Paper-based Platform Research Articles

Electroanalytical paper-based device for reliable detection and quantification of sugars in milk

Knowing the level of sugars in food and beverages is essential because they are related to diseases such as diabetes, and obesity, among others. In this regard, an approach has been designed, characterized, and applied to develop the first all-in-one paper-based microfluidic analytical device for the quantification of sugars in milk samples. In particular, the powerful combination of the paper-based platform, the facile manufacturing, and the on-demand customization, allowed to obtain a stand-alone platform that was capable to store all the reagents necessary for the assay, to treating the sample by removing major interferences due to lipids and proteins, and to visualize the results in minutes. A wax-patterned chromatographic paper was finely designed to provide a reagent-free platform for the use of non-specialists applied towards the analysis of sugars' content (lactose as the main sugar). Sugars were electrochemically quantified down to 0.16 g L−1 with a repeatability of 5%. To strengthen the efficacy of the novel platform, the electrochemical paper-based analytical device has been applied to commercial milk, including skimmed, semi-skimmed, whole, and lactose-free, confirming satisfactory performance with analytical reliability. This paper-based architecture opens novel avenues for portable (bio)sensing of other relevant species, not only in the agri-food field.

A COVID19-selective pH-paper test: Ultrafast and highly accurate antibody-free viral detection in native saliva

COVID-19 is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). SARS-CoV-2 has led to high mortality worldwide, with social and financial effects expected to persist for years to come. Since asymptomatic individuals cause a large portion of transmission, actions taken to curb the COVID-19 pandemic mostly rely on procedures aimed at detecting viral-related molecules in infected carriers. Currently, leading available detection methods fall short in reliability or point-of-care mass screening applicability.Here, we present an unprecedented antibody-free smart pH paper-based seconds-long detection platform against the virus-related enzyme 3CLpro as a saliva biomarker of SARS-CoV-2 infection. The selective proteolytic activity of 3CLpro is directly detected from native saliva using a peptide substrate-embedded pH-paper platform. 3CLpro presence in infected individuals leads to an ultrafast pH-drop in the paper matrix, thus leading to a sharp color change as direct means of detection.Ultrafast detection, simplicity, no requirement of surface chemistry by sensitive biomolecules, long-term stability, and point-of-care compatibility for COVID-19 mass screening were demonstrated. Forty-two subjects were tested, exhibiting highly sensitive and specific detection of SARS-CoV-2 infection. Finally, we foresee that this universal approach could be implemented for the multiplexed detection of other viral infections by detecting specific viral proteases.Importantly, since our approach does not require immune-specific antibodies for specific detection, the overall platform is extremely cost-efficient, less than 2 USD cents per assay, and suitable for the worldwide mass screening of viral infections, particularly in remote and developing world locations. Moreover, we propose an extremely easy-to-use and produce practical test strip design.

Gold Nanotapes and Nanopinecones in a Quantitative Lateral Flow Assay for the Cancer Biomarker Carcinoembryonic Antigen.

Colorectal cancer is the third most common malignancy and the second leading cause of cancer death globally. Multiple studies have linked levels of carcinoembryonic antigen in patient serum to poor disease prognosis. Hence, the ability to detect low levels of carcinoembryonic antigen has applications in earlier disease diagnosis, assessment, and recurrence monitoring. Existing carcinoembryonic antigen detection methods often require multiple reagents, trained operators, or complex procedures. A method alleviating these issues is the lateral flow assay, a paper-based platform that allows the detection and quantification of target analytes in complex mixtures. The tests are rapid, are point-of-care, possess a long shelf life, and can be stored at ambient conditions, making them ideal for use in a range of settings. Although lateral flow assays typically use spherical gold nanoparticles to generate the classic red signal, recent literature has shown that alternate morphologies to spheres can improve the limit of detection. In this work, we report the application of alternative gold nanoparticle morphologies, gold nanotapes (∼35 nm in length) and gold nanopinecones (∼90 nm in diameter), in a lateral flow assay for carcinoembryonic antigen. In a comparative assay, gold nanopinecones exhibited a ∼2× improvement in the limit of detection compared to commercially available spherical gold nanoparticles for the same antibody loading and total gold content, whereas the number of gold nanopinecones in each test was ∼3.2× less. In the fully optimized test, a limit of detection of 14.4 pg/mL was obtained using the gold nanopinecones, representing a 24-fold improvement over the previously reported gold-nanoparticle-based carcinoembryonic antigen lateral flow assay.

