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Electrochemical paper-based microfluidics has attracted much attention due to the promise of transforming point-of-care diagnostics by facilitating quantitative analysis with low-cost and portable analyzers. Such devices harness capillary flow to transport samples and reagents, enabling bioassays to be executed passively. Despite exciting demonstrations of capillary-driven electrochemical tests, conventional methods for fabricating electrodes on paper impede capillary flow, limit fluidic pathways, and constrain accessible device architectures. This account reviews recent developments in paper-based electroanalytical devices and offers perspective by revisiting key milestones in lateral flow tests and paper-based microfluidics engineering. The study highlights the benefits associated with electrochemical sensing and discusses how the detection modality can be leveraged to unlock novel functionalities. Particular focus is given to electrofluidic platforms that embed electrodes into paper for enhanced biosensing applications. Together, these innovations pave the way for diagnostic technologies that offer portability, quantitative analysis, and seamless integration with digital healthcare, all without compromising the simplicity of commercially available rapid diagnostic tests., (© 2024 The Authors. Small published by Wiley‐VCH GmbH.)

We developed a simple, paper-based device that enables sensitive detection by mass spectrometry (MS) without solid phase extraction or other sample preparation. Using glass fiber filter papers within a 3D printed holder, the device employs electrokinetic manipulations to stack, separate, and desalt charged molecules on paper prior to spray into the MS. Due to counter-balanced electroosmotic flow and electrophoresis, charged analytes stack on the paper and desalting occurs in minutes. One end of the paper strip was cut into a sharp point and positioned near the inlet of a MS. The stacked analyte bands move toward the paper tip with the EOF where they are ionized by paper spray. The device was applied to analysis of PFAS in tap water with sub part-per-trillion detection limits in less than ten minutes with no sample pretreatment. Analysis of opioids in urine also occurs in minutes. The crucial parameters to enable stacking, separation, and MS ionization of both positively and negatively charged analytes were determined and optimized. Experimental and computational modeling studies confirm the electrokinetic stacking and analyte transport mechanisms. On-paper separations were carried out by stacking analyte bands at different locations depending on their electrophoretic mobility, achieving baseline separation in some cases., (© 2024 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.)

Salmonella, the most prevalent food-borne pathogen, poses significant medical and economic threats. Swift and accurate on-site identification and serotyping of Salmonella is crucial to curb its spread and contamination. Here, a synthetic biology cascade reaction is presented on a paper substrate using CRISPR-Cas12a and recombinase polymerase amplification (RPA), enabling the programming of a standard toehold RNA switch for a genome of choice. This approach employs just one toehold RNA switch design to differentiate between two different Salmonella serotypes, i.e., S. Typhimurium and S. Enteritidis, without the need for reengineering the toehold RNA switch. The sensor exhibits high sensitivity, capable of visually detecting as few as 100 copies of the whole genome from a model Salmonella pathogen on a paper substrate. Furthermore, this robust assay is successfully applied to detect whole genomes in contaminated milk and lettuce samples, demonstrating its potential in real sample analysis. Due to its versatility and practical features, genomes from different organisms can be detected by merely changing a single RNA element in this universal cell-free cascade reaction., (© 2024 Wiley‐VCH GmbH.)

Abstract This study identifies important factors for designing an effective biomimetic paper‐based fog harvesting substrate by examining the harvesting properties of different surfaces, including glass, polyethylene, and superhydrophobic paper. In laboratory‐scale fogging tests, the wetting behavior of the substrates is characterized, and the importance of the tilt angle of the respective surface relative to the fog flow is elaborated. Because successful fog harvesting requires both efficient accumulation of water droplets on the surface (by condensation and collision) and sufficient but not excessive roll‐off of the liquid, the amount of water finally collected is clearly related to the pinning effect, which should prevent the smallest droplets from being carried away by the wind but must not lead to full and permanent wetting of the surface. Coalescence is identified as a major phenomenon to improve droplet roll‐off. In this context, superhydrophobic paper indicates to be a more effective water collector than glass or polyethylene, especially when oriented vertically, since it allows the droplets to roll off very efficiently. Finally, the addition of glass particles to the superhydrophobic coating is proposed as a means of enhancing pinning and improving the fog harvesting efficiency.

Microfluidic paper-based analytical devices (µPADs) are indispensable tools for disease diagnostics. The integration of electronic components into µPADs enables new device functionalities and facilitates the development of complex quantitative assays. Unfortunately, current electrode fabrication methods often hinder capillary flow, considerably restricting µPAD design architectures. Here, laser-induced graphenization is presented as an approach to fabricate porous electrodes embedded into cellulose paper. The resulting electrodes not only have high conductivity and electrochemical activity, but also retain wetting properties for capillary transport. Paper-based electrofluidics, including a lateral flow device for injection analysis of alkaline phosphatase in serum and a vertical flow device for quantitative detection of HPV16 with a CRISPR-based assay are demonstrated. It is expected that this platform will streamline the development of diagnostic devices that combine the operational simplicity of colorimetric lateral flow tests with the added benefits and possibilities offered by electronic signaling., (© 2023 The Authors. Advanced Materials published by Wiley-VCH GmbH.)

Abstract The synergy resulting from the high conductivity of graphene and catalytic properties of metal nanoparticle has been a resource to improve the activity and functionality of electrochemical sensors. This work focuses on the simultaneous synthesis of copper nanoparticles (CuNPs) and laser‐induced graphene (LIG) derived from paper, through a one‐step laser processing approach. A chromatography paper substrate with drop‐casted copper sulfate is used for the fabrication of this hybrid material, characterized in terms of its morphological, chemical, and conductive properties. Appealing conductive properties are achieved, with sheet resistance of 170 Ω sq−1 being reached, while chemical characterization confirms the simultaneous synthesis of the conductive carbon electrode material and metallic copper nanostructures. Using optimized laser synthesis and patterning conditions, LIG/CuNPs‐based working electrodes are fabricated within a three‐electrode planar cell, and their electrochemical performance is assessed against pristine LIG electrodes, demonstrating good electron transfer kinetics appropriate for electrochemical sensing. The sensor's ability to detect glucose through a non‐enzymatic route is optimized, to assure good sensing performance in standard samples and in artificial sweat complex matrix.

