Sensor Chip Research Articles

Molecularly imprinted fluorescence sensor chip for lactate measurement

Lactate measurements provide an opportunity to conveniently evaluate bodily functions and sports performance. A molecularly imprinted fluorescence biochip provides an innovative way to achieve lactate measurement and overcomes the limitations of enzyme-based sensors. To realize this goal, ZnO quantum dots (QDs), a biocompatible sensing material, were combined with selective receptors comprised of molecularly imprinted polymers (MIPs). The lactate-selective imprinted polymers were formed using 3-aminopropyltriethoxysilane (APTES) and 5-indolyl boronic acid monomers. Furthermore, a new solid-phase sensing platform that overcomes the limitations of liquid-based sensors was developed to detect lactate in real-time. The platform consists of the biosensor chip with a thin-film sensing layer, an ultraviolet (UV) excitation source, and a portable light detector. The final sensor has a sensitivity of 0.0217 mmol L-1 for 0–30 mmol L-1 of lactate in phosphate-buffered saline (PBS) with a correlation coefficient of 0.97. The high sensor sensitivity and selectivity demonstrates the applicability of the ZnO QDs and synthetic receptors for sweat analysis.

Quantitative Investigation of Layer-by-Layer Deposition and Dissolution Kinetics by New Label-Free Analytics Based on Low-Q-Whispering Gallery Modes

A new instrument for label-free measurements based on optical Low-Q Whispering Gallery Modes (WGMs) for various applications is used for a detailed study of the deposition and release of Layer-by-Layer polymer coatings. The two selected coating pairs interact either via hydrogen bonding or electrostatic interactions. Their assembly was followed by common Quartz Crystal Microbalance (QCM) technology and the Low-Q WGMs. In contrast to planar QCM sensor chips of 1 cm, the WGM sensors are fluorescent spherical beads with diameters of 10.2 µm, enabling the detection of analyte quantities in the femtogram range in tiny volumes. The beads, with a very smooth surface and high refractive index, act as resonators for circular light waves that can revolve up to 10,000 times within the bead. The WGM frequencies are highly sensitive to changes in particle diameter and the refractive index of the surrounding medium. Hence, the adsorption of molecules shifts the resonance frequency, which is detected by a robust instrument with a high-resolution spectrometer. The results demonstrate the high potential of the new photonic measurement and its advantages over QCM technology, such as cheap sensors (billions in one Eppendorf tube), simple pre-functionalization, much higher statistic safety by hundreds of sensors for one measurement, 5–10 times faster analysis, and that approx. 25, 000 fewer analyte molecules are needed for one sensor. In addition, the deposited molecule amount is not superposed by hydrated water as for QCM. A connection between sensors and instruments does not exist, enabling application in any transparent environment, like microfluidics, drop-on slides, Petri dishes, well plates, cell culture vasculature, etc.

Simultaneous and Rapid Detection of Glucose and Insulin: Coupling Enzymatic and Aptamer-Based Assays.

Diabetes management demands precise monitoring of key biomarkers, particularly insulin (I) and glucose (G). Herein, we present a bioelectronic chip device that enables the simultaneous detection of I and G in biofluids within 2 min. This dual biosensor chip integrates aptamer-based insulin sensing with enzymatic glucose detection on a single platform, employing a four-electrode sensor chip. The insulin voltammetric sensor employs a G-quadraplex methylene-blue-modified aptamer, while the amperometric biocatalytic glucose sensor utilizes a second-generation mediator-based approach. Simultaneous reagent-less sensing of I and G has been achieved by addressing key challenges. These include combining different surface chemistries, assay formats, and detection principles at closely spaced working electrodes and the substantially different concentration levels of the I and G targets. An attractive analytical performance, with no apparent crosstalk, is demonstrated for the simultaneous detection of millimolar G concentrations and picomolar I concentrations in single microliter serum or saliva sample droplets. This dual biosensor offers rapid, cost-effective, and reliable monitoring, addressing the unmet need for integrated multiplexed diabetes biomarker detection in decentralized settings. Such integration of enzymatic and aptamer-based bioassays could greatly expand the scope of decentralized testing in healthcare beyond diabetes care.

