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Microfluidic lab‐on‐a‐chip (LOC) devices have become essential tools for multitudes of applications in various research fields. 3D printing of microfluidic LOC devices offers many advantages over more traditional manufacturing processes, including rapid prototyping and single‐step fabrication of complex 3D structures. In this work, 3D‐printed microfluidic devices are designed and fabricated for optical chromatography and sorting. Optical chromatography is performed by inserting a single‐mode optical fiber into the device creating a counter‐propagating laser beam to the fluid flow. Particles are separated depending on refractive index and size. To demonstrate optical sorting, a cross‐type sorter 3D‐printed microfluidic device is fabricated that directs the laser beam perpendicular to the flow direction. Design features such as a sloping channel and a channel configuration for 3D hydrodynamic focusing (to aid in controlled sample flow and particle position) help to optimize sorting performance. Stable optofluidic trapping and sorting are successfully achieved using the fabricated microfluidic devices. These results highlight the tremendous potential of 3D printing of microfluidic LOC devices for applications aimed at the optofluidic manipulation of micron‐sized particles. [ABSTRACT FROM AUTHOR]

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The inception of microfluidic devices marks a confluence of diverse scientific domains, including physics, biology, chemistry, and fluid mechanics. These multidisciplinary roots have catalyzed the evolution of microfluidic devices, which serve as versatile platforms for various chemical and biological processes. Notably, microfluidic devices have garnered attention as efficient reactors, offering distinct benefits such as minimized spatial requirements for reactions, reduced equipment costs, and accelerated residence times. These advantages, among others, have ignited a compelling interest in harnessing microfluidic technology for the conception, refinement, and production of various nanomaterials and nanocomposites, pivotal within both industrial and medicinal sectors. This comprehensive exposition delves into multifaceted aspects of nanomaterial synthesis, underscoring the transformative role of microfluidic methodologies as a departure from conventional techniques. The discourse navigates through intricate considerations surrounding the preparation of nanomaterials, elucidating how the microfluidic paradigm has emerged as a promising alternative. This paper serves as an illuminating exploration of the juncture between microfluidic innovation and nanomaterial synthesis. It traverses the transformative potential of microfluidics in revolutionizing traditional approaches, heralding a new era of precision engineering for advanced materials with applications spanning industrial to medicinal domains. [ABSTRACT FROM AUTHOR]

This article reviews the recent progress in fabricating microfluidic devices and soft robots using direct ink writing (DIW) three-dimensional (3D) printing with silicone elastomers. Additive manufacturing, especially 3D printing, has become an alternative method to traditional soft lithography for producing microchannels, establishing a new standard in the field of microfluidics. This approach offers unprecedented opportunities for digital control, automation, and the elimination of manual assembly. Among different 3D printing technologies, DIW 3D printing facilitates the accurate deposition of liquid silicone precursors on various substrates in the air or liquid media, enabling the fabrication of microfluidic structures using a one-part room-temperature-vulcanizing (RTV) silicone sealant and two-part addition-curing silicone elastomers. The effectiveness of DIW 3D printing is demonstrated through (1) creating microchannels on various substrates, (2) printing interconnected, multilayer microchannels without the need for sacrificial support materials or extensive post-processing steps, and (3) integrating electronic components into microchannels during the printing process. In this article, overviews of the fabrication of microfluidic devices using 3D printing are provided first, followed by a discussion of different criteria and approaches for DIW 3D printing of silicone-based elastomeric structures in open-air and embedded media. Next, the structure–property relations of silicone-based microfluidic devices are discussed. Then, examples of DIW-fabricated silicone microfluidic devices and soft robotics are showcased, highlighting the unique benefits and opportunities of the methods. Finally, current challenges and future directions in DIW 3D printing of microfluidic systems are discussed. [ABSTRACT FROM AUTHOR]

3D printing has revolutionized the fabrication and rapid prototyping of microfluidic devices. However, it remains challenging to achieve optically transparent microfluidic chips with 3D printing, which limits their applicability in high-resolution imaging applications. We present a paradigm-shifting, low-cost, and generalizable post-processing method to address this challenge. Our method is centered around the implementation of a novel post-processing equipment "Spinning Desicurer" which integrates solvent-free resin removal, surface smoothing, and efficient surface curing. Our method produces microfluidic devices with high optical transparency and can be readily used to image microscopic objects such as cells and microparticles with fine details. [ABSTRACT FROM AUTHOR]

The Special Issue of Micromachines, titled "Nanomaterials for Micro/Nanodevices," explores the advancements and applications of nanomaterials in micro- and nano-scale devices. The issue features ten papers that highlight the unique properties of nanomaterials and their role in enhancing device performance. From bio-inspired nanomaterials to superhydrophobic surfaces and novel materials like nanostructured spinel chromites, the issue covers a wide range of topics that showcase the potential of nanomaterials in driving future technological innovations. Researchers and practitioners can gain valuable insights from these studies to further develop nanomaterial applications in various fields. [Extracted from the article]

The velocity and trajectory of particles moving along the corrugated (rough) surface under the action of gravity is obtained by a modified Method of Fundamental Solutions (MFS). This physical situation is found often in biological systems and microfluidic devices. The Stokes equations with no-slip boundary conditions are solved using the Green's function for Stokeslets. In the present study, the velocity of a moving particle under the action of the gravity force is not known and becomes a part of the MFS solution. This requires an adjustment of the matrix of the MFS linear system to include the unknown particle velocity and incorporate in the MFS the balance of hydrodynamic and gravity forces acting on the particle. The study explores the combination of the regularization of Stokeslets and placement of Stokeslets outside the flow domain to ensure the accuracy and stability of computations for particles moving in proximity to the wall. The MFS results are compared to prior published approximate analytical and experimental results to verify the effectiveness of this methodology to predict the trajectory of particles, including their deviation from the vertical trajectory, and select the optimal set of computational parameters. The developed MFS methodology is then applied to the sedimentation of a pair of two spherical particles in proximity to the corrugated wall, in which case, the analytical solution is not available. The MFS results show that particles in the pair deviate from the trajectory of a single particle: the particle located below moves farther away from vertical wall, and the particle located above shifts closer to the wall. [ABSTRACT FROM AUTHOR]

Long-term live cell imaging requires sophisticated and fully automated commercial-stage incubators equipped with specified inverted microscopes to regulate temperature, CO2 content, and humidity. In this study, we present a CO2-free on-stage incubator specifically designed for use across various cell culture platforms, enabling live cell imaging applications. A simple and transparent incubator was fabricated from acrylic sheets to be easily placed on the stages of most inverted microscopes. We successfully performed live-cell imaging of cholangiocarcinoma (CCA) cells and HeLa cell dynamics in both 2D and 3D microenvironments over three days. We also analyzed directed cell migration under high serum induction within a microfluidic device. Interesting phenomena such as "whole-colony migration", "novel type of collective cell migration" and "colony formation during cell and colony migration" are reported here for the first time, to the best of our knowledge. These phenomena may improve our understanding of the nature of cell migration and cancer metastasis. [ABSTRACT FROM AUTHOR]