Bioelectronic implants delivering electrical stimulation offer an attractive alternative to traditional pharmaceuticals in electrotherapy. However, achieving simple, rapid, and cost-effective personalization of these implants for customized treatment in unique clinical and physical scenarios presents a substantial challenge. This challenge is further compounded by the need to ensure safety and minimal invasiveness, requiring essential attributes such as flexibility, biocompatibility, lightness, biodegradability, and wireless stimulation capability. Here, a flexible, biodegradable bioelectronic paper with homogeneously distributed wireless stimulation functionality for simple personalization of bioelectronic implants is introduced. The bioelectronic paper synergistically combines i) lead-free magnetoelectric nanoparticles (MENs) that facilitate electrical stimulation in response to external magnetic field and ii) flexible and biodegradable nanofibers (NFs) that enable localization of MENs for high-selectivity stimulation, oxygen/nutrient permeation, cell orientation modulation, and biodegradation rate control. The effectiveness of wireless electrical stimulation in vitro through enhanced neuronal differentiation of neuron-like PC12 cells and the controllability of their microstructural orientation are shown. Also, scalability, design flexibility, and rapid customizability of the bioelectronic paper are shown by creating various 3D macrostructures using simple paper crafting techniques such as cutting and folding. This platform holds promise for simple and rapid personalization of temporary bioelectronic implants for minimally invasive wireless stimulation therapies., (© 2024 Wiley‐VCH GmbH.)

Abstract Paper‐based devices have attracted considerable attention in point‐of‐care testing (POCT) due to their simple operation and portability. The performance of paper‐based POC assays is further enhanced by coupling with functional nucleic acids (FNAs), which are able to selectively recognize and bind to targets, amplify and transduce signals. Several high‐performance paper‐based POC assays have been developed, resulting from the different spatial structures of the paper‐based device and detection strategies using different FNAs. In this review, we first introduce FNAs and paper‐based devices, including their concepts, classifications and advances. The following section focuses on the application of these FNAs in POC assays using paper‐based devices, taking into account their spatial one‐, two‐ and three‐dimensional structures. Finally, the challenges and perspectives of the application of FNAs in paper‐based POCT are discussed.

Abstract Paper, an inexpensive material with natural biocompatibility, non‐toxicity, and biodegradability, allows for affordable and cost‐effective substrates for unconventional advanced electronics, often called papertronics. On the other hand, polymeric elastomers have shown to be an excellent success for substrates of soft bioelectronics, providing stretchability in skin wearable technology for continuous sensing applications. Although both materials hold their unique advantageous characteristics, merging both material properties into a single electronic substrate reimagines paper‐based bioelectronics for wearable and patchable applications in biosensing, energy generation and storage, soft actuators, and more. Here, a breathable, light‐weighted, biocompatible engineered stretchable paper is reported via coaxial nonwoven microfibers for unconventional bioelectronic substrates. The stretchable papers allow intimate bioconformability without adhesive through coaxial electrospinning of a cellulose acetate polymer (sheath) and a silicone elastomer (core). The fabricated cellulose‐silicone fibers exhibit a greater percent strain than commercially available paper while retaining hydrophilicity, biocompatibility, combustibility, disposable, and other natural characteristics of paper. Moreover, the nonwoven stretchable cellulose‐silicone fibrous mat can adapt conventional printing and fabrication process for paper‐based electronics, an essential aspect of advanced bioelectronic manufacturing.

Abstract Urinary tract infections (UTIs) are the most common nosocomial infection in North America leading to over $12 billion in annual health care costs. UTIs can significantly reduce the quality of life and, in severe cases, result in sepsis and mortality. According to Public Health Ontario, over 80% of long‐term care home (LTCH) residents with asymptomatic bacteriuria are treated with antibiotics, however, less than 50% of the antibiotic treatments for UTIs show clinical benefit. Current confirmatory processes for UTIs are primarily dependent on the completion of urine cultures which can result in a delay of more than 24 h. Therefore, there is a need to develop new efficient diagnostic methods to provide timely test results and prevent multidrug resistance. Emerging nanomaterials with special physical and chemical properties have demonstrated great potential in rapid detection of UTI‐associated bacteria. This review paper provides a thorough analysis of current diagnostic tools for UTIs. Emerging nanostructured biosensors are reviewed to elucidate the most recent progress in the detection of uropathogens. It is believed that advanced biosensors integrated with nanotechnology will contribute to the timely diagnosis of UTIs and improve the accuracy of the results, which will lead to better treatment of this prevalent clinical condition.

Electroextraction (EE) encompasses a range of sample preparation methods whose effectiveness, selectivity, and efficiency are significantly influenced by the physical-chemical characteristics of analytes, samples, and instrumental conditions. This article explores, for the first time, various strategies aimed at enhancing the extraction efficiency of a recent approach of EE utilizing a paper point (PP) combined with a hollow fiber (HF) (abbreviated as PP-HF-EE) to extract various cationic and anionic model compounds from water samples. The study also explores, experimentally, the impact of agitation, organic filter composition, PP diameter, and PP brand on extraction performance, and proves that all these factors are quite important, especially when digital image analysis is utilized for determination. Furthermore, this work demonstrates the ease and feasibility of simultaneously extracting cations and anions using PP-HF-EE and proposes a straightforward method to enhance analyte concentration on the vertex of the PP through a base-to-vertex focusing. Lastly, it is demonstrated, using capillary electrophoresis coupled to a UV-Vis detector, that for PP-HF-EE, the extraction efficiency and pre-concentration factor are less dependent on other parameters when multiple PPs per sample are utilized, with signal enhancement values of up to 111 and 339 for nortriptyline and haloperidol, respectively. All the findings and strategies presented herein constitute significant contributions that can facilitate future research in method development, particularly in the utilization of PP-HF-EE and similar EE approaches., (© 2024 Wiley‐VCH GmbH.)

Disposable wearable electronics are valuable for diagnostic and healthcare purposes, reducing maintenance needs and enabling broad accessibility. However, integrating a reliable power supply is crucial for their advancement, but conventional power sources present significant challenges. To address that issue, a novel paper-based moist-electric generator is developed that harnesses ambient moisture for power generation. The device features gradients for functional groups and moisture adsorption and architecture of nanostructures within a disposable paper substrate. The nanoporous, gradient-formed spore-based biofilm and asymmetric electrode deposition enable sustained high-efficiency power output. A Janus hydrophobic-hydrophilic paper layer enhances moisture harvesting, ensuring effective operation even in low-humidity environments. This research reveals that the water adsorption gradient is crucial for performance under high humidity, whereas the functional group gradient is dominant under low humidity. The device delivers consistent performance across diverse conditions and flexibly conforms to various surfaces, making it ideal for wearable applications. Its eco-friendly, cost-effective, and disposable nature makes it a viable solution for widespread use with minimal environmental effects. This innovative approach overcomes the limitations of traditional power sources for wearable electronics, offering a sustainable solution for future disposable wearables. It significantly enhances personalized medicine through improved health monitoring and diagnostics., (© 2024 The Author(s). Small published by Wiley‐VCH GmbH.)

