Chemosensors

The functionalization of biosensor interfaces constitutes a crucial aspect of biosensing systems, as it directly governs key characteristics, including sensitivity, selectivity, accuracy, and rapidity. Among the diverse range of functionalization strategies available for biosensor interfaces, the click reaction has emerged as an exceptionally straightforward and stable approach for modifying electrodes and sensing films. Notably, the electro-click reaction enables the reagent-free functionalization of the biosensing interface, offering significant advantages, such as high speed, selectivity, and minimal pollution. Consequently, this strategy has garnered substantial attention and is widely regarded as a promising avenue for enhancing biosensor interface functionalization. Within this comprehensive review, we commence by presenting the latest advancements in functionalized biosensor interfaces, organizing the regulatory strategies into distinct categories based on the mediators employed, ranging from nanomaterials to biomolecules. Subsequently, we provide a comprehensive summary with an emphasis on recently developed electro-click strategies for functionalizing electrochemical and optical biosensor interfaces, covering both principles and applications. It is our anticipation that gaining a profound understanding of the principles and applications underlying electro-click strategies for biosensor interface functionalization will facilitate the design of highly selective and sensitive biosensor systems for diverse domains, such as clinical, pharmaceutical, environmental, and food analyses. Full article

Quantum tunneling electrical probes, consisting of a pair of nanoelectrodes with a gap width of less than 5 nm, can be used as a robust electrical sensing platform for the detection of various nanoscale objects. To achieve this, stable and gap-width-controllable electrodes are essential. Although various methods, including lithography and electrochemical strategies, have been proposed for the fabrication of tunneling electrodes, the ability to precisely control the gap width and ensure reproducibility is still lacking. Here, we report a feedback-controlled electrochemical etching approach to fabricate the tunneling electrodes with a controlled nanogap. The connected nanoelectrodes, derived from a dual-barrel nanopipette, were subjected to a controlled electrochemical etching process from a short-circuited state to a tunneling gap. The resulting tunneling electrodes exhibited solvent-response current–voltage electrical behavior, which was well fitted with the Simons model, indicating the formation of tunneling electrodes. Overall, a success rate of more than 60% could be achieved to obtain the tunneling gaps. Furthermore, to verify the function of tunneling electrodes, we used the etched-tunneling electrodes for free-diffusing protein detection, showing the potential of etched-tunneling electrodes as single-molecule sensors. Full article

At present, the majority of water testing is carried out in the laboratory, and portable field methods for the quantification of elements in natural waters remain to be established. In contrast, portable instruments like portable X-ray fluorescence (pXRF) analysis and portable laser-induced breakdown spectroscopy (pLIBS) have become routine analytical methods for the quantification of elements in solids. This study aims to show that pLIBS can also be used for chemical compositional measurements of natural waters. Bottled mineral waters were selected as sample materials. A surface-enhanced liquid-to-solid conversion technique was used to improve the detection limits and circumvent the physical limitations in liquid analysis. The results show that low to medium mineralised waters can be analysed quantitatively for their ions using the documented method. For more highly concentrated samples, typically above an electrical conductivity (EC) of 1000 µS/cm, further adjustment is required in the form of self-absorption correction. However, water with a conductivity up to this limit can be analysed for the main cations (Li⁺, Na⁺, Mg²⁺, K⁺, Ca²⁺, and Sr²⁺) as well as the main anions (SO₄²⁻ and Cl⁻) using the documented method. This study demonstrates that there is significant potential for developing field-based pLIBS as a tool for quantitative water analysis. Full article

Electrochemical sensors have the advantages of being sensitive, stable, selective, simple, fast, and cost-efficient, and they have attracted much attention in food analysis. Electrode modification materials are very important for the performance of electrochemical sensors. This review summarizes the type of electrode modification material (metal nanoparticles/metal oxides, conductive polymers, carbon materials, and the metal-organic framework and its composite materials) and the application progress of electrochemical sensors in food analysis, mainly including the detection of food additives, pesticide residues, veterinary drugs residue, heavy metals, and mycotoxins in food in the recent ten years. Moreover, the application of electrochemical sensors is prospected. Full article

Two-dimensional (2D) inorganic compounds, MXenes, are the most promising candidate for chemical sensors and environmental remediation. Since the first synthesis of Ti₃C₂T_x MXene from the Ti₃AlC₂ MAX phase in 2011, 2D materials have been attracting significant attention from a wide range of scientific communities because of their unique physicochemical properties. The attractive properties of MXenes motivated us to explore the new wave of front-end research and applications. Over the past 12 years, there have been more than 10,000 theoretical and experimental studies on MXenes. All these publications have primarily focused on Ti₃C₂T_x MXene because of its fascinating material properties and tunability towards target applications. To provide readers with a fundamental understanding of this emerging 2D material, this review discusses the recent trends in the design of Ti₃C₂T_x MXene for gas sensors and energy harvesting applications. For the most updated information, this review focuses on important findings and applications reported in the last decade. Full article

High-performance microelectromechanical system (MEMS) oxygen sensors were realized by successful preparation of Au nanofilms over TiO₂ thin films through successive sputtering on commercial MEMS microhotplates. Oxygen sensing performance of 3 and 6 nm thick Au over TiO₂ thin films were compared with that of pure TiO₂ thin films. It was shown that 6 nm thick Au over TiO₂ thin films have the best sensitivity toward oxygen. The prepared TiO₂ thin films were characterized using SEM, EDS, XPS, and a gas testing instrument. The results show that Au decoration has little influence on the surface morphologies of TiO₂ thin films. However, Au decoration has a strong influence on the surface properties of the composite films. The favorable performance of 6 nm Au-doped TiO₂ thin films is attributed to factors such as catalytical performance, height of Schottky contact, and number of oxygen vacancies. This work makes contributions to low power consumption and high-performance oxygen sensors for Internet of Things applications. Full article

Salmonella is one of the leading causes of foodborne illnesses worldwide, with poultry products being a major source of contamination. Thus, the detection of salmonella in commercial poultry products is crucial to minimize the effects on public health. Electrochemical sensors are promising tools for bacteria detection due to their sensitivity, simplicity, and potential for on-site analysis. In this work, a three-dimensional (3D) printed electrochemical immunosensor for the determination of Salmonella typhimurium in fresh chicken through a sandwich immunoassay employing biotinylated anti-S. typhimurium antibody followed by streptavidin labeled with Cd/Se ZnS quantum dots (QDs) is presented. The device features three carbon-black polylactic acid electrodes and a holder, and the quantification of S. typhimurium is performed by anodic stripping voltametric (ASV) determination of the Cd(II) released after acidic dissolution of the QDs. To enhance sensitivity, an electroplated bismuth film was deposited on the working electrode, achieving a detection limit of 5 cfu/mL in a total assay time of 25 min, whereas 5 h of sample pre-enrichment was required for the detection of 1 cfu/25 mL of chicken rinse and chicken broth. The method is accurate, with %recovery values ranging from 93.3 to 113% in fresh chicken samples, and repeatable with intra- and inter- assay coefficient of variations <2 and 5%, respectively, indicating the suitability of the proposed immunosensor for the detection of S. typhimurium at the point-of-need. Full article

Novel photoluminescent carbon dots (CDs) were synthesized through a facile hydrothermal method using Hibiscus tea extract as a natural carbon source and boric acid as a boron source. The optical and physicochemical properties of the as-synthesized nitrogen- and boron-doped CDs (NB-CDs) were characterized using UV–Visible (UV–Vis), photoluminescence (PL) spectroscopy, Fourier-transform infrared (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). The as-synthesized NB-CDs showed spherical morphology of approximately 6.2 ± 0.5 nm with quantum yield (9.2%), high aqueous solubility, strong photo-stability, and excitation-dependent PL behavior. The obtained NB-CDs exhibited high stability over a wide pH range and high ionic strength. Additionally, NB-CDs exhibited PL enhancement response with excellent sensitivity toward multi-metal ions, including Ag⁺, Cd²⁺, and Cr³⁺ ions, with very low detection limits of 44.5, 164.4, and 54.6 nM, respectively, with a wide concentration range of 0–10 μM. Upon testing the cytotoxicity of the NB-CDs at a concentration of 20 μg/mL for 24 h, we found no obvious inhibition of cell viability. Therefore, the proposed sensor method can be successfully applied to detect Ag⁺, Cd²⁺, and Cr³⁺ ions in cell imaging as well as in real water environmental samples. Full article

With the unprecedented development of green and renewable energy sources, the proportion of clean hydrogen (H₂) applications grows rapidly. Since H₂ has physicochemical properties of being highly permeable and combustible, high-performance H₂ sensors to detect and monitor hydrogen concentration are essential. This review discusses a variety of fiber-optic-based H₂ sensor technologies since the year 1984, including: interferometer technology, fiber grating technology, surface plasma resonance (SPR) technology, micro lens technology, evanescent field technology, integrated optical waveguide technology, direct transmission/reflection detection technology, etc. These technologies have been evolving from simply pursuing high sensitivity and low detection limits (LDL) to focusing on multiple performance parameters to match various application demands, such as: high temperature resistance, fast response speed, fast recovery speed, large concentration range, low cross sensitivity, excellent long-term stability, etc. On the basis of palladium (Pd)-sensitive material, alloy metals, catalysts, or nanoparticles are proposed to improve the performance of fiber-optic-based H₂ sensors, including gold (Au), silver (Ag), platinum (Pt), zinc oxide (ZnO), titanium oxide (TiO₂), tungsten oxide (WO₃), Mg₇₀Ti₃₀, polydimethylsiloxane (PDMS), graphene oxide (GO), etc. Various microstructure processes of the side and end of optical fiber H₂ sensors are also discussed in this review. Full article

Analytical chemistry relies on the qualitative and quantitative analysis of multivariate data obtained from various measurement techniques. However, artifacts such as missing data, noise, multiplicative and additive effects, and peak shifts can adversely affect the accuracy of chemical measurements. To ensure the validity and accuracy of results, it is crucial to preprocess the data and correct for these artifacts. This paper proposes a fusion recalibration algorithm, called Spectral Offset Recalibration (SOR), that combines the Extended Multiplicative Signal Correction (EMSC) and Correlation-Optimized Warping (COW) algorithms to address both multiplicative and additive effects and peak shifts. The algorithm incorporates prior spectroscopic knowledge to down-weight or disregard spectral regions with strong absorption or significant distortion caused by peak alignment algorithms. Experimental validation on wood NIR datasets and simulated datasets demonstrates the effectiveness of the proposed method. The fusion recalibration approach offers a comprehensive solution for accurate analyses and predictions in analytical chemistry by mitigating the impact of artifacts. Full article

A new green-validated and highly sensitive electrochemical method for the determination of molnupiravir (MOV) has been developed using cyclic voltammetry. The proposed analytical platform involves the use of a disposable laboratory-made screen-printed reduced graphene oxide 2.5% modified electrode (rGO-SPCE 2.5%) for the first time to measure MOV with high specificity. The surface morphology of the sensor was investigated by using a scanning electron microscope armed with an energy-dispersive X-ray probe. The fabricated sensor attained improved sensitivity when sodium dodecyl sulfate (SDS) surfactant (3 µM) was added to the supporting electrolyte solution of 0.04 M Britton–Robinson buffer at pH 2. The electrochemical activity of rGO-SPCE was examined in comparison with two different working electrodes in order to demonstrate that it was the most competitive sensor for MOV monitoring. The method was validated using differential pulse voltammetry according to ICH guidelines, resulting in good precision, accuracy, specificity, and robustness over a concentration range of 0.152–18.272 µM, with a detection limit of 0.048 µM. The stability investigation demonstrated that rGO-SPCE 2.5% can provide high-stability behavior towards the analyte throughout a six-week period under refrigeration. The fabricated rGO-SPCE 2.5% was successfully employed for the measurement of MOV in pharmaceutical capsules and human biofluids without the interference of endogenous matrix components as well as the commonly used excipient. Full article

Sweat, as a biofluid that is easy to extract and contains a variety of biomarkers, can provide various types of physiological information for health monitoring. In recent years, research on wearable sensors for sweat sensing has been emerging continuously. Wearable sweat sensing will probably become an alternative method to traditional chemical analysis. This is due to its advantages of portability, non-invasiveness, comfort, and continuous monitoring. Since the inception of this research field, wearable sweat sensors have achieved significant development in terms of materials, structures, systems, and application directions. Research interests are gradually evolving from single biomarker detection to the pursuit of multi-channel, multi-modal system-level architecture. The analysis of physiological signals has also developed from single signal characterization to omics analysis using multiple physiological information sources. Based on the changes mentioned above, this paper mainly introduces the latest researches of wearable sweat sensors from the aspects of strategy, architecture, material, system, data processing, etc., and tries to summarize the trends of sweat sensors. Finally, this paper analyzes the challenges faced by the sensing platform and possible methods for optimization. Full article

This paper is a comprehensive review of the techniques for the detection of pancreatic enzymes, which are common biochemical indicators of pancreatitis, including amylase, trypsin, chymotrypsin, elastase, and lipase. Pancreatitis is a disease with self-digestion due to the abnormal activation of digestive enzymes in the pancreas. Hospitalization is often required due to the lack of convenient therapeutic agents. The main recent results are reported in this review, especially the techniques that enable portability and Point-of-Care testing (POCT). This is because timely diagnosis at the early stage and avoiding recurrence after recovery are the keys to treatment. It is also important to reduce the rate of misdiagnosis and to avoid overtreatment. Various detection methods are discussed, with particular attention given to the implementation of chemical sensing and probe design. The new sensing technology for digestive enzymes makes it possible to perform early screening for pancreatitis in remote areas or in one’s own home. Full article

Traditionally, analytical chemistry and diagnosis relied on wet laboratories and skilled professionals utilizing sophisticated instruments for sample handling and analysis. However, with the development of novel materials and sensing techniques, there has been a significant shift towards the use of standalone sensors, allowing tests to be conducted on-site or even in real time, leading to cost- and time-efficiency. With their widespread adoption globally, smartphones have emerged as an ideal platform for such sensors, boasting extensive sensor capabilities, advanced processing power, and communication functionalities. Smartphone-based assays make use of optical and electrochemical sensors, utilizing built-in cameras, ambient light sensors, and other features for optical sensing, while the micro-USB port, Bluetooth, and wireless connection facilitate data transmission and analog voltage application for electrochemical sensing. Previous overview papers have explored smartphone-based sensing in specific domains; this review provides a comprehensive examination of recent advancements in smartphone-based sensors, encompassing both optical and electrochemical sensing methods. The review provides the fundamental principles of these sensors and their implementation using smartphones, showcases recent applications, and presents innovative designs that take advantage of the inherent functionalities and sensor capabilities of smartphones. The review concludes by offering an outlook on the prospects of smartphone-based sensing and includes a reflective section emphasizing the potential impact of sensors in chemical and biological analyses. This comprehensive resource aims to provide information to researchers and practitioners interested in using smartphones for cutting-edge analytical methodologies. Full article

Electrochemical detection, with its advantages of being rapid, multi-time point, compatible with cost-effective fabrication methods, and having the potential for miniaturization and portability, has great promise for point-of-care drug monitoring. However, a continuing challenge concerns the robust and sensitive electrochemical detection of pharmaceutical analytes from biological fluids. These complex matrices, such as saliva, sweat, interstitial fluid, urine, and blood/serum, contain multiple components that can contribute to an increased background or reduced analyte signal. In this mini-review, we discuss progress on electrochemical sensing in complex biofluids. We first introduce the challenge of drug titration in the management of various health conditions and provide an overview of the motivation for improved therapeutic drug monitoring, including current limitations. We then review progress on pharmaceutical drug detection from these biofluids with a focus on sample preprocessing, electrode modification for signal amplification, and/or electrode passivation to minimize fouling. Finally, we highlight promising strategies that have enabled robust drug quantification for clinical relevance and that may be useful for field-use systems. Full article

