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Highlighted with bio‐degradability, paper‐based flexible pressure sensors receive significant attention in the field of wearable devices for a sustainable future. However, it remains a challenge to possess considerable sensing performance in high humidity and underwater environments, because its structure rapidly breaks down after the hydrophilic cellulose absorbs water. In this study, a facile chemical vapor deposition method is employed to conformally coat a thin hydrophobic layer onto the cellulose fibers, resulting in an encapsulating paper with high moisture tolerance. The well‐maintained porous structure reserves the superior breathability of the paper. A micro‐convex‐structured sensor layer impregnated with MXene serves as the sensing layer. As a result, an all‐paper‐based pressure sensor with high moisture tolerance and breathability is fabricated. This sensor features a broad sensing range (0–60 kPa), acceptable sensitivities (39.58 kPa−1 (0–1.01 kPa), 11.95 kPa−1 (1.01–60 kPa)), a low detection limit of ≈2.8 Pa, response and recovery time (93 and 69 ms), reliable hydrophobic breathability, and excellent repeatability (10 000 cycles). Moreover, this sensor can be safely worn on human skin and can monitor physiological signals in real‐time in different environments (including air, humid environments, and even underwater), providing a reliable, economical, and environmentally friendly solution for wearable technology. [ABSTRACT FROM AUTHOR]

The discriminative detection of volatile primary aliphatic diamines (VPADs) is a relevant and timely issue. This paper explores the distinctive optical features of H-type and J-type aggregates on paper-based (PB) films, namely H-PB and J-PB films, respectively, of a Lewis acidic Zn(salen)-type complex upon chemisorption of vapors of ditopic VPADs versus those of monotopic volatile amines. While volatile monotopic Lewis bases upon chemisorption give rise to mono-adducts accompanied by enhancement of the fluorescence, in contrast, VPADs act as ditopic bases forming di-adducts with distinct optical properties, leading to fluorescence quenching. This behavior enables the sensitive and discriminative detection of VPAD vapors from those of volatile monoamines. For example, for ethylenediamine (EDA), using J-PB films, sensitive detection is achieved with a LOD down to 6.6 ppm, lower than the OSHA permissible exposure limit of 10 ppm for EDA, and a linear dynamic range up to 100 ppm. Instead, H-PB films enable the detection of EDA vapors at higher ppm concentrations (up to 3000 ppm) with a linearity of up to 1000 ppm. Thus, the combination of both H-PB and J-PB films of the Zn(salen)-type complex represents a unique example of the sensitive and discriminative detection of EDA vapors in such a wide concentration range. [ABSTRACT FROM AUTHOR]

This study developed a novel paper-based sensor for the simultaneous analysis of ascorbic acid (AA) and hydroquinone (HQ). The sensor utilized polyvinyl alcohol (PVA)-stabilized silver nanoparticles (AgNPs-PVA) as the reagent probe and PVA media acted as the filter for separation of the analytes. Polydimethylsiloxane (PDMS) and ethanol serve as the stationary phase and eluent, respectively, exploiting the differences in analyte reactions and solubility to achieve their separation on the filter paper. The circular sensor's central zone was AA's detection area, while HQ was detected in the outer ring region. AA induced an immediate color change in the test kit, whereas HQ required a 20-minute elution with ethanol followed by colorimetric analysis. All analytes exhibited relative standard deviations of repeatability and reproducibility below 2.7% and 9.5%, respectively. Under optimal conditions, the linear detection range for HQ was 0.2-2.0 mg⋅L− 1, while AA was 0.1-2.0 mg⋅L− 1. The detection limit was determined to be 0.05 mg⋅L− 1 for AA and 0.1 mg⋅L− 1 for HQ. The recoveries of AA and HQ in cosmetic cream samples ranged from 80 to 110%. The accuracy of the sensor's measurements was further validated by comparison with the HPLC-DAD method. [ABSTRACT FROM AUTHOR]

Abstract Rifampicin-resistant tuberculosis (RR-TB) is a critical issue with significant implications for patient care, public health, and TB control efforts that necessitate comprehensive strategies for detection. This study presents a novel point-of-care diagnostic tool for RR-TB detection employing a peptide nucleic acid (PNA)-paper-based sensor combined with isothermal recombinase polymerase amplification (RPA). The sensor targets mutations in codons 516, 526, and 531 of the rpoB gene, the top three common mutations associated with rifampicin-resistant strains. PNA probes specifically recognised wild-type sequences, generating a visual signal through a reverse hybridisation assay. The absence of a signal was observed when the mutant strains were detected because of the inability to bind the mutant sequence. Our proof-of-concept assay displayed high accuracy (100% for detecting mutations at codons 516, 526, and 531), a short turnaround time (110 min), no cross-reactivity with other bacterial pathogens, and ultrasensitivity. This PNA-paper-based sensor model can be a valuable diagnostic tool for RR-TB detection, providing an accessible diagnostic platform that can be advantageous in resource-limited settings where sophisticated laboratory infrastructure may be lacking.