A label-free optical biosensor-based point-of-care test for the rapid detection of Monkeypox virus

Diagnostic approaches that combine the high sensitivity and specificity of laboratory-based digital detection with the ease of use and affordability of point-of-care (POC) technologies could revolutionize disease diagnostics. This is especially true in infectious disease diagnostics, where rapid and accurate pathogen detection is critical to curbing the spread of disease. We have pioneered an innovative label-free digital detection platform that utilizes Interferometric Reflectance Imaging Sensor (IRIS) technology. IRIS leverages light interference from an optically transparent thin film, eliminating the need for complex optical resonances to enhance the signal by harnessing light interference and the power of signal averaging in shot-noise-limited operation In our latest work, we have further improved our previous 'Single-Particle' IRIS (SP-IRIS) technology by allowing the construction of the optical signature of target nanoparticles (whole virus) from a single image. This new platform, 'Pixel-Diversity' IRIS (PD-IRIS), eliminated the need for z-scan acquisition, required in SP-IRIS, a time-consuming and expensive process, and made our technology more applicable to POC settings. Using PD-IRIS, we quantitatively detected the Monkeypox virus (MPXV), the etiological agent for Monkeypox (Mpox) infection. MPXV was captured by anti-A29 monoclonal antibody (mAb 69-126-3) on Protein G spots on the sensor chips and were detected at a limit-of-detection (LOD) - of 200 PFU/mL (∼3.3 aM). PD-IRIS was superior to the laboratory-based ELISA (LOD - 1800 PFU/mL) used as a comparator. The specificity of PD-IRIS in MPXV detection was demonstrated using Herpes simplex virus, type 1 (HSV-1), and Cowpox virus (CPXV). This work establishes the effectiveness of PD-IRIS and opens possibilities for its advancement in clinical diagnostics of Mpox at POC. Moreover, PD-IRIS is a modular technology that can be adapted for the multiplex detection of pathogens for which high-affinity ligands are available that can bind their surface antigens to capture them on the sensor surface.

Smartphone-based colorimetric paper chip sensor using single-atom nanozyme for the detection of carbofuran pesticide residues in vegetables

Carbofuran (CBF), which exhibit high toxicity, persistent residues, ease of accumulation, and resistance to degradation, pose serious threats to human health and harm the ecological environment. Therefore, there is an urgent need to develop a rapid and accurate method for detecting CBF. In this work, a low-cost, portable, and easy-to-use paper chip biosensor was developed, integrating smartphones for the detection of CBF pesticide residues. This biosensor facilitates rapid on-site testing, meeting the needs for immediate analysis. CBF has the ability to inhibit acetylcholinesterase (AChE) activity. In the presence of AChE, acetylthiocholine (ATCh) is hydrolyzed to produce thiocholine (TCh). TCh, in turn, can inhibit the catalytic activity of Ni-N-C single-atom nanozymes (SAzyme) synthesized using Ni(OH)2 nanochip as a metal precursor, which possess high peroxidase activity. Consequently, the concentration of CBF can be determined by observing the resultant color changes. The results showed that this sensor had a good linear response in the range of CBF concentration from 10 to 500 ng/mL, and the LOD was as low as 8.79 ng/mL. In testing three actual samples—Chinese cabbage, cabbage, and lettuce—the recoveries ranged from 81.09% to 125.27%. This demonstrated that the proposed smartphone-based colorimetric paper chip sensor, utilizing Ni-N-C SAzyme, offers an immediate, convenient, and rapid new strategy for detecting CBF.

Electroactivated SERS Nanoplatform for Rapid and Sensitive Detection and Identification of Tumor-Derived Exosome miRNA.

Exosomal miRNA expression derived from tumor cells provides a valuable and promising noninvasive modality for the early diagnosis and assessment of the efficacy of cancer treatment. However, accurate detection and identification of miRNA within exosomes have been challenging due to its low abundance and the complexity and tedious extraction with large sample volumes in the separation process. Here, we developed an electrically activated nanoplatform for rapid and sensitive detection and identification of exosome miRNA, through triggering miRNA release by opening exosomes that were captured on the electrode surface using a slightly applied electric field (50 mV), and simultaneously detected them with surface-enhanced Raman spectroscopy (SERS) in situ. The method possessed superior specificity and sensitivity for exosomal miRNA detection, with a low detection concentration of 0.5 nM. The SERS sensor chips also showed a superior sensing performance of exosomal miRNA in complex body fluids such as urine and blood. We found that exosomal miRNA contents derived from tumor cells were significantly higher than those in normal cells, and importantly, the concentrations of exosomes secreted from three different cell lines were distinctly augmented after mild electrical stimulation (ES) treatment. Furthermore, the miRNA expression within exosomes was upregulated after the ES treatment of cells. The developed approach and SERS detection platform for exosomal miRNA are promising for noninvasive and precise screening, classification, and monitoring of cancer.