This review examines recent advancements in electrochemical immunosensors for the detection of organophosphate pesticides, focusing on strategies to enhance sensitivity and selectivity. The widespread use of these pesticides has necessitated the development of rapid, accurate, and field-deployable detection methods. We discuss the fundamental principles of electrochemical immunosensors and explore innovative approaches to improve their performance. These include the utilization of nanomaterials such as metal nanoparticles, carbon nanotubes, and graphene for signal amplification; enzyme-based amplification strategies; and the design of three-dimensional electrode architectures. The integration of these sensors into microfluidic and lab-on-a-chip devices has enabled miniaturization and automation, while screen-printed and disposable electrodes have facilitated on-site testing. We analyze the challenges faced in real sample analysis, including matrix effects and the stability of biological recognition elements. Emerging trends such as the application of artificial intelligence for data interpretation and the development of aptamer-based sensors are highlighted. The review also considers the potential for commercialization and the hurdles that must be overcome for widespread adoption. Future research directions are identified, including the development of multi-analyte detection platforms and the integration of sensors with emerging technologies like the Internet of Things. This comprehensive overview provides insights into the current state of the field and outlines promising avenues for future development in organophosphate pesticide detection. [ABSTRACT FROM AUTHOR]

Microfluidics are crucial for managing small-volume analytical solutions for various applications, such as disease diagnostics, drug efficacy testing, chemical analysis, and water quality monitoring. The precise control of flow control devices can generate diverse flow patterns using pneumatic control with solenoid valves and a microcontroller. This system enables the active modulation of the pneumatic pressure through Arduino programming of the solenoid valves connected to the pressure source. Additionally, the incorporation of solenoid valve sets allows for multichannel control, enabling simultaneous creation and manipulation of various microflows at a low cost. The proposed microfluidic flow controller facilitates accurate flow regulation, especially through periodic flow modulation beneficial for droplet generation and continuous production of microdroplets of different sizes. Overall, we expect the proposed microfluidic flow controller to drive innovative advancements in technology and medicine owing to its engineering precision and versatility. [ABSTRACT FROM AUTHOR]

Particle separation and sorting techniques based on microfluidics have found extensive applications and are increasingly gaining prominence. This research presents the design and fabrication of a microfluidic device for separating cells using deterministic lateral displacement (DLD), enabling accuracy and continuity while being size-based. Nevertheless, it remains demanding, to completely reverse the detrimental effects of the boundaries that disturb the fluidic flow in the channel and reduce particle separation efficiency. This study introduces a novel approach to enhance the boundary structure of channels. By using this design, separation efficiency is boosted, and the fluid behavior around the walls is improved. The boundary correction (BC) enhances the operation of the microchannel and is very effective in microchannels. With boundary correction, the device exhibited improved separation efficiencies, but in its absence, separation efficiencies dropped. The collected microscopic images of the isolation of prostate cancer cell lines and red blood cells revealed promising outcomes. The efficiency of circulating tumor cell (CTC) throughput in the microfluidic channel, quantified as the ratio or proportion of tumor cells exiting the channel to cells entering it, exceeds 93%. Moreover, the efficiency of CTC isolation, expressed as the proportion of tumor cells from the upper outlet of the microfluidic channel to all cells, is over 89%. Additionally, the efficiency of red blood cell isolation, evaluated as the ratio of red blood cells from the lower outlet of the microfluidic channel to all cells, surpasses 77%. While using the same DLD separator without boundary correction reduced the separation efficiency by around 5%. [ABSTRACT FROM AUTHOR]

Bioartificial livers have showcased significant value in the treatment of acute liver failure (ALF). Current efforts are directed toward overcoming challenges in the development of microcarriers, with a specific emphasis on integrating higher‐density liver cells to enhance detoxification capabilities. Here, inspired by the radial filtration model in hepatic lobules, ion‐specific silk fibroin microcarriers are proposed with biomimetic niches for cultivating functional liver cells at high density. These biomimetic microcarriers are generated by capillary microfluidic device with controllable adjustments of ion type or concentration within the aqueous phase. When cultivating human induced pluripotent stem cell ‐differentiated mature liver cells on these recrystallized microcarriers, notably enhanced cell proliferation activity, as well as increased metabolic and secretory functionality is observed. Based on these features, the microcarrier‐integrated bioreactor can effectively reduce hepatic transaminase levels and significantly improve urea, albumin production, and survival rate in rabbit ALF models is demonstrated. Thus, it is believed that the biomimetic microcarriers and their derived bioreactor may hold potential for clinical applications in managing ALF and other liver diseases. [ABSTRACT FROM AUTHOR]

Cavitation and its effects are well investigated, especially single bubble cavitation and its collapse near rigid and elastic boundaries. In our current article, we investigated novel experiments of a single cavitation bubble near an oscillatory boundary. We generated the cavitation bubble by laser focusing in water. A flat glass plate was fixed to the shaft of the magnetostriction oscillator coil. We investigated the dynamics of bubbles at two relative wall distances (ratio of the distance between the bubble center and plate surface to the maximum radius of the bubble) of the bubble from the glass plate in combination with four modes of oscillation. Each mode has specific frequency and amplitude of oscillation. The high-speed camera captured the dynamics of the bubble using the back-illumination method with a framing rate of 120Kfps and simultaneously we used an optical CMOS sensor to measure the oscillation of the glass plate. We presented a clear comparison among the bubble dynamics near stationary and oscillating plates with parameters such as oscillating modes and direction. We correlated the dynamics of the bubble with the motion of the plate. In addition, we highlighted the differences including the characteristics of bubble shape and jetting that occurred during the collapse phase. The comparison of the time histories of the bubble's equivalent size postulated that the bubble's collapse times vary significantly in some cases compared to the bubble's dynamics near the stationary plate. In all cases, we noticed the shortening of the bubble's collapsing time, i.e. accelerated collapses. In our findings, we noticed a collapse times reduction of about 4–15%. Our finding signifies the importance of introducing the oscillation of the boundaries to obtain effective energy concentration over the time during the collapse. Our study also suggests that forced oscillation of boundaries is undesirable for destructive cavitation effects. The method we suggested for the manipulation of bubble dynamics holds potential for enhancing the efficiency of applications such as lithotripsy in biomedical devices, actuation and micro pumping in microfluidic devices, and effective semiconductor surface cleaning. Not but least, obtained results can be used as benchmark in future for validating numerical methods. [ABSTRACT FROM AUTHOR]

Ketones, such as beta-hydroxybutyrate (BHB), are important metabolites that can be used to monitor for conditions such as diabetic ketoacidosis (DKA) and ketosis. Compared to conventional approaches that rely on samples of urine or blood evaluated using laboratory techniques, processes for monitoring of ketones in sweat using on-body sensors offer significant advantages. Here, we report a class of soft, skin-interfaced microfluidic devices that can quantify the concentrations of BHB in sweat based on simple and low-cost colorimetric schemes. These devices combine microfluidic structures and enzymatic colorimetric BHB assays for selective and accurate analysis. Human trials demonstrate the broad applicability of this technology in practical scenarios, and they also establish quantitative correlations between the concentration of BHB in sweat and in blood. The results represent a convenient means for managing DKA and aspects of personal nutrition/wellness. [ABSTRACT FROM AUTHOR]