A novel paper-based colorimetric sensor using parylene C for Al (III) detection on a smartphone platform

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

Sensitive and cost-effective colorimetric sensor based on enzyme mimic MoS2@CoTiO3 nanocomposite for detection of hydrogen peroxide in milk and tap water

Although hydrogen peroxide (H2O2) is essential for biochemical reactions and industrial processes but excessive levels can be hazardous to health. As a result, developing a reliable, selective, and sensitive H2O2 detection method remains challenging. This study proposes an inexpensive, portable, and rapid colorimetric sensor for quick H2O2 detection based on a filter paper-based platform and novel nanozymes named Molybdenum disulfide and Cobalt titanate (MoS2@CoTiO3) nanocomposite.Different analytical techniques were used to evaluate the interaction between the material and analyte, including UV-Visible spectrophotometry, Fourier transform infrared spectroscopy, Scanning electron microscopy, X-Ray diffraction, Zeta potential, and Dynamic light scattering. The characterization study proved the proposed material's appropriateness for sensing purposes. The combined action of MoS2 and CoTiO3 components revealed intrinsic peroxidase-like activity, allowing for the visible oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB). Several optimization parameters were evaluated, including TMB concentration (25 mM), incubation time (20 min), pH (7.0), and nanocomposite (3.0 mg) and gel (0.2 g) concentrations. Consequently, due to its peroxidase-like activity, the MoS2@CoTiO3 nanocomposite achieved a lower detection limit (LOD) of 0.01 µM. The platform displayed adequate selectivity against potential interferants in biological samples, with excellent recovery rates ranging from 93.3 % to 98.3 %. The use of low-cost paper-based porous substrates for sensing has proven to be a versatile option for onsite health and environmental monitoring, providing an alternative to costly and complicated instrumentation.

Point-of-Care Devices for Viral Detection: COVID-19 Pandemic and Beyond.

The pandemic of COVID-19 and its widespread transmission have made us realize the importance of early, quick diagnostic tests for facilitating effective cure and management. The primary obstacles encountered were accurately distinguishing COVID-19 from other illnesses including the flu, common cold, etc. While the polymerase chain reaction technique is a robust technique for the determination of SARS-CoV-2 in patients of COVID-19, there arises a high demand for affordable, quick, user-friendly, and precise point-of-care (POC) diagnostic in therapeutic settings. The necessity for available tests with rapid outcomes spurred the advancement of POC tests that are characterized by speed, automation, and high precision and accuracy. Paper-based POC devices have gained increasing interest in recent years because of rapid, low-cost detection without requiring external instruments. At present, microfluidic paper-based analysis devices have garnered public attention and accelerated the development of such POCT for efficient multistep assays. In the current review, our focus will be on the fabrication of detection modules for SARS-CoV-2. Here, we have included a discussion on various strategies for the detection of viral moieties. The compilation of these strategies would offer comprehensive insight into the detection of the causative agent preparedness for future pandemics. We also provide a descriptive outline for paper-based diagnostic platforms, involving the determination mechanisms, as well as a commercial kit for COVID-19 as well as their outlook.

Development of a Low-Cost Paper-Based Platform for Coffee Ring-Assisted SERS.

The need for highly sensitive, low-cost, and timely diagnostic technologies at the point of care is increasing. Surface-enhanced Raman spectroscopy (SERS) is a vibrational spectroscopic technique that is an advantageous technique to address this need, as it can rapidly detect analytes in small or dilute samples with improved sensitivity compared to conventional Raman spectroscopy. Despite the many advantages of SERS, one drawback of the technique is poor reproducibility due to variable interactions between nanoparticles and target analytes. To overcome this limitation, coupling SERS with the coffee ring effect has been implemented to concentrate and localize analyte-nanoparticle conjugates for improved signal reproducibility. However, current coffee ring platforms require laborious fabrication steps. Herein, we present a low-cost, two-step fabrication process for coffee ring-assisted SERS, utilizing wax-printed nitrocellulose paper. The platform was designed to produce a highly hydrophobic paper substrate that supports the coffee ring effect and tested using gold nanoparticles for SERS sensing. The nanoparticle concentration and solvent were varied to determine the effect of solution composition on ring formation and center clearance. The SERS signal was validated using 4-mercaptobenzoic acid (MBA) and tested with Moraxella catarrhalis bacteria to ensure functionality for chemical and biological applications. The limit of detection using MBA is 41.56 nM, and the biochemical components of the bacterial cell wall were enhanced with low spectral variability. The developed platform is advantageous due to ease of fabrication and use, representing the next step toward implementing low-cost coffee ring-assisted SERS for point-of-care sensing.