A broadband hyperspectral image sensor with high spatio-temporal resolution

Hyperspectral imaging provides high-dimensional spatial–temporal–spectral information showing intrinsic matter characteristics1–5. Here we report an on-chip computational hyperspectral imaging framework with high spatial and temporal resolution. By integrating different broadband modulation materials on the image sensor chip, the target spectral information is non-uniformly and intrinsically coupled to each pixel with high light throughput. Using intelligent reconstruction algorithms, multi-channel images can be recovered from each frame, realizing real-time hyperspectral imaging. Following this framework, we fabricated a broadband visible–near-infrared (400–1,700 nm) hyperspectral image sensor using photolithography, with an average light throughput of 74.8% and 96 wavelength channels. The demonstrated resolution is 1,024 × 1,024 pixels at 124 fps. We demonstrated its wide applications, including chlorophyll and sugar quantification for intelligent agriculture, blood oxygen and water quality monitoring for human health, textile classification and apple bruise detection for industrial automation, and remote lunar detection for astronomy. The integrated hyperspectral image sensor weighs only tens of grams and can be assembled on various resource-limited platforms or equipped with off-the-shelf optical systems. The technique transforms the challenge of high-dimensional imaging from a high-cost manufacturing and cumbersome system to one that is solvable through on-chip compression and agile computation.

Stannous Chloride-Modified Glass Substrates for Biomolecule Immobilization: Development of Label-Free Interferometric Sensor Chips for Highly Sensitive Detection of Aflatoxin B1 in Corn.

This study presents the development of stannous chloride (SnCl2)-modified glass substrates for biomolecule immobilization and their application in fabricating sensor chips for label-free interferometric biosensors. The glass modification process was optimized, identifying a 5% SnCl2 concentration, a 45 min reaction time, and a 150 °C drying temperature as conditions for efficient protein immobilization. Based on the SnCl2-modified glass substrates and label-free spectral-phase interferometry, a biosensor was developed for the detection of aflatoxin B1 (AFB1)-a highly toxic and carcinogenic contaminant in agricultural products. The biosensor realizes a competitive immunoassay of a remarkable detection limit as low as 26 pg/mL of AFB1, and a five-order dynamic range. The biosensor performance was validated using real corn flour samples contaminated with Aspergillus flavus. The proposed approach not only provides a powerful tool for AFB1 detection for food safety monitoring but also demonstrates the potential of SnCl2-modified substrates as a versatile platform for the development of next-generation biosensors.

First test beam of the DMAPS-based proton tracker at the pMBRT facility at the Curie Institute

Objective.Proton radiotherapy's efficacy relies on an accurate relative stopping power (RSP) map of the patient to optimise the treatment plan and minimize uncertainties. Currently, a conversion of a Hounsfield Units map obtained by a common x-ray computed tomography (CT) is used to compute the RSP. This conversion is one of the main limiting factors for proton radiotherapy. To bypass this conversion a direct RSP map could be obtained by performing a proton CT (pCT). The focal point of this article is to present a proof of concept of the potential of fast pixel technologies for proton tracking at clinical facilities.Approach.A two-layer tracker based on the TJ-Monopix1, a depleted monolithic active pixel sensor (DMAPS) chip initially designed for the ATLAS, was tested at the proton minibeam radiotherapy beamline at the Curie Institute. The chips were subjected to 100 MeV protons passing through the single slit collimator (0.4×20mm2) with fluxes up to1.3×107p s-1 cm-2. The performance of the proton tracker was evaluated with GEANT4 simulations.Main results.The beam profile and dispersion in air were characterized by an opening of 0.031 mm cm-1, and aσx=0.172mm at the position of the slit. The results of the proton tracking show how the TJ-Monopix1 chip can effectively track protons in a clinical environment, achieving a tracking purity close to 70%, and a position resolution below 0.5 mm; confirming the chip's ability to handle high proton fluxes with a competitive performance.Significance.This work suggests that DMAPS technologies can be a cost-effective alternative for proton imaging. Additionally, the study identifies areas where further optimization of chip design is required to fully leverage these technologies for clinical ion imaging applications.