Heavy metal contamination especially in aqueous media has become an important risk to human health and environment. Therefore, due to the broad distribution of barium (Ba2+) and strontium (Sr2+) ions in the environment and wide variety of their harmful health effects for human, development of efficacious systems for their accurate and selective determination is of great importance. Aiming to develop a point-of-care and easy-to-use sensing device, a paper-based colorimetric sensing device was designed for simultaneous measurement of Ba2+ and Sr2+ ions standing on the basis of the color change of sodium rhodizonate (SR) in the presence of various concentrations of the target analytes. These color changes were photographed using a smartphone, and after analyzing with Photoshop 2022 software, the average variations in the intensities of colors (RGB (red, green, blue) model) were used to draw the calibration curves. The quantitative identification of Ba2+ and Sr2+ ions in a single solution was carried out by masking one of them at a moment. The average color intensities (G) displayed a linear relationship with the concentration of the analytes in the ranges of 5––300 ppm and 5–350 ppm with the limit of detection (LOD) values of 3.64 and 4.75 ppm for Ba2+ and Sr2+ ions, respectively. Moreover, the selectivity of the proposed analytical device was assessed; SR was selective for the target analytes versus the other ions causing a considerable color change. Furthermore, the practical application of this colorimetric device was investigated by the excellent performance in real samples indicating its potential for field applications. [ABSTRACT FROM AUTHOR]

The development of portable and cost-effective sensing system for Hg2+ quantitation is highly demanded for environmental monitoring. Herein, an on-site, rapid and portable smartphone readout device based Hg2+ sensing system integrating nitrogen-doped carbon quantum dots (NCDs) modified paper strip was proposed, and the physicochemical properties of NCDs were characterized by high resolution TEM, FTIR, UV–vis absorption spectrum and fluorescence spectral analysis. The modified paper strip was prepared via "ink-jet" printing technology and exhibits sensitive fluorescence response to Hg2+ with fluorescence color of bright blue (at the excitation/emission wavelength of 365/440 nm). This portable smartphone-based sensing platform is highly selective and sensitive to Hg2+ with the limit of detection (LOD) of 10.6 nM and the concentration range of 0–130 nM. In addition, the recoveries of tap water and local lake water were in the range of 89.4% to 109%. The cost-effective sensing system based on smartphone shows a great potential for trace amounts of Hg2+ monitoring in environmental water samples. [ABSTRACT FROM AUTHOR]

Heavy metals are particularly damaging contaminants in the environment, and even trace concentrations represent a risk to human health due to their toxicity. To detect the heavy metals of Mn2+ and Co2+ ions, a novel selective reusable paper-based Fluorescence naked-eye sensor based on naphthalene cationic Schiff base (NCSB) was synthesized and confirmed using FT-IR, 1 H-NMR, and MS tools. Based on a blue to colorless color change in the aqueous solution, the NCSB sensor is utilized to Mn2+ and Co2+ cations selectively among other metal ions (Fe2+, Cu2+, Mg2+, Ni2+, Zn2+, Cd2+, Hg2+, Pb2+, Sn2+ and Cr3+). In the aqueous medium, the NCSB sensor displayed high sensitivity, with limits of detection (LOD) values of 0.014 µM (14.08 nM) and 0.041 µM (41.47 nM) for Mn2+ and Co2+ cations, respectively. The paper-based sensor naked-eye detected Mn2+ and Co2+ cations in water at concentrations as low as 0.65 µM (65 nM) and 0.086 µM (86 nM), respectively. It was discovered that 5 min of incubation time and a pH range of 7 to 11 were optimal for the complexation reaction between the Mn2+ and Co2+ ions and the NCSB sensor. Through a static quenching process, the interaction of the different metal ions with the Schiff base group in the NCSB molecule results in the development of a ground-state non-fluorescent complex. NCSB sensor was also successfully applied in analysis of Mn2+ and Co2+ in environmental water with good recoveries of 94.8–105.9%. The theoretical calculations based on density functional theory (DFT) studies are in support of experimental interpretations. The links between the input factors and the anticipated response were evaluated using the quadratic model of the response surface methodology (RSM) modeling. [ABSTRACT FROM AUTHOR]

The wide range of pressure detection and the exceptional linearity are essential performance parameters for flexible pressure sensors, enabling them to adapt to diverse scenarios and acquire information accurately. However, currently available "ultra‐wide range" piezoresistive sensors lack an optimal solution that effectively balances sensing properties, device thickness, and process cost. This study proposes a distinctive approach by introducing a Janus conductive structure assembled with dual resistive sensitive layers. The design allows for a pressure‐induced staged transformation of the current transport path, effectively mitigating variations and saturation in sensor resistance over a wide pressure range. The resulting piezoresistive sensor demonstrates an unprecedented detection range of 0–3800 kPa, showcasing remarkable sensitivity of 4.11 kPa−1 and outstanding linearity of 99.9% within the range of 0–1000 kPa. Additionally, the sensor boasts a thickness of only ≈200 µm, made possible through the utilization of a cellulose nanofibers material matrix. These performance achievements stand at the forefront when compared to existing reports. This research explores the potential applications of these sensors and extended arrays in the domains of human health and motion monitoring. It investigates their utility in gait analysis for assisted posture correction, as well as in the assessment and rehabilitation of gait instability. [ABSTRACT FROM AUTHOR]

