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A simple strategy to rapidly detect glucose was developed by utilizing core (Fe3O4)–shell (Pt) magnetic nanoparticles (Fe3O4@Pt NPs) as a nanoenzyme and a paper-based colorimetric sensor. In the presence of H2O2, Fe3O4@Pt NPs catalyze the redox reaction of 3,3′,5,5′-tetramethylbenzidine (TMB) and generate a colour change from colourless to blue. On this basis, a colorimetric glucose sensing method assisted by glucose oxidase (GOx) was developed. Under the optimal conditions, the detection limits of the proposed assay for H2O2 and glucose were 0.36 µM and 1.27 µM, respectively. Furthermore, the fabricated colorimetric method was successfully applied to analyze glucose concentrations by using a paper device as a measuring platform without a spectrometer. In addition, this method exhibited satisfactory recovery for glucose detection in human serum samples and urine samples, which satisfied the requirements for normal detection of real samples. This study provides a good candidate for health monitoring of glucose and also expands the applications of nanoenzymes and paper-based colorimetric assays in point-of-care testing.

A dual-mode lab-on-paper device based on BiVO4/FeOOH nanocomposites as an efficient generating photoelectrochemical (PEC)/colorimetric signal reporter has been successfully constructed by integration of the lab-on-paper sensing platform and PEC/colorimetric detection technologies for sensitive detection of carcinoembryonic antigen (CEA). Concretely, the BiVO4/FeOOH nanocomposites were in situ synthesized onto the paper-working electrode (PWE) through hydrothermal synthesis of the BiVO4 layer on cellulose fibers (paper-based BiVO4) which were initially modified by Au nanoparticles for improving the conductivity of three dimensional PWE, and then the photo-electrodeposition of FeOOH onto the paper-based BiVO4 to construct the paper-based BiVO4/FeOOH for the portable dual-mode lab-on-paper device. The obtained nanocomposites with an FeOOH needle-like structure deposited on the BiVO4 layer exhibits enhanced PEC response activity due to its effective separation of the electron–hole pair which could further accelerate the PEC conversion efficiency during the sensing process. With the introduction of CEA targets onto the surface of nanocomposite-modified PWE assisted by the interaction with the CEA antibody from a specific recognition property, a signal-off PEC signal state with a remarkable photocurrent response decreasing trend can be achieved, realizing the quantitative detection of CEA with the PEC signal readout mode. By means of a smart origami paper folding, the colorimetric signal readout is achieved by catalyzing 3,3′,5,5′-tetramethylbenzidine (TMB) to generate blue oxidized TMB in the presence of H2O2 due to the satisfied enzyme-like catalytic activity of the needle-like structure, FeOOH, thereby achieving the dual-mode signal readout system for the proposed lab-on-paper device. Under the optimal conditions, the PEC and colorimetric signals measurement were effectively carried out, and the corresponding linear ranges were 0.001–200 ng·mL−1 and 0.5–100 ng·mL−1 separately, with the limit of detection of 0.0008 and 0.013 ng·mL−1 for each dual-mode. The prepared lab-on-paper device also presented a successful application in serum samples for the detection of CEA, providing a potential pathway for the sensitive detection of target biomarkers in clinical application.

A dual-mode lab-on-paper device based on BiVO4/FeOOH nanocomposites as an efficient generating photoelectrochemical (PEC)/colorimetric signal reporter has been successfully constructed by integration of the lab-on-paper sensing platform and PEC/colorimetric detection technologies for sensitive detection of carcinoembryonic antigen (CEA). Concretely, the BiVO4/FeOOH nanocomposites were in situ synthesized onto the paper-working electrode (PWE) through hydrothermal synthesis of the BiVO4 layer on cellulose fibers (paper-based BiVO4) which were initially modified by Au nanoparticles for improving the conductivity of three dimensional PWE, and then the photo-electrodeposition of FeOOH onto the paper-based BiVO4 to construct the paper-based BiVO4/FeOOH for the portable dual-mode lab-on-paper device. The obtained nanocomposites with an FeOOH needle-like structure deposited on the BiVO4 layer exhibits enhanced PEC response activity due to its effective separation of the electron–hole pair which could further accelerate the PEC conversion efficiency during the sensing process. With the introduction of CEA targets onto the surface of nanocomposite-modified PWE assisted by the interaction with the CEA antibody from a specific recognition property, a signal-off PEC signal state with a remarkable photocurrent response decreasing trend can be achieved, realizing the quantitative detection of CEA with the PEC signal readout mode. By means of a smart origami paper folding, the colorimetric signal readout is achieved by catalyzing 3,3′,5,5′-tetramethylbenzidine (TMB) to generate blue oxidized TMB in the presence of H2O2 due to the satisfied enzyme-like catalytic activity of the needle-like structure, FeOOH, thereby achieving the dual-mode signal readout system for the proposed lab-on-paper device. Under the optimal conditions, the PEC and colorimetric signals measurement were effectively carried out, and the corresponding linear ranges were 0.001–200 ng·mL−1 and 0.5–100 ng·mL−1 separately, with the limit of detection of 0.0008 and 0.013 ng·mL−1 for each dual-mode. The prepared lab-on-paper device also presented a successful application in serum samples for the detection of CEA, providing a potential pathway for the sensitive detection of target biomarkers in clinical application. [ABSTRACT FROM AUTHOR]

In this work, indoxyl-glucoside was used as the substrate to develop a cost-effective, paper-based analytical device for the fluorescent and colorimetric dual-mode detection of β-glucosidase activity through a smartphone. The β-glucosidase can hydrolyze the colorless substrate indoxyl-glucoside to release indoxyl, which will be self-oxidized to generate green products in the presence of oxygen. Meanwhile, the green products emit bright blue-green fluorescence under ultraviolet–visible light irradiation at 365 nm. Fluorescent or colorimetric images were obtained by a smartphone, and the red-green-blue channels were analyzed by the Adobe Photoshop to quantify the β-glucosidase activity. Under the optimum conditions, the relative fluorescent and colorimetric signals have a good linear relationship with the activity of β-glucosidase, in the range of 0.01–1.00 U/mL and 0.25–5.00 U/mL, and the limits of detection are 0.005 U/mL and 0.0668 U/mL, respectively. The activities of β-glucosidase in a crude almond sample measured by the fluorescent and colorimetric methods were 23.62 ± 0.53 U/mL and 23.86 ± 0.25 U/mL, respectively. In addition, the spiked recoveries of normal human serum and crude almond samples were between 87.5% and 118.0%. In short, the paper-based device, combined with a smartphone, can provide a simple, environmentally friendly, and low-cost method for the fluorescent and colorimetric dual-mode detection of β-glucosidase activity.

The generation of DNase type I 3′OH DNA ends is closely related to the harm of endogenous reactive oxygen species (ROS) and environmental genotoxic agents. The evaluation of this type of DNA damage plays an important role in clinical intervention and environmental toxicity assessment. Terminal deoxynucleotidyl transferase (TdT)-assisted isothermal amplification (TAIA) offers a facile and versatile way to detect DNase type I 3′OH DNA ends. Its ability of templated-independent isothermal amplification is one unique feature. Here, we reported a paper-based analytical device (PAD) coupled with a smartphone for the detection of DNase type I 3′OH DNA ends using TAIA and colorimetric signal readout. We achieved the integration of cell lysis, DNA extraction, TAIA, horseradish peroxidase (HRP)-enabled colorimetric reaction, and signal readout. This device could achieve a limit of detection of 264 cells with a total assay time of less than 45 min. By combining PAD with a smartphone, the integrated platform could be used for the visual and quantitative analysis of DNA damages with the advantages of ease-to-use, fast response, inexpensive, and instrument free. Furthermore, successful assessment of the genotoxicity in wastewater effluents suggested the great promise of the integrated platform for on-site testing in practical applications.