A visual electrochemiluminescence sensor based on the combination of distance-readout strategy and nanozymes catalyzing precipitation

BackgroundNanozyme is a kind of biomimetic enzyme with unique properties and catalytic function of nanomaterials. Various nanozymes have been applied in the development of visual biosensors because of its excellent stability and availability. Nevertheless, the current applications of nanozymes primarily focus on colorimetric sensing based on color changes, which is susceptible to external factors interference including sample solution color and ambient light. Incorporating a distance-readout strategy with nanozymes presents a promising avenue for the advancement of innovative visual biosensing technologies in the future. ResultsA visual electrochemiluminescence (ECL) sensor was developed by combining the distance-readout strategy with nanozymes catalyzing precipitation for the first time. The detection is based on the ECL length change induced by nanozymes. This sensor chip comprises a square detection area and a visual ECL channel area. A peroxidase-mimic, core-shell hollow Fe3O4@PDA@ZIF-67, was modified in the detection region. The substrate 4-chloro-1-naphthol was rapidly catalyzed by nanozymes to form purple precipitate benzo-4-chlorohexanedione, leading to an increase in impedance within the detection region. Consequently, the detection area's partial voltage rose while the visual channel's dropped, resulting in a shorter ECL length. As a proof-of-concept experiment, the visual distance-readout ECL sensor was utilized for the quantitative detection of H2O2. The alteration in ECL length exhibited a good linear relationship with H2O2 concentration (logarithm) within the range of 300 nM to 300 μM, with the limit of detection (LOD) of 87 nM. SignificanceThis work developed a novel approach for the application of nanozymes in analytical chemistry. Compared with common colorimetric sensing, this method is more convenient and intuitive, which can effectively eliminate potential interference from humans and the environment during signal acquisition. Because biocatalytic precipitation can be formed through multiple sensing processes, this strategy holds great promise as a portable and cost-effective tool with diverse applications.

A Lab Prototype for Rapid Electrochemical Detection of Escherichia coli in Water Using Modified Screen-Printed Electrodes.

Recognizing the need for a hand-held device capable of quantitatively measuring the concentration of bacteria in water, this paper describes a label-free method for rapid detection of Escherichia coli (E. coli) in water via H2O2 decomposition using screen-printed electrodes (SPE) modified with nanostructured metal oxide layers. The study encompasses sensor preparation, bacteria culture, synthesis and characterization of nanostructures, and development of a readout circuitry for lab prototyping. During sensing measurements, the bacteria are first made to interact with H2O2 and subsequently, the H2O2 solution is exposed on the sensing surface. The electrochemical sensors are fabricated by modifying the working electrode of SPE with nanostructured metal oxide layers of MnO2 and TiO2 as these play a crucial role in the detection of E. coli in water. The sensing experiments of MnO2-modified SPE show a significant response to bacteria with a sensitivity of 0.82 mV.mL/log CFU and a limit of detection (LOD) of 1.8 CFU/mL, while the TiO2-modified SPE exhibits a linear response over a wide range of bacterial concentrations with a sensitivity of 1.12 mV·mL/log CFU and a limit of detection of 2.23 CFU/mL. Both sensors demonstrate a rapid response, stability, repeatability, and a recovery time of 70 ms. Additionally, selectivity with respect to other bacteria, wastewater components such as glucose, ammonium sulfate, and sodium carbonate, and testing with RO, DI, and tap water samples are conducted to evaluate the sensors' performance. A detailed sensing mechanism has been developed to comprehend the results, including chemical and biological reactions, metal oxide interfaces, morphology, and other surface studies of the sensing surface. A prototype comprising a sensor chip, an Arduino board, and other necessary circuit components is tested with various bacterial solutions. This enables its use for on-field rapid detection of bacteria in water using smaller volumes and a portable system.