Facile Synthesis of Iron and Nitrogen Co-Doped Carbon Dot Nanozyme as Highly Efficient Peroxidase Mimics for Visualized Detection of Metabolites.

Visual detection based on nanozymes has great potential for the rapid detection of metabolites in clinical analysis or home-based health management. In this work, iron and nitrogen co-doped carbon dots (Fe,N-CDs) were conveniently synthesized as a nanozyme for the visual detection of glucose (Glu) or cholesterol (Chol). Using inexpensive and readily available precursors, Fe,N-CDs with peroxidase-like activity were conveniently prepared through a simple hydrothermal method. Co-doping of Fe and N atoms enhanced the catalytic activity of the nanozyme. The nanozyme had a low Michaelis constant (Km) of 0.23 mM when hydrogen peroxide (H2O2) was used as the substrate. Free radical trapping experiments revealed that the reactive oxygen species (ROS) generated in the nanozyme-catalyzed process were superoxide anion radicals (•O2-), which can oxidize colorless 3,3',5,5'-tetramethylbenzidine (TMB) to generate blue oxidation product (ox-TMB) with characteristics absorbance at 652 nm. Based on this mechanism, a colorimetric sensor was constructed to detect H2O2 ranging from 0.1 μM to 200 μM with a detection limit (DL) of 75 nM. In the presence of glucose oxidase (Gox) or Chol oxidase (Chox), Glu or Chol was oxidized, respectively, and generated H2O2. Based on this, indirect detection of Glu and Chol was realized with linear detection ranges of 5-160 μM and 2-200 μM and DLs of 2.8 μM and 0.8 μM, respectively. A paper-based visual detection platform was fabricated using Fe,N-CDs as nanozyme ink to prepare testing paper by inkjet printing. Using a smartphone to record the RGB values of the testing paper after the reaction, visual detection of Glu and Chol can be achieved with linear detection ranges of 5-160 μM (DL of 3.3 μM) and 2-200 μM (DL of 1.0 μM), respectively.

Hinge-like paper-based dual-channel enzyme-free ratiometric fluorescent microfluidic platform for simultaneous visual detection of carbaryl and glyphosate

On-site multi-pesticide residues detection is particularly urgent and challenging. Here, we fabricated an enzyme-free ratiometric fluorescent detection system in combination with a hinge-like dual-channel 3D microfluidic paper analytical device (3D μPAD) for simultaneous visual detection of carbaryl and glyphosate. Blue-emission 1-naphthol (Em. 470 nm) was hydrolyzed from carbaryl, while yellow-emission 2,3-diaminophenazine (Em. 570 nm) was produced with the aid of Cu2+ for glyphosate sensing. Inner-filter effect between 1-naphthol or 2,3-diaminophenazine and green-emission carbon dots (Em. 510 nm) realized two ratiometric fluorescent detection systems. Remarkable color variation of green–blue for carbaryl (50.00–1100 μΜ) and yellow–green for glyphosate (5.00–600 μΜ) were observed on a dual-channel 3D μPAD without crosstalk. Their detection limits were 1.11 and 0.63 μΜ, respectively. The strategy realized simultaneous visual detection of carbaryl and glyphosate in food/herbal with excellent accuracy (spiked recoveries, 91.00–107.2%), high precision (RSD ≤ 8.43%), and superior selectivity.

Facile preparation of a dual-emission paper-based fluorescent sensor based on carbon quantum dots and rhodamine B for dual-mode detection of Hg2+

In this study, carbon quantum dots (CQDs) and rhodamine B (RhB) were physically mixed to construct a highly selective and sensitive ratiometric fluorescent sensor (CQDs@RhB) for the quantitative and visual detection of Hg2+. After adding Hg2+, the emission peak of CQDs at 445 nm was quenched and the peak of RhB at 575 nm remained unchanged; the ratio of the two emission peaks had a linear relationship with the Hg2+ concentration. The CQDs@RhB had a detection range of 0–15 µM and the limit of detection (LOD) is 65.93 nM and a color change from blue to pink was visible to the naked eye under ultraviolet light. The study revealed a static quenching mechanism of CQDs@RhB. The established method was successfully applied to the detection of Hg2+ in real water and rice samples with satisfactory results. In addition, a portable fluorescent paper-based sensor platform was developed using computer software assistance. The relationship with Hg2+ concentration was constructed by converting the pictures obtained under ultraviolet light to RGB color mode for visualization and quantitative detection of Hg2+. This study provides a valuable strategy for constructing a rapid detection system for Hg2+ in the field.

Ce4+-based self-validated portable platform for highly selective and anti-interference visual sensing of phosphate

Construction of a convenient and multi-responsive sensor for visual and real-time detecting of phosphate (Pi) is important to monitor the eutrophication pollution or drinking water quality. Herein, we developed a highly selective and anti-interference fluorescent and colorimetric dual-mode sensor for Pi detection. Since only the Ce4+ ion was used as the center with copper nanoclusters (CuNCs) and 3,3′,5,5′-Tetramethylbenzidine (TMB) as the signal carriers, the construction of the sensor was significantly simplified. The dissociated Ce4+ showed ability of triggering the CuNCs aggregation-induced emission (AIE) and oxidase-like enzyme, independently bringing red fluorescence (AIE of CuNCs) and blue color (oxidized TMB) signals. With the presence of Pi, the strong binding between Pi and Ce4+ through P-O-Ce bond quenched both the fluorescent and colorimetric signals. More significantly, the selective and anti-interference ability were effectively improved by self-validation between fluorescent and colorimetric modes. Meanwhile, combining with smartphone, the Pi lowered at 1 μM could be visually detected. Based on the fluorescent and colorimetric outputs could be directly quantified by the naked eye, a paper-based dual-mode visualization platform was constructed. The reliable dual-mode also showed robust analysis of the Pi in environmental water, indicating its great potential as a simple and efficient tool for field monitoring.

A rapid and sensitive smartphone colorimetric sensor for detection of ascorbic acid in food using the nanozyme paper-based microfluidic chip

Ascorbic acid is very important to human health because of its excellent antioxidant effect. Developing sensitive and on-site detection methods is therefore in high demand. In this work, a portable paper-based colorimetric sensor with a smartphone platform with an ultrahigh sensitivity has been designed for on-site and quantitative analysis of ascorbic acid based on AuNPs nanozyme activity. The developed excellent peroxidase-like nanozymes, could effectively catalyze the oxidation of chromogenic substrates by H2O2. Herein, the AuNPs nanozyme activity are embedded on paper pieces to construct paper-based microfluidic chips for visual detection. Meanwhile, a smartphone platform is integrated for the signal readout. Using ascorbic acid as an analyte model, the proposed paper-based analysis platform shows a reliable and sensitive detection of ascorbic acid with a low detection limit of 0.406 μmol/L. The platform also works well in various real samples. This analysis method is facile in design, showing a great application potential for on-site and mass screening of ingredients in the environment and in foods.

Advancement in Paper-Based Electrochemical Biosensing and Emerging Diagnostic Methods.

The utilization of electrochemical detection techniques in paper-based analytical devices (PADs) has revolutionized point-of-care (POC) testing, enabling the precise and discerning measurement of a diverse array of (bio)chemical analytes. The application of electrochemical sensing and paper as a suitable substrate for point-of-care testing platforms has led to the emergence of electrochemical paper-based analytical devices (ePADs). The inherent advantages of these modified paper-based analytical devices have gained significant recognition in the POC field. In response, electrochemical biosensors assembled from paper-based materials have shown great promise for enhancing sensitivity and improving their range of use. In addition, paper-based platforms have numerous advantageous characteristics, including the self-sufficient conveyance of liquids, reduced resistance, minimal fabrication cost, and environmental friendliness. This study seeks to provide a concise summary of the present state and uses of ePADs with insightful commentary on their practicality in the field. Future developments in ePADs biosensors include developing novel paper-based systems, improving system performance with a novel biocatalyst, and combining the biosensor system with other cutting-edge tools such as machine learning and 3D printing.

Paper-based colorimetric detection of COVID-19 using aptasenor based on biomimetic peroxidase like activity of ChF/ZnO/CNT nano-hybrid

Corona Virus Disease 2019 (COVID-19) as the infectious disease caused the pandemic disease around the world through infection by SARS-CoV-2 virus. The common diagnosis approach is Quantitative RT-PCR (qRT-PCR) which is time consuming and labor intensive. In the present study a novel colorimetric aptasensor was developed based on intrinsic catalytic activity of chitosan film embedded with ZnO/CNT (ChF/ZnO/CNT) on 3,3′,5,5′-tetramethylbenzidine (TMB) substrate. The main nanocomposite platform was constructed and functionalized with specific COVID-19 aptamer. The construction subjected with TMB substrate and H2O2 in the presence of different concentration of COVID-19 virus. Separation of aptamer after binding with virus particles declined the nanozyme activity. Upon addition of virus concentration, the peroxidase like activity of developed platform and colorimetric signals of oxidized TMB decreased gradually. Under optimal conditions the nanozyme could detect the virus in the linear range of 1–500 pg mL and LOD of 0.05 pg mL. Also, a paper-based platform was used for set up the strategy on applicable device. The paper-based strategy showed a linear range between 50 and 500 pg mL with LOD of 8 pg mL. The applied paper based colorimetric strategy showed reliable results for sensitive and selective detection of COVID-19 virus with the cost-effective approach.

Promising carbonized polymer dots for visually sequential sensing of Cu2+ and S2−

Carbonized polymer dots (CPDs) are formed by combining lignite, which primarily forms carbon cores, with polyvinylpyrrolidone, citric acid and tryptophan, which primarily produce short polymer chains and surface functional groups. These CPDs display a unique core–shell structure, excellent optical stability, superior fluorescence intensity, high quantum yield (QY) and outstanding biocompatibility allowing them to be well suited for application as fluorescent sensors. CPDs can be employed both as smart sensing systems for visual detection and absorption of Cu2+ and S2− through hydrogel sensors and as fluorescent inks for information security and anti-counterfeiting. More importantly, the paper-based platform and smartphone assistance enable visual real-time on-site quantification of Cu2+ and S2−, which offers an effective tool for fast and accurate Cu2+ and S2− identification and information encryption with high selectivity and sensitivity. In addition, with its good biocompatibility and low cytotoxicity, the CPDs have been successfully utilized for imaging Cu2+ and S2− in MG-63 cells, thus making a positive contribution to the analysis and imaging of the effects of Cu2+ and S2− in relevant biological processes and promoting better diagnosis and treatment of diseases.

Dual-Mode Paper Biosensing Platform Based on Oxidase-Like CoFeMn Nanozymes for Point-of-Care Detection of Glutathione

A paper-based biosensing platform is a point-of-care (POC) analysis toolkit for detection of various biomarkers. Nonetheless, its lack of high sensitivity, selectivity, and multi-signal readout poses a high degree of challenge. Herein, we introduce an interesting colorimetric-temperature dual-signal readout biosensor based on multifunctional CoFeMn biomimetic oxidase. Due to the cost-effectiveness, no additional detector requirement, dual-signal readout capacity, and darker signal change, CoFeMn hydroxide is innovatively fabricated by a facile hydrothermal method using Mn as an active center to construct a multifunctional signal tag for mimicking the structure of oxidase. This strategy allows CoFeMn hydroxide to exhibit an unusual oxidase-like activity, transforming O2 into ·OH in the absence of H2O2 and resulting in the generation of a colorimetric temperature dual signal by oxidizing 3,3′,5,5′-tetramethylbenzidine (TMB). We used glutathione (GSH) as the analyst and successfully applied this biosensor to determine GSH, which showed excellent analytical performance of rapidity, high specificity, sensitivity, and accuracy. Employing the colorimetric and temperature test strips, these toolkits are designed to visualize GSH. Benefiting from a relatively independent signal transduction pathway, the constructed test strip POC devices display satisfactory coupling efficiency and are further employed to monitor GSH in tumor cells. This research will be conducive to the rational design of a mimetic oxidase-based dual-response nanoprobe in paper-based POC devices, the exploration of more nanomaterial-derived mimetic oxidase, and the extension of their applications in medical diagnosis.

A Novel Approach for Glycosylated Hemoglobin Testing Using Microchip Affinity Electrophoresis.