Neurotransmitters are essential chemical messengers required for proper brain function, and any changes in their concentrations can lead to neuronal diseases. Therefore, sensitive and selective detection is crucial. This study presents a fast and simple colorimetric method for dopamine detection using three reagent solutions: AgNP and MPA, Ag/Au nanocomposite, and mercaptophenylacetic acid. TEM images showed a narrow distribution of Ag and Au nanoparticles with average sizes of 20 nm and 13 nm, respectively, with gold nanoparticles bound to the edges of silver nanoparticles. A paper-based biosensor was created using manual wax printing for the colorimetric detection of dopamine. Visual detection onsite showed color changes with both the silver nanoparticles and mercaptophenylacetic acid mixture and the silver–gold nanoparticle composite. Electrochemical detection using a glassy carbon electrode modified with 8 mM mercaptophenylacetic acid demonstrated high selectivity and sensitivity towards dopamine, with a peak in the range of 0.7–0.9 V. Interferences were minimized, ensuring high sensitivity and selective detection of dopamine. [ABSTRACT FROM AUTHOR]

Inductive contact force sensors, known for their high precision and anti-interference capabilities, hold significant potential applications in fields such as wearable and medical monitoring devices. Most of the current research on inductive contact force sensors employed novel nanomaterials as sensitive elements to enhance their sensitivity and other performance characteristics. However, sensors developed through such methods typically involve complex preparation processes, high costs, and difficulty in biodegradation, which limit their further development. This article introduces a new flexible inductive contact force sensor using paper as a sensitive element. Paper inherently possesses micro- and nanostructures on its surface and interior, enabling it to sensitively convert changes in contact force into changes in displacement, making it suitable for use as the sensor's sensitive element. Additionally, the advantages of paper also include its great flexibility, low cost, wide availability, and biodegradability. Performance testing on this flexible sensor showed good repeatability, hysteresis, sensitivity, and consistency. When used in experiments for monitoring human motion and respiration, this sensor also exhibited great detection performance. The proposed inductive paper-based flexible contact force sensor, with its simple structure, easy manufacturing process, cost-effectiveness, eco-friendliness, and good sensing performance, provides new insights into research for contact force sensors. [ABSTRACT FROM AUTHOR]

A one-shot CO2 laser-based strategy to generate conductive reduced graphene oxide (rGO) decorated with nanoceria (nCe) is proposed. The 2D/0D rGO-nCe films, integrated as catalytic sensing layers in paper-based sensors, were employed for on-site monitoring of indoor fogging treatments against Listeria monocytogenes (Lm), a ubiquitous pathogenic bacterium. The rGO-nCe laser-assisted synthesis was optimized to preserve the rGO film morphological and electron-transfer features and simultaneously integrate catalytic nCe. The films were characterized by microscopical (SEM), spectroscopical (EDX, Raman, and FTIR), and electrochemical techniques. The most performing film was integrated into a nitrocellulose substrate, and the complete sensor was assembled via a combination of xurography and stencil printing. The rGO-nCe sensor's catalytic activity was proved toward the detection of H2O2, obtaining sensitive determination (LOD = 0.3 µM) and an extended linear range (0.5–1500 µM). Eventually, the rGO-nCe sensor was challenged for the real-time continuous monitoring of hydrogen peroxide aerosol during no-touch fogging treatment conducted following the EU's recommendation for biocidal product use. Treatment effectiveness was proved toward three Lm strains characterized by different origins, i.e., type strain ATCC 7644, clinical strain 338, and food strain 641/6II. The sensor allows for discrimination and quantification treatments at different environmental biocidal amounts and fogging times, and correlates with the microbiological inhibition, promoting the proposed sensor as a useful tool to modulate and monitor no-touch treatments. [ABSTRACT FROM AUTHOR]