Laser Construction TiOx-Ag heterostructure interface for high sensitive coupling resonance enhanced fluorescence in bacterial nucleic acid amplification sensor chip

Coupled resonance at the noble metals and metal oxides heterogeneous interface can enhance the fluorescence of molecules. This fascinating direction provides high value for the preparation and engineering design of fluorescence sensing platforms in nucleic acid sensing, pathogen detection and biological imaging. Here, an integrated nucleic acid amplification sensor chip consists of an array of silver nanoparticles/oxygen vacancy titanium oxide (TiOx-Ag) heterostructure substrates. The femA gene of Staphylococcus aureus was amplified and detected by enhancement fluorescence on the integrated chip. The TiOx-Ag heterostructure array was prepared by a laser method, the enhanced fluorescence performance was investigated in detail using calcein as a probe. The optical, electronic structure and plasmonic local field analysis indicate the strong coupling between the fluorescence molecule and the TiOx-Ag crystal plane, which inspired the excellent fluorescence signal of calcein, with an enhancement factor of up to 5. Staphylococcus aureus was detected by the above chip with a detection limit as low as 157 cfu/mL. These methods were applied to the detection of spiked serum samples with good detected performances, providing a powerful tool for rapid and reliable diagnosis of pathogens in medical institutions.

Implementation of Wide Angle FoV Radar Module for ADAS Systems

In this study, we propose the wide field of view (FoV) radar module for autonomous vehicles. The proposed wide FoV radar (WFR) module was constructed using of an RF module comprising wide beamwidth microstrip patch antennas, an AWR1642 radar sensor chip, and a control module. To achieve a wide FoV of 150° using the fabricated radar module, the 3-dB beamwidth characteristic of the applied microstrip patch antenna had to wider than 150°. The patch antenna was designed using a comb-line structure along 10-by-1 array structure, each radiator characterized by a shorted patch structure, such as a planar inverted-F antenna. The designed antenna was then fabricated on the same board surface as the sensor chip. To identify the characteristics of the implemented radar module, a trihedral corner reflector with a radar-cross-section of 180 m2 was used as the reflector target, and the CA-CFAR (cell averaging constant false alarm rate) target detection algorithm was applied. The measurement results, showed good detection performance of the radar in the view angle of 150°, from -75° to +75°, and a broad bandwidth of 4 GHz in the 77–81 GHz millimeter band. Therefore, the proposed WFR is applicable for used in blind spot detection sensors in autonomous vehicles.

A piezoresistive-based 3-axial MEMS tactile sensor and integrated surgical forceps for gastrointestinal endoscopic minimally invasive surgery

In robotic-assisted surgery (RAS), traditional surgical instruments without sensing capability cannot perceive accurate operational forces during the task, and such drawbacks can be largely intensified when sophisticated tasks involving flexible and slender arms with small end-effectors, such as in gastrointestinal endoscopic surgery (GES). In this study, we propose a microelectromechanical system (MEMS) piezoresistive 3-axial tactile sensor for GES forceps, which can intuitively provide surgeons with online force feedback during robotic surgery. The MEMS fabrication process facilitates sensor chips with miniaturized dimensions. The fully encapsulated tactile sensors can be effortlessly integrated into miniature GES forceps, which feature a slender diameter of just 3.5 mm and undergo meticulous calibration procedures via the least squares method. Through experiments, the sensor’s ability to accurately measure directional forces up to 1.2 N in the Z axis was validated, demonstrating an average relative error of only 1.18% compared with the full-scale output. The results indicate that this tactile sensor can provide effective 3-axial force sensing during surgical operations, such as grasping and pulling, and in ex vivo testing with a porcine stomach. The compact size, high precision, and integrability of the sensor establish solid foundations for clinical application in the operating theater.