Effective management of diabetes largely benefits from early diagnosis followed by intensive long-term regulation of blood glucose. The levels of glycohemoglobin (HbA1 and HbA1c) have been used as standard biomarkers to assess long-term blood glucose concentrations for diabetes diagnosis and management. Gold standard laboratory methods for HbA1 and HbA1c testing are often costly and not widely available. Moreover, currently available point-of-care (POC) immunoassay-based glycohemoglobin tests may produce inaccurate test results for patients with co-existing diseases such as hemoglobin disorders and anemia. Here, we report a POC platform, HemeChip-GHb, for quantitative HbA1 detection leveraging paper-based affinity electrophoresis. We describe the design and development of the HemeChip-GHb test. Feasibility and accuracy of the HemeChip-GHb system were demonstrated by testing blood samples collected from healthy donors, patients with prediabetes, and patients with diabetes. HbA1 levels measured with HemeChip-GHb show 0.96 correlation to the levels reported from the clinical standard HPLC tests, and with a bias of -0.72% based on Bland-Altman analysis. 99.6% of the HbA1 levels for paired HemeChip-GHb and HPLC fell within A and B zones of no difference in clinical outcome based on error grid analysis. Using HemeChip-GHb we achieved accurate diabetes status detection with sensitivity and specificity of 100%. We presented a novel POC paper-based affinity electrophoresis platform that has the potential for accurately diagnosing diabetes, and addressing an unmet need for accurate and affordable diagnostics in resource-challenged environments.

Biomarker Detection in Early Diagnosis of Cancer: Recent Achievements in Point-of-Care Devices Based on Paper Microfluidics

Microfluidics is very crucial in lab-on-a-chip systems for carrying out operations in a large-scale laboratory environment on a single chip. Microfluidic systems are miniaturized devices in which the fluid behavior and control can be manipulated on a small platform, with surface forces on the platform being greater than volumetric forces depending on the test method used. In recent years, paper-based microfluidic analytical devices (μPADs) have been developed to be used in point-of-care (POC) technologies. μPADs have numerous advantages, including ease of use, low cost, capillary action liquid transfer without the need for power, the ability to store reagents in active form in the fiber network, and the capability to perform multiple tests using various measurement techniques. These benefits are critical in the advancement of paper-based microfluidics in the fields of disease diagnosis, drug application, and environment and food safety. Cancer is one of the most critical diseases for early detection all around the world. Detecting cancer-specific biomarkers provides significant data for both early diagnosis and controlling the disease progression. μPADs for cancer biomarker detection hold great promise for improving cure rates, quality of life, and minimizing treatment costs. Although various types of bioanalytical platforms are available for the detection of cancer biomarkers, there are limited studies and critical reviews on paper-based microfluidic platforms in the literature. Hence, this article aims to draw attention to these gaps in the literature as well as the features that future platforms should have.

Combining microfluidic paper-based platform and metal–organic frameworks in a single device for phenolic content assessment in fruits

A microfluidic paper-based device (µPAD) has been combined with metal–organic frameworks (MOFs) for total phenolic compounds (TPC) quantification in fruit samples for the first time. The performance of the µPAD, based upon the vertical flow approach, was enhanced in order to determine the TPC content with high accuracy in fruit samples. The method was based on the traditional Folin-Ciocalteu Index using gallic acid or oenotannin as reference phenolic compounds. This novel design and construction of the device are in agreement with the principles of Green Chemistry avoiding wax technology (lower toxicity). The analytical parameters that affect the colorimetric method (using digital imaging of the colored zone) performance were optimized including design, sample volume, and MOF amount. Then, the analytical features of the developed method were investigated such as dynamic range (1.6–30 mg L−1), limit of detection (0.5 mg L−1), and precision (RSD < 9%). Besides, the in-field analysis is achievable with a color stability up to 6 h after the loading process of the sample and storage stability for at least 15 days without performance losses (under vacuum at − 20 °C). Furthermore, the MOF ZIF-8@paper was characterized to study its composition and the successful combination. The feasibility of the proposed method was demonstrated by determining the TPC in 5 fruit samples using oenotannin as reference solute. The accuracy was validated by comparison of the data with the results obtained with the recommended protocol proposed by the International Organisation of Vine and Wine (OIV).Graphical

Colorimetric detection of SARS‐CoV‐2 variants with paper‐based analytical devices

Colorimetric detection of SARS‐CoV‐2 variants with paper‐based analytical devices