Strontium-90 (90Sr) is a major radioactive component that has attracted great attention, but its detection remains challenging since there are no specific energy rays indicative of its presence. Herein, a biosensor that is capable of rapidly detecting Sr2+ ions is demonstrated. Simple colorimetric method for sensitive detection of Sr2+ with the help of single-stranded DNA was developed by preparing MnO2 nanorods as oxidase mimic catalysis 3,3′,5,5′-tetramethylbenzidine (TMB). Under weakly acidic conditions, MnO2 exhibited a strong oxidase-mimicking activity to oxidize colorless TMB into blue oxidation products (oxTMB) with discernible absorbance signals. Nevertheless, the introduction of a guanine-rich DNA aptamer inhibited MnO2-mediated TMB oxidation and reduced oxTMB formation, resulting in blue fading and diminished absorbance. Upon the addition of strontium ions to the system, the aptamers formed a stable G-quadruplex structure with strontium ions, thereby restoring the oxidase-mimicking activity of MnO2. Under the best experimental conditions, the absorbance exhibits a linear relationship with the Sr2+ concentration within the range 0.01–200 μM, with a limit of detection of 0.0028 µM. When the concentration of Sr2+ from 10−8 to 10−6 mol L−1, a distinct color change gradient could be observed in paper-based sensor. We successfully applied this approach to determine Sr2+ in natural water samples, obtaining recoveries ranging from 97.6 to 103% with a relative standard deviation of less than 5%. By providing technical solutions for detection, our work contributed to the effective monitoring of transportation of radioactive Sr in the environment. [ABSTRACT FROM AUTHOR]

Detection of mycotoxins in food is essential due to their potential harm to human and animal health. However, developing affordable and rapid methods for their detection, particularly with the necessary selectivity to differentiate between various mycotoxins, remains a challenge. Herein, we present low-cost paper-based sensing platforms modified with curcumin, a natural polyphenolic compound, for the electrochemical and optical detection of ochratoxin A (OTA). By exploiting the fluorescence quenching effect of OTA on curcumin through Förster energy transfer, we successfully conducted optical detection with LODs of 0.09 ng mL−1 and a linear range of 0.5 to 15 ng mL−1. Additionally, by using electrochemical impedance spectroscopy and a portable instrument, we detected OTA with a limit of detection (LOD) as low as 0.045 ng mL−1. These sensitivity levels meet the requirements established by food regulatory agencies for monitoring food quality in relation to OTA contamination. Our curcumin-modified paper-based sensors offer a compelling combination of simplicity in manufacturing and cost-effectiveness, underscoring their potential for routine food quality monitoring, especially concerning ochratoxin A.

Flexible paper-based force sensors have garnered significant attention for their important potential applications in healthcare wearables, portable electronics, etc. However, most studies have only used paper as the flexible substrate for sensors, not fully exploiting the potential of paper's micro-nanostructure for sensing. This article proposes a novel approach where paper serves both as the sensitive element and the flexible substrate of force sensors. Under external mechanical forces, the micro-nanostructure of the conductive-treated paper will change, leading to significant changes in the related electrical output and thus enabling sensing. To demonstrate the feasibility and universality of this new method, the article takes paper-based capacitive pressure sensors and paper-based resistive strain sensors as examples, detailing their fabrication processes, constructing sensing principle models based on the micro-nanostructure of paper materials, and testing their main sensing performance. For the capacitive paper-based pressure sensor, it achieves a high sensitivity of 1.623 kPa−1, a fast response time of 240 ms, and a minimum pressure resolution of 4.1 Pa. As for the resistive paper-based strain sensor, it achieves a high sensitivity of 72 and a fast response time of 300 ms. The proposed new method offers advantages such as high sensitivity, simplicity in the fabrication process, environmental friendliness, and cost-effectiveness, providing new insights into the research of flexible force sensors. [ABSTRACT FROM AUTHOR]

This work discusses surface modification of cellulose paper specimens for compatibility with nitrogen and sulfur co‐doped carbon dots (NSCDs) for lead ion sensing. The interaction of carbon dots (CDs) and cellulose fibers was investigated using silane or chitosan‐modified cellulose papers. It was found that modified papers could reduce undesirable redistribution of CDs, during paper drying. Also, only chitosan‐modified filter paper was suitable for the successful immobilization of NSCDs. The effect of paper type, chitosan amount, pH, and NSCDs concentration was also studied, and a Whatman No. 42 filter paper modified with chitosan (1% w/v), pH 8.0, and an NSCD concentration of 2.5 g L−1 being selected for further studies. The sensor exhibited high selectivity for lead(II) compared with other metal ions because lead(II) resulted in the most significant changes in the emitted light intensity. Variations in NSCDs fluorescence were measured using a fluorescence imaging system. The NSCDs‐paper sensor showed a linear relationship between mean fluorescence intensity and lead(II) in the concentration range of 5.00–1.25 × 102 μmol L−1 with a correlation coefficient (R2) of 0.9988 and a detection limit of 4.50 μmol L−1. The suggested method showed satisfying results for lead(II) determination in different samples as a fast and low‐cost approach with on‐site application. [ABSTRACT FROM AUTHOR]