The first step in blood testing necessitates blood separation to obtain an adequate volume of plasma. Traditional centrifugation is bulky, expensive and electricity-powered, which is not suitable for micro-scale blood plasma separation in point-of-care testing (POCT) cases. Microfluidic paper-based plasma separation devices present a promising alternative for plasma separation in such occasions. However, they are limited in terms of plasma yield, which hinders analyte detection. Herein, we proposed a humidity-enhanced paper-based microfluidic plasma separation method to address this issue. Specifically, paper was first treated by blood-typing antibodies, then samples of whole blood were introduced into the prepared paper. After waiting for 5 min for RBC agglutination and plasma wicking under high humidity, micro-scale plasma separation from whole blood was achieved. As a result, an extremely high plasma yield of up to 60.1% could be separated from whole blood through using Xuan-paper. Meanwhile, the purity of plasma could reach 99.99%. Finally, this innovative approach was effortlessly integrated into distance-based glucose concentration detection, enabling rapid determination of blood glucose levels through naked-eye observation. Considering the simplicity and inexpensiveness of this method, we believe that this technology could be integrated to more paper-based microfluidic analytical devices for rapid and accurate detection of plasma analytes in POCT. [ABSTRACT FROM AUTHOR]

The ability to cost-effectively produce large surface area microfluidic devices would bring many smallscale technologies such as microfluidic artificial lungs (μALs) from the realm of research to clinical and commercial applications. However, efforts to scale up these devices, such as by stacking multiple flat μALs have been labor intensive and resulted in bulky devices. Here, we report an automated manufacturing system, and a series of cylindrical multi-layer lungs manufactured with the system and tested for fluidic fidelity and function. A roll-to-roll (R2R) system to engrave multiple-layer devices was assembled. Unlike typical applications of R2R, the rolling process is synchronized to achieve consistent radial positioning. This allows the fluidics in the final device to be accessed without being unwrapped. To demonstrate the capabilities of the R2R manufacturing system, this method was used to manufacture multi-layer μALs. Gas and blood are engraved in alternating layers and routed orthogonally to each other. The proximity of gas and blood separated by gas permeable PDMS permits CO2 and O2 exchange via diffusion. After manufacturing, they were evaluated using water for pressure drop and CO2 gas exchange. The best performing device was tested with fresh whole bovine blood for O2 exchange. Three μALs were successfully manufactured and passed leak testing. The top performing device had 15 alternating blood and gas layers. It oxygenated blood from 70% saturation to 95% saturation at a blood flow of 3 mL min−1 and blood side pressure drop of 234 mmHg. This new roll-to-roll manufacturing system is suitable for the automated construction of multi-layer microfluidic devices that are difficult to manufacture by conventional means. With some upgrades and improvements, this technology should allow for the automatic creation of large surface area microfluidic devices that can be employed for various applications including large-scale membrane gas exchange such as clinical-scale microfluidic artificial lungs. [ABSTRACT FROM AUTHOR]

Presumptive drug screening enables timely procurement of search and arrest warrants and represents a crucial first step in crime scene analysis. Screening also reduces the burden on forensic laboratories which often face insurmountable backlogs. In most scenarios, on-site presumptive drug screening relies on chemical field tests for initial identification. However, even when used appropriately, these test kits remain limited to subjective colorimetric analysis, produce false positive or negative results with excessive sample quantities, and are known to cross-react with numerous innocuous substances. Previous efforts to develop microfluidic devices that incorporate these chromogenic indicator reagents address only a few of the many challenges associated with these kits. This is especially true for samples where the drug of interest is present as a lacing agent. This work describes the development of a centrifugal microfluidic device capable of integrating facile sample preparation, by way of a 3D printed snap-on cartridge amenable to microwave assisted extraction, followed by chromatographic separation and chromogenic detection on-disc. As cannabis is among the most widely used controlled substance worldwide, and displays strong interference with these indicator reagents, mock samples of laced marijuana are used for a proof-of-concept demonstration. Post extraction, the microdevice completes high throughput metering just prior to simultaneous reaction with four of the most commonly employed microchemical tests, followed by objective image analysis in CIELAB (a device-independent color model). Separation and recovery of a representative controlled substance with 93% efficiency is achieved. Correct identification, according to hierarchical cluster analysis, of three illicit drugs (e.g., heroin, phencyclidine, and cocaine) in artificially laced samples is also demonstrated on-disc. The cost effective microdevice is capable of complete automation post-extraction, with a total analysis time (including extraction) of <8 min. Finally, sample consumption is minimized, thereby preventing the complete destruction of forensic evidence. [ABSTRACT FROM AUTHOR]

Endothelial cells (ECs) line the inner walls of blood vessels, respond to shear stress by elongating in the direction of flow. Engineering aligned ECs in vitro is essential for modeling human vascular diseases and for drug testing. Current microfluidic approaches mainly rely on unidirectional laminar flow, uniform coating of surfaces to improve cellular adhesion or alteration of the surface topography. Challenges persist due to shear stress‐induced changes in cellular behavior, especially in complex multicellular environments and the time needed for the cells to align and polarize inside the microfluidic conduits. Generally, protein coating processes and physical treatments are also not compatible with the steps required for the assembly of microfluidic devices. This approach employs aerosol jet printing (AJP) to precisely pattern poly(3,4‐ethylenedioxythiophene) polystyrene sulphonate (PEDOT:PSS) within microfluidic chambers in a single step. It is shown that the PEDOT:PSS is biocompatible and facilitates EC adhesion, patterning, elongation, and alignment. Under capillary flow, the cells retain their pattern‐induced morphology over 7 d, confirming the efficacy of the approach in promoting cellular organization, eliminating the need for external pumps. Furthermore, it is demonstrated that the PEDOT:PSS pattern retains structural integrity and electrical stability following oxygen plasma treatment, required for assembling of fully enclosed microfluidic devices. [ABSTRACT FROM AUTHOR]

Three‐dimensional Printing (3DP) and computer‐assisted design (CAD) are a boon for producing high‐quality analytical and electrochemical devices using low‐cost components. This review briefly explains various 3D printing techniques. The focus is on the fabrication of integrated miniature devices developed through the 3DP process, mainly by the Fused deposition modelling (FDM) technique. Examples of integrated electrochemical devices are presented to highlight the potential of 3DP. Special emphasis is given to surface activation of 3D printed electrodes to enhance their electrochemical activity and various activation methods. This paper discusses the opportunities and future applications in developing all‐in‐one miniature electrochemical devices that might lead to on‐site environmental measurements, point‐of‐care tests, and the development of portable instruments with reduced sample volume. [ABSTRACT FROM AUTHOR]

The synergy of integrating semiconductors and MOF photocatalysts is the chief motive for this review paper. This merit has been combined with the microfluidic platforms, which are the cutting‐edge technology of synthesis. The microfluidic synthesis of semiconductors and MOF photocatalysts are categorized according to morphology and linker, respectively. Enhancing the effectiveness of photocatalysis comes along with adding a proper amount of electron acceptor or hole scavenger, combing electrochemical with photocatalytic degradation, and optimizing the photocatalyst band gap. Moreover, approaches for improving photocatalytic activity of MOFs can be classified as functionalization of organic linkers/metal centers, sensitization, incorporation of nanoparticles, and hybridization with semiconductors. Finally, the current applications of microfluidic devices, from the detection of water quality parameters to the elimination of water contaminants, have been addressed. [ABSTRACT FROM AUTHOR]