Pt thin-film resistance thermo detectors with stable interfaces for potential integration in SiC high-temperature pressure sensors

Due to the excellent mechanical, chemical, and electrical properties of third-generation semiconductor silicon carbide (SiC), pressure sensors utilizing this material might be able to operate in extreme environments with temperatures exceeding 300 °C. However, the significant output drift at elevated temperatures challenges the precision and stability of measurements. Real-time in situ temperature monitoring of the pressure sensor chip is highly important for the accurate compensation of the pressure sensor. In this study, we fabricate platinum (Pt) thin-film resistance temperature detectors (RTDs) on a SiC substrate by incorporating aluminum oxide (Al2O3) as the transition layer and utilizing aluminum nitride (AlN) grooves for alignment through microfabrication techniques. The composite layers strongly adhere to the substrate at temperatures reaching 950 °C, and the interface of the Al2O3/Pt bilayer remains stable at elevated temperatures of approximately 950 °C. This stability contributes to the excellent high-temperature electrical performance of the Pt RTD, enabling it to endure temperatures exceeding 850 °C with good linearity. These characteristics establish a basis for the future integration of Pt RTD in SiC pressure sensors. Furthermore, tests and analyses are conducted on the interfacial diffusion, surface morphological, microstructural, and electrical properties of the Pt films at various annealing temperatures. It can be inferred that the tensile stress and self-diffusion of Pt films lead to the formation of hillocks, ultimately reducing the electrical performance of the Pt thin-film RTD. To increase the upper temperature threshold, steps should be taken to prevent the agglomeration of Pt films.

Pressure Visualization and Quantification Photonic Skin Based on Flexible Optical Fiber Combiner

AbstractThe integration of pressure quantification and visualization enhances pressure perception, accuracy, and efficiency. Current solutions require improvements in quantization accuracy, structural simplicity, and integration. We proposed a novel photonic skin comprising a 3 × 1 flexible optical fiber combiner, integrating red, green, and blue light emitting diode (LED) chips through three flexible optical fibers. Under pressure, changes in the optical fibers' transmission loss alter the output light intensity ratio, thus inducing a color shift at the combiner's output. This visible change can be precisely quantified using a color sensor chip. Performance metrics include sensing range up to 33N, sensitivity between 0.04 and 0.24 dB N−1, detection limit below 0.08 N, response time of 500 ms, recovery time of 400 ms, and durability exceeding 2000 cycles. A compact flexible circuit board manages light source driving, data acquisition, and wireless communication, forming a wearable photonic skin system. This system enables visual recognition and quantitative measurement of pressure across diverse scenarios, including different tactile modes, multi‐position pressure, finger bending, and neck movement. For oral occlusion force detection, the spatial separation of the sensing and visualization areas enables the system to simultaneously provide accurate measurements and intuitive visual assessment.

Optical fibre based artificial compound eyes for direct static imaging and ultrafast motion detection

Natural selection has driven arthropods to evolve fantastic natural compound eyes (NCEs) with a unique anatomical structure, providing a promising blueprint for artificial compound eyes (ACEs) to achieve static and dynamic perceptions in complex environments. Specifically, each NCE utilises an array of ommatidia, the imaging units, distributed on a curved surface to enable abundant merits. This has inspired the development of many ACEs using various microlens arrays, but the reported ACEs have limited performances in static imaging and motion detection. Particularly, it is challenging to mimic the apposition modality to effectively transmit light rays collected by many microlenses on a curved surface to a flat imaging sensor chip while preserving their spatial relationships without interference. In this study, we integrate 271 lensed polymer optical fibres into a dome-like structure to faithfully mimic the structure of NCE. Our ACE has several parameters comparable to the NCEs: 271 ommatidia versus 272 for bark beetles, and 180o field of view (FOV) versus 150–180o FOV for most arthropods. In addition, our ACE outperforms the typical NCEs by ~100 times in dynamic response: 31.3 kHz versus 205 Hz for Glossina morsitans. Compared with other reported ACEs, our ACE enables real-time, 180o panoramic direct imaging and depth estimation within its nearly infinite depth of field. Moreover, our ACE can respond to an angular motion up to 5.6×106 deg/s with the ability to identify translation and rotation, making it suitable for applications to capture high-speed objects, such as surveillance, unmanned aerial/ground vehicles, and virtual reality.