A novel assay platform consisting of a microfluidic sliding double-track paper-based chip and a hand-held Raspberry Pi detection system is proposed for determining the albumin-to-creatine ratio (ACR) in human urine. It is a clinically important parameter and can be used for the early detection of related diseases, such as renal insufficiency. In the proposed method, the sliding layer of the microchip is applied and the sample diffuses through two parallel filtration channels to the reaction/detection areas of the microchip to complete the detection reaction, which is a simple method well suited for self-diagnosis of ACR index in human urine. The RGB (red, green, and blue) value intensity signals of the reaction complexes in these two reaction zones are analyzed by a Raspberry Pi computer to derive the ACR value (ALB and CRE concentrations). It is shown that the G + B value intensity signal is linearly related to the ALB and CRE concentrations with the correlation coefficients of R2 = 0.9919 and R2 = 0.9923, respectively. It is additionally shown that the ALB and CRE concentration results determined using the proposed method for 23 urine samples were collected from real suffering chronic kidney disease (CKD) patients are in fine agreement with those acquired operating a traditional high-reliability macroscale method. Overall, for point-of-care (POC) CKD diagnosis and monitoring in clinical applications, the results prove that the proposed method offers a convenient, real time, reliable, and low-spending solution for POC CKD diagnosis.

Rapid and sensitive detection of tetracycline (TC) in the aquatic environment is important for the environmental ecosystem and human health. Herein, we presented on the first attempt to construct a fast‐responding gating system by using horseradish peroxidase (HRP)‐loaded functional RNA superstructures (HRP@3D RNA). Proteins were directly loaded into 3D RNA by the rolling circle transcription (RCT) reaction. We found that the specificity of aptamer‐ligand interaction could serve as a triggered manner to release the loaded HRP from 3D RNA. The above general scheme showed a few minutes of rapid release kinetics. According to the controlled‐release mechanism, we designed a disposable origami paper‐based analytical device (doPAD) coupled with HRP@3D RNA for colorimetric detection of TC. This doPAD can realize target recognition and signal readout by taking advantage of the unique spatial control advantages of 3D origami, thus generating a signal of color change that is positively related to the concentration of TC. This doPAD achieved the quantitative analysis of TC with a limit of detection of 10 nM within 41 min. We envision that the platform will be widely used in the field of environmental monitoring and biosensing. [ABSTRACT FROM AUTHOR]

Rapid and sensitive detection of acrylamide in food samples is important for food safety and public health. Here, we describe a disposable origami paper-based analytical device (denoted doPAD) for colorimetric detection of acrylamide. This device uniquely exploits 3D origami folding paper for spatial control of the target recognition and signal readout, thus resulting in a positive correlation between the signals and the analytes. Under optimal conditions, the device achieved the quantitative analysis of acrylamide with a limit of detection of 1.13 μg/L within 120 min (including a derivatization time of 90 min and an assay time of 21 min). Furthermore, our method allowed the rapid and sensitive detection of acrylamide in complex food matrices. We envision that the platform described will find useful applications in the fields of food safety and environmental health.

We report on a novel colorimetric sensor system for highly sensitive detection of formaldehyde (FA) in the gas phase. The sensor is constructed with paper towel as a substrate coated with the sulfuric acid salt of hydroxylamine ((NH2OH)2·H2SO4) together with two pH indicators, bromophenol blue and thymol blue. Upon exposure to FA, the hydroxylamine will react with the absorbed FA to form a Schiff base (H2C=N-OH), thus releasing a stoichiometric amount of sulfuric acid, which in turn induces a color change of the pH indicator. Such a color change was significantly enriched by incorporating two pH indicators in the system. With the optimized molar ratio of the two pH indicators, the color change (from brown to yellow, and to red) could become so dramatic as to be visible to the eye depending on the concentration of FA. In particular, under 80 ppb of FA (the air quality threshold set by WHO) the color of the sensor substrate changes from brown to yellow, which can even be envisioned clearly by the naked eyes. By using a color reader, the observed color change can be measured quantitatively as a function of the vapor concentration of FA, which produces a linear relationship as fitted with the data points. This helps estimate the limit of detection (LOD), to be 10 ppb under an exposure time of 10 min, which is much lower than the air quality threshold set by WHO. The reported sensor also demonstrates high selectivity towards FA with no color change observed when exposed to other common chemicals, including solvents and volatile organic compounds. With its high sensitivity and selectivity, the proposed paper-based colorimetric sensor thus developed can potentially be employed as a low-cost and disposable detection kit that may find broad application in detecting FA in indoor air and many other environments.

Microfluidic paper-based analytical devices are emerging as promising options for on-the-spot detection of chemical contaminants in water. The coupling of these devices with digital imaging technology has attracted immense interest in developing portable sensor applications. However, the potential of digital techniques still remains to be fully explored. In this work, we integrate digital imaging with microfluidic paper-based analytical devices to develop a portable colorimetric assay for iron. The experimental conditions are optimised using image analysis and the effects of imaging equipment and colorimetric analysis methods on the readout of devices are studied using numerical, graphical and statistical techniques. The experimental results are obtained for the estimation of iron contamination in water samples using a colorimetric assay based on iron (III)-thiocyanate reaction. The digital image acquisition approach using smartphone as imaging equipment is adopted for on-the-spot colorimetric data collection. Image processing techniques are employed to estimate the iron concentration in water from digital images. Greyscale colour intensity obtained from a digital image is identified as a readout of the analytical device and employed for quantitative assessment. The limit of detection for iron is estimated to be 0.26 ppm. The microfluidic approach offers good recovery and repeatability with relative standard deviation of 1.4%. The maximum percentage difference for intensities between the image analysis methods is 4.94% and that between the imaging equipment is 9.96%. The gradients of regression lines for pairwise equipment and method outputs with zero intercept range from 0.9931 to 1.0162 with high values of coefficients of determination. The correlation coefficient values for various paired comparisons (>0.99) suggest strong agreement. Statistical test results suggest no significant differences between methods and between imaging equipment (significance level 0.05). The findings suggest the efficacy of digital imaging and colorimetric analysis for paper-based analytical devices. [ABSTRACT FROM AUTHOR]

The detection of iodide ions (I−), despite challenges due to low concentrations and potential masking, is crucial for studying physiological processes and diagnosing diseases. A colorimetric sensor was developed to improve I− ion monitoring and facilitate on-site detection based on filter paper, which is a cost-effective platform. The sensor observed color changes in response to the exposure of hydrogen peroxide (H2O2), 3,3′,5,5′-tetramethylbenzidine (TMB), from colorless to yellowish brown. The sensor demonstrated a detection limit of 0.125 × 10−6 M for I− ions in a relatively wide range of 0.01 to 15 × 10−6 M under optimized conditions including gel concentration, temperature, incubation time, TMB and H2O2 concentration, and pH. Furthermore, the proposed sensor was successfully employed in a variety of applications, such as biological (urine and blood serum), food (egg yolk and snacks), and environmental samples (tap water). The study established effective recoveries in complex media for visual on-site I− ion monitoring, indicating the developed assay as a potent, affordable, and practical platform. [ABSTRACT FROM AUTHOR]

This work reports the development of low-cost and rapid multiplexed colorimetric assay of antioxidants (total phenolics, antioxidant capacity, flavonoids and anthocyanins) in wines at daisy-shaped fluidic paper-based analytical devices (PADs). The desired fluidic patterns were formed on paper by pen drawing and colorimetric reagents were immobilized at the 6 peripheral test zones. The sample was added at the central sample zone, migrated to the test zones and reacted with the immobilized reagents producing characteristic colors that were captured and analyzed. The paper-based approach was applied to the analysis of several wine samples and the results were statistically correlated to standard solution-based colorimetric assays, indicating that it could be reliably used for ranking wines according to their antioxidants content. In addition, the paper-based analytical methodology is simple, instrument-free, portable, cost-effective, rapid and environment friendly. [Display omitted] • Daisy-shaped paper-based analytical devices (PADs) were fabricated by pen drawing. • The PADs were used for a sextuple antioxidant/phenolics/anthocyanins/flavonoids assay. • Reagents were added to the 6 peripheral test zones and sample was added to the central sample zone. • The results of the assay for 18 wines correlated well with those of solution-based assays (R2 > 0.97). • The paper-based analytical methodology is simple, instrument-free, portable, cost-effective, rapid and environment friendly. [ABSTRACT FROM AUTHOR]