As sustainable and eco-friendly replacements to conventional paper, rewritable paper is a very attractive alternative for communication, information circulation, and storage. Development is made for rewritable paper using chromogenic materials that change its color in presence of external stimuli. However, the new techniques have faced several major challenges including feasible operational method, eco-friendly approach. Herein, a simple, convenient, and eco-friendly strategy is described for the preparation of rewritable paper substrate, and multi colored ink for efficient use in writing, painting or printing purpose. In addition, writing with "invisible ink" on the rewritable paper can be realized for potential anti-counterfeiting application. The written, painted, or printed information on the paper substrate can be easily erased using an aqueous solution. Thus, the original paper can be retrieved and the paper substrate can be reused multiple times. Besides, the written or printed information can be retained for a prolonged time at ambient conditions. Overall, this approach shows the rewritable paper as a prototype of multicolor writing/painting application, offering a sustainable solution for reducing paper waste and promoting environmental stewardship., (© 2024 Wiley‐VCH GmbH.)

Abstract Cellulose paper has emerged as an ideal sensing element for wearable pressure sensors owing to its inherent flexibility, high porosity, and light weight. However, traditional paper‐based pressure sensors use metal‐based materials as electrodes, which significantly limits the unique advantages of paper, particularly in terms of degradability. In this study, a degradable pressure sensor is designed by combining the highly conductive poly(3,4‐ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) Xuan paper electrode with a low‐conductivity PEDOT:PSS tissue paper sensitive layer. Notably, Xuan paper, also called rice paper, has been a prominent substrate owing to its softness and good durability. By introducing a perforated structure in the sensitive layer, a novel sensing mechanism, conductivity conversion under pressure, is realized to improve the sensitivity. The obtained sensor exhibits a high sensitivity (13.9 kPa−1 at < 8.3 kPa, 151 kPa−1 at 8.3–20.8 kPa), ensuring that it can precisely monitor the full‐range human activities. Additionally, as the sensor does not rely on metal materials, it can degrade in water or fire without causing any negative environmental impacts. These findings establish a new approach to producing highly sensitive degradable sensors, which hold significant potential for application in green electronics, paper‐based sensing matrices, new prosthetics, and other fields.

Transparent paper manufactured from wood fibers is emerging as a promising, cost-effective, and carbon-neutral alternatives to plastics. However, fully exploring their mechanical properties is one of the most pressing challenges. In this work, a strong yet tough transparent paper with superior folding endurance is prepared by rationally altering the native fiber structure. Microwave-assisted choline chloride/lactic acid deep eutectic solvent (DES) pulping is first utilized to isolate wood fibers from spruce wood. During this process, the S1 layer within the fibers is partially disrupted, forming protruding microfibrils that play a crucial role in enhancing cellulose accessibility. Subsequently, carboxymethylation treatment is applied to yield uniformly swollen carboxymethylated wood fibers (CM fibers), which improves the interaction between CM fibers during papermaking. The as-prepared transparent paper not only shows a 90% light transmittance (550 nm) but also exhibits impressive mechanical properties, including a folding endurance of over 26 000, a tensile strength of 248.4 MPa, and a toughness of 15.6 MJ m -3 . This work provides a promising route for manufacturing transparent paper with superior mechanical properties from wood fibers and can extend their use in areas normally dominated by high-performance nonrenewable plastics., (© 2024 Wiley‐VCH GmbH.)

Although paperless technologies are becoming ubiquitous, paper and paper-based materials remain one of the most widely used resources, predicted to exceed an annual total of 460 million metric tons by 2030. Given the environmental challenges, deleterious impact on natural resources, and waste associated with conventional wood-based paper manufacturing, developing more sustainable strategies to source, produce, and recycle paper from natural materials is essential. Here, the development and production of reusable and recyclable paper are reported. This approach offers a pathway for easily producing natural pollen grains via ecofriendly, economical, scalable, and low-energy fabrication routes. It is demonstrated that the pollen-based paper exhibits high-quality printability, readability, and erasability, enabling its reuse. Based on the pH-responsive morphological responses of engineered pollen materials, a method for hygro stable printing and on-demand unprinting is presented. The reusability of the pollen paper renders it more advantageous than conventional single-print wood-based paper. This study thus provides possible pathways to utilize non-allergenic pollen, which is renewable and naturally abundant, as a sustainable source of reusable paper. While this work primarily deals with paper, the methods described here can be extended to produce other products such as cartons and containers for the storage and transport of liquid and solid materials., (© 2022 Wiley-VCH GmbH.)

Abstract Health monitoring using wearable artificial intelligence (AI) sensors with sensing and cognitive capabilities has garnered significant attention. The development of self‐contained AI sensors that can operate with low power consumption, akin to the human brain, is necessary. Physical reservoir computing (PRC), which mimics the human brain using physical phenomena, offers a low‐power consumption architecture. Nevertheless, creating a flexible and easily disposable sensors using PRC capable of processing optical signals with sub‐second response times suitable for biological signals presents a challenge. In this study, a disposable and flexible paper‐based optoelectronic synaptic devices are designed, which are composed of nanocellulose and ZnO nanoparticles, for PRC. This device exhibits synaptic photocurrent in response to optical input. To assess its performance, a classification and time‐series forecasting tasks are conducted. The memory capacity of short‐term memory task, indicating the device's ability to store past information, is 1.8. The device can recognize handwritten digits with an accuracy of 88%. These results highlight the potential of the device for PRC. In addition, subjecting the device to 1000 rounds of bending do not affect its accuracy. Furthermore, the device burn in a few seconds, much like regular office paper, demonstrating its disposability.

Lithium (Li) metal is regarded as the most promising anode for next-generation batteries with high energy density. However, the uncontrolled dendrite growth and infinite volume expansion during cycling seriously hinder the application of Li metal batteries (LMBs). Herein, an inorganic/organic protective layer (labeled as BPH), composed of in situ formed inorganic constituents and PVDF-HFP, is designed on the 3D carbon paper (CP) surface by hot-dipping method. The BPH layer can effectively improve the mechanical strength and ionic conductivity of the SEI layer, which is beneficial to expedite the Li-ion transfer of the entire framework and achieve stable Li plating/stripping behavior. As a result, the modified 3D CP (BPH-CP) exhibits an ultrahigh average Coulombic efficiency (CE) of ≈99.7% over 400 cycles. Further, the Li||LiFePO 4 (LFP) cell exhibits an extremely long-term cycle life of over 3000 cycles at 5 C. Importantly, the full cell with high mass loading LiFePO 4 (20 mg cm -2 ) or LiNi 0.8 Co 0.1 Mn 0.1 O 2 (NCM, 16 mg cm -2 ) cathode exhibits stable cycling for 100 or 150 cycles at 0.5 C with high-capacity retention of 86.5% or 82.0% even at extremely low N/P ratio of 0.88 or 0.94. believe that this work enlightens a simple and effective strategy for the application of high-energy-density and high-rate-C LMBs., (© 2024 Wiley‐VCH GmbH.)

Paper is a readily available material in nature. Its recyclability, eco-friendliness, portability, flexibility, and affordability make it a favored substrate for researchers seeking cost-effective solutions. Electronic devices based on solution process are fabricated on paper and banknotes using PVK and SnO 2 nanoparticles. The devices manufactured on paper substrates exhibit photosynaptic behavior under ultraviolet pulse illumination, stemming from numerous interactions on the surface of the SnO 2 nanoparticles. A light-modulated artificial synapse device is realized on a paper at a low voltage bias of -0.01 V, with an average recognition rate of 91.7% based on the Yale Face Database. As a security device on a banknote, 400 devices in a 20 × 20 array configuration exhibited random electrical characteristics owing to the local morphology of the SnO 2 nanoparticles and differences in the depletion layer width at the SnO 2 /PVK interface. The security Physically Unclonable Functions (PUF) key based on the current distribution extracted at -1 V show unpredictable reproducibility with 50% uniformity, 48.7% inter-Hamming distance, and 50.1% bit-aliasing rates. Moreover, the device maintained its properties for more than 210 days under a curvature radius of 8.75 mm and bias and UV irradiation stress conditions., (© 2024 Wiley‐VCH GmbH.)

Accurate quantification of disease-signature microRNAs (miRNAs) in biomedical samples is in high demand for clinical diagnosis but still challenging because of the low abundance of miRNAs and complicating interferences in the milieus. Here, we report a multi-amplification strategy based on paper-spray mass spectrometry (PS MS) for the analysis of miRNAs in blood. A toehold-mediated DNA-strand-displacement reaction (TSD) is employed to amplify the signal chain and to ensure the specificity. The signal chain is then cleaved by UV light to release signal molecules for detection. Moreover, the paper spray method can efficiently filter out interfering substances in the blood and further enhance the sensitivity of detection. This concept is successfully demonstrated in the prototypical detection of the cancer biomarker miRNA-141 in blood and serum. The proposed TSD-PS MS approach provides an efficient method for the sensitive detection of oligonucleotides at low concentration in complicated milieus., (© 2021 Wiley-VCH GmbH.)

Abstract Miniaturized paper‐based electrochemical sensors were fabricated using kraft paper and CO2 laser, dispensing the need for chemical reagents and controlled atmospheric conditions. This study initially evaluated the paper type and laser processing parameters, enhancing the electrodes′ robustness, electrochemical response, and electrical resistance. The sensors were also treated by applying −1 V for 60 s in 1.0 mol L−1 KCl, which is a simple and rapid procedure. The electrochemical treatment increased the electroactive area and roughness, confirmed by scanning electron microscopy. These aspects helped modulate the sensors′ electrochemical response for nitrite determination, improving selectivity and sensitivity for this compound. The sensors also showed repeatability and batch‐to‐batch reproducibility, with 2.2 and 10 % RSD, respectively. Therefore, this work brings a protocol to fabricating competitive electrochemical sensors through a sustainable strategy, opening possibilities for designing new analytical systems.

Abstract An increase in the environmental and health concerns over fluorochemical‐based, wax‐based, and extrusion‐based paper coatings has led to a growing interest in bio‐based, biodegradable, and repulpable alternatives to obtain water‐ and oil‐repellent coatings. Reported herein is a fluorine‐free, plastic‐free, and cost‐effective water and grease resistant paper coating approach that utilizes blends of corn‐starch (S) and a novel chitosan‐graft‐polydimethylsiloxane (CP) copolymer. The hydrophobic and oleophobic performance of the S/CP‐coated paper was evaluated by varying the ratio of S and CP in the overall blend. The S/CP‐coated papers were observed to have low cobb60 values (water absorptivity) of 13 ± 0.9 g m−2 and an excellent kit rating (oil resistance) of 12/12. The S/CP‐coated paper substrate surface profile was analyzed via scanning electron microscopy (SEM). The repulpability of the coated paper is also demonstrated by washing the coating materials from the paper and recovering the pulp.

Abstract This study reports the selective hydroxylation of macroscopic carbon surfaces that renders initially hydrophobic carbon fiber paper hydrophilic for more than one year (62 weeks) so far. This long time of sustained hydrophilicity is unprecedented and transforms the utility of macroscopic carbon materials. Quantification of surface oxygenates of a systematic series of 13 chemical treatments reveals that surface hydroxyls are predictors of long‐lasting hydrophilicity. The rapid, mild, acid‐free, transition‐metal‐free treatment does not leave surface residues, inhibits overoxidation of graphitic carbon beyond hydroxyls, and introduces the highest edge density on carbon surfaces, without altering the mesostructure of carbon fiber network architectures and without lowering the flexural strength of carbon fiber paper. Graphitic edges are required for enhanced stability of surface oxygenates that retain a threshold amount of adsorbed water, which is necessary for keeping carbon fiber paper hydrophilic. Application of hydrophilic carbon fiber paper as high‐surface‐area working electrode supports for alkaline water oxidation catalyzed by [NiFe]‐layered double hydroxide nanosheets demonstrates a factor of 60 higher mass activity compared to catalysis on flat basal‐plane highly ordered pyrolytic graphite electrodes.

Abstract Enhanced and rapid surveillance for diseases is critical to public health and meeting United Nations' Sustainable Development Goal for Good Health and Well‐being by allowing for targeted and accelerated prevention and control response strategies. Human malaria, caused by Plasmodium spp. and transmitted by mosquitoes is no exception. Advances in sustainable materials provide an opportunity to improve fast, sustainable, and equitable testing assays. Here, naturally abundant polymers and biomaterials, such as cellulose nanocrystals (CNCs) and chitosan, were used to increase antibody density deposition on the assay detection line when compared to traditional free antibody deposition, and thus the sensitivity, of easily assembled rapid tests designed to detect Plasmodium vivax infective (sporozoite) parasites in mosquitoes, a critical indicator of malaria transmission. The immobilization of antibodies onto chitosan‐coated CNCs allowed for antigen detection with a lower number of antibodies used in each test; likewise, the immobilization allowed to directly place the CNC‐Ab without the traditionally needed blockers layer on the paper like bovine serum albumin (BSA). This bio‐based prototype of a paper‐based dipstick assay shows a promising pathway for the development of rapid disease surveillance tools using sustainable and globally available materials.

Distorted urea levels indicate several liver, kidney, or metabolic diseases; however, traditional clinical urea detection relies on urease-based methods enslaved to well-known limitations of high-price, unstable properties, complicated sample pretreatment and analysis procedures, and difficult visual real-time monitoring. Herein, nonenzymatic paper-based fluorescent materials (UFP-BP) are strategically integrated with an on-demand fluorescent-sensor (UFP) self-aggregated nanoparticle on commercial filter paper for pre-dilution-free and visual real-time urea monitoring. The UFP is synthesized and self-aggregated into the fluorescent nanoparticles for selective urea recognition. Then, the nanoparticles are interstitially loaded on filter paper to nanoengineer the UFP-BP, achieving selective quantitative urea detection in the normal concentration range (10-1000 mm). UFP and UFP-BP can successfully monitor urea levels in real rat urine, artificial simulants, and milk. The proposed sensing platform, integrated with smartphones, offers accurate, quantitative, nonenzymatic, noninvasive, pre-dilution-free, on-site, rapid, low-cost, easy-to-operate, real-time visual urea detection in food samples and human body fluids. The designed sensing system can provide early warnings of abnormal nitrogen-based health issues., (© 2024 Wiley‐VCH GmbH.)

Laser-induced graphene (LIG) technology has provided a new manufacturing strategy for the rapid and scalable assembling of triboelectric nanogenerators (TENG). However, current LIG-based TENG commonly rely on polymer films, e.g., polyimide (PI) as both friction material and carbon precursor of electrodes, which limit the structural diversity and performance escalation due to its incapability of folding and creasing. Using specialized PI paper composed of randomly distributed PI fibers to substantially enhance its foldability, this work creates a new type of TENG, which are structurally foldable and stackable, and performance tailorable. First, by systematically investigating the laser power-regulated performance of single-unit TENG, the open-circuit voltage can be effectively improved. By further exploiting the folding process, multiple TENG units can be assembled together to form multi-layered structures to continuously expand the open-circuit voltage from 5.3 to 34.4 V cm -2 , as the increase of friction units from 1 to 16. Last, by fully utilizing the unique structure and performance, representative energy-harvesting and smart-sensing applications are demonstrated, including a smart shoe to recognize running motions and power LEDs, a smart leaf to power a thermometer by wind, a matrix sensor to recognize writing trajectories, as well as a smart glove to recognize different objects., (© 2024 The Authors. Advanced Science published by Wiley‐VCH GmbH.)

Lignin has been extensively researched as a cathode active material in secondary batteries. In the present work, the energy storage potential of lignin naturally present in papers made of softwood chemi-thermomechanical pulp (CTMP) is explored. More specifically, effects from softwood CTMP fines on the electrochemical characteristics have been studied. Compared to pulp fibers, fines are higher in lignin content and have higher specific surface area. It was expected that this would be positive for the electrode performance; however, the result points to the opposite. The fines do not significantly contribute to a higher lignin specific capacity, and they deteriorate the cycling stability. Higher fines content was found to result in a higher oxidative activity as well as more abundant competing reactions. These competing reactions are believed to be linked to the cycle stability. Therefore, we hypothesize that the electrochemical stability of lignin can be better understood by studying differences between fines and fiber lignin. As the theoretical specific capacity of this material is about 20 times larger than obtained here, identification of the reasons for this capacity discrepancy is needed to realize the full potential of lignin-based paper batteries., (© 2024 The Authors. ChemSusChem published by Wiley-VCH GmbH.)

Abstract Flexible conducting materials are required for the design and fabrication of a host of applications involving flexible electronic items. A flexible substrate like paper or polymer is generally employed for deposition of metal by a variety of processes. Among many physical properties, the roughness of the substrate is considered an important parameter, although, its exact role on effective conductivity of the coating is not known. Nor any study has been carried out to understand how the three‐dimensional porous structure of the substrate surface affects the microscopic packing of grains that constitute the metal coating. With the objective of elucidating the effect of substrate roughness on the conductivity of paper electrodes, we have used six different commonly available papers for vacuum coating with copper. For a smooth substrate, the grains that constitute the coating appear spherical, however, turns ellipsoidal as the substrate roughness and heterogeneity is increased; ellipsoidal grains result in higher packing efficiency leading to higher conductivity. We have also presented a model to relate the packing efficiency to the asphericity, polydispersity, and skewness of size distribution of grains.

Abstract Wearable sensors are establishing themselves as options for real‐time continuous health monitoring in health care and wellness. In particular, the use of flexible interfaces that conform to the skin have attracted considerable interest for the extraction of meaningful pathophysiological information through continuous and painless sampling and analysis of biofluids. In contrast, conventional techniques for biomarkers analysis are difficult to adapt to real‐time portable monitoring due to their invasive sampling protocols, biosample preparation and reagent stabilization. Here a shelf‐stable, non‐invasive, paper‐based colorimetric wearable lactate sensor is reported. This sensor exploits the ability of silk to control the concentration, print, and functionally preserve labile transducing biomolecules in the format of a shelf‐stable digital patch for optical readout. This novel approach overcomes major challenges associated with the commercialization of colorimetric wearable sensors (e.g., enzyme thermal instability, narrow sensing range, low sensitivity, and qualitative response) by showing a combination of unprecedented stability (i.e., up to 2 years in refrigerated conditions), wide sensing range, and high sensitivity. Additionally, real‐time quantitative signal readouts are achieved using machine learning‐driven image analysis enabling physiological status evaluation with a simple smartphone camera.

Abstract Nano‐silver conductive inks have attracted the attention of researchers due to their high electrical conductivity, good chemical stability, and wide applicability. As the mainstream conductive ink, it is mostly used in inkjet printing, but its application is limited due to the high sintering temperature. In this paper, silver nanoparticles were synthesized by reducing silver nitrate with sodium borohydride. Using silver nanoparticles as basic conductive fillers and graphene or copper nanoparticles as auxiliary conductive fillers, silver conductive inks, silver/graphene conductive inks and silver/copper conductive inks suitable for micro‐direct writing printing were prepared. Electrode patterns were printed on photo paper by micro‐pen writing printing. The prepared paper electrode can detect nitrate using electrochemical analysis. The results show that the paper electrodes prepared with the three conductive inks can be used for the analysis of potassium ferricyanide and potassium nitrate. The minimum square resistance of paper electrodes prepared with silver conductive ink is 0.11 Ω/sq. It can be cycled 60 times in electrochemical applications with small standard deviation and high reproducibility and stability. Analysis and detection can also be performed in nitrate concentrations ranging from 60 μM to 1000 μM. This low silver‐containing, green, and low resistivity flexible electrode offers a solution for the simplicity and economy of electronic devices.

Lithium-air battery (LAB) is regarded as one of the most promising energy storage systems. However, the challenges arising from the lithium metal anode have significantly impeded the progress of LAB development. In this study, cellulose-based filter paper (FP) is utilized as a separator for ambient Li-air batteries to suppress dendrite growth and prevent H 2 O crossover. Thermogravimetric analysis and molecular spectrum reveal that FP enables ambient Li-air battery operation due to its surface functional groups derived from cellulose. The oxygen-enriched surface of cellulose not only enhances ion conductivity but also captures water and confines solvent molecules, thereby mitigating anode corrosion and side reactions. Compared with commercial glassfiber (GF) separator, this cellulose-based FP separator is cheaper, renewable, and environmentally friendly. Moreover, it requires less electrolyte while achieving prolonged and stable cycle life under real air environment conditions. This work presents a novel approach to realizing practical Li-air batteries by capturing water on the separator's surface. It also provides insights into the exploration and design of separators for enabling practical Li-air batteries toward their commercialization., (© 2024 Wiley‐VCH GmbH.)

Achieving thermochromic afterglow (TCAG) in a single material for advanced information encryption remains a significant challenge. Herein, TCAG in carbon dots (CDs)-inked paper (CDs@Paper) is achieved by tuning the temperature-dependent dual-mode afterglow of room temperature phosphorescence (RTP) and thermally activated delayed fluorescence (TADF). The CDs are synthesized through thermal treatment of levofloxacin in melting boric acid with postpurification via dialysis. CDs@Paper exhibit both TCAG and excitation-dependent afterglow color properties. The TCAG of CDs@Paper exhibits dynamic color changes from blue at high temperatures to yellow at low temperatures by adjusting the proportion of the temperature-dependent TADF and phosphorescence. Notably, two-photon afterglow in CDs-based afterglow materials and time-dependent two-photon afterglow colors are achieved for the first time. Moreover, leveraging the opposite emission responses of phosphorescence and TADF to temperature, CDs@Paper demonstrate TCAG with temperature-sensing capabilities across a wide temperature range. Furthermore, a CDs@Paper-based 3D code containing color and temperature information is successfully developed for advanced dynamic information encryption., (© 2024 The Author(s). Advanced Materials published by Wiley‐VCH GmbH.)

Capturing short-lived intermediates at the molecular level is key to understanding the mechanism and dynamics of chemical reactions. Here, we have developed a paper-in-tip bipolar electrolytic electrospray mass spectrometry platform, in which a piece of triangular conductive paper incorporated into a plastic pipette tip serves not only as an electrospray emitter but also as a bipolar electrode (BPE), thus triggering both electrospray and electrolysis simultaneously upon application of a high voltage. The bipolar electrolysis induces a pair of redox reactions on both sides of BPE, enabling both electro-oxidation and electro-reduction processes regardless of the positive or negative ion mode, thus facilitating access to complementary structural information for mechanism elucidation. Our method enables real-time monitoring of transient intermediates (such as N,N-dimethylaniline radical cation, dopamine o-quinone (DAQ) and sulfenic acid with half-lives ranging from microseconds to minutes) and transient processes (such as DAQ cyclization with a rate constant of 0.15 s -1 ). This platform also provides key insights into electrocatalytic reactions such as Fe (III)-catalyzed dopamine oxidation to quinone species at physiological pH for neuromelanin formation., (© 2024 Wiley-VCH GmbH.)

Silver nanoparticles (AgNPs) are in situ synthesized for the first time on microfibrillated silk (MFS) exfoliated from domesticated Philosamia cynthia ricini (eri) and Bombyx mori (mulberry) silkworm silk fibers. The process is rapid (hours time), does not rely on harmful chemicals, and produces robust and flexible AgNPs coated MFS (MFS-AgNPs) protein papers with excellent handling properties. None of these can be achieved by approaches used in the past to fabricate AgNPs silk systems. MFS bonds the AgNPs strongly, providing good support and stabilization for the NPs, leading to strong wash fastness. The mechanical properties of the MFS-AgNPs papers largely do not change compared to the MFS papers without nanoparticles, except for some higher concentration of AgNPs in the case of mulberry silk. The improved tensile properties of eri silk papers with or without AgNPs compared to mulberry silk papers can be attributed to the higher degree of fibrillation achieved in eri silk and its inherent higher ductility. MFS-AgNPs from eri silk also exhibit strong antibacterial activity. This study provides the basis for the development of smart protein papers based on silk fiber and functional nanomaterials., (© 2020 Wiley-VCH GmbH.)

Abstract The fabrication of flexible catalytic films with isolated single/dual‐atomic sites and their integration in wearable electronics is challenging. Herein, an efficient method to prepare atomically dispersed binary Ni/Co‐decorated flexible carbon nanofiber (NiCo‐CNF) film using formamide‐derived cyano‐specific NiCo‐NC as nanofillers was developed. The optimized Ni1Co1‐CNF catalytic film, having large‐area, high density of adjacent Ni‐N4 and Co‐N4 active sites, and good mechanical properties under repeated bending and release conditions, possessed high catalytic activity towards oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). The ORR/OER potential difference (ΔE10) for Ni1Co1‐CNF at 10.0 mA cm−2 was highly comparable with the Pt/C+RuO2 mixture. In addition, flexible Ni1Co1‐CNF‐assembled Zn‐air battery displayed very good mechanical robustness and cycling stability. Our work may inspire the fabrication of other atomic metal‐decorated films for membrane electrocatalysis.

Electrochemical aptamer-based (E-AB) sensors offer a powerful and general means for analyte detection in complex samples for various applications. Paper-based E-AB sensors could enable portable, low-cost, and rapid detection of a broad range of targets, but it has proven challenging to fabricate suitable three-electrode systems on paper. Here, we demonstrate a simple, economic, and environmentally friendly strategy for fabricating aptamer-modified paper electrochemical devices (PEDs) via ambient vacuum filtration. The material, shape, size, and thickness of the three-electrode PED system can be fully customized. We developed aptamer-modified PEDs that enable sensitive and specific detection of small molecules in minimally processed biosamples. The sensitivity and stability of the PEDs are comparable to E-AB sensors based on commercial gold electrodes. We believe our strategy can lead to the development of high performance PEDs for the on-site detection of a variety of analytes., (© 2020 Wiley-VCH GmbH.)

Abstract Metal–organic frameworks (MOFs) derived nanostructures receive immense research focus due to its high porosity, conductivity, and structural tailrolability features. In this work, porous Zeolitic Imidazole Framework‐67 (ZIF‐67) to synthesize cobalt phosphide/carbon composite (ZCoPC) that serves as a positive electrode is utilized. Furthermore, porous and conductive office paper derived carbon (OPC) are utilized as a negative electrode to make a hybrid system. The metalloid characteristics, high conductivity, and good porosity of ZCoPC material makes it a high‐performance battery like electrode. ZCoPC electrode achieves maximum specific capacity of 192.6 mAh g−1 at 1 A g−1 using 1 m potassium hydroxide (KOH) electrolyte. Furthermore, surface and diffusion charge participation investigation are also undergone for ZCoPC electrode that helps in determining the actual charge dynamics occurring in the electrode. In addition, a supercapattery device is assembled using ZCoPC as battery electrode and OPC as supercapacitor electrode. The as fabricated OPC//ZCoPC hybrid supercapattery device delivers extraordinary energy density of 31.6 Wh kg−1 with a power density of 700 W kg−1 and also a long cycle life of 92.3% even after 10,000 charge–discharge cycles. Hence, these outcomes demonstrate that the synergy of porous MOF derived metal phosphide and OPC electrodes are beneficial for supercapattery devices.

Detection of biomarkers is essential for diagnosis and prognosis of diseases for healthcare teams to provide timely appropriate treatments. Reliable, inexpensive, and sensitive devices are desirable to serve this purpose. Paper-based analytical devices (PADs) have gained enormous attention during the past decade as point-of-care devices for biomarker detection due to their simplicity, portability, and biocompatibility. Importantly, the devices highly comply with the WHO "ASSURED" concept (i.e. Affordable, Sensitive, Specific, User-friendly, Rapid and Robust, Equipment free, and Deliverable to end-users). Thus, PADs could be sustainably alternative tools for biomarker detection, especially in resources-constraint areas where budget, skillful operators, and health infrastructure are limited. First, this review introduces overviews of biomarkers, their detection and brief history of PADs. Second, description of common fabrication and detection techniques in PADs are provided. Then, it highlights recent state of the art technologies and applications of PADs for various biomarker detection published during 2018 to May 2019. Applications for tumor marker, cardiac and coronary heath disease, and metabolic disorder biomarker detection are tabulated and selected examples are described in details. Finally, it discusses the current challenges, advances, and novel applications of PADs. The review would be valuable for healthcare workers using PADs as cost-effective point-of-care devices for biomarker detection and for researchers working on future developments of the devices., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The erratic, intermittent, and unpredictable nature of sweat production, resulting from physiological or psychological fluctuations, poses intricacies to consistently and accurately sample and evaluate sweat biomarkers. Skin-interfaced microfluidic devices that rely on colorimetric mechanisms for semi-quantitative detection are particularly susceptible to these inaccuracies due to variations in sweat secretion rate or instantaneous volume. This work introduces a skin-interfaced colorimetric bifluidic sweat device with two synchronous channels to quantify sweat rate and biomarkers in real-time, even during uncertain sweat activities. In the proposed bifluidic-distance metric approach, with one channel to measure sweat rate and quantify collected sweat volume, the other channel can provide an accurate analysis of the biomarkers based on the collected sweat volume. The closed channel design also reduces evaporation and resists contamination from the external environment. The feasibility of the device is highlighted in a proof-of-the-concept demonstration to analyze sweat chloride for evaluating hydration status and sweat glucose for assessing glucose levels. The low-cost yet highly accurate device provides opportunities for clinical sweat analysis and disease screening in remote and low-resource settings. The developed device platform can be facilely adapted for the other biomarkers when corresponding colorimetric reagents are exploited., (© 2023 The Authors. Advanced Science published by Wiley-VCH GmbH.)

Personalized healthcare management is an emerging field that requires the development of environment-friendly, integrated, and electrochemical multimodal devices. In this study, the concept of integrated paper-based biosensors (IFP -Multi ) for personalized healthcare management is introduced. By leveraging ink printing technology and a ChatGPT-bioelectronic interface, these biosensors offer ultrahigh areal-specific capacitance (74633 mF cm -2 ), excellent mechanical properties, and multifunctional sensing and humidity power generation capabilities. More importantly, the IFP -Multi devices have the potential to simulate deaf-mute vocalization and can be integrated into wearable sensors to detect muscle contractions and bending motions. Moreover, they also enable monitoring of physiological signals from various body parts, such as the throat, nape, elbow, wrist, and knee, and successfully record sharp and repeatable signals generated by muscle contractions. In addition, the IFP -Multi devices demonstrate self-powered handwriting sensing and moisture power generation for sweat-sensing applications. As a proof-of-concept, a GPT 3.5 model-based fine-tuning and prediction pipeline that utilizes recorded physiological signals through IFP -Multi is showcased, enabling artificial intelligence with multimodal sensing capabilities for personalized healthcare management. This work presents a promising and ecofriendly approach to developing paper-based electrochemical multimodal devices, paving the way for a new era of healthcare advancements., (© 2023 The Authors. Advanced Science published by Wiley-VCH GmbH.)

Weighing paper-assisted magnetic ionic liquid headspace single-drop microextraction using microwave distillation followed by gas chromatography-mass spectrometry was successfully developed to determine the essential oil components in lavender. The magnetic ionic liquid 1-octyl-3-methylimidazolium tetrachloroferrate was successfully synthesized and used as the optimal extraction solvent. An aliquot of 9 μL of magnetic ionic liquid could be stably suspended on the weighing paper for long time extraction. The increase of the extractant volume resulted in a significantly enhanced in extracting efficiency of the weighing paper-assisted magnetic ionic liquid headspace single-drop microextraction than traditional headspace single-drop microextraction method. In this experiment, the optimal conditions were 1-octyl-3-methylimidazolium tetrachloroferrate as the extraction solvent, extraction time of 12 min, microwave power of 600 W, cyclohexane as back-extractant and sample amount of 30 mg. The developed method was successfully applied to analyze 16 lavender samples from three different harvest years. A total of 39 compounds in lavender were identified and the principal component analysis provided a clear separation between those lavender samples harvested in different years. The results indicated that the proposed weighing paper-assisted magnetic ionic liquid headspace single-drop microextraction is a novel, fast, simple and sensitive microextration technique for the determination of the essential oil components in lavender., (© 2020 Wiley-VCH GmbH.)

Abstract Electronic paper devices, also known as electrochromic devices, are known for their ability to change color and remain in a particular color state even after the electric power is turned off. Traditional devices such as electrochromic windows use mechanisms such as electrophoresis or intercalation and use special materials such as anhydrous electrolytes and transparent conductive materials (TCMs). As a result, these devices can sometimes be relatively difficult to assemble, especially in developing countries where such materials are difficult to obtain. Recently, some improvements are made by using alternative electrode positioning that do not require TCM. Here, a novel multicolor display module that is recyclable, can be fabricated from readily available materials, and can be scaled according to the desired screen size is presented. The presented device is a semi‐open electrochemical device that uses pH indicator dyes and an aqueous electrolyte solution in combination with readily available stainless steel sheet.

The ongoing pandemic of coronavirus disease 2019 (COVID‐19) caused by severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has caused millions of deaths worldwide. However, most SARS‐CoV‐2 detection methods depend on time‐consuming sample preparation and large detection instruments. Herein, a method employing nonbleeding pH paper to achieve both RNA extraction and visual isothermal amplification is proposed, enabling rapid, instrument‐free SARS‐CoV‐2 detection. By taking advantage of capillary forces, pH‐paper‐based RNA extraction can be accomplished within 1 min without need for any equipment. Further, the pH paper can mediate dye‐free visual isothermal amplification detection. In less than a 46‐min sample‐to‐answer time, pH‐paper‐based extraction and visual detection (termed pH‐EVD) can consistently detect 1200 genome equivalents per microliter of SARS‐CoV‐2 in saliva, which is comparable to TaqMan probe‐based quantitative reverse transcription PCR (RT‐qPCR). Through coupling with a chemically heated incubator called a smart cup, the instrument‐free, pH‐EVD‐based SARS‐CoV‐2 detection method on 30 nasopharyngeal swab samples and 33 contrived saliva samples is clinically validated. Thus, the pH‐EVD method provides simple, rapid, reliable, low‐cost, and instrument‐free SARS‐CoV‐2 detection and has the potential to streamline onsite COVID‐19 diagnostics.

Bladder cancer is the fourth most common cancer in men, and it is becoming a prevalent malignancy. Most of the regular clinical examinations are prompt evaluations with cystoscopy, renal function testing, which require high-precision instrument, well-trained operators, and high cost. In this study, a microfluidic paper-based analytical device (μPAD) was fabricated to detect nuclear matrix protein 22 (NMP22) and bladder cancer antigen (BTA) from the urine samples. Urine samples were collected from 11 bladder cancer patients and 10 well-beings as experiment and control groups, respectively, to verify the working efficiency of μPAD. A remarkable checkout efficiency of up to 90.91% was found from the results. Meanwhile, this method is feasible for home-based self-detection from urine samples within 10 min for the total process, which provides a new way for quick, economical, and convenient tumor diagnosis, prognosis evaluation, and drug response., (© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Diffusion of colored dye on water saturated paper substrates has been traditionally exploited with great skill by renowned water color artists. The same physics finds more recent practical applications in paper-based diagnostic devices deploying chemicals that react with a bodily fluid yielding colorimetric signals for disease detection. During spontaneous imbibition through the tortuous pathways of a porous electrolyte saturated paper matrix, a dye molecule undergoes diffusion in a complex network of pores. The advancing front forms a strongly correlated interface that propagates diffusively but with an enhanced effective diffusivity. We measure this effective diffusivity and show that it is several orders of magnitude greater than the free solution diffusivity and has a significant dependence on the solution pH and salt concentration in the background electrolyte. We attribute this to electrically mediated interfacial interactions between the ionic species in the liquid dye and spontaneous surface charges developed at porous interfaces, and introduce a simple theory to explain this phenomenon., (© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A complete mathematical model for electromigration in paper-based analytical devices is derived, based on differential equations describing the motion of fluids by pressure sources and EOF, the transport of charged chemical species, and the electric potential distribution. The porous medium created by the cellulose fibers is considered like a network of tortuous capillaries and represented by macroscopic parameters following an effective medium approach. The equations are obtained starting from their open-channel counterparts, applying scaling laws and, where necessary, including additional terms. With this approach, effective parameters are derived, describing diffusion, mobility, and conductivity for porous media. While the foundations of these phenomena can be found in previous reports, here, all the contributions are analyzed systematically and provided in a comprehensive way. Moreover, a novel electrophoretically driven dispersive transport mechanism in porous materials is proposed. Results of the numerical implementation of the mathematical model are compared with experimental data, showing good agreement and supporting the validity of the proposed model. Finally, the model succeeds in simulating a challenging case of free-flow electrophoresis in paper, involving capillary flow and electrophoretic transport developed in a 2D geometry., (© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Microfluidic paper-based analytical devices (μPADs) allow user-friendly and portable chemical determinations, although they provide limited applicability due to insufficient sensitivity. Several approaches have been proposed to address poor sensitivity in μPADs, but they frequently require bulky equipment for power and/or read-outs. Universal serial buses (USB) are an attractive alternative to less portable power sources and are currently available in many common electronic devices. Here, USB-powered μPADs (USB μPADs) are proposed as a fusion of both technologies to improve performance without adding instrumental complexity. Two ITP USB μPADs were developed, both powered by a 5 V potential provided through standard USB ports. The first device was fabricated using the origami approach. Its operation was analyzed experimentally and numerically, yielding a two-order-of-magnitude sample focusing in 15 min. The second ITP USB μPAD is a novel design, which was numerically prototyped with the aim of handling larger sample volumes. The reservoirs were moved away from the ITP channel and capillary action was used to drive the sample and electrolytes to the separation zone, predicting 25-fold sample focusing in 10 min. USB μPADs are expected to be adopted by minimally-trained personnel in sensitive areas like resource-limited settings, the point-of-care and in emergencies., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Exosome quantification is important for estimation of informative messengers (e.g., proteins, lipids, RNA, etc.) involving physiological and pathological effects. This work aimed to develop a simple and rapid distance-based paper portable device using exosome-capture vesicles (polydiacetylene conjugated with antiCD81) for exosome quantification in cell cultures. This novel concept relied on distinct aggregation of exosomes and exosome-capture vesicles leading to different solvent migration. Distances of the migration were used as signal readouts, which could be detected by naked eye. PDA-antiCD81 as exosome-capture vesicles were optimized (e.g., size, reaction ratio, and concentration) and the paper designs were investigated (e.g., diameter of sample reservoir and lamination layer) to enhance the solvent stop-flow effects. Finally, exosome screening on three cell culture samples (COLO1, MDA-MB-231, and HuR-KO1 subclone) was demonstrated. The method could linearly measure exosome concentrations in correlation with solvent migration distances in the range of 10 6 -10 10 particles/mL (R 2  > 0.98) from the cell culture samples. The exosome concentration measurements by the developed device were independently assessed by nanoparticle tracking analysis. Results demonstrated no statistically significant difference (p > 0.05) by t-test. This low-cost and rapid device allows a portable platform for exosome quantification without the requirement of expensive equipment and expertise of operation. The developed device could potentially be useful for quantification of other biomarker-related extracellular vesicles., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)