A study of multiple solid-state dewetting of sputtered Au ultra-thin films for chip-based LSPR sensor applications

This article proposes a lithography-free technique to fabricate Au NPs on glass substrates using multiple solid-state dewetting (SSD) of sputtered Au ultra-thin films for LSPR sensor chip applications. We studied the influence of initial film thickness and the number of repeated process cycles on the morphology and LSPR sensing performance. This fabrication process allowed control over particle size, gap spacing, and density of the Au NPs, which influenced the LSPR peak position as observed using field emission scanning electron microscopy (FE-SEM) and UV–Vis–NIR spectrophotometry. To demonstrate LSPR sensing performance, the refractive index (RI) sensitivity was evaluated by measuring the wavelength shift of the LSPR peak in a series of glycerol/phosphate-buffered saline (PBS) mixtures, varying the refractive index from 1.33909 to 1.37409. The results showed that RI sensitivity and the figure of merit (FOM) for all prepared samples ranged from 37.191 ± 12.26–73.592 ± 9.70 and 0.35 ± 0.12–0.75 ± 0.02, respectively. An increase in repeated process cycles tended to decrease RI sensitivity and FOM. The best LSPR performance was achieved with an 8 nm initial film thickness after the first cycle, with an RI sensitivity of 70.937 ± 2.60 and an FOM of 0.75 ± 0.02, attributed to optimal Au size and density. Additionally, the binding efficiency response to human IgG with high regeneration cycles was demonstrated, highlighting the potential for biosensor applications.

A miniaturized microfluidic nanoplasmonic sensor with cavity reflection enhancement for ultrasensitive molecular interaction analysis

Molecular binding kinetics quantification is pivotal in the design of antibodies, small-molecule drugs, and early diagnosis of complex disease. This study presents a portable microfluidic system, featuring a nanoplasmonic sensor with cavity reflection enhancement (NSCRE), designed for the ultrasensitive detection and analysis of molecular interactions. This device comprises liquid flow paths, generic fiber spectrometers, a versatile NSCRE sensor chip, and a novel data analysis system. Furthermore, a neural network data processing system is developed based on a deep learning model to decrease significant data fluctuations caused by air segments. This “all-in-one” platform, integrating multifunctional, easy-to-use, and renewable NSCRE biosensors, boasts detection capabilities for both slow and rapid kinetics. It can automatically monitor interactions between molecules across a broad range of molecular weights (0.259–150 kDa), allowing for real-time, ultra-sensitive, and highly selective analysis. In addition, the platform with CRE effect facilitates a 7.2-fold increase in reflection intensity signals compared to that of a sensor without CRE. The immunoglobulin G detection with a limit of detection of 73 pM based on this device, showing a 50-fold increase in sensitivity compared to previously reported values. The miniaturized automatic detection system paves a new path for the use of molecular interaction analysis in life science research, drug discovery, early diagnosis, and other fields.

Integrated Amorphous Carbon Film Temperature Sensor with Silicon Accelerometer into MEMS Sensor.

Amorphous carbon (a-C) has promising potential for temperature sensing due to its outstanding properties. In this work, an a-C thin film temperature sensor integrated with the MEMS silicon accelerometer was proposed, and a-C film was deposited on the fixed frame of the accelerometer chip. The a-C film was deposited by DC magnetron sputtering and linear ion beam, respectively. The nanostructures of two types of films were observed by SEM and TEM. The cluster size of sp2 was analyzed by Raman, and the content of sp2 and sp3 of the carbon film was analyzed by XPS. It showed that the DC-sputtered amorphous carbon film, which had a higher sp2 content, had better temperature-sensitive properties. Then, an integrated sensor chip was designed, and the structure of the accelerometer was simulated and optimized to determine the final sizes. The temperature sensor module had a sensitivity of 1.62 mV/°C at the input voltage of 5 V with a linearity of 0.9958 in the temperature range of 20~150 °C. The sensitivity of the sensor is slightly higher than that of traditional metal film temperature sensors. The accelerometer module had a sensitivity of 1.4 mV/g/5 V, a nonlinearity of 0.38%, a repeatability of 1.56%, a total thermomechanical noise of 509 μg over the range of 1 to 20 Hz, and an average thermomechanical noise density of 116 µg/√Hz, which is smaller than the input acceleration amplitude for testing sensitivity. Under different temperatures, the performance of the accelerometer was tested. This research provided significant insights into the convenient procedure to develop a high-performance, economical temperature-accelerometer-integrated MEMS sensor.