the sensing window was achieved, allowing quantitative analysis of various proline concentrations using a constant reaction time. Only the sensing window and sample loading area were exposed to limit sample evaporation and contamination from the external environment. The LOD of the fabricated sensor was 23 μM, which is approximately 29-fold lower than that of the previously proposed paper sensor (657 μM). Samples were extracted from A. thaliana plants subjected to drought stress for proline detection. The proline concentrations measured using the developed paper sensor and a spectrophotometric method were not statistically significant at a confidence level of 95%. Therefore, the developed sensor can be applied to measure proline concentrations precisely in the field with a low detection limit. The developed paper-based sensor can be used to detect the early stages of drought in plants and thus improve crop productivity. Image 1 • An enclosed multilayer paper-based microfluidic sensor for proline quantification is manufactured. • The enclosed multilayer sensor structure avoids sample evaporation and contamination. • The sensor detects proline with a LOD of 23 μM. • The sensor is suitable for the early detection of drought stress in plants. • The measured proline concentration is similar to that measured by spectrometry. [ABSTRACT FROM AUTHOR]

A new paper-based analytical device based on bulk ion-selective optodes (ISOs) for dual Ag+ and Hg2+ detection has been developed. A plasticized PVC hydrophobic phase composed of 25,27-di(benzothiazolyl)-26,28-hydroxycalix[4]arene (CU1) as an ion-selective ionophore, potassium tetrakis(4-chlorophenyl)borate as an ion-exchanger and chromoionophore XIV as a lipophilic pH indicator was entrapped in the pores of cellulose paper. This paper strip showed higher selectivity for Ag+ and Hg2+ over common alkali, alkaline earth and some transition metal ions with a color change from blue to yellow. With the proposed sensor, Ag+ and Hg2+ can be measured with the range of 1.92 × 10−6 to 5.00 × 10−3 M for Ag+ and 5.74 × 10−7 to 5.00 × 10−5 M for Hg2+ with a limit of detection of 1.92 × 10−6 M for Ag+ and 5.74 × 10−7 M for Hg2+. The proposed sensor was successfully applied to determine the amount of mercury in various water sources and the amount of silver in cleaning product samples containing silver nanoparticles (AgNPs). The results were in good agreement with inductively couple plasma-optical emission spectrometric measurements (ICP-OES). Image 1 • Paper-based bulk ion-selective optode (ISOs) was fabricated. • Benzothiazole calix[4]arene was employed as an ionophore. • The sensor was used for dual colorimetric Ag+ and Hg2+ detection. • High selectivity for Ag+ and Hg2+ over other metal ions was achieved. [ABSTRACT FROM AUTHOR]

[Display omitted] • Products of urease catalyzes urea induce color change of Prussian blue nanoparticles. • A paper-based sensor depending on the Prussian blue pH sensitivity is developed. • Smartphone captures color signals of the sensor to achieve rapid detection of urea. Depending on the pH sensitivity of Prussian blue nanoparticles (PB NPs) and the specificity of urease-catalyzed urea, a paper-based colorimetric sensor was developed using urease, PB NPs, and cellulose filter paper. With the assistance of a smartphone, the rapid detection of urea can be realized. Under the optimal conditions, the linear range of the paper-based sensor for detection of urea is 0.5–5.0 mM, and the limit of detection is 0.27 mM. The RSD values of within-batch and between-batch repeatability are 2.5 % and 0.9 %, respectively. The method was successfully applied to the detection of urea in spiked milk samples and artificial urine sample, and the recoveries are in the range of 91.8–107.9%. The developed paper-based colorimetric sensor is a simple, economic, and rapid method that can be used for the determination of urea in real samples, particularly in resource-poor regions. [ABSTRACT FROM AUTHOR]

Carbon cloth and carbon paper have unique characteristics such as conductivity, mechanical strength, porosity, reduced dimensions, and adjustable size and shape. With these materials, different simple modification strategies can be employed, with emphasis on the direct growth of metal-based catalysts through single-step hydrothermal methods. Thus, owing to these interesting features, highly efficient, versatile, and disposable electrochemical (bio)sensors based on carbon cloth and carbon paper have been designed for biomolecules, biomarkers, and hazardous and chemical compounds detection in clinical, environmental and food samples, as well as in industrial products. Moreover, the advantage of facile integration in miniaturized and portable devices, envisages their successful application in point-of-care diagnostics and in-situ measurements. Therefore, this review highlights the main advances and the current research gaps concerning the design of these novel electroanalytical tools. • CC and CP present high electrical conductivity, porosity, and adjustable size/shape. • Single-step hydrothermal methods are the most used for CC and CP modification. • CC and CP (bio)sensors successfully used in clinical, environmental and food analysis. • Excellent performance of CP and CC (bio)sensors reaching sub-micromolar levels of LOD. • Facile integration in miniaturized and portable devices for in-situ measurements. [ABSTRACT FROM AUTHOR]

[Display omitted] • A series of two-armed indole appended Schiff base conjoined 1,2,3-Triazole based click derived bis-organosilane and bis-organosilatrane is synthesized. • The designed Schiff bases are developed as colorimetric, fluorescent and paper-based selective sensors for Al(III). • The binding capabilities are in sighted by using absorption and emission titrations that determine the 4 and 5 high sensitivity and ultratrace low detection limits of 1.41 × 10−9 M and 0.17 × 10−9 M. • The insights into the optical signal changes are discussed. Metal ions have significant roles in diagnosis, industry, human health, and the environment. To design and develop new lucid molecular receptors for the selective detection of metal ions is important for environmental and medical applications. In the present work, two-armed indole appended Schiff bases conjoined with 1,2,3-Triazole bis-organosilane and bis-organosilatrane skelton sensors for naked eye colorimetric and fluorescent detection sensors for Al(III) are developed. The introduction of Al(III) in sensor 4 and 5 show red shift in UV–visible spectra, changes in fluorescence spectra and immediate color change from colorless to dark yellow. Furthermore, the pH and time response studies were explored for both sensors 4 & 5. The sensors 4 and 5 exhibited significantly low detection limit (LOD) in nano-molar range 1.41 × 10−9 M and 0.17 × 10−9 M respectively from emission titration. The LOD form absorption titration was found to be 0.6 × 10−7 M for sensor 4 and 0.22 × 10−7 M for sensor 5. In addition, the sensing model is developed as paper based sensor for its practical applicability. The theoretical calculations were performed on Gaussian 03 program by relaxing the structures using Density functional theory. [ABSTRACT FROM AUTHOR]

A highly efficient, flexible and cost-effective ammonia (NH 3) gas sensor is developed on a biodegradable paper substrate. The polyaniline (PANI) film as an active sensing material was deposited by a simple in-situ polymerization method and optimized for NH 3 detection. The PANI film was investigated using X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) for structural and morphological properties. The sensor was tested for its efficiency to detect the NH 3 gas over the concentration range of 12–1000 ppm at room temperature. The sensor showed excellent repeatability, stability and selectivity towards NH 3 detection. At concentrations of 12 ppm (lower level), 200 ppm (intermediate level), and 1000 ppm (higher level), the sensor exhibited effective response values of 3.60, 6.85, and 9.33, respectively. The sensor exhibited a quick response time of 30–9 s when subjected to 12–1000 ppm of NH 3. The sensor can detect ammonia gas in real-time, which makes it useful for identifying rapid changes in NH 3 concentration. The sensor response was reduced by 5.5% towards 200 ppm NH 3 despite a significant variation in relative humidity from 20% to 80%. Based on these results, our flexible PANI sensor is a viable option for efficient and cost-effective on-site NH 3 detection. [Display omitted] • We fabricated a room temperature operational, highly sensitive and selective polyaniline based ammonia gas sensor. • The sensor is fabricated over the bio-degradable paper substrate which makes it flexible and cost-effective. • The sensor exhibited a linear response with increasing NH 3 concentration along with excellent repeatability and stability. • The effect of relative humidity on the sensor response has been thoroughly investigated. [ABSTRACT FROM AUTHOR]

Environmentally friendly humidity sensors with high sensing performance are considered crucial components for various wearable electronic devices. We developed a rapid-response and durable Paper Cellulose Fiber/Graphene Oxide Matrix (PCFGOM) humidity sensor using an all-carbon functional material. The fabricated sensor demonstrated a high sensitivity to humidity through an electrical impedance measurement, with an increase in response to humidity ranging from 10% to 90% at 1 kHz and 10 kHz, respectively, along with a response time of 1.2 s and a recovery time of 0.8 s. The stability of the sensor was also examined, with consistent performance over a period of 24 h. This novel sensor was employed in several applications, including non-contact proximity sensing, environmental humidity detection, and human respiration detection, to showcase its potential. Moreover, this work represents a significant milestone in developing inexpensive and eco-friendly humidity sensors, given the abundance of paper and graphene in nature and their biocompatibility. • This paper reports on Paper Cellulose Fiber Graphene Oxide Matrix (PCFGOM) humidity sensor. • The PCFGOM humidity sensor is Low-cost, effective, and environmentally friendly. • PCFGOM humidity sensor exhibits a linear response for humidity ranges from 10% to 90% • PCFGOM humidity sensor has a 1.3 s response time and 0.8 s recovery time. • PCFGOM humidity sensor is durable and stable for greater than 24 hrs. [ABSTRACT FROM AUTHOR]

• Nano Ge as structure-directing agent facilitates the formation of nanofiber-like PANI. • The porous filter paper was chosen as a substrate (pore size: 15–20 μm). • The PANI/Ge-based sensor can achieve the high gas response of 1098.6% (50 ppm NH 3). In this paper, we proposed a flexible paper sensor based on nano-sized polyaniline/germanium (PANI/Ge) film to detect ammonia (NH 3) gas. The results indicate that hydrogenated Ge polycrystalline nanomaterial acts as a structure-directing agent, assisting the growth of nanofiber-like PANI. In the sensing experiments, the response of the PANI/Ge sensor is up to 1098.6% (50 ppm NH 3) with the response/recovery time at 72 s/111 s. Moreover, the sensor exhibits good reversibility and selectivity at room temperature. The improvement of sensing performances can be attributed to two aspects: Ge regulates the morphology of PANI, and the rough and porous filter paper as substrate increases specific surface area of the film. It demonstrates that the as-prepared PANI/Ge sensor has a potential application in low-cost disposable devices for NH 3 detection. [ABSTRACT FROM AUTHOR]

Ion-selective electrodes (ISEs) are an efficient and versatile tool for ion detection. However, portability and applicability for field applications are often limited by the need of a conditioning step, and high cost of the needed bulky reference electrode. Herein, the traditional conditioning protocol of ISEs has been eliminated and a paper-based solid-contact ISE (PBSC-ISE) has been integrated with a paper-based solid-contact reference electrode (PBSC-RE) in a single strip format for on-site analysis. The PBSC-RE is based on the copolymer methyl methacrylate-co-decyl methacrylate (MMA-DMA) (support matrix), combined with ionic liquids (ILs) to create and maintain a stable potential that is un-affected by a change in ionic activity. This single-strip ready-to-use sensor yields a Nernstian response towards Na +, K + , and I − ions with submicromolar limits of detection, and is able to be used for multiplex analysis. [ABSTRACT FROM AUTHOR]

An organometallic dye, europium tetrakis dibenzoylmethide triethylammonium (EuD 4 TEA) and gold nanoparticles (Au NPs) impregnated paper based sensor platform have been utilized for development of fluorescence turn-on cyanide assay in aqueous media. The ordinary filter paper with 6 μ m pore size were employed as solid support that facilitates impregnation of EuD 4 TEA and gold nanoparticles and provides durability. Detection mechanism relying on two processes (i) dissolution of gold nanoparticles causing fluorescence recovery and (ii) ligand exchange of triethyl amine with CN group stimulating cyanide specific fluorescence enhancement. The paper platform exhibit naked eye distinguishable color transition upon CN − addition from 10 −2 to 10 −12 M. To standardize the methodology a homemade image processing algorithm has been developed that enabling calibration of color change and quantify CN − concentration. The described algorithm is applicable to Android smart phones and facilitate transforming these devices into a quantitative cyanide detector. The overall methodology provides instrument free cyanide detection and therefore rapid control of water quality and safety at off-field conditions. [ABSTRACT FROM AUTHOR]

The recently emergent laser induced graphene paper (LIGP) has endowed the large-scale assembly of 2D electronics with freestanding and multifunctional natures. Liquid sensors, a crucial component in next-generation smart devices, were developed in this report through LIGP technology. Attributed to the one-step process of computer-aided laser scribing, the new sensor was fulfilled easily with arbitrary 2D shapes, sizes and array modalities. In comparison to indirect sensing manners existed majorly in polymer binder/substrate enabled carbon devices, the novel LIGP sensors with self-supported graphitic structures evidently showed multiple superiorities, including faster response, greater reproducibility, and higher sensitivity for micro-volume liquid detections. Benefiting from the laser-process dependent structures, we further proved the tunable sensing characteristics relying dominantly on specific surface area, a critical factor for introducing capillary pressure to facilitate liquid infiltration and electrical disruption. Additionally, a dual-mode liquid-recognition strategy based on both time and speed was creatively proposed for identification of various liquids. With successful utilization of 5 × 5 LIGP array for mapping the distribution of different fluid emissions on composite structures, we highly anticipate the escalation of LIGP sensors for commercialization, roll-to-roll manufacturing, and multimodal safety-assurance applications. Freestanding laser induced graphene paper (LIGP) based liquid sensors were fabricated for fast response, micro-volume detection, and accurate liquid identifications. The laser power dependent specific surface area dominantly controls the capillary pressure for disrupting the conducting network, showing clear superiority to other matrix swelling based mechanisms. This further guarantees the assembly of LIGP array for large-area deployment and leakage mapping applications. Image 1 [ABSTRACT FROM AUTHOR]

Flexible sensor of flower-like PANI coated filter paper was prepared by spraying for the first time, achieving the highly sensitive and fast detection of nitroaromatic explosives. Response fluctuation does not exceed 7% during the bending process and the decreases of responses are less than 7.9% after 2000 bends of 40° due to the interlaced flower-like PANI fibers. The spraying method is suitable for economical, efficient and large-scale preparation of paper-based flexible sensors. • The flexible sensor of flower-like PANI coated filter paper was prepared by spraying for the first time. • The response time and recovery time to TNT, PA and DNT are no more than 8.1 and 1.9 s, respectively. • The theoretical detection limit for TNT and PA is 0.094 and 0.029 ppb, respectively. • Response fluctuation of flexible sensors does not exceed 7% in the bending process and the decreases of responses are less than 7.9% after 2,000 bends of 40°. Both bending stability and high sensitivity are two important problems to be solved in developing flexible sensors. The flexible sensor based on flower-like polyaniline coated filter paper (PCFP) was developed by spraying for the first time, achieving the non-contact and fast detection of nitroaromatic explosives. Hierarchical structure, high permeability of filter paper and the interaction between amino groups of PANI and nitro groups of nitroaromatic explosives contributed to the sensitive and fast response to 2, 4, 6-trinitrotoluene (TNT), picric acid (PA) and 2, 4-dinitrotoluene (DNT) at room temperature. The responses of PCFP to TNT, PA and DNT run up to about 237.7, 100.6 and 80.1%, respectively. The average response time and recovery time to TNT, PA and DNT are no more than 8.1 and 1.9 s, respectively. The theoretical limit of detection for TNT and PA is 0.094 and 0.029 ppb, respectively. More importantly, the special interlaced flower-like structures of polyaniline contributed to the good flexural stability. The response fluctuation to TNT, PA and DNT do not exceed 7% in the bending process and the decreases of responses are less than 7.9% after 2000 bends of 40°. In addition, the spraying method is suitable for economical, efficient and large-scale preparation of paper-based flexible sensors. [ABSTRACT FROM AUTHOR]

Abstract A high-sensitivity fluorescence visualization paper-based sensor is developed and used to achieve specific detection and analysis of three organophosphorus pesticides (OPPs: dimethoate, dichlorvos, and demeton) in a "Turn-off-on" detection mode. The fluorescence visualization paper-based sensor is established through combining double quantum dots (QDs) with high-activity nanoporphyrins (QDs-nanoporphyrin), realizing double nanometer signal amplification and producing different color change responses to these three OPPs. In particular, this approach is based on Partial least squares discriminant analysis (PLSDA) for fingerprint spectrum analysis of three kinds of organophosphorus pesticides in complex matrix (apple and cabbage). Therefore, different concentrations of pesticide residues can be quickly identified at the same time with 100% accuracy for both training set and prediction set. In summary, this method has high selectivity and stability, and thus provides a new approach for the identification of organophosphorus residues in complex systems. Graphical abstract For a new method, not only the double nano signal amplification effect of dual QDs fluorescent color interval variability, but also nano-porphyrin high activity is employed to construct a high-sensitivity fluorescent visualization paper chip sensor, which is characterized in based on the "Turn-off-on" detection mode and producing different color change responses. fx1 Highlights • A paper sensor based on double quantum dots-nanoporphyrin is designed. • The high-sensitivity sensor is fluorescence-visualized based on "off-on" model. • Providing a new theoretical guidance for real-time monitoring of pesticide residues. [ABSTRACT FROM AUTHOR]

• A paper-based piezoresistive sensor with advantages of low-cost, portability, flexibility and disposability was developed. • The resulting device exhibited rapid response and recovery speed (0.6 s and 0.2 s, respectively). • The device was applied to monitoring human physiological signals. A paper-based pressure sensor constructed by sandwiching a piezoresistive film between two pieces of paper substrates with silver electrodes is reported in this work. The resulting devices exhibited rapid response and recovery speed, and the response and recovery times were 0.6 s and 0.2 s, respectively, under a pressure of approximately 1.5 kPa. In addition, the device can be especially sensitive to pressures less than 3 kPa. Finally, the devices were used to monitor physiological signals, including the motions of fingers, vocal cord vibration and wrist pulse. The advantages of paper-based devices, such as low cost, portability and flexibility, will have great potential for expanding the application of resultant sensors in wearable medical devices. [ABSTRACT FROM AUTHOR]