[Display omitted] • This review advances in the development of colorimetric and fluorometric paper-based devices (PADs) • PADs with metal nanoparticles and quantum dots employed as sensing probes in the point-of-care diagnosis. • PADs are integrated with desktop scanners and smartphones measure the grey scale/RGB values for quantitative measurement. • This innovative paper-based detection platforms for diverse diagnostic scenarios and their utility in resource-limited settings. This review paper comprehensively explores recent advancements in the development of colorimetric and fluorometric paper-based analytical devices (PADs) for rapid point-of-care diagnosis of specific disease biomarkers. The paper elucidates the principles of colorimetry and fluorometry, focusing on their application in the detection of various biomolecules. Notably, metal nanoparticles (NPs) and quantum dots (QDs) emerge as versatile sensing probes in these platforms. The fabrication of nanomaterials (NMs) on paper substrates is extensively discussed, covering techniques such as dip-coating, drop-casting, wax printing, inkjet printing and screen printing. The integration of PADs with portable devices is explored, including gray scale and RGB measurements using desktop scanners, smartphones and color detector apps for enhanced colorimetric and fluorometric analysis. The application of PADs with metal NPs for the detection of a wide array of biomolecules is highlighted. The versatility of these devices is demonstrated in detecting nucleic acids, proteins, amino acids, bio thiols, urea, uric acid, antigens, antibodies, glucose, creatinine, bilirubin, vitamins and bacteria. The potential for point-of-care diagnosis in diverse healthcare settings is underscored, emphasizing the simplicity, cost-effectiveness and rapidity of these paper-based diagnostic platforms. This review provides an overview of the NMs-enabled colorimetric and fluorometric PADs, offering insights into the fabrication techniques, integration with portable devices and diverse applications in the field of biomarker detection. The amalgamation of metal nanoparticles and quantum dots with paper-based devices holds promising prospects for advancing point-of-care diagnostics of specific disease biomarkers. [ABSTRACT FROM AUTHOR]

The monitoring of foodborne bacterial contamination requires simple and convenient biosensors. This work describes a novel paper-based colorimetric biosensor for the rapid and sensitive bacteria detection. The biosensor was constructed via the encapsulation of D-alanyl-D-alanine capped gold nanoparticles (DADA-AuNPs) in a modified paper that was fabricated by the freeze-drying of TEMPO-oxidized cellulose nanofibers/cationic guar gum composite hydrogel-modified filter paper. The results indicated that the size of DADA-AuNPs largely determined the color of their aqueous system and they exhibited light red to dark red as their size increased from around 6 to 36 nm. All these different sized DADA-AuNPs turned into colorless when encountered with either S. aureus or E. coli. In particular, the smaller the DADA-AuNPs size, the faster the discoloration. The encapsulation of DADA-AuNPs into modified paper negligibly changed their responsiveness towards bacteria. In comparison to the original filter paper and oven-dried hydrogel-modified filter paper, the freeze-dried hydrogel-modified paper was demonstrated to be a better substrate for the encapsulation of DADA-AuNPs since they could be loaded with a larger amount of DADA-AuNPs in a faster way and showed a better perceivable color. This work demonstrated a promising paper-based colorimetric biosensor for the facile and rapid detection of bacteria. [Display omitted] [ABSTRACT FROM AUTHOR]

In this work, indoxyl-glucoside was used as the substrate to develop a cost-effective, paper-based analytical device for the fluorescent and colorimetric dual-mode detection of β-glucosidase activity through a smartphone. The β-glucosidase can hydrolyze the colorless substrate indoxyl-glucoside to release indoxyl, which will be self-oxidized to generate green products in the presence of oxygen. Meanwhile, the green products emit bright blue-green fluorescence under ultraviolet–visible light irradiation at 365 nm. Fluorescent or colorimetric images were obtained by a smartphone, and the red-green-blue channels were analyzed by the Adobe Photoshop to quantify the β-glucosidase activity. Under the optimum conditions, the relative fluorescent and colorimetric signals have a good linear relationship with the activity of β-glucosidase, in the range of 0.01–1.00 U/mL and 0.25–5.00 U/mL, and the limits of detection are 0.005 U/mL and 0.0668 U/mL, respectively. The activities of β-glucosidase in a crude almond sample measured by the fluorescent and colorimetric methods were 23.62 ± 0.53 U/mL and 23.86 ± 0.25 U/mL, respectively. In addition, the spiked recoveries of normal human serum and crude almond samples were between 87.5% and 118.0%. In short, the paper-based device, combined with a smartphone, can provide a simple, environmentally friendly, and low-cost method for the fluorescent and colorimetric dual-mode detection of β-glucosidase activity. [ABSTRACT FROM AUTHOR]

The metal-organic frameworks (MOFs) nanozyme-mediated paper-based analytical devices (PADs) have shown great potential in portable visual determination of phenolic compounds in the environment. However, most MOF nanozymes suffer from poor dispersibility and block-like structure, which often prompts deposition and results in diminished enzymatic activity, severely hindering their environmental applications. Here, we proposed colorimetric PADs for the visual detection of dichlorophen (Dcp) based on its significant inhibitory effect on the two-dimensional (2D) MOF nanozyme activity. Specifically, we synthesized a 2D Cu TCPP (Fe) (defined as 2D-CTF) MOF nanozyme exhibiting excellent dispersibility and remarkable peroxidase-like (POD-like) activity, which could catalyze the oxidation and subsequent color change of 3,3′,5,5′-tetramethylbenzidine even under neutral conditions. Notably, the POD-like activity of 2D-CTF demonstrated a unique response to Dcp because of the occupation of Fe–N 4 active sites on the 2D-CTF. This property enables the use of 2D-CTF as a highly efficient catalyst to develop colorimetric PADs for naked-eye and portable detection of Dcp. We believe that the proposed colorimetric PADs offer an efficient method for Dcp assay and open fresh avenues for the advancement of colorimetric sensors for analyzing of phenolic toxic substances in real samples. [ABSTRACT FROM AUTHOR]

A dual colorimetric/electrochemical sensor integrated with a microfluidic paper-based analytical device (μPAD) is created for rapid and sensitive detection of cabaryl in fruit. For colorimetric sensor, quercetin modified silver nanoparticle (QCT-AgNPs) is synthesized via self-reduction, resulting in the color change from green to dark green in the presence of cabaryl, which can be readily observed via naked eyes. This colorimetric sensor provides a linear response of 5 – 50 μM quantified by Image J software. For electrochemistry, AgNPs/MXene nanocomposite electrode offers high electrocatalytic activity towards the detection of carbarly with a linear range of 0 – 60 µM and a detection limit of 0.01 µM. The limit of detection values obtained from this dual sensor are lower than a cut-off of carbaryl residue in food, which is 7 mg.kg−1 (35 µM) verifying the desired sensitivity of this platform. Ultimately, this dual sensor is successfully applied for on-site detection of carbaryl in the orange samples read out on the smartphone with satisfactory results. [Display omitted] • Dual colorimetric/electrochemicl sensor is developed on μPAD for cabaryl sensor • QCT-AgNPs is synthesized by self-reduction and applied for colorimetric detection. • AgNPs/MXene modified electrode provided high electrochemical sensitivity. • This platform is applied for on-site carbaryl detection in fruits on smartphone. [ABSTRACT FROM AUTHOR]

An ammonium chloride–Congo red (NH4Cl-CR) solution is presented as a potential sensing solution for aldehydes. Monofunctional aldehydes such as formaldehyde, acetaldehyde, benzaldehyde, and isobutyraldehyde caused changes in the pH of the sensing solution, producing a color transition from red-orange to violet to blue. This distinguished them from the other compounds, thereby acting as a qualitative test for the functional group. The NH4Cl-CR solution was also employed in making filter paper-based and silica gel-based sensors for formaldehyde and acetaldehyde vapors. These sensors responded positively towards the aldehyde gases through a color transition from pink to blue. The NH4Cl-CR mixture provides a simple and easy-to-handle reagent for the detection of both liquid and gaseous aldehydes which has potential applications in environmental monitoring.