Neurotransmitters are essential chemical messengers required for proper brain function, and any changes in their concentrations can lead to neuronal diseases. Therefore, sensitive and selective detection is crucial. This study presents a fast and simple colorimetric method for dopamine detection using three reagent solutions: AgNP and MPA, Ag/Au nanocomposite, and mercaptophenylacetic acid. TEM images showed a narrow distribution of Ag and Au nanoparticles with average sizes of 20 nm and 13 nm, respectively, with gold nanoparticles bound to the edges of silver nanoparticles. A paper-based biosensor was created using manual wax printing for the colorimetric detection of dopamine. Visual detection onsite showed color changes with both the silver nanoparticles and mercaptophenylacetic acid mixture and the silver–gold nanoparticle composite. Electrochemical detection using a glassy carbon electrode modified with 8 mM mercaptophenylacetic acid demonstrated high selectivity and sensitivity towards dopamine, with a peak in the range of 0.7–0.9 V. Interferences were minimized, ensuring high sensitivity and selective detection of dopamine.

Inductive contact force sensors, known for their high precision and anti-interference capabilities, hold significant potential applications in fields such as wearable and medical monitoring devices. Most of the current research on inductive contact force sensors employed novel nanomaterials as sensitive elements to enhance their sensitivity and other performance characteristics. However, sensors developed through such methods typically involve complex preparation processes, high costs, and difficulty in biodegradation, which limit their further development. This article introduces a new flexible inductive contact force sensor using paper as a sensitive element. Paper inherently possesses micro- and nanostructures on its surface and interior, enabling it to sensitively convert changes in contact force into changes in displacement, making it suitable for use as the sensor’s sensitive element. Additionally, the advantages of paper also include its great flexibility, low cost, wide availability, and biodegradability. Performance testing on this flexible sensor showed good repeatability, hysteresis, sensitivity, and consistency. When used in experiments for monitoring human motion and respiration, this sensor also exhibited great detection performance. The proposed inductive paper-based flexible contact force sensor, with its simple structure, easy manufacturing process, cost-effectiveness, eco-friendliness, and good sensing performance, provides new insights into research for contact force sensors.

Glyphosate is one of the most effective herbicides and is extensively used in agriculture to improve crop production. However, its toxicity and carcinogenicity stimulate the development of potent, rapid, and highly selective sensors for glyphosate. In this study, we have successfully developed a rational and effective method for detecting glyphosate concentrations in the nanomolar range through luminescence enhancement. For this purpose, we synthesized NH2-MIL-88B (Fe) (MIL = Material Institute Lavoisier) metal–organic framework (MOF)-based nanocrystals (NCs) using the hydrothermal method and applied it for glyphosate detection in an aqueous medium. The MOF NCs contain coordinative ligands (2-aminoterephthalic acid) and metal clusters. The Fe clusters act as luminescence quenchers, suppressing emission from the MOF due to photoinduced electron transfer (PET) from the ligand to Fe3+ ions. The phosphate group of glyphosate competes with the carboxylate of the ligand in the MOF. As a result, the coordination between ligand molecules and Fe metal clusters in the MOF weakens, causing the ligand molecules to separate from the Fe cluster. This process diminishes the PET and regenerates the ligand emission at 450 nm. The luminescence enhancement exhibits high selectivity toward glyphosate and shows minimal interference from various pesticides and metal ions. The limit of detection was calculated as 198 nM, and the performance of the detection probe was evaluated in drinking water. Finally, MOF NCs-coated circular paper strips were prepared and successfully applied to detect glyphosate at femtomolar concentrations. [ABSTRACT FROM AUTHOR]

Paper-based sensors overcome the drawbacks of conventional sensors in terms of their flexibility, portability, and stability compared to conventional sensors. Moreover, as a noninvasive bodily fluid, saliva contains various biomarkers related to physical status, which makes it perfectly matched with to use of paper-based sensors to manufacture a convenient and inexpensive disposable sensing device. This review focuses on the recent advances and progress in the design of paper-based salivary sensors and their applications. The first part mainly discusses various paper-based sensors and their advanced compositions, including dipstick assay, lateral flow assay, and microfluidic analytical device. Different detection methods in salivary biomarker detection are specially introduced in the secondary section, then their multiple potential applications and prospects are summarized. The sensor has excellent advantages for saliva detection, provides a reliable platform for point-of-care tests and telemedicine, and epically promotes the development of the medical Internet of Things. [ABSTRACT FROM AUTHOR]

Moisture detection through naked eye is important in various fields, including pharmaceuticals, fuels, materials, and agriculture. In this study, we demonstrate the use of a strategically designed organic molecule, 2AMBP, for the detection of moisture in organic solvents and real‐life samples. The principle behind this sensory system involves fluoride‐induced deprotonation followed by water‐induced re‐protonation. The deprotonated form of 2AMBP displays a color‐changing response (yellow to pink) even in trace amounts of water (LOD: 0.0207 % by spectrophotometric analysis), making it a highly sensitive probe for detecting moisture. We show that the anionic receptor moieties of 2AMBP can be employed for the quantification of water impurity in various real‐life samples, and we develop inexpensive, reusable, dye‐coated paper sensor for quick onsite moisture detection and quantification. Interestingly, a smart phone camera can be used to provide relative RGB values that directly correlate to the amount of moisture present in the sample. The 2AMBP‐F‐ exhibits significant changes in fluorescence properties in the presence and absence of water, which makes it an effective fluorescent switch for detecting moisture. Overall, 2AMBP is a highly sensitive, sustainable material that can be conveniently used by laymen for moisture detection without the need for specific instruments or expertise. [ABSTRACT FROM AUTHOR]