This paper presents a novel centrifugal microfluidic approach (so-called lab-on-a-CD) for magnetic circulating tumor cell (CTC) separation from the other healthy cells according to their physical and acquired chemical properties. This study enhances the efficiency of CTC isolation, crucial for cancer diagnosis, prognosis, and therapy. CTCs are cells that break away from primary tumors and travel through the bloodstream; however, isolating CTCs from blood cells is difficult due to their low numbers and diverse characteristics. The proposed microfluidic device consists of two sections: a passive section that uses inertial force and bifurcation law to sort CTCs into different streamlines based on size and shape and an active section that uses magnetic forces along with Dean drag, inertial, and centrifugal forces to capture magnetized CTCs at the downstream of the microchannel. The authors designed, simulated, fabricated, and tested the device with cultured cancer cells and human cells. We also proposed a cost-effective method to mitigate the surface roughness and smooth surfaces created by micromachines and a unique pulsatile technique for flow control to improve separation efficiency. The possibility of a device with fewer layers to improve the leaks and alignment concerns was also demonstrated. The fabricated device could quickly handle a large volume of samples and achieve a high separation efficiency (93%) of CTCs at an optimal angular velocity. The paper shows the feasibility and potential of the proposed centrifugal microfluidic approach to satisfy the pumping, cell sorting, and separating functions for CTC separation. [ABSTRACT FROM AUTHOR]

Vascular diseases are widespread, and sometimes such life-threatening medical disorders cause abnormal blood flow, blood particle damage, changes to flow dynamics, restricted blood flow, and other adverse effects. The study of vascular flow is crucial in clinical practice because it can shed light on the causes of stenosis, aneurysm, blood cancer, and many other such diseases, and guide the development of novel treatments and interventions. Microfluidics and computational fluid dynamics (CFDs) are two of the most promising new tools for investigating these phenomena. When compared to conventional experimental methods, microfluidics offers many benefits, including lower costs, smaller sample quantities, and increased control over fluid flow and parameters. In this paper, we address the strengths and weaknesses of computational and experimental approaches utilizing microfluidic devices to investigate the rheological properties of blood, the forces of action causing diseases related to cardiology, provide an overview of the models and methodologies of experiments, and the fabrication of devices utilized in these types of research, and portray the results achieved and their applications. We also discuss how these results can inform clinical practice and where future research should go. Overall, it provides insights into why a combination of both CFDs, and experimental methods can give even more detailed information on disease mechanisms recreated on a microfluidic platform, replicating the original biological system and aiding in developing the device or chip itself. [ABSTRACT FROM AUTHOR]

The microfluidic measurement of capillary flow can be used to evaluate the response of biological samples to stimulation, where distance and velocity are altered. Melt-extruded multi-bored microfluidic capillaries allow for high-throughput testing with low device cost, but simple devices may limit control over sample flow when compared to the more complex "lab-on-a-chip" devices produced using advanced microfluidic fabrication methods. Previously, we measured the dynamics of global haemostasis stimulated by thrombin by dipping straight vertical microcapillaries into blood, but only the most rapid response could be monitored, as flow slowed significantly within 30 s. Here, we show an innovative method to extend both the stimulation process and flow measurement time without increasing the cost of the device by adding simple loops to the flexible extruded device. The loops enable longer time-scale measurements by increasing resistance to flow, thereby reducing the dependence on high stimulus concentrations for rapid reactions. The instantaneous velocity and equilibrium heights of straight and looped vertical microcapillary films were assessed with water, plasma and whole blood, showing that the loops create additional frictional resistances, reduce flow velocity and prolong residence times for increased time scales of the stimulation process. A modified pressure balance model was used to capture flow dynamics with the added loop. Looped devices loaded with thrombin and collagen showed an improved detection of blood stimulation responses even with lower stimulus concentrations, compared to straight vertical capillaries. Thrombin-activated blood samples in straight capillaries provided a maximum measurement zone of only 4 mm, while the looped design significantly increased this to 11 mm for much longer time scale measurements. Our results suggest that extending stimulation times can be achieved without complex microfluidic fabrication methods, potentially improving concentration–response blood stimulation assays, and may enhance the accuracy and reliability. We conclude adding a loop to low-cost extruded microfluidic devices may bring microfluidic devices closer to delivering on their promise of widespread, decentralized low-cost evaluation of blood response to stimulation in both research and clinical settings. [ABSTRACT FROM AUTHOR]

In microfluidic reactors designed for the synthesis of nanomaterials, hydrodynamics and mixing performance play a crucial role in the characteristics of the synthesized nanoparticles. In the current study, CFD simulation is utilized to shed light on flow characteristics inside a spiral microfluidic device and the way it affects the mixing during ZnO synthesis. Before microfabrication, the optimal number of spiral loops and flow rate in the microfluidic reactor was determined through mixing index calculation according to the CFD results in terms of the concentration distribution. Furthermore, this synthesis method is compared with batch nanoparticle fabrication techniques. In the microfluidic system, the concentrations of precursors were 50 times more diluted rather than batch methods. The droplet-based microfluidic ZnO synthesis was eight-fold faster than batch synthesis. The ZnO nanoparticles were characterized by XRD, SEM, and FTIR techniques. The outcomes of the FTIR analysis demonstrated that both the batch and microfluidic samples exhibit identical vibrational peaks. The experiments showed that the microfluidic system is reliable for controlling size. Besides, the CFD results indicated that a spiral micromixer with five loops provides sufficient mixing. The acquired findings from the characterization analyses can lead us toward a clue that once the ZnCl 2 /NaOH concentration ratio is greater than unity, a narrower size distribution of ZnO particles is probable. Consequently, the microfluidic reactor can be an efficient method for nanomaterial construction owing to the minimization of energy consumption and independence of the operational synthesis temperature. [ABSTRACT FROM AUTHOR]

Understanding the propulsion of a swimmer in a large group of individuals holds the key to unravelling the intriguing dynamics of active matter collective motion. Here, we develop a two-dimensional (2-D) self-assembled rotor, powered by bacterial flagella. At a water–air interface, the average direction of rotation of a rotor is fixed. When the chiral rotor is put into a 2-D bacterial suspension, we examine the average and fluctuation of the angular velocity of the rotor. Remarkably, the average angular velocity of a rotor is found to increase up to 3 times when the density of surrounding bacterial suspension increases and the increase is nonlinear. In a dense suspension of bacteria, the existence of a rotor disrupts vortices in the surrounding active turbulence, and the acceleration of the rotor is independent of the activity level of the surrounding free bacteria. The nonlinear acceleration thus results from hydrodynamic interaction with surrounding crowdedness that can be quantitatively explained by hydrodynamic simulation. The simultaneity between the acceleration of rotor and free bacteria in active turbulence suggests that crowding-induced acceleration may promote the onset of instability. The result will inspire new active-matter-based microfluidic devices with improved transport properties. [ABSTRACT FROM AUTHOR]

Stereolithography enables the fabrication of three-dimensional (3D) freeform structures via light-induced polymerization. However, the accumulation of ultraviolet dose within resin trapped in negative spaces, such as microfluidic channels or voids, can result in the unintended closing, referred to as overcuring, of these negative spaces. We report the use of injection continuous liquid interface production to continuously displace resin at risk of overcuring in negative spaces created in previous layers with fresh resin to mitigate the loss of Z-axis resolution. We demonstrate the ability to resolve 50-µm microchannels, breaking the historical relationship between resin properties and negative space resolution. With this approach, we fabricated proof-of-concept 3D free-form microfluidic devices with improved design freedom over device material selection and resulting properties. [ABSTRACT FROM AUTHOR]

