Search Results (1,072)

Background/Objectives: The question addressed in the current work is to develop a simulation of a pharmaceutical process (DNA encapsulation within lipid nanoparticles using a microfluidic micromixer) which will be of utility to the end users (laboratory-scale formulation development). The simulation and the microfluidic approach also address sustainability issues, such as reducing the environmental impact of the process itself, and reducing the need for physical testing. The paper details the implementation and validation, taking into account key performance indicators and control parameters. Methods: The main method applied for simulation development is a novel multi-agent approach to incorporate stochastic probabilistic behavior, combined with theoretical definitions from the process experts and relevant literature, and data/results from laboratory-scale experiments with different parameter configurations. Results: The simulation was implemented as a representation of the real physical process, reproducing the relationships between process parameters (flow rates) and experimental key performance indicators (capsule diameter, poly dispersion index, encapsulation efficiency). The simulation results demonstrated a general agreement with the empirical results and provided useful predictive insights for the laboratory experiments. Conclusions: The simulation has potential as a support tool for laboratory experiments to reduce physical testing and indicate the most promising configurations on which to focus, with potential savings in time, resources and other costs. Full article

Oil analysis is one of the main means to obtain the working status of important friction pairs in ship and Marine engineering equipment at present. Analyzing the wear mechanism by analyzing the particle size, morphology, properties and other characteristics of metal abrasive particles in the oil is an important basis for achieving health monitoring and scientific maintenance of ship and Marine engineering equipment. Classifying the abrasive particles in the oil according to their particle size is an important step in sample pretreatment. This paper proposes a two-stage sorting microfluidic chip for wear debris based on magnetophoresis. By setting up external permanent magnets in a stepwise manner in the primary and secondary sorting areas, gradient magnetic fields of different magnitudes were formed. The effects of different sample flow rates, sheath fluid flow rates and sheath flow ratios on the pre-focusing before sorting and the sorting effect were studied. The primary sorting of ferromagnetic metal wear particles larger than 50 µm and the secondary sorting of those smaller than 50 µm have been achieved. The primary sorting can serve as an early warning for abnormal equipment wear, while the secondary sorting can provide data support for the scientific formulation of maintenance plans based on equipment requirements. This work provides a new idea and method for the rapid determination of lubricating oil contamination in engineering equipment. Full article

Chronic kidney disease (CKD) is a progressively worsening condition that erodes renal function over time, reduces quality of life, and can ultimately culminate in kidney failure with far-reaching systemic complications. In addition to reduced filtration, worsening kidney function disrupts mineral homeostasis and leads to CKD–mineral and bone disorder (CKD-MBD). Dysregulated calcium handling and maladaptive endocrine responses contribute to bone pathology and increase cardiovascular calcification risk; therefore, serial calcium monitoring remains clinically relevant for longitudinal CKD management. Conventional calcium measurements are typically obtained with centralized analyzers or laboratory assays (e.g., colorimetry and electrode/optical readouts). Despite high accuracy, the required instrumentation, controlled operating conditions, and pretreatment steps complicate rapid point-of-care deployment, especially when only microliter-scale biofluids are available. Accordingly, this study develops a finger-actuated microfluidic colorimetric platform capable of determining calcium ion concentrations in human biofluids, such as whole blood, serum, and urine. The platform integrates a three-dimensional PMMA/paper microchip with a compact reader that maintains stable temperature control while enabling CMOS-based optical detection. With just 6 μL of sample, a brief finger press propels the biofluid across an internal filtration layer, generating serum or cleaned urine that subsequently reacts with a pre-deposited murexide reagent. Under optimized conditions (1.6% reagent, 50 °C, 3 min), the signal follows a strong logarithmic relationship with calcium concentration (Y = 47.273 ln X + 28.890; R² = 0.9905), supporting quantification over 1–40 mg/dL and a detection limit of 0.2 mg/dL. Across 80 clinical CKD specimens spanning serum, whole blood, and urine, results aligned closely with the NM-BAPTA reference assay, with R² values exceeding 0.97. Full article