[Display omitted] • A dual-optical method for 2,4-D detection is developed. • oxTMB-mediated colorimetric and ratiometric fluorescent assay was demonstrated. • A high-throughput PAD was fabricated for on-site rapid visual detection. • Dual signals can prove each other with high accuracy. • The proposed platform had facile, portable, and visual advantages in POCT. High-throughput and accurate monitoring of pesticide residues is extremely crucial, but remains challenging. Herein, oxidized 3,3′,5,5′-tetramethylbenzidine (oxTMB) mediated dual-optical sensing-based paper analytical device (PAD) was unveiled for on-site visual detection of 2,4-dichlorophenoxyacetic acid (2,4-D) in real samples. Colorimetric blue oxTMB (652 nm) can be reduced to colorless TMB by ascorbic acid (AA). Meanwhile, oxTMB was demonstrated for the first time to switch oxidation and condensation reactions between o -phenylenediamine and AA to produce yellow-emission (564 nm) and blue-emission (429 nm) probes. Thus, colorimetric and ratiometric fluorescent dual-mode detection system was developed for 2,4-D detection by combining with alkaline phosphatase (ALP) initiating AA generation (ascorbic acid-2-phosphate as the substrate). Notably, the developed method can correct itself to improve the accuracy due to the dual-response signals. Using the principle, ALP-loaded PAD (array 3 × 10) was designed for efficient and high-performance detection of 2,4-D in turnip and cauliflower with good sensitivity (0.09 μg/mL for colorimetry, 0.06 μg/mL for fluorometry), satisfactory recovery (98.0 %–107.2 %), and high consistency (relative error ≤ 3.1 %). This work demonstrated a promising strategy for high-throughput visual detection of 2,4-D, which may provide a new pathway for the further development of dual-mode sensing platforms to efficiently detect other targets for food safety. [ABSTRACT FROM AUTHOR]

• Surface molecularly imprinted polymer with selective recognition capability to butachlor was fabricated. • A colorimetric paper chip combined with the smartphone was developed to detect butachlor in mung bean. • The sensor has highly selective and sensitive to butachlor with LOD is 1.43 ng/g. • The sensor is simple, cheap, portable and widely used for fast detection. A microfluidic paper chip colorimetric detection system based on surface molecular imprinting of zinc ferrite nanoparticles was established, and the detection images were obtained by smartphone for gray value analysis and determination of butachlor. The best functional monomers and addition ratio were selected by quantum chemical simulation calculation, the properties of the prepared molecularly imprinted polymers were analyzed, and the detection conditions were optimized. The linear range, sensitivity, and selectivity of the method were evaluated. The results showed that under the optimum conditions, the concentration of 2–80 ng/g had a good linear relationship (R2 is 0.9953), the detection limit was 1.43 ng/g, the specificity was good, and the whole detection process did not exceed 20 min. The microfluidic paper chip was applied to detect butachlor in mung bean samples. The results showed that the recovery was 93.4–106.4 %, and the relative standard deviation was less than 5.6 %. [ABSTRACT FROM AUTHOR]

Paper-based ion-selective optodes (ISOs) allow for low-cost ion measurements using widely accessible optical detectors such as smartphones, representing an attractive analytical platform for medical testing and environmental monitoring. Previously reported paper-based ISOs rely on plasticized PVC membranes or PVC/plasticizer-free adsorption layers containing hydrophobic sensing chemicals. In this paper, we studied a new format of paper-based ISOs, in which a plasticizer phase containing sensing chemicals is deposited onto cellulose paper without using a hydrophobic polymer like PVC. Compared to ISOs without plasticizers and polymers, the plasticizer-based ISOs show much higher pH sensitivity when using chromoionophore I and tetrakis[3,5-bis(trifluoromethyl)phenyl]borate as the sensing chemicals. When the sensing layer further contains a solid ionophore with high molecular rigidity, the plasticizer-based ISOs for cations also exhibit enhanced sensitivity than the plasticizer-free ISOs. However, when the ionophore is a liquid at room temperature or has a long alkyl chain, the plasticizer-based and plasticizer-free ISOs have comparable responses because the ionophore behaves as a pseudo-plasticizer. Compared to ISOs with both plasticizers and polymers, the elimination of hydrophobic polymers like PVC makes inkjet printing more efficient and preserves the capillary action of the porous paper. By using the newly launched Samba cartridge with smaller nozzles, the plasticizer-based and polymer-free optodes for sodium, potassium, and calcium ions are prepared by inkjet printing for the first time. In an example application, the inkjet-printed plasticizer-based and polymer-free ISOs are used for colorimetric measurements of urine calcium. • Plasticizer-based and polymer-free ion-selective optodes are fabricated on cellulose paper. • The use of plasticizers enhances the optode performance compared to plasticizer-free optodes. • Inkjet printing of the plasticizer-based optode ink is realized using the newly launched Samba cartridge. • The inkjet-printed optodes are used for colorimetric calcium measurements in urine. [ABSTRACT FROM AUTHOR]

A novel assay platform consisting of a microfluidic sliding double-track paper-based chip and a hand-held Raspberry Pi detection system is proposed for determining the albumin-to-creatine ratio (ACR) in human urine. It is a clinically important parameter and can be used for the early detection of related diseases, such as renal insufficiency. In the proposed method, the sliding layer of the microchip is applied and the sample diffuses through two parallel filtration channels to the reaction/detection areas of the microchip to complete the detection reaction, which is a simple method well suited for self-diagnosis of ACR index in human urine. The RGB (red, green, and blue) value intensity signals of the reaction complexes in these two reaction zones are analyzed by a Raspberry Pi computer to derive the ACR value (ALB and CRE concentrations). It is shown that the G + B value intensity signal is linearly related to the ALB and CRE concentrations with the correlation coefficients of R2 = 0.9919 and R2 = 0.9923, respectively. It is additionally shown that the ALB and CRE concentration results determined using the proposed method for 23 urine samples were collected from real suffering chronic kidney disease (CKD) patients are in fine agreement with those acquired operating a traditional high-reliability macroscale method. Overall, for point-of-care (POC) CKD diagnosis and monitoring in clinical applications, the results prove that the proposed method offers a convenient, real time, reliable, and low-spending solution for POC CKD diagnosis. [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]