Increasing evidences demonstrate the role of sensory innervation in bone metabolism, remodeling and repair, however neurovascular coupling in bone is rarely studied. Using microfluidic devices as an indirect co-culture model to mimic in vitro the physiological scenario of innervation, our group demonstrated that sensory neurons (SNs) were able to regulate the extracellular matrix remodeling by endothelial cells (ECs), in particular through sensory neuropeptides, i.e. calcitonin gene-related peptide (CGRP) and substance P (SP). Nonetheless, still little is known about the cell signaling pathways and mechanism of action in neurovascular coupling. Here, in order to characterize the communication between SNs and ECs at molecular level, we evaluated the effect of SNs and the neuropeptides CGRP and SP on ECs. We focused on different pathways known to play a role on endothelial functions: calcium signaling, p38 and Erk1/2; the control of signal propagation through Cx43; and endothelial functions through the production of nitric oxide (NO). The effect of SNs was evaluated on ECs Ca2+ influx, the expression of Cx43, endothelial nitric oxide synthase (eNOS) and nitric oxide (NO) production, p38, ERK1/2 as well as their phosphorylated forms. In addition, the role of CGRP and SP were either analyzed using respective antagonists in the co-culture model, or by adding directly on the ECs monocultures. We show that capsaicin-stimulated SNs induce increased Ca2+ influx in ECs. SNs stimulate the increase of NO production in ECs, probably involving a decrease in the inhibitory eNOS T495 phosphorylation site. The neuropeptide CGRP, produced by SNs, seems to be one of the mediators of this effect in ECs since NO production is decreased in the presence of CGRP antagonist in the co-culture of ECs and SNs, and increased when ECs are stimulated with synthetic CGRP. Taken together, our results suggest that SNs play an important role in the control of the endothelial cell functions through CGRP production and NO signaling pathway. [ABSTRACT FROM AUTHOR]

Microfluidic devices with open lattice structures, equivalent to a type of porous media, allow for the manipulation of fluid transport processes while having distinct structural, mechanical, and thermal properties. However, a fundamental understanding of the design principles for the solid structure in order to achieve consistent and desired flow patterns remains a challenge, preventing its further development and wider applications. Here, through quantitative and mechanistic analyses of the behavior of multi-phase phenomena that involve gas–liquid–solid interfaces, we present a design framework for microfluidic devices containing porous architectures (referred to as poroFluidics) for deterministic control of multi-phase fluid transport processes. We show that the essential properties of the fluids and solid, including viscosity, interfacial tension, wettability, as well as solid manufacture resolution, can be incorporated into the design to achieve consistent flow in porous media, where the desired spatial and temporal fluid invasion sequence can be realized. Experiments and numerical simulations reveal that different preferential flow pathways can be controlled by solid geometry, flow conditions, or fluid/solid properties. Our design framework enables precise, multifunctional, and dynamic control of multi-phase transport within engineered porous media. [ABSTRACT FROM AUTHOR]

The paper-based culture platform developed by Whitesides readily incorporates tissue-like structures into laboratories with established workflows that rely on monolayer cultures. Cell-laden hydrogels are deposited in these porous scaffolds with micropipettes; these scaffolds support the thin gel slabs, allowing them to be evaluated individually or stacked into thick constructs. The paper-based culture platform has inspired many basic and translational studies, each exploring how readily accessible materials can generate complex structures that mimic aspects of tissues in vivo. Many of these examples have relied on static culture conditions, which result in diffusion-limited environments and cells experiencing pericellular hypoxia. Perfusion-based systems can alleviate pericellular hypoxia and other cell stresses by continually exposing the cells to fresh medium. These perfusion systems are common in microfluidic and organ-on-chip devices supporting cells as monolayer cultures or as 3D constructs. Here, we introduce a continuous flow delivery system, which uses parts readily produced with 3D printing to provide a self-contained culture platform in which cells in paper or other scaffolds are exposed to fresh (flowing) medium. We demonstrate the utility of this device with examples of cells maintained in single cell-laden scaffolds, stacks of cell-laden scaffolds, and scaffolds that contain monolayers of endothelial cells. These demonstrations highlight some possible experimental questions that can be enabled with readily accessible culture materials and a perfusion-based device that can be readily fabricated. [ABSTRACT FROM AUTHOR]

Electrochemical sensors provide an affordable and reliable approach towards the detection and monitoring of important biological species ranging from simple ions to complex biomolecules. The ability to miniaturize electrochemical sensors, coupled with their affordability and simple equipment requirements for signal readout, permits the use of these sensors at the point-of-care where analysis using non-invasively obtainable biofluids is receiving growing interest by the research community. This paper describes the design, fabrication, and integration of a 3D printed Mg2+ potentiometric sensor into a 3D printed microfluidic device for the quantification of Mg2+ in low-sample volume biological fluids. The sensor employs a functionalized 3D printable photocurable methacrylate-based ion-selective membrane affixed to a carbon-mesh/epoxy solid-contact transducer for the selective determination of Mg2+ in sweat, saliva and urine. The 3D printed Mg2+ ion-selective electrode (3Dp-Mg2+-ISE) provided a Nernstian response of 27.5 mV per decade with a linear range of 10 mM to 39 μM, covering the normal physiological and clinically relevant levels of Mg2+ in biofluids. 3Dp-Mg2+-ISEs selectively measure Mg2+ over other biologically present cations – sodium, potassium, calcium, ammonium – as well as provide high stability in the analytical signal with a drift of just 13 μV h−1 over 10 hours. Comparison with poly(vinylchloride)-based Mg2+-ISEs showed distinct advantages to the use of 3Dp-Mg2+-ISEs, with respect to stability, resilience towards biofouling and importantly providing a streamlined and rapid approach towards mass production of selective and reliable sensors. The miniaturization capabilities of 3D printing coupled with the benefits of microfluidic analysis (i.e., low sample volumes, minimal reagent consumption, automation of multiple assays, etc.), provides exciting opportunities for the realization of the next-generation of point-of-care diagnostic devices. [ABSTRACT FROM AUTHOR]

Polyploid giant cancer cells (PGCCs) contribute to the genetic heterogeneity and evolutionary dynamics of tumors. Their size, however, complicates their isolation from mainstream tumor cell populations. Standard techniques like fluorescence-activated cell sorting (FACS) rely on fluorescent labeling, introducing potential challenges in subsequent PGCC analyses. In response, we developed the Isosceles Trapezoidal Spiral Microchannel (ITSμC), a microfluidic device optimizing the Dean drag force (FD) and exploiting uniform vortices for enhanced separation. Numerical simulations highlighted ITSμC's advantage in producing robust FD compared to rectangular and standard trapezoidal channels. Empirical results confirmed its ability to segregate larger polystyrene (PS) particles (avg. diameter: 50 μm) toward the inner wall, while directing smaller ones (avg. diameter: 23 μm) outward. Utilizing ITSμC, we efficiently isolated PGCCs from doxorubicin-resistant triple-negative breast cancer (DOXR-TNBC) and patient-derived cancer (PDC) cells, achieving outstanding purity, yield, and viability rates (all greater than 90%). This precision was accomplished without fluorescent markers, and the versatility of ITSμC suggests its potential in differentiating a wide range of heterogeneous cell populations. [ABSTRACT FROM AUTHOR]

Microfluidic chips hold vast potential for applications in fields such as DNA analysis, drug screening, cell culture and biosensing. However, microfluidic chips are susceptible to disruption and damage from bubbles. Current bubble removal methods suffer from limitations including narrow applicability, poor biocompatibility, limited bubble containment volume, low degassing rates, manufacturing complexity and integration challenges. Addressing these issues, this study presents the development of a bubble filtration microfluidic chip inspired by the stomatal pore structure in plant leaves, which prevents air propagation between conduits. Surface wettability theory and surface tension principles were utilized to investigate the mechanism of bubble filtration by plant stomatal pores. A cellulose/PVA hydrogel was introduced to enable the microfluidic chip to effectively filter bubbles. The design and in situ formation method of the bubble filtration chip were developed, and the chip was fabricated using micro-nanofabrication processes. Performance evaluation of the bubble filtration microfluidic chip demonstrated that with a gel film thickness of 20 μm, the microfluidic chip exhibits high gas leak threshold and minimal flow loss. The resulting biomimetic bubble filtration microfluidic chip features a simple structure, compact size, and independence from auxiliary equipment, making it suitable for portable microfluidic devices. [ABSTRACT FROM AUTHOR]