The detection of biogenic amines released from degraded meats is an effective method for evaluating meat freshness. However, existing traditional methods like titration are deemed tedious, while the use of sophisticated analytical instruments is not amenable to field testing. Herein, a cyanostilbene-based fluorescent array was rapidly fabricated using macroarray synthesis on a cellulose paper surface to detect amines liberated from spoiled beef, fish, and chicken. The fluorescence changes of immobilized molecules from the interaction with gaseous amines were used to monitor changes in freshness levels. Thanks to the high-throughput nature of macroarray synthesis, a set of highly responsive molecules such as pyridinium and dicyanovinyl moieties were quickly revealed. Importantly, this method offers flexibility in sensing applications including (1) sensing by individual sensor molecules, where the fluorescence response correlated well with established titration methods, and (2) collective sensing whereby chemometric analysis was used to provide a cutoff of freshness with 73–100% accuracy depending on meat types. Overall, this study paves the way for a robust and cost-effective tool for monitoring meat freshness. [ABSTRACT FROM AUTHOR]

This research explores the dynamics of a fluidically loaded Bi-Material cantilever (B-MaC), a critical component of μPADs (microfluidic paper-based analytical devices) used in point-of-care diagnostics. Constructed from Scotch Tape and Whatman Grade 41 filter paper strips, the B-MaC's behavior under fluid imbibition is examined. A capillary fluid flow model is formulated for the B-MaC, adhering to the Lucas–Washburn (LW) equation, and supported by empirical data. This paper further investigates the stress–strain relationship to estimate the modulus of the B-MaC at various saturation levels and to predict the behavior of the fluidically loaded cantilever. The study shows that the Young's modulus of Whatman Grade 41 filter paper drastically decreases to approximately 20 MPa (about 7% of its dry-state value) upon full saturation. This significant decrease in flexural rigidity, in conjunction with the hygroexpansive strain and coefficient of hygroexpansion (empirically deduced to be 0.008), is essential in determining the B-MaC's deflection. The proposed moderate deflection formulation effectively predicts the B-MaC's behavior under fluidic loading, emphasizing the measurement of maximum (tip) deflection using interfacial boundary conditions for the B-MaC's wet and dry regions. This knowledge of tip deflection will prove instrumental in optimizing the design parameters of B-MaCs. [ABSTRACT FROM AUTHOR]

In this paper, the behavior of the Bi-Material Cantilever (B-MaC) response deflection upon fluidic loading was experimentally studied and modeled for bilayer strips. A B-MaC consists of a strip of paper adhered to a strip of tape. When fluid is introduced, the paper expands while the tape does not, which causes the structure to bend due to strain mismatch, similar to the thermal loading of bi-metal thermostats. The main novelty of the paper-based bilayer cantilevers is the mechanical properties of two different types of material layers, a top layer of sensing paper and a bottom layer of actuating tape, to create a structure that can respond to moisture changes. When the sensing layer absorbs moisture, it causes the bilayer cantilever to bend or curl due to the differential swelling between the two layers. The portion of the paper strip that gets wet forms an arc, and as the fluid advances and fully wets the B-MaC, the entire B-MaC assumes the shape of the initial arc. This study showed that paper with higher hygroscopic expansion forms an arc with a smaller radius of curvature, whereas thicker tape with a higher Young's modulus forms an arc with a larger radius of curvature. The results showed that the theoretical modeling could accurately predict the behavior of the bilayer strips. The significance of paper-based bilayer cantilevers lies in their potential applications in various fields, such as biomedicine, and environmental monitoring. In summary, the novelty and significance of paper-based bilayer cantilevers lie in their unique combination of sensing and actuating capabilities using a low-cost and environmentally friendly material. [ABSTRACT FROM AUTHOR]

The increasing prevalence of arsenic (As3+) in water and its health impacts necessitate advanced detection methods. Similarly, monitoring L-Cysteine, a vital thiol-containing amino acid, is crucial for assessing physiological processes and disorders. This study presents a novel method for detecting As3+ and L-Cysteine in food samples using 4-amino-3-(D-galactopentitol-1-yl)-5-mercapto-1,2,4-triazole (AMTPP) functionalized silver nanoparticles (AMTPP-AgNPs) by UV/Vis spectrophotometric method and smartphone-assisted inkjet-printed paper-based sensors. AMTPP-AgNPs, synthesized through a detailed process, show exceptional selectivity and sensitivity to As3+ and L-Cysteine, undisturbed by other metal ions and amino acids. Characterization techniques like FTIR, DLS, Zeta Potential, AFM, and SEM detailed their morphological and interaction properties. Optimizing detection parameters, such as response time, pH, and temperature, improved sensitivity and achieved low detection limits. The limits of detection (LODs) were 0.0052 μM for L-cysteine and 0.0092 μM for As3+, as calculated using UV–Vis spectrophotometric methods. The method also demonstrated high recovery rates in spiked meat and corn samples. This research offers a cost-effective, rapid method for on-site food analysis, significantly aiding environmental and public health monitoring. [Display omitted] • Novel AMTPP functionalized silver nanoparticles were synthesized. • Dual detection strategies based on AMTPP-AgNPs. • Inkjet printed paper sensor developed for detection of As3+ and cysteine. • Qualitative and quantitative determination of As3+ and cysteine in food samples. [ABSTRACT FROM AUTHOR]

Rapid detection of plant viruses is crucial for ensuring the safety of agricultural production. In this study, a paper-based molecularly imprinted polymers (MIPs) sensor was developed for visual detection of tobacco mosaic virus (TMV). Two types of MIPs were synthesized as artificial antibodies: paper-based MIPs and monoclonal MIPs. The sandwich strategy achieved high sensitivity (with a limit of detection of 4.8 fM) and high selectivity (with an imprinting factor of 5.25) for TMV detection. This sensor eliminated the need for costly and unstable biological agents such as natural antibodies and DNA, enabling detection visible to the naked eye within 10–20 min. Overall, the paper-based MIPs sensor costs as little as 8.6 cents (1 cents for smaller sizes) and is easy to store and cut. This approach provides a new method for the rapid field detection of plant viruses such as TMV and is crucial for ensuring the safety of agricultural production. • Paper-based sandwich MIPs sensor. • Low-cost sensors as low as 8.6 cents each. • High sensitivity (LOD 4.8 fM) and specificity (IF 5.25). • Naked eyes detection under visible light or UV light within 10–20 min. [ABSTRACT FROM AUTHOR]

A novel fluorescent probe was fabricated using fluorescein-based ionic liquids (ILs) to effectively achieve rapid and accurate detection of Hg2+ and CH 3 Hg+ in food. A probe developed by addition of modified fluorescein into the functionalised ILs presented a promising sensitivity toward Hg2+ and CH 3 Hg+ at concentrations of 0.4 and 60 nM, respectively. In addition, the novel probe could achieve visual and timely detection of Hg2+ and CH 3 Hg+ by the naked eyes at concentrations of 0.1 and 1 μM, respectively. The probe could also overcome the interference of potential ions and common organic ligands and detect Hg2+ and CH 3 Hg+ in real food samples, such as green tea and liquor. The probe could be converted into a paper-based sensor to visually detect Hg2+ and CH 3 Hg+ at levels as low as 10 nM. [Display omitted] • The probe could achieve visual and real-time monitoring for trace Hg2+ and CH 3 Hg+. • The probe improved sensitivity through electrostatic attraction of ionic liquids. • Satisfactory recoveries were obtained in various complex real samples. • This probe could be easily assembled into a paper strip as a portable tool. [ABSTRACT FROM AUTHOR]

• Paper-based sensor detects perchlorate using albumin-conjugated gold nanoparticles. • Colorimetric detection method integrates with smartphone for on-site analysis. • Eco-friendly and cost-effective solution for rural and industrial areas. Perchlorate, a prevalent and dangerous contaminant, is being increasingly found in untreated wastewater from urban areas and industrial discharges, as well as in unmonitored surface and groundwater sources. The urgent need for the creation of straightforward, efficient, and environmentally friendly sensing techniques to detect perchlorate in water. Cellulosic paper-based sensors show great promise as sustainable tools for detecting chemical pollutants. The study aimed to develop and evaluate the effectiveness of a paper-based sensor for detecting perchlorate levels in water samples. The approach showcased a reliable perchlorate colorimetric detection method, integrating digital smartphone imagery with paper-based sensors. The sensor employs a colorimetric assay that relies on the modification of gold nanoparticles with egg albumin protein, a material derived from biological sources. A digital smartphone facilitates on-site colorimetric data collection, and image processing methods are used to determine the presence of perchlorate in water samples based on these digital pictures. The grayscale color intensity derived from digital images is utilized for quantitative analysis. Comprehensive parametric evaluations were conducted to examine the stability and selectivity of the color intensities obtained from the sensor. The limits of detection and quantification are established at 2.86 µg/L and 9.55 µg/L, respectively. This study delivers a facile, highly sensitive, and cost-effective technique for the detection of perchlorate, particularly advantageous in industrial and rural settings where advanced detection devices are scarce. [Display omitted] [ABSTRACT FROM AUTHOR]

Norfloxacin (NOR) and levofloxacin (LEV) are the two most frequently used fluoroquinolones (FQs) in clinic. Their residues seriously endanger the ecosystem and human health. Due to their similarity in structure and properties, it is urgent to develop an efficient and sensitive strategy for detection and differentiation. Herein, we synthesized a novel ratiometric fluorescent sensor for the first time by combining N, S co-doped carbon dots (CDs) and the precursors of Tb-MOFs through a facile one-pot method. The introduction of CDs effectively facilitated the energy transfer between Tb3+ and FQs, overcoming the limitation that single Tb-MOFs could not identify similar antibiotics. Specifically, the presence of NOR resulted in reverse signal response through the inner filter effect and antenna effect. The synergistic effect of these two mechanisms contributed to achieving signal amplification accompanied by a distinguishable color transition. The limit of detection (LOD) was 0.036 μM. Different from NOR, the addition of LEV reduced the electron density of the system, weakened the coordination ability of Tb3+ with LEV, and induced a single signal response with Tb3+ fluorescence intensity as a reference signal (LOD = 0.383 μM). Furthermore, the method proved to be rapid and visual, allowing for the straightforward analysis of FQs residues in water, food matrices, and biological samples with satisfactory precision. By integrating N, S-CDs@Tb-MOFs with flexible substrates, the paper-based sensor facilitated the visual quantitative determination of FQs by reading RGB values. The developed sensor presents a promising strategy for the identification and real-time monitoring of antibiotics. [Display omitted] • A novel ratiometric fluorescent sensor was developed by in-situ encapsulation. • The introduction of CDs can trigger a dual-mode sensing strategy to identify FQs. • The method can simultaneously realize the fluorescent and visual detection of FQs. • The sensor exhibited reliability and practicability in real samples. • The paper-based device shows great potential for visual determination of FQs. [ABSTRACT FROM AUTHOR]

Printing technology for electronic devices has garnered considerable attention owing to its rapid and massive productivity under ambient conditions. In this study, a facile approach is proposed for manufacturing cellulose paper-based strain sensors with Ni/multi-walled carbon nanotube (MWCNT) composites using roll stamping technology. This process enables the fabrication of stable sensing structures owing to the formation of stable Ni core-enveloping structures in the MWCNT interlacing network. In particular, the rheological properties of the composites revealed shear thinning and thixotropic behavior, which resulted in fine printing of the sensing electrodes. Furthermore, the shape of the printed patterns, imparted by the pattern morphology, significantly influenced the strain-sensing performance. In particular, the Ni/MWCNT composite-based strain sensor exhibited a higher gauge factor of 13.9, with a high sensing recovery of 90.4% and stability over 23,500 bending cycles. [ABSTRACT FROM AUTHOR]

An aptamer is a synthetic oligonucleotide, referring to a single-stranded deoxyribonucleic acid or ribonucleic acid ligand produced by synthesis from outside the body using systematic evolution of ligands by exponential enrichment (SELEX) technology. Owing to their special screening process and adjustable tertiary structures, aptamers can bind to multiple targets (small molecules, proteins, and even whole cells) with high specificity and affinity. Moreover, due to their simple preparation and stable modification, they have been widely used to construct biosensors for target detection. The paper-based sensor is a product with a low price, short detection time, simple operation, and other superior characteristics, and is widely used as a rapid detection method. This review mainly focuses on the screening methods of aptamers, paper-based devices, and applicable sensing strategies. Furthermore, the design of the aptamer-based lateral flow assay (LFA), which underlies the most promising devices for commercialization, is emphasized. In addition, the development prospects and potential applications of paper-based biosensors using aptamers as recognition molecules are also discussed. [ABSTRACT FROM AUTHOR]

Flexible and wearable sensors are of paramount importance in applications like electronic skin, health monitoring, and human–computer interactions. However, mass production of flexible sensors with versatile, high-performance, low-cost, and easy-to-dispose features remains a huge challenge. Herein, based on a strategy of bionics inspired by the slit receptors in arthropods, a flexible paper-based sensor with macrocracks is developed. And a large number of irregular microdomes are formed on the surfaces of folded paper, which attributes to the conductive composites constructed by carbon nanomaterials and poly-(dimethylsiloxane) (PDMS). Macrocracks and microdomes are helpful to achieve outstanding dual mechanical strain/pressure signal sensing functions. The materials used and the fabricating method employed are cost-efficient and convenient. As a result, the paper-based sensor exhibits a gauge factor of 64 within the strain range of 1% and excellent stability over 1500 cycles. When serving as a pressure sensor, it shows a high sensitivity of 1.4 kPa–1 in the range within 0.5 kPa. Also, the paper-based sensor shows an environmentally friendly feature and can be almost disposed of naturally, indicating that the bioinspired sensor could serve as disposable green flexible electronics, which has potential usage in wearable applications. [ABSTRACT FROM AUTHOR]