Detection of bisulfite (HSO 3 −) in food and beverages has vital importance because the excessive amount leads to ill effects on the human body. Colorimetric and fluorometric chromenylium-cyanine-based chemosensor CyR was synthesized and applied for high selective and sensitive analysis of HSO 3 − in red wine, rose wine and, granulated sugar with high recovery ranges and very fast response time without any interference from other competitive species. The limits of detection (LOD) for the UV–Vis and fluorescence titrations were found as 11.5 μM and 3.77 μM, respectively. The on-site and very rapid methods based on paper strips and smartphone which depend on the color changes from yellow to green have been successfully developed to analyze HSO 3 − concentration (10−5-10−1 M for paper strip and 163–1205 μM for smartphone). CyR and the bisulfite-adduct formed in the nucleophilic addition reaction with HSO 3 − were verified by FT-IR, 1H NMR, and MALDI-TOF results as well as Single-Crystal X-Ray Crystallography for CyR. [Display omitted] • Chromenylium-cyanine based probe (CyR) was constructed for bisulfite determination. • CyR platform was decorated with glyoxal group to provide selectivity for bisulfite. • Probe is the first example of NIR Spectrophotometric probes for bisulfite analysis. • Bisulfite was quantified in red wine, rose wine and granulated sugar. • Paper strips and smartphone-based methods have been developed to analyze bisulfite. [ABSTRACT FROM AUTHOR]

In this study, we developed a low-cost, handheld optical biosensor for measuring blood urea nitrogen (BUN) levels in fingertip blood. This biosensor can connect to a cloud-enabled smartphone for remote monitoring of renal diseases. The biosensor features a simple, stackable and multilayer paper-based strip design, which not only achieves a linear optical fast response to BUN concentration but also reduces the complexity of the optical reader. Excellent detection performance was obtained via a unique photoelectric detection algorithm. The proportional function for calculating the analyte concentration was established using blood samples with different BUN concentrations, resulting in a wide detection range of 2.46–38.14 mM and a low detection limit of 0.03 mM. Clinical sample testing demonstrated the biosensor's high reliability, showing strong agreement with the bulky biochemistry analyzer (gold standard), with a correlation coefficient R2 = 0.9635. It is also capable of connecting to a cloud-enabled smartphone via Bluetooth to transmit test data, which has an easy-to-use interface, thus enabling proactive health management or remote diagnosis. We believe that the proposed BUN biosensor can be a big boost to the daily monitoring of renal diseases and has promising prospects in contributing to the development of the IoMT. • We developed a low-cost, handheld BUN optical biosensor for renal surveillance in fingertip blood. • The sensor achieves a linear optical fast response through a multi-layer test strip. • Reflection spectroscopy is utilized for colorimetric quantification with high sensitivity. • The biosensor has high reliability and can greatly promote the daily monitoring of kidney diseases. [ABSTRACT FROM AUTHOR]

At present, most countries or regions use commercial centrifuges for centrifugation, but this is out of reaching for limited-resource areas. To overcome this problem, a portable electric yo-yo as centrifuge was firstly proposed to obtain serum, and this device can be combined with paper-based analytical devices for enzyme-linked immunosorbent assay (ELISA) analysis from human whole blood. In this study, inflammatory biomarkers C-reactive protein (CRP) and serum amyloid A (SAA) were used as target biomarker to verify the performance of the proposed method. The results shows good performance and their detection limits were determined to be 580 pg/mL for CRP and 800 pg/mL for SAA, respectively. We believe this method provides a new platform of low cost and fast detection for inflammatory biomarkers in the limited-resource settings. Using electric yo-yo device to implement inflammatory biomarkers detection in whole blood paper-based microfluidic immunoassay chip. [Display omitted] • A low-cost, portable and effective electric yo-yo centrifugal device is firstly proposed for blood centrifugation. • Paper-based microfluidic immunoassay chip used for inflammatory biomarkers analysis in whole blood. • The method shows good potential to on-site/limited-resource testing. [ABSTRACT FROM AUTHOR]

• Synthesis of novel oxazolidine derivatives with ionochromic properties. • Application of the oxazolidine molecules for photodetection of metal ions by colorimetric and fluorometric methods. • Selective sensing of Fe3+ and Ag+ in aqueous solution by development of metal ion chemosensors. • Preparation of ionochromic papers with the printing ability of security marks by using metal ion solutions as the ink. Photodetection of metal ions in different environments is a noteworthy research. Some sensitive oxazolidine derivatives were synthesized and their responsivities toward different metal ions were investigated. The OX 1 and OX 2 derivatives were synthesized from 2,3,3-trimethylindolenin and 1,1,2-trimethylbenz[e]indole, respectively. In addition, two hydroxyl and naphthalene functionalities were applied to both of the OX 1 and OX 2 derivatives to obtain OX 1 -OH and OX 2 -OH and also OX 1 -Naph and OX 2 -Naph derivatives, respectively. Investigation of ionochromic properties of oxazolidine derivatives showed their potential applications as highly-selective and sensitive optical chemosensors for detection of metal ions. The results showed colorimetric and fluorometric photodetection of Fe3+ ions in aqueous solution, where OX 2 -NaPh displayed selective photodetection of Ag+ in addition to Fe3+. For the development of paper-based colorimetric/fluorometric metal ion chemosensors and also high-security anticounterfeiting technology, ionochromic cellulosic papers based on oxazolidine derivatives were prepared via layer-by-layer coating strategy, which showed fluorescence emission in different colors with impregnation in aqueous solution of Fe3+ or Ag+. In addition, the Fe3+ and Ag+ aqueous solutions were used as anticounterfeiting ink for handwriting and printing on the ionochromic papers with pink, cyan blue, and dark blue fluorescence emissions of the written or printed marks. Therefore, the prepared ionochromic cellulosic papers have potential applications as colorimetric/fluorometric metal ion chemosensors and also in anticounterfeiting technology based on ionochromic security papers. Photodetection of metal ions by development of fluorometric/colorimetric chemosensors, and also anticounterfeiting technology based on oxazolidine derivatives. [Display omitted] [ABSTRACT FROM AUTHOR]

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Alpha-fetoprotein (AFP) is a fetal protein that can indicate congenital anomalies such as Down syndrome and spinal canal blockage when detected at abnormal levels in pregnant women. Current AFP detection methods rely on invasive blood or serum samples, which require sophisticated equipment. From the many solutions proposed, colorimetric paper-based assays excel in point-of-care settings. The concept of paper-based ELISA (p-ELISA) enhances traditional methods, aligning with the ASSURED criteria for diagnostics in resource-limited regions. Despite success in microfluidic paper-based assay devices, laser printing remains underexplored for p-ELISA. Additionally, modifying the paper surface provides an additional layer of sensitivity enhancement. In this study, we developed a novel laser-printed paper-based ELISA (LP-pELISA) for rapid, sensitive, and noninvasive detection of AFP in saliva samples. The LP-pELISA platform was fabricated by printing hydrophobic barriers on filter paper using a laser printer, followed by depositing hydroxyapatite (HAp) as an immobilization material for the antibodies. The colorimetric detection was achieved using AuNPs functionalized with anti-AFP antibodies and silver nitrate enhancement. The LP-pELISA exhibited a linear response for AFP detection in both buffer and saliva samples over a range of 1.0–800 ng mL−1, with a limit of detection (LOD) reaching 1.0 ng mL−1. The assay also demonstrated good selectivity, repeatability, reproducibility, and stability. The LP-pELISA was further validated by testing spiked human saliva samples, showing its potential for point-of-care diagnosis of congenital disabilities. The LP-pELISA is a noninvasive platform showcasing simplicity, cost-effectiveness, and user-friendliness, utilizing laser printing, hydroxyapatite modification, and saliva samples to efficiently detect AFP. Beyond its application for AFP, this method's versatility extends to other biomarkers, positioning it as a catalyst for the evolution of paper-based biosensors. The LP-pELISA holds promise as a transformative tool for point-of-care diagnostics, fostering advancements in healthcare with its innovative technology. [Display omitted] • The study introduces laser printing to create paper-based ELISA. • Hydroxyapatite was used to immobilize antibody binding and enhance assay performance. • Colorimetric detection using silver-enhanced AuNPs for rapid and sensitive readout. • The LP-pELISA shows a high Greenness score aligning with ecofriendly practices. [ABSTRACT FROM AUTHOR]

A novel tetrahedral DNA nanostructure (TDN) functionalized paper-based colorimetric sensor was developed for ultrasensitive analysis of mercury ion (Hg2+). On the paper-based platform, TDN was used as scaffold to anchor aptamer to improve the capture efficiency owing to the controllably specific orientation, low steric hindrance effect and well-defined spacing. In the absence of Hg2+, biotinylated aptamer would bind with streptavidin-labeled HRP. Whereas, in the presence of Hg2+, aptamer would preferentially bind to Hg2+ owing to the higher binding constant of T–Hg–T than that of T–A, which consequently leading to the biotinylated aptamer releasing from TDN. After introducing TMB-H 2 O 2 solution, strong variation of color signal could be observed. Therefore, the quantitative analysis of Hg2+ was carried out by using smartphone to monitor the color intensity on paper chip. The proposed strategy exhibits good linearity over a wide range of 10–13–10–7 M with a low detection limit of 30 fM. And this method had been successfully applied in real water samples. Our strategy provided a versatile, low-cost and user-friendly paper-based monitoring platform for rapid and ultrasensitive analysis of heavy metal ions and thus had potential applications in food safety and public health. [Display omitted] • A sensitive paper-based platform based on tetrahedral DNA nanostructure. • DNA nanostructure confers controllable anchoring aptamer in a consistently specific orientation and well-defined spacing. • Employment of high affinity of aptamer toward target mercury ion with 30 fM detection limit. • The developed platform is simplicity, rapidity, user-friendly, low cost and sensitive monitor food quality. [ABSTRACT FROM AUTHOR]

• A new spiropyran probe was designed and synthesized by modifying a bis(pyridin-2-ylmethyl)amino group as the acceptor at 5-position. • The probe displays a remarkable property of selective naked-eye recognizing copper ions in aqueous media and on test paper strips. • The linking of Cu2+ to the probe caused a dramatic change from colorless to pink. • Job's plot analysis displayed the coordination ratio between the probe and copper ions is 2:1. Using a strategy of modifying a bis(pyridin-2-ylmethyl) amino group in the 5-position, a new spiropyran dye ((1′-ethyl-3′,3′-dimethyl-N, N-bis(pyridin-2-ylmethyl) was synthesized. The dye was able to distinguish copper ions with remarkable selectivity by naked eye on paper strips and in aqueous media. Copper ions are selectively coupled to the receptor, which stimulates the opening of the spirocycle. Consequently, the π -electrons are localized on the spiropyran and a new absorption peak appears between 450 and 600 nm. Due to its functional properties, the receptor facilitates the rapid, selective, and sensitive detection of copper ions with a detection limit of 19 nM. According to Job's plot analysis, the correlation ratio between the probe and copper ions appears to be 2:1. Further, the probe was successfully applied to test papers strips that demonstrated distinct colors changes in response to different concentrations of copper ions. [Display omitted] [ABSTRACT FROM AUTHOR]

This study reports an economical and portable point-of-care (POC) monitoring device based on artificial multi-enzyme cascade systems for multiple detection purposes. The device was made up of a disposable three dimensional microfluidic paper-based analytical device (3D μPAD) with multiple detection zones and a smartphone readout. On-paper synthesis of a multifunctional mimetic composite, based on the CeO 2 nanoparticles embedded in the amino-functionalized Fe metal-organic frameworks (CeO 2 @NH 2 -MIL-88B(Fe)), for cascade reactions was the main achievement of this work. The 3D μPAD was applied for simultaneous quantification of glucose, fructose, sucrose and maltose, and the detection process consisted of the enzymatic reaction of each sugar by anchored enzymes on the metal-organic frameworks (MOF) and successive oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB). Utilizing the new artificial mimicking system improved the color development uniformity and resulted in a reliable detection tool, with excellent detection limits in the range of 20–280 μM. It was directly applied to analyze the sugars levels of human total blood, urine, semen, honey and juice samples with the relative errors of less than 7.7% compared with the HPLC method. The cost-effective and easy-to-use μPAD has a great potential to be used in either medical diagnostics or the food industry. Also, it can be considered as a competitive POC method for patients in disadvantaged communities or emergencies. [ABSTRACT FROM AUTHOR]

Given the pandemic situation, there is an urgent need for an accurate test to monitor antibodies anti-SARS-CoV-2, providing crucial epidemiological and clinical information to monitor the evolution of coronavirus disease in 2019 (COVID-19) and to stratify the immunized and asymptomatic population. Therefore, this paper describes a new cellulose-based test strip for rapid and cost-effective quantitative detection of antibodies to SARS-CoV2 virus by colorimetric transduction. For this purpose, Whatman paper was chemically modified with sodium metaperiodate to introduce aldehyde groups on its surface. Subsequently, the spike protein of the virus is covalently bound by forming an imine group. The chemical control of cellulose paper modification was evaluated by Fourier transform infrared spectroscopy, thermogravimetry and contact angle analysis. Colorimetric detection of the antibodies was performed by a conventional staining method using Ponceau S solution as the dye. Color analysis was performed after image acquisition with a smartphone using Image J software. The color intensity varied linearly with the logarithm of the anti-S concentration (from 10 ng/mL to 1 μg/mL) in 500-fold diluted serum samples when plotted against the green coordinate extracted from digital images. The test strip was selective in the presence of nucleocapsid antibodies, urea, glucose, and bovine serum albumin with less than 15% interference, and detection of antibodies in human serum was successfully performed. Overall, this is a simple and affordable design that can be readily used for mass population screening and does not require sophisticated equipment or qualified personnel. [ABSTRACT FROM AUTHOR]

A simple colorimetric paper-based sensor array (optical tongue), which can quickly and accurately identify and discriminate twenty-five kinds of heavy metal ions, is developed. It functions by immobilizing six metal indicators on the paper substrate using polyvinyl chloride. Exposing the device to the aqueous solution of metal ions produces a unique colorimetric signature for each ion, enabling discrimination of the ions by visual inspection. Further analysis of the colorimetric patterns by chemometrics data analysis methods leads to a clustering map for accurate classifying of the metal ions at different concentrations (10.0, 5.0, 2.5, and 1.0 mg L−1). In addition, the device was applied to analyze binary and ternary mixtures of metal ions as well. An interesting feature of this tasting device is speciation analysis of an element of different oxidation states and their mixtures. Beside to qualitative analysis, it represented quantitative analysis ability, e.g., for Zn2+ and Co2+, in the concentration ranges of 0.10–10.00 mg L−1 (R2 = 0.99) and 0.25–12.50 mg L−1 (R2 = 0.99) and detection limits of 0.03 and 0.08 mg L−1, respectively. This optoelectronic tongue shows promising results to be used potentially of on-site analysis of water for its quality. • An optical tongue, which can quickly identify and discriminate 25 heavy metal ions. • Immobilizing of the indicators on the paper surface hinders licking of the indicators. • The device can analyze sample solution, without need to any pretreatment. • The device produces a unique colorimetric signature for each ion. • Has potentially in on-site analysis of water for its quality. [ABSTRACT FROM AUTHOR]

To ensure safe drinking water, it is necessary to have a simple method by which the probable pollutants are detected at the point of distribution. Nitrite contamination in water near agricultural locations could be an environmental concern due to its deleterious effects on the human population. The development of a frugal paper-based microfluidic sensor could be desirable to achieve the societal objective of providing safe drinking water. This work describes the development of a facile and cost-effective microfluidic paper-based sensor for quantitative estimation of nitrite in aquatic environments. A simple punching machine was used for fabrication and rapid prototyping of paper-based sensors without the need of any specialized equipment or patterning techniques. A reusable 3D printed platform served as the support for simultaneous testing of multiple samples. The nitrite estimation was carried out with smartphone-assisted digital image acquisition and colorimetric analysis. Under optimized experimental conditions, the variation in average grayscale intensity with concentration of nitrite was linear in the range from 0.1 to 10 ppm. The limits of detection and quantitation were 0.12 ppm and 0.35 ppm respectively. The reproducibility, expressed as relative standard deviation was 1.31%. The selectivity of nitrite detection method was determined by performing interference studies with commonly existing co-ions in water, such as bicarbonates, chloride and sulphate. The paper-based sensor was successfully applied for estimation of nitrite in actual water samples and showed high recoveries in the range of 83.5–109%. The results were in good agreement with those obtained using spectrophotometry. The developed paper-based sensor method, by virtue of its simplicity, ease of fabrication and use, could be readily extended for detection of multiple analytes in resource-limited settings. [ABSTRACT FROM AUTHOR]

Aflatoxin B 1 (AFB 1) is a powerful carcinogen, and the pollution it causes has become a global public health safety issue. Therefore, microfluidic paper-based analytical devices (μPADs) with smartphones to read colorimetric signals were constructed for rapid AFB 1 detection. The colorimetric mechanism of μPADs was based on the common starch–iodine reaction, and the addition of gelatin/chitosan enhanced the colorimetric effect. During detection and analysis, the competitive analysis occurred in the process of AFB 1 monoclonal antibody's recognition of free AFB 1 and functionalized antigen. The glucose oxidase-labeled IgG was used as the secondary antibody. Hydrogen peroxide, an oxidation product of the glucose, caused a chroma change in μPADs. Simultaneously, the change in chroma was consistent with the change in AFB 1 concentration. Under the best optimized conditions, the limits of detection and quantitation of AFB 1 in the buffer were 9.45 and 12.00 ng mL−1, respectively. A comparison of the detection performance of commercial kits with that of the method introduced herein confirmed the superiority of our method in actual food samples with known AFB 1 concentrations. This colorimetric μPADs analysis met the detection requirements of some countries, such as China, and had great potential for development in the direction of daily extensive food safety control and environmental monitoring. [Display omitted] • Portable and low-cost smartphone-based microfluidic paper-based analytical devices (μPADs). • The colorimetric μPAD detection system can detect aflatoxin B1 as low as 9.45 ng mL−1 through Lab data analysis. • The colorimetric mechanism is based on the common starch–iodine reaction. • The addition of gelatin and chitosan mixture enhances the colorimetric effect. [ABSTRACT FROM AUTHOR]

Purpose – The purpose of this study was to develop an accurate, selective, low-cost and user-friendly colorimetric pad to detect formaldehyde at low concentration. Design/methodology/approach – 1-phenyl-1,3-butanedione, a reactive chemical, was selected to develop the colorimetric pad for indoor air formaldehyde measurement. Silica nanoparticle impregnated with the reactive chemical was coated on the cellulose filter surface to increase the reactive site. A certified formaldehyde permeation tube was used to generate six varied concentrations between 0.01 and 0.10 ppm in a test chamber. The color intensity on the pads was measured using an image processing program to produce a formaldehyde concentration reading chart. The colorimetric pad was tested for optimum reaction time, accuracy, precision, stability, selectivity and shelf life. Findings – The color of the pads changed from white to yellow and the color intensity varied with the concentrations and appeared to be stable after exposure to formaldehyde for 8 hours. At room temperature, the stability of the pad was 7 days, and shelf life was 120 days. The accuracy, precision and bias of the pad were 12.38%, 0.032 and 6.0%, respectively. Carbonyl compounds, benzene and toluene did not interfere with the reading of this developed colorimetric pad. Originality/value – The developed colorimetric pad meets NIOSH's criteria for an overall accuracy of ±25%, bias = 10%. They were accurate at low concentrations, user-friendly and had low cost compared to an electronic direct reading instrument (cost of chemicals and materials was 21.50 Bath or 0.69 USD per piece) so that favorable for the use of general people for health protection.

[Display omitted] • High-efficiency (2 orders of magnitude), reproducible (RSD 2.5%), fast (within 2 min) parallel electric stacking PAD was created; • The wet real-time photographic colorimetry results of the parallel PAD system are insensitive to the changes of light conditions; • On-line colorimetric detection of pigments in drinks and off-line MS/MS detection of serum amino acids are used to demonstrate their applicability. A microfluidic paper-based analytical device (PAD) with both pre-concentration and parallel operation functions is of great promise for sensitive and high throughput detection. In this paper, a fast and multiplexed PAD was designed based on wax-screen-printing with glass fiber paper substrate and validated by image-based colorimetry. Driven by the same DC power supply, parallel electrokinetic stacking with the PAD of 8 channels can be completed within 2 min, and each channel can be loaded with different samples. Enrichment factor of 2 orders of magnitude was demonstrated with RSD below 2.5% between the chips and the channels of a chip. Reproducible and multiplexed stacking operations of this PAD provide a solid foundation for online calibration and sample detection on the same chip at the same time. Applications of this PAD was demonstrated by online colorimetric detection of food pigments from beverages and offline MS/MS detection of amino acids from a serum sample. Besides high-throughput and sensitive point-of-care test detection, this PAD method could also find applications for efficient pre-separation and pre-concentration of complex samples. [ABSTRACT FROM AUTHOR]

Paper-based analytical devices (PADs) with four new designs could be fabricated using commercially available home-based scan-and-cut printer. They serve for miniaturised platforms for chemical analysis. Replication analysis of a sample together with the calibration (using the analyte standards at different concentrations) can be completed in a single run, by utilising smartphone as the detector. Some new approaches for choosing detection zones were suggested. The four proposed PAD designs here were used as models in microliter scale operation to demonstrate the well-known chemistries of colorimetric determinations of iron, phosphate, and hardness using 1,10-phenanthroline and simple aqueous guava leaf extract; molybdate, and EBT-EDTA complexometric titration, respectively, through calibrations: where Blue (B) value = 88.2log [Fe3+] - 80.8, R2 = 0.989; B value = 1.75 [Fe3+] + 0.198, R2 = 0.999; Grey scale (I) value = 1.77 [Fe3+] – 1.22, R2 = 0.997; Red (R) value = 16.1log [PO 4 3−] + 8.95, R2 = 0.999; Hue (H) value = 43.3log [Ca2+] + 233, R2 = 0.994, respectively. For the hardness, using one of the PAD designs, true titration was also possible. Applications of the proposed devices and procedures were demonstrated for real world samples with validation. Additionally, kinetic study of the molybdenum blue for phosphate was demonstrated using one of the PADs. [Display omitted] • New designs of paper based analytical devices (PADs) by simple fabrication. • The PADs for replication analysis of a sample within a single run with smartphone. • Via video recorded by smartphone allows new way for optimisation. • Demonstrated for real world uses with iron, phosphate, and hardness as model assays. • Reengineered PADs as powerful analytical tools in low resource settings. [ABSTRACT FROM AUTHOR]

Mercury contamination in the environment has reached alarming levels. Due to its persistence and bioaccumulation, mercury is one of the most widespread toxic heavy metals found in air, water and food. Thus, it is mandatory to monitor mercury and its compounds, and the availability of sensitive and rapid biosensors is highly valuable. We developed a low-cost biosensor for orthogonal detection of mercury(II) integrating three different biorecognition principles on a three-leaf paper: i) a mercury-specific bioluminescent Escherichia coli bioreporter strain expressing NanoLuc luciferase as reporter protein, ii) a purified β-galactosidase (β-gal) enzyme which is irreversibly inhibited by mercury and other metal ions, and iii) an Aliivibrio fischeri bioluminescent strain which is used to quantitatively assess sample toxicity and correct the analytical signal accordingly. Both sensory elements and substrates, Furimazine for the bioluminescent reporter strain and chlorophenol red-β-D-galactopyranoside for colorimetric detection of β-gal, were integrated in the paper sensor to provide a stable all-in-one disposable cartridge which can be easily snapped into a smartphone with a clover-shaped 3D printed housing. This is the first integration of bioluminescence and colorimetric detection on a smartphone-paper sensor, providing a readout within 15 and 60 min for the colorimetric and bioluminescent detection respectively. The biosensor was applied to water samples spiked with different concentrations of mercury, interferents and toxic chemicals providing a limit of detection for Hg(II) at the ppb levels. [Display omitted] • Orthogonal smartphone biosensor for mercury detection. • Colorimetric enzyme sensor and bioluminescent bacterial bioreporters on a paper sensor. • Mercury(II) detection within 60 min at ppb levels. • Applicable to toxic and complex samples. [ABSTRACT FROM AUTHOR]

This work presents a novel cellulose-based aptasensor for the colorimetric detection of a cancer biomarker, osteopontin (OPN), in point-of-care (PoC) analysis. For this purpose, the cellulose paper was chemically modified with (mercaptopropyl)methyldimetoxisilane to attach the thiolated aptamer, which acts as a biological detection layer. The surface modification was checked by Fourier transform infrared spectroscopy and thermogravimetric analysis. Colorimetric detection was performed using a conventional staining solution, Bradford reagent. The color analysis was performed by evaluating the RGB coordinates provided by the ImageJ program from the photographs taken with a smartphone. Overall, the biosensor shows good sensitivity with a wide linear range (R > 0.998) of 5–1000 ng/mL and a detection limit lower than 5 ng/mL in buffer and commercial human serum solution, after 30 min of incubation. In addition, this aptasensor shows good selectivity to some interfering species such as bovine serum albumin and recombinant OPN. Analytical data obtained from spiked serum samples confirm the accuracy of the method. Importantly, it is a broad-spectrum method that tends to meet the criteria of REASSURED (real-time connectivity, ease of sampling, affordability, specificity, ease of use, speed and robustness, device freedom, and deliverability) for global testing. [Display omitted] • Development of a cellulose-based colorimetric test strip for the detection of a cancer biomarker. • Aptamer as a biological recognition layer for an OPN detection. • Bradford as a detection reagent. • Visual quantitative detection of a cancer biomarker. [ABSTRACT FROM AUTHOR]

The microfluidic paper-based analytical devices (μPADs) have grown-up swiftly over the decade due to its low cost, simple fabrication procedure, resource-limitedness, non-toxicity and their environmentally benign nature. The μPADs, also identified as point-of-care devices or health care devices have successfully applied in several fields such as diagnostics, biological, food safety, environmental, electrochemical and most importantly colorimetric/fluorimetric sensors, owing to the attractive passive motions of analyte without any external forces. In recent years, a large number of colorimetric and fluorimetric probes have been reported that can selectively recognize the analytes in μPADs. However, there is no organized review on its structure-activity relationship. In this review, we have focused to summarize the colorimetric and fluorimetric probes utilized in μPADs. This review discuss about the relationships between the structure and functions of various probes as signaling units of the efficient μPADs. The probes including nanomaterials, nanozymes, polymers and organic molecules, their structural activity with regard to sensing performances along with their limit of detection are also discussed. This review is expected to assist readers for better understanding of the sensing mechanisms of various chemo and bio-probes utilized in μPADs, as well as promote their advancement in the field. On the other hand, this review also helps the researchers for enhancement of μPADs and paves way for synergistic application of existing molecular probes as an effective diagnostic tool for the worldwide pandemic novel corona virus COVID-19. [Display omitted] • Traditional fabrications methods for µPADs are summarized. • Discusses about the hindrances of commercial wax printing method for fabrication of µPADs. • Various sensory materials are categorized and discussed along with their structure activity properties. • Highlights about the most promising material that could be a probable probe for µPADs. • The vision towards employing µPADs for COVID19 diagnosis is also discussed. [ABSTRACT FROM AUTHOR]

Rapid and sensitive detection of acrylamide in food samples is important for food safety and public health. Here, we describe a disposable origami paper-based analytical device (denoted doPAD) for colorimetric detection of acrylamide. This device uniquely exploits 3D origami folding paper for spatial control of the target recognition and signal readout, thus resulting in a positive correlation between the signals and the analytes. Under optimal conditions, the device achieved the quantitative analysis of acrylamide with a limit of detection of 1.13 μg/L within 120 min (including a derivatization time of 90 min and an assay time of 21 min). Furthermore, our method allowed the rapid and sensitive detection of acrylamide in complex food matrices. We envision that the platform described will find useful applications in the fields of food safety and environmental health. [ABSTRACT FROM AUTHOR]

[Display omitted] • The TPA-SB sensor showed rapid absorbance, excellent selectivity, and high sensitivity towards Hg2+ ions. • The TPA-SB sensor could detect Hg2+ ions from colourless to reddish-orange via naked-eye, exhibiting fluorescence OFF response to Hg2+ ions. • The detection limit achieved for Hg2+ ions (0.27 nM). • Low-cost, easy-to-make filter paper strips are developed to detect Hg2+ ions for field application. • Solid-supported TPA-SB@SiO 2 was developed and demonstrated for onsite analysis. A new, sensitive and highly selective chemosensor (N, N-diphenyl-4-(E)-(E)-thiophen-2-ylmethylene)hydrazono)methyl) aniline (TPA-SB) for Hg2+ was designed and synthesised by combining the triphenylamine motif and thiophene group. The TPA-SB exhibited a remarkable colour change from light yellow to reddish-orange with Hg2+, which was visible to the naked eye. The detection limit of Hg2+ was 0.27 nM. We fabricated a TPA-SB-coated paper sensor to detect Hg2+ rapidly, with excellent selectivity and sensitivity. Adding KI to TPA-SB-Hg2+ recovered the colour and retained the probe TPA-SB as a reversible sensor for real-time applications in solution and paper matrix. Further, we developed a solid-supported adsorbent (TPA-SB-SiO 2) and utilised it for the complete removal (100%) of Hg2+ ions from the mercury-contaminated water. Based on the NMR titration, ESI – MS, Job's plot and DFT study, probable binding mode and biding ratio (1:1) of TPA-SB with Hg2+ have been proposed. Importantly, we can apply the present sensing system for recognising Hg2+ ions in Escherichia coli cells. [ABSTRACT FROM AUTHOR]

The reaction-based system enables the detection of glyphosate in real samples by the color change. [Display omitted] • Two new colorimetric sensors were developed for detection of glyphosate (Glyp). • The sensing mechanism between the sensors and Glyp were clearly presented. • The sensors were successfully applied to detect Glyp in real samples. • Paper strips were fabricated to visualize Glyp in solutions. Glyphosate is widely used herbicides and causes several diseases in humans. Therefore, the detection of glyphosate is curial and urgent. Studies on the detection of glyphosate in literature are often based on inhibition of the enzyme acetylcholinesterase. In this study, we developed two simple colorimetric sensors, BP-Cl and CP-Cl, by linking 3-chloro-4-methylpyridine with 4-(dimethylamino)cinnamaldehyde or 4-(dimethylamino)benzaldehyde in a one-step reaction. The colorimetric and optical sensing properties of these compounds were investigated by the naked-eye and UV–Vis spectrophotometer in ACN/HEPES buffer (5 mM pH 8.0, 1:1 v/v). The sensors displayed high sensitivity and selectivity for glyphosate by color changes, which ranged from colorless to yellow for BP-Cl and yellow to orange for CP-Cl. The detection limits of BP-Cl and CP-Cl by the naked-eye detection were found as 15 µM and 10 µM. On the other hand, the detection limits of BP-Cl and CP-Cl via UV–Vis measurements were calculated as 0.847 µM and 1.23 µM, respectively. Moreover, the sensors were able to monitor glyphosate in water samples using the naked-eye, UV–Vis spectroscopy, and filter paper strips. [ABSTRACT FROM AUTHOR]