Open microfluidic systems offer significant advantages, including the elimination of external pumps and facilitating fluid access at any point along the channel. However, their deployment in harsh environments is commonly compromised due to the delicate nature of hydrophilic chemical coatings and the vulnerability of open microchannels to clogging and contamination. Here, a bioinspired, demand-responsive mode-switchable strategy is proposed to enhance the mechanical durability of open microfluidic systems. Specifically, under harsh conditions or when long-term storage is necessary, this strategy allows the open microfluidic device to transition to a protective mode simply through releasing the strain, thereby preserving the integrity of the structure and hydrophilic coatings. The stretched open microfluidic mode enables spontaneous liquid spreading along a hydrophilic microchannel scribed by femtosecond laser. This mode-switchable strategy provides the open microfluidic device with robustness to maintain spontaneous liquid flow, even under severe testing conditions such as 2000 cycles of cotton swab rubbing, sand impact, sandpaper abrasion, tape peeling, twisting, and finger rubbing. A proof-of-concept application involving blood type analysis on this mode-switchable open microfluidic device showcases its superior mechanical durability under severe environmental conditions. The proposed strategy paves the way for the broader use of open microfluidic devices in various practical applications. [ABSTRACT FROM AUTHOR]

Compartmentalization is a vital aspect of living cells to orchestrate intracellular processes. In a similar vein, constructing dynamic and responsive sub-compartments is key to synthetic cell engineering. In recent years, liquid-liquid phase separation via coacervation has offered an innovative avenue for creating membraneless organelles (MOs) within artificial cells. Here, we present a lab-on-a-chip system to reversibly trigger peptide-based coacervates within cell-mimicking confinements. We use double emulsion droplets (DEs) as our synthetic cell containers while pH-responsive elastin-like polypeptides (ELPs) act as the coacervate system. We first present a high-throughput microfluidic DE production enabling efficient encapsulation of the ELPs. The DEs are then harvested to perform multiple MO formation-dissolution cycles using pH as well as temperature variation. For controlled long-term visualization and modulation of the external environment, we developed an integrated microfluidic device for trapping and environmental stimulation of DEs, with negligible mechanical force, and demonstrated a proof-of-principle osmolyte-based triggering to induce multiple MO formation-dissolution cycles. In conclusion, our work showcases the use of DEs and ELPs in designing membraneless reversible compartmentalization within synthetic cells via physicochemical triggers. Additionally, presented on-chip platform can be applied over a wide range of phase separation and vesicle systems for applications in synthetic cells and beyond. Compartmentalization within living cells is vital to orchestrate intracellular processes, but effective compartmentalization and organization within synthetic cells remains a key challenge. Here, the authors report a lab-on-a-chip system to reversibly trigger the formation of peptide-based coacervates as membraneless organelles via pH/temperature/osmolyte variations within cell-mimicking confinements. [ABSTRACT FROM AUTHOR]

Inertial microfluidic devices have gained attention for point-of-need (PoN) sample preparation. Yet, devices capable of simultaneous particle-bacteria solution exchange and separation are low in throughput, hindering their applicability to PoN settings. This paper introduces a microfluidic centrifuge for high-throughput solution exchange and separation of microparticles, addressing the need for processing large sample volumes at elevated flow rates. The device integrates Dean flow recirculation and inertial focusing of microparticles within 24 curved microchannels assembled in a three-layer configuration via in-plane and out-of-plane parallelization. We studied solution exchange and particle migration using singleplex and duplex samples across devices with varying curve numbers (2-curve, 8-curve, and 24-curve). Processing 5 and 10 μm microparticles at flow rates up to 16.8 ml/min achieved a solution exchange efficiency of 96.69%. In singleplex solutions, 10 and 5 μm particles selectively migrated to inner and outer outlets, demonstrating separation efficiencies of 99.7% and 90.3%, respectively. With duplex samples, sample purity was measured to be 93.4% and 98.6% for 10 and 5 μm particles collected from the inner and the outer outlets, respectively. Application of our device in biological assays was shown by performing duplex experiments where 10 μm particles were isolated from Salmonella bacterial suspension with purity of 97.8% while increasing the state-of-the-art particle solution exchange and separation throughput by 16 folds. This parallelization enabled desirable combinations of high throughput, low-cost, and scalability, without compromising efficiency and purity, paving the way for sample preparation at the PoN in the future. [ABSTRACT FROM AUTHOR]

Textile-based microfluidic biosensors represent an innovative fusion of various multidisciplinary fields, including bioelectronics, material sciences, and microfluidics. Their potential in biomedicine is significant as they leverage textiles to achieve high demands of biocompatibility with the human body and conform to the irregular surfaces of the body. In the field of microfluidics, fabric coated with hydrophobic materials serves as channels through which liquids are transferred in precise amounts to the sensing element, which in this case is a biosensor. This paper presents a condensed overview of the current developments in textile-based microfluidics and biosensors in biomedical applications over the past 20 years (2005–2024). A literature search was performed using the Scopus database. The fabrication techniques and materials used are discussed in this paper, as these will be key in various modifications and advancements in textile-based microfluidics. Furthermore, we also address the gaps in the application of textile-based microfluidic analytical devices in biomedicine and discuss the potential solutions. Advances in textile-based microfluidics are enabled by various printing and fabric manufacturing techniques, such as screen printing, embroidery, and weaving. Integration of these devices into everyday clothing holds promise for future vital sign monitoring, such as glucose, albumin, lactate, and ion levels, as well as early detection of hereditary diseases through gene detection. Although most testing currently takes place in a laboratory or controlled environment, this field is rapidly evolving and pushing the boundaries of biomedicine, improving the quality of human life. [ABSTRACT FROM AUTHOR]

Filamentous fungi and fungal-like organisms contribute to a wide range of important ecosystem functions. Evidence has shown the movement of liquid across mycelial networks in unsaturated environments, such as soil. However, tools to investigate liquid movement along hyphae at the level of the single cell are still lacking. Microfluidic devices permit the study of fungal and fungal-like organisms with cellular resolution as they can confine hyphae to a single optical plane, which is compatible with microscopy imaging over longer timescales and allows for precise control of the microchannel environment. The aim of this study was to develop a method that enables the visualization and quantification of liquid movement on hyphae of fungal and fungal-like microorganisms. For this, the fungal–fungal interaction microfluidic device was modified to allow for the maintenance of unsaturated microchannel conditions. Fluorescein-containing growth medium solidified with agar was used to track liquid transported by hyphae via fluorescence microscopy. Our key findings highlight the suitability of this novel methodology for the visualization of liquid movement by hyphae over varying time scales and the ability to quantify the movement of liquid along hyphae. Furthermore, we showed that at the cellular level, extracellular movement of liquid along hyphae can be bidirectional and highly dynamic, uncovering a possible link between liquid movement and hyphal growth characteristics. We envisage that this method can be applied to facilitate future research probing the parameters contributing to hyphal liquid movement and is an essential step for studying the phenomenon of fungal highways. [ABSTRACT FROM AUTHOR]