Molecular point-of-care testing (POCT) for respiratory infections has undergone remarkable advancement over the past two decades, driven by technological innovation and urgent clinical needs highlighted by the COVID-19 pandemic. This comprehensive systematic review was conducted following PRISMA 2020 guidelines, synthesizing evidence from 254 peer-reviewed studies published between 2006 and 2026, with detailed analysis of the 30 most relevant papers selected through a rigorous four-stage screening process. The review examines the evolution of molecular POCT technologies, including reverse transcription polymerase chain reaction (RT-PCR), loop-mediated isothermal amplification (LAMP), recombinase polymerase amplification (RPA), and CRISPR-based detection systems. Key findings demonstrate that modern molecular POCT platforms achieve diagnostic performance comparable to laboratory-based testing, with sensitivities ranging from 88% to 100% and specificities from 98% to 100%, while delivering results in 15 to 80 min. These technologies enable rapid, accurate detection of major respiratory pathogens, including SARS-CoV-2, influenza A/B, respiratory syncytial virus (RSV), and atypical bacteria. The integration of microfluidic systems, portable devices, and smartphone-based analysis has expanded access to testing in resource-limited settings, emergency departments, and wearable platforms. This review provides critical insights for clinicians, researchers, and policymakers regarding the current state, clinical applications, and future directions of molecular POCT for respiratory infections. Full article

Stimulated Raman scattering (SRS) with Raman crystals is widely recognized as an effective technical approach for achieving high-efficiency lasers at specific wavelengths. However, due to crystal size limitations, it is challenging to generate large-energy Raman lasers while simultaneously considering the laser damage threshold of optical components. To overcome this limitation, in this paper we describe the successful fabrication of a large-aperture barium nitrate Raman gain medium using the directional template growth technique. Employing this large-aperture Raman medium and a 532 nm pulse laser as the excitation source, a large-energy, high-efficiency yellow–orange waveband laser system was constructed. When injected with 886.7 mJ pump energy at 532 nm, the Raman laser achieved a maximum output energy of 556.2 mJ, corresponding to an optical-to-optical conversion efficiency of 62.7%. This represents a significant advancement in single-pulse energy for barium nitrate Raman lasers. Large-energy yellow–orange wavelength lasers have applications in the clinical treatment of skin diseases and microfluidic chip manufacturing. Full article

Microfluidics-based preparation methods for cell-laden hydrogel microspheres are well-suited for large-scale comparative analysis of single or few cells. However, in existing studies, the preparation of cell-laden hydrogel microspheres and the cell culture process are typically separated, requiring the fabricated microspheres to be eluted and transferred from the preparation device to cell culture dishes or plates for cultivation. This transfer process can easily compromise sterility, while conventional cell culture methods consume more reagents and cause microsphere stacking, hindering single-cell observation and analysis. To address these issues, this paper presents an integrated microfluidic chip that sequentially enables droplet generation with cell encapsulation, gel droplet solidification, hydrogel microsphere trapping, and microsphere-based cell culture and analysis, facilitating the cultivation and observation of single or small numbers of cells. Integrating cell-laden microsphere preparation and 3D cell culture within a sealed chip structure reduces contamination risks associated with cell transfer, enables automation of multiple cell analysis workflows, and minimizes reagent and sample consumption. Using polydimethylsiloxane (PDMS) with good gas permeability and processability as the chip material, biocompatible fluorinated oil was selected as the oil phase for microsphere preparation. A mild sodium alginate-calcium ion gelation system was employed, where calcium ions were released under acidic conditions after droplet generation to trigger solidification, yielding uniform hydrogel microspheres. Under optimized conditions, the single-cell encapsulation efficiency for test samples of human myeloid leukemia cells (K562) was 33.8% ± 1.8%, with a size uniformity coefficient of variation (CV) reaching 3.85%. Cells encapsulated within hydrogel microspheres were cultured in 286 on-chip independent cell culture chambers, achieving >95% viability after 24 h. Full article

This paper investigates a novel optical method that uses a high-responsivity a-Si:H photodiode for label-free detection of luminescence from HeLa cervical cancer cells excited by a blue LED. We examine the energy distribution of the energy-gap density of states (DOS) from the photodiode’s long-time transient current, which shows exponential decay kinetics in the HeLa cell reaction. We analysed the transient response of a-Si:H p-i-n photodiode upon the illumination of the analyte with a pulsed blue LED light to better understand the HeLa cells activity and the fundamental defect kinetics processes in the a-Si:H material. Results suggest that the characteristic very low-level, time-varying light response of HeLa cells is due to chemiluminescence within cells, resulting from the reaction between nitric oxide (NO) and hydrogen peroxide (H₂O₂). Given the low signal intensity and noise, we applied a Savitzky–Golay (SG) filter to post-process the data. By reducing noise without attenuating chemiluminescent peaks, the Savitzky–Golay filter enabled accurate, reproducible quantification of the photocurrent response, reflecting the kinetics of cellular reactions. Further studies and more precise measurement instruments are needed for this real-time, label-free, non-destructive method, which applies SG-filtered signal processing to microfluidic optical biosensors. Full article

Countercurrent electrophoresis (CCEP) is a technology that forms a steady focus in the separation channel through the coupling of electric field migration and reverse fluid flow, so as to realize the synchronous concentration and separation of substances. This paper reviews the evolution of CCEP from its theoretical origin, device design to microfluidic integration and optimization. Compared with traditional capillary electrophoresis, CCEP has higher processing flux, continuous operation ability and separation resolution, and has been successfully applied to isotope enrichment, protein recovery and complex matrix analysis. This paper further discusses the methods derived from it, such as isoelectric focusing (CACE), conductance gradient focusing (CGF) and electric field gradient focusing (EFGF), which expand the analysis ability and application scenarios of CCEP. Although the technology still faces challenges such as system stability, operation complexity and detection dependence, with the development of microfluidic, intelligent control and new material technology, CCEP shows broad development prospects in biomedicine, environmental monitoring and nuclide separation. Full article

Aberrant glycosylation is linked to several diseases, making glycoproteins and their glycoforms promising biomarkers. Traditional methods like mass spectrometry offer high sensitivity but are costly, time-consuming, and unsuitable for point-of-care testing. Electrochemical biosensors emerge as an attractive alternative due to their simplicity, affordability, portability, and rapid response. This review focuses on electrochemical strategies developed to assess the glycosylation level of a specific glycoprotein or biological structure rather than merely glycoprotein or cell concentration, as in previous reviews. Approaches include the use of aptamers, boronic acid derivatives, antibodies, and lectins, often combined with nanomaterials for enhanced sensitivity. Applications span the diagnosis/prognosis of several illnesses such as diabetes, congenital disorders of glycosylation, cancer, and neurodegenerative diseases. Innovative designs incorporate microfluidic and paper-based platforms for faster, low-cost analysis, while strategies using dual-signal acquisition or competitive assays improve accuracy. Despite promising sensitivity and selectivity, most sensors require multi-step protocols and lack of validation in clinical samples. Future research should focus on simplifying procedures, integrating microfluidics, and exploring novel capture or detection probes such as metal complexes or metal–organic frameworks. Overall, electrochemical sensors hold significant potential for point-of-care testing, enabling rapid and precise evaluation of glycosylation status, which could drive cell-based biomarker discovery and disease diagnostics. Full article

Ion chromatography (IC) serves as a pivotal technique in trace ion analysis, and the separation performance of IC is largely determined by the properties of stationary phases. In contrast to silica-based matrices, polymer-based stationary phases have garnered significant interest owing to their outstanding pH stability and mechanical robustness. However, unmodified polymer matrices usually lack necessary ion exchange functions and selectivity; therefore, precise functional modification is the key to improving their chromatographic separation performance. This paper provides a systematic overview of recent advances in the synthesis and functional modification of polymer-based anion exchange chromatography stationary phases over the past few years. Firstly, the types and characteristics of polymer matrices commonly used for functional modification are summarized; secondly, the origin and improvement of common synthesis methods such as microporous membrane emulsification, droplet microfluidics, suspension polymerization, emulsion polymerization, soap-free emulsion polymerization, precipitation polymerization, dispersion polymerization, and seed swelling are introduced according to the molding methods of polymer matrices; furthermore, the principles, characteristics, and development status of mainstream functionalization strategies, including chemical derivatization, surface grafting, latex agglomeration, and hyperbranching, are emphasized. Finally, the existing challenges and prospective development trends in this field are discussed and outlooked, with the purpose of offering insights for the targeted design and practical application of high-performance polymer-based anion exchange chromatography stationary phases. Full article

Surface plasmon resonance (SPR) sensors based on photonic crystal fibers (PCFs) hold significant promise for high-precision detection in biochemical and chemical sensing. However, achieving high sensitivity in low-refractive-index (RI) aqueous environments remains a formidable challenge due to weak light-matter interactions. To address this limitation, this paper designs and proposes a novel dual-channel D-shaped PCF-SPR sensor tailored for the refractive index range of 1.34–1.40. The sensor incorporates a dual-layer gold/titanium dioxide film, with gold nanoparticles deposited on the surface to synergistically enhance both propagating and localized surface plasmon resonance effects. Furthermore, a D-shaped polished structure integrated with double-sided microfluidic channels is employed to significantly strengthen the interaction between the guided-mode electric field and the analyte. Finite element method simulations demonstrate that the proposed sensor achieves an average wavelength sensitivity of 5733 nm/RIU and a peak sensitivity of 15,500 nm/RIU at a refractive index of 1.40. Notably, the introduction of gold nanoparticles contributes to an approximately 1.47-fold sensitivity enhancement over conventional structures. This work validates the efficacy of hybrid plasmonic nanostructures and optimized waveguide design in advancing RI sensing performance. Full article

This paper presents a multichannel electronics measurement system that uses microwave sensors to perform real-time microplastics assessment in aqueous environments. The system is capable of simultaneously reading up to four microwave sensors, enabling the use of multiple sensors that target microplastic particles with different sizes and properties. The multichannel capability allows the measurement of multiple MW sensors integrated with different microfluidic channel designs while targeting different MPs’ dimension ranges, although experimental validation in this work was limited to a single sensor. Each readout channel is implemented combining radio-technology-integrated circuits with a microprocessor that has advanced analog peripherals used for signal conditioning and acquisition. An ADF4351 wideband frequency synthesizer is used for excitation signal generation while an ADL5902 power detector converts the sensor output to a DC voltage. Baseline removal and amplification of the power detector output is realized with a MSP430FR2355 microprocessor which is also responsible for its acquisition at 40 kHz and digital decimation. Characterization results show the system’s capability to generate excitation signals between 700 MHz and 3.5 GHz with power levels around 0 dBm. Sensor output can be detected with a power between −50 dBm and −5 dBm and a 230 Hz bandwidth. A compact form factor of 15 cm × 10 cm × 3 cm was realized together with a low power consumption of 6.6 W. Validation was realized with a previously developed microwave sensor, demonstrating the detection of polyethylene spheres with 400 μm diameters animated in 10 mL/min flux within the microfluidics device. Full article

Microfluidic paper-based analytical devices (µPADs) convert ordinary cellulose into an active analytical platform where capillary gradients shape transport, surface chemistry guides recognition, and embedded electrodes or optical probes translate biochemical events into readable signals. Progress in fabrication—from wax and stencil barriers to laser-defined grooves, inkjet-printed conductive lattices, and 3D-structured multilayers—has expanded reaction capacity while preserving portability. Detection strategies span colorimetric fields that respond within porous fibers, fluorescence and ratiometric architectures tuned for low abundance biomarkers, and electrochemical interfaces resilient to turbidity, salinity, and biological noise. Applications now include diagnosing human body fluids, checking food safety, monitoring the environment, and testing for pesticides and illegal drugs, often in places with limited resources. Researchers are now using learning algorithms to read minute gradients or currents imperceptible to the human eye, effectively enhancing and assisting the measurement process. This perspective article focuses on the newest advancements in the design, fabrication, material selection, testing methods, and applications of µPADs, and it explains how they work, where they can be used, and what their future might hold. Full article

Along with the growing demands for personalized medicine and public health surveillance, diagnostic technologies capable of rapid and accurate pathogen nucleic acid testing in home settings are becoming increasingly crucial. Paper-based microfluidic chips (μPADs) have emerged as a potential core platform for enabling molecular testing at home, owing to their advantages of low cost, portability, and independence from complex instrumentation. However, significant challenges remain in the current μPADs systems regarding nucleic acid extraction efficiency, isothermal amplification stability, and signal readout standardization, which hinder their practical and large-scale application. This review systematically summarizes recent research progress in μPADs for home-based nucleic acid testing from four key aspects: extraction–amplification–detection system integration, with a particular focus on the synergistic effects and development trends of critical technologies such as material engineering, fluid control, signal transduction, and intelligent readout. We further analyze typical application cases of this technology in the rapid screening of infectious disease. Promising optimization pathways are proposed, focusing on standardized manufacturing, cold-chain-independent storage, and AI-assisted result interpretation, aiming to provide a feasible framework and forward-looking perspectives for constructing home-based molecular diagnostic systems. Full article

Escherichia coli (E. coli) is a well-established indicator of faecal pollution and a potent pathogen linked to numerous gastrointestinal and systemic illnesses. Ensuring public safety requires rapid and sensitive detection methods capable of real-time, on-site deployment. Many conventional techniques are either laborious, time-intensive, costly, or require complex infrastructure, limiting their applicability in field settings. Raman spectroscopy offers label-free molecular fingerprinting; however, its inherently weak scattering signals restrict its effectiveness as a standalone technique. Surface-Enhanced Raman Spectroscopy (SERS) overcomes this limitation by exploiting plasmonic enhancement from nanostructured metallic substrates—most commonly gold, silver, copper, and aluminium. Despite the commercial availability of SERS-active substrates, challenges remain in achieving high reproducibility, long-term stability, and true field applicability, necessitating the development of integrated lab-on-chip platforms and portable, handheld Raman devices. This review critically examines recent advances in SERS-based E. coli detection across water and perishable food products with particular emphasis on the evolution of SERS substrate design, the incorporation of biosensing elements, and the integration of electrochemical and microfluidic systems. By contrasting conventional SERS approaches with next-generation biosensing strategies, this paper outlines pathways toward robust, real-time pathogen detection technologies suitable for both laboratory and field applications. Full article