The integration of sensing devices into cell culture systems is a topic of great interest in the study of pathologies and complex biological mechanisms in real-time. In particular, the fit-for-purpose microfluidic devices called organ-on-chip (OoC), which host living engineered organs that mimic in vivo conditions, benefit greatly from the integration of sensors, enabling the monitoring of specific chemical-physical parameters that can be correlated with biological processes. In this context, copper is an essential trace element whose total concentration may be associated with specific pathologies, and it is therefore important to develop reliable analytical techniques in cell systems. Copper can be determined by using the anodic stripping voltammetry (ASV) technique, but its applicability in cell culture media presents several challenges. Therefore, in this work, the performance of ASV in cell culture media was evaluated, and an acidification protocol was tested to improve the voltammetric signal intensity. A Transwell^® culture model with Caco-2 cells was used to test the applicability of the developed acidification protocol by performing an off-line measurement. Finally, a microfluidic device was designed in order to perform the acidification of the cell culture medium in an automated manner and then integrated with a silicon microelectrode to perform in situ measurements. The resulting sensor-integrated microfluidic chip could be used to monitor the concentration of copper or other ions concentration in an organ-on-chip model; these functionalities represent a great opportunity for the non-destructive strategic experiments required on biological systems under conditions close to those in vivo. Full article

Molecularly imprinted polymers (MIPs) and aptamers (Apts) are widely used in substance detection due to their specific recognition abilities. However, both of them have limitations in terms of stability or sensitivity. Therefore, an increasingly employed strategy is to combine MIPs and aptamers to form mixed components for detecting various substances, such as viruses, bacteria, proteins, heavy-metal ions, and hormones. The aim of this review is to provide a comprehensive summary of the scientific research conducted on the construction and application of aptamer–MIP multiple-recognition components in the past five years. It also aims to analyze their research and development strategies, construction mechanisms, advantages, and potential applications, as well as limitations and current challenges that need to be addressed. Full article

Elaboration of biosensors on the base of organic transistors with embedded biomolecules which can operate in an aqueous environment is of paramount importance. Electrolyte-gated organic field-effect transistors demonstrate high sensitivity in detection of various analytes. In this paper, we demonstrated the possibility of quantitative fast specific determination of virus particles by an aptasensor based on EGOFET. The sensitivity and selectivity of the devices were examined with the influenza A virus as well as with control bioliquids like influenza B, Newcastle disease viruses or allantoic fluid with different dilutions. The influence of the semiconducting layer thickness on EGOFETs sensory properties is discussed. The fabrication of a multi-flow cell that simultaneously registers the responses from several devices on the same substrate and the creation of a multi-sensor flow device are reported. The responses of the elaborated bioelectronic platform to the influenza A virus obtained with application of the portable multi-flow mode are well correlated with the responses obtained in the laboratory stationary mode. Full article

In this paper, a method is described to perform ion concentration measurements on both sides of an inserted contact lens, without physical contact with the eye or the contact lens. The outer surface of an eye is covered with a tear film that has multiple layers. The central aqueous layer contains electrolytes and proteins. When a contact lens is inserted, it becomes localized in the central layer, which creates two layers known as the pre-lens tear film (PLTF) and the post-lens tear film (PoLTF). The PoLTF is in direct contact with the sensitive corneal epithelial cells which control electrolyte concentrations in tears. It is difficult to measure the overall electrolyte concentration in tears because of the small 7 μL volume of bulk tears. No methods are known, and no method has been proposed, to selectively measure the concentrations of electrolytes in the smaller volumes of the PLTF and the PoLTF. In this paper, we demonstrate the ability to localize fluorophores on each side of a contact lens without probe mixing or diffusion across the lens. We measured the concentration of sodium in the region of the PoLTF using a sodium-sensitive fluorophore positioned on the inner surface of a contact lens. The fluorescence measurements do not require physical contact and are mostly independent of eye motion and fluorophore concentration. The method is generic and can be combined with ion-sensitive fluorophores for the other electrolytes in tears. Instrumentation for non-contact measurements is likely to be inexpensive with modern opto-electronic devices. We expect these lenses to be used for measurements of other ions in the PLTF and the PoLTF, and thus become useful for both research and in the diagnosis of infections, keratitis and biomarkers for diseases. Full article