The incorporation of engineered muscle‐tendon junction (MTJ) with organ‐on‐a‐chip technology provides promising in vitro models for the understanding of cell‐cell interaction at the interface between muscle and tendon tissues. However, developing engineered MTJ tissue with biomimetic anatomical interface structure remains challenging, and the precise co‐culture of engineered interface tissue is further regarded as a remarkable obstacle. Herein, an interwoven waving approach is presented to develop engineered MTJ tissue with a biomimetic "M‐type" interface structure, and further integrated into a precise co‐culture microfluidic device for functional MTJ‐on‐a‐chip fabrication. These multiscale MTJ scaffolds based on electrospun nanofiber yarns enabled 3D cellular alignment and differentiation, and the "M‐type" structure led to cellular organization and interaction at the interface zone. Crucially, a compartmentalized co‐culture system is integrated into an MTJ‐on‐a‐chip device for the precise co‐culture of muscle and tendon zones using their medium at the same time. Such an MTJ‐on‐a‐chip device is further served for drug‐associated MTJ toxic or protective efficacy investigations. These results highlight that these interwoven nanofibrous scaffolds with biomimetic "M‐type" interface are beneficial for engineered MTJ tissue development, and MTJ‐on‐a‐chip with precise co‐culture system indicated their promising potential as in vitro musculoskeletal models for drug development and biological mechanism studies. [ABSTRACT FROM AUTHOR]

The Organ-on-a-Chip is a microfluidic device designed to replicate human organ and tissue conditions. Temperature regulation is crucial for mimicking physiological processes and ensuring cellular viability in Organ-on-a-Chip platforms. This article focuses on employing system identification to mathematically model thermal regulation in a new Organ-on-a-Chip. A controlled environment box was constructed for testing, using infrared and negative temperature coeficient sensors for intrim temperature analysis. Data collected from the cell culture chamber were processed and analyzed in MATLAB®. System identification led to the selection of a transfer function, and a descriptive equation for Organ-on-a-Chip temperature was obtained. The study revealed temperature differences between ambient and culture chamber temperatures, emphasizing the importance of real-time analysis. Mathematical modeling and in silico tests play a crucial role in predicting physiological behavior, allowing complex interactions to be simulated. The obtained temperature equation can be refined and applied in various 3D models. indicating innovation in the integration of Organ-on-a-Chip in medicine and biomedical engineering. [ABSTRACT FROM AUTHOR]

Infectious diseases caused by bacteria, viruses, fungi, and parasites pose a significant societal challenge. In response, scientists are developing advanced technology to enhance the prevention, diagnosis, and treatment of such diseases. One such promising technology is microfluidic systems, which are utilized in organ‐on‐a‐chip systems to replicate the microenvironments of organs. These systems have potential applications in drug screening, disease modeling, and personalized medicine. This review provides an overview of recent advances in organ‐on‐a‐chip platforms and their potential for preventing and diagnosing various infections. After discussing traditional techniques employed in studying infectious diseases, the role of microfluidic platforms in detecting infections is delved in. It is expound on advanced microfluidic‐based strategies for infection diagnosis, such as the polymerase chain reaction‐based microfluidic devices, enzyme linked immunosorbent assay‐based microfluidic devices, hierarchical nanofluidic molecular enrichment systemand µWestern blotting‐based microfluidic devices, and smartphone‐based microfluidic devices. Additionally, future research challenges and perspectives are discussed on microfluidic systems in biomedical and regenerative medicine applications. Consequently, microfluidic platforms have the potential to serve as fundamental frameworks for understanding infectious diseases, thereby leading to personalized regenerative medicine. hierarchical nanofluidic molecular enrichment system [ABSTRACT FROM AUTHOR]

The study of heat and mass transfer in a Hele-Shaw cell rotating around a perpendicular axis has various advanced technological applications. These include the design of microfluidic devices and continuous-flow chemical microreactors, to name a couple. In this setup configuration, the quasi-two-dimensional design allows for recording the density field using optical methods, and the rotation enables control of this field through spatially distributed inertial forces. As is known, in the limit of an infinitely thin layer, the Coriolis force vanishes within a standard mathematical model. However, experimental observations of fluid flow in a rotating Hele-Shaw cell indicate the opposite. In this paper, we show that the correct derivation of the equation of motion under the Hele-Shaw approximation leads to the appearance of a Boussinesq-type term for the Coriolis force. To study the effect of the Coriolis buoyancy, we consider the problem of fluid stability during the internal generation of a transfer component, which can be either the concentration of the dissolved substance or the temperature of the medium. The careful study of system dynamics involves linear stability analysis, weakly nonlinear analysis, and direct numerical simulation. The general properties of the disturbance spectrum are analyzed. The branching of solutions near the first bifurcation is studied using the technique of multiple time scales. A stationary convection is replaced by an oscillatory one under the action of the Coriolis force, as demonstrated by weakly nonlinear analysis. Finally, we investigate the nonlinear dynamics using direct numerical simulation. [ABSTRACT FROM AUTHOR]

This study introduces the first experimental analysis of shear cavitation in a microscale backward-facing step (BFS) configuration. It explores shear layer cavitation under various flow conditions in a microfluidic device with a depth of 60 μm and a step height of 400 μm. The BFS configuration, with its unique characteristics of upstream turbulence and post-reattachment pressure recovery, provides a controlled environment for studying shear-induced cavitation without the complexities of other microfluidic geometries. Experiments were conducted across four flow patterns: inception, developing, shedding, and intense shedding, by varying upstream pressure and the Reynolds number. The study highlights key differences between microscale and macroscale shear cavitation, such as the dominant role of surface forces on nuclei distribution, vapor formation, and distinct timescales for phenomena like shedding and shockwave propagation. It is hypothesized that vortex strength in the shear layer plays a significant role in cavity shedding during upstream shockwave propagation. Results indicate that increased pressure notably elevates the mean thickness, length, and intensity within the shear layer. Instantaneous data analysis identified two vortex modes (shedding and wake modes) at the reattachment zone, which significantly affect cavitation shedding frequency and downstream penetration. The wake mode, characterized by stronger and lower-frequency vortices, transports cavities deeper into the channel compared to the shedding mode. Additionally, vortex strength, proportional to the Reynolds number, affects condensation caused by shockwaves. The study confirms that nuclei concentration peaks in the latter half of the shear layer during cavitation inception, aligning with the peak void fraction region. [ABSTRACT FROM AUTHOR]

The present study focuses on the unsteady flow of a viscoelastic Maxwell nanofluid with couple stress in a circular microchannel under the combined action of periodic pressure and magnetic field. The Green's function method is applied to the unsteady Cauchy momentum equation to derive the velocity field. We strive to check out the analytical solutions of the current model by validating them with existing results. In addition, the effects of several dimensionless parameters (such as the couple stress parameter γ, the Deborah number De, and the dimensionless frequency ω) on the streaming potential and the electrokinetic energy conversion (EKEC) efficiency of the three waveforms (cosine, square, and triangular) are portrayed via graphical illustrations. Within the range of parameters chosen in this study, the results demonstrate that increasing the value of the Deborah number or decreasing the dimensionless frequency can effectively enhance the streaming potential. The velocity field and EKEC efficiency are improved with increasing couple stress parameters. Furthermore, our investigation is extended to compare the EKEC efficiency for square and triangular waveforms when the couple stress parameters are set to 20 and 40, respectively. The results also indicate that increasing the couple stress parameter significantly improves the EKEC efficiency, particularly in the context of the square waveform. These findings will provide valuable assistance in the design of periodic pressure-driven microfluidic devices. [ABSTRACT FROM AUTHOR]

In this study, a novel approach for enhancing the rapid spreading of free liquid film on lithium niobate (LiNbO3) substrate under megahertz (MHz) surface acoustic wave (SAW) excitation is presented by treating it with surfactants. Through the design of a specific interdigital transducer structure, it was discovered that exciting the SAW at a frequency of 32.3 MHz can achieve optimal spreading performance for water droplets on the surface of surfactant-treated LiNbO3 substrate. The maximum average velocity reaches 1.76 mm/s at position P2 = 1250 μm in the water film front, and the stable film spreading speed shows a 204.9% increase compared to the existing research. Simultaneously, through the investigation of the spreading experiment phenomenon of silicone oil and de-ionized water droplets at varying frequencies, we have discovered the dynamic mechanism of "reverse phase" propagation in liquid film for the first time. This entails that the advancing edge of the wetting film demonstrates a spreading motion law that is opposite to the traditional spreading phenomena, with the spreading velocity in the central exceeding that on both sides. Our research demonstrates that this microfluidic device developed by SAWs enhances the spreading efficiency of the free films, enabling rapid expansion of the target liquid to form a high-surface area film layer. This advancement holds promise for overcoming the limitations of low sensitivity and short response time in the field of rapid pathological diagnosis in contemporary medicine. [ABSTRACT FROM AUTHOR]

This study provides a critical understanding of controlling solute distribution in microfluidic systems by examining the effects of symmetric and asymmetric zeta potentials under magnetohydrodynamic (MHD) pulsatile electroosmotic flow. These findings are vital for enhancing the efficiency of microfluidic devices used in lab-on-a-chip applications. The aim of this study is to explore the modulation of solute transport in MHD pulsatile electroosmotic microchannel flow, focusing on both symmetric and asymmetric wall zeta potentials. Using the Debye–Hückel approximation, the Poisson–Boltzmann equation is obtained. Subsequently, the convection–diffusion equation is solved using the velocity profile, with Aris's method of moments to derive the moment equations. These equations are then solved using a finite difference scheme. The mean concentration is calculated employing Hermite polynomials. We examined the effects of key parameters such as the electroosmotic parameter (κ), the Hartmann number (Ha), and zeta potentials on the dispersion coefficient (DT), mean concentration distribution (Cm), skewness, and kurtosis. We consider three situations: symmetric ( ζ 1 = ζ 2 ), partially asymmetric ( ζ 1 = 1.0 , ζ 2 = 0.0), and fully asymmetric ( ζ 1 = 1.0 , ζ 2 = − 1.0) zeta potentials. Our results reveal that asymmetric zeta potentials lead to faster dispersion, with DT decreasing with increasing κ for symmetric potentials and increasing for asymmetric ones. As the Hartmann number increases, dispersion decreases for both symmetric and asymmetric zeta potentials while the peak of mean concentration rises. The mean concentration profile exhibits Gaussian behavior at both small and large times, with anomalous behavior in the intermediate region. For symmetric zeta potentials, Gaussianity is observed at t = 0.001 in the diffusive regime and at t = 10.0 in Taylor's regime, while for asymmetric potentials, Gaussianity occurs at t = 0.03 and t = 3.0, indicating that large-time Gaussian behavior is approximately 3.33 times faster and dispersion becomes transient for asymmetric potentials. [ABSTRACT FROM AUTHOR]

A theoretical and numerical investigation of electrokinetic flow is performed in a nanochannel with the charged symmetric corrugated surfaces. The perturbation and numerical solutions of electrokinetic flow variables are given, and the effects of corrugation geometry, such as wave amplitude and wave number, on the electrokinetic flow characteristics are systematically examined. The results show that the electrokinetic flow recirculation may occur easily at wave crest due to the electroviscous effect. The velocity profile is strongly dependent on wave number, but the maximum or minimum velocity may be insusceptible to wave number. Furthermore, the distributions of streaming potential and energy conversion efficiency are also investigated. We find that, for some special geometry of corrugations, the streaming current and conversion efficiency obtained from the present corrugated nanochannel are higher than that from the smooth nanochannel. Specially, when the dimensionless wave number is 0.5/π, the magnitude of streaming potential is enhanced about 29% at δ = 0.5 and the peak value of conversion efficiency is enhanced about 2% at δ = 0.1. We believe that the optimal corrugation geometry parameters can be of benefit in designing a microfluidic device with higher streaming current and conversion efficiency. [ABSTRACT FROM AUTHOR]

In this article, the role of slip-dependent (SD) zeta potential in the hydrodynamic characteristics of mixed electromagnetohydrodynamic (EMHD) and electroosmotic driven flow of couple stress fluid within a rotating microfluidic channel is theoretically investigated. This work is the first to analyze the hydrodynamic characteristics of slip-independent (SI) and slip-dependent (SD) zeta potentials in a rotating microchannel including a detailed analysis of Ekmann spirals in the microchannel. Ekmann spirals show the effect of rotational flow caused by different parameters, particularly, the slip parameter and the Hartmann number being the most significant ones. Ekmann plot variations, observed under both SI and SD model cases, show a significant effect on rotating flow dynamics. The effect of pertinent parameters on the rotational flow velocity, centerline velocity, and volumetric flow rate is graphically depicted. The findings of this research reveal that the SD zeta potential plays a crucial role in determining the rotating flow velocity and volume flow transport. The normalized transverse centerline in the magnitude flow velocity increases with the couple stress parameter and decreases with the slip parameter for both SI and SD model cases. Notably, the magnitude of the normalized transverse flow rate increases with rotational parameter values. In contrast, it decreases with an increase in the slip parameter under the SD model case. The outcomes of this study can be directly used in applications like transportation of biofluid models in Lab-On-a-Chip (LOC) devices and microfluidic systems under certain conditions. [ABSTRACT FROM AUTHOR]

Glioblastoma multiforme (GBM) is the most severe form of brain cancer in adults, characterized by its complex vascular network that contributes to resistance to conventional therapies. Thermal therapies, such as magnetic hyperthermia (MHT), emerge as promising alternatives, using heat to selectively target tumor cells while minimizing damage to healthy tissues. The organ-on-a-chip can replicate this complex vascular network of GBM, allowing for detailed investigations of heat dissipation in MHT, while computational simulations refine treatment parameters. In this in silico study, tumor-on-a-chip models were used to optimize MHT therapy by comparing heat dissipation in normal and abnormal vascular networks, considering geometries, flow rates, and concentrations of magnetic nanoparticles (MNPs). In the high vascular complexity model, the maximum velocity was 19 times lower than in the normal vasculature model and 4 times lower than in the low-complexity tumor model, highlighting the influence of vascular complexity on velocity and temperature distribution. The MHT simulation showed greater heat intensity in the central region, with a flow rate of 1 µL/min and 0.5 mg/mL of MNPs being the best conditions to achieve the therapeutic temperature. The complex vasculature model had the lowest heat dissipation, reaching 44.15 °C, compared to 42.01 °C in the low-complexity model and 37.80 °C in the normal model. These results show that greater vascular complexity improves heat retention, making it essential to consider this heterogeneity to optimize MHT treatment. Therefore, for an efficient MHT process, it is necessary to simulate ideal blood flow and MNP conditions to ensure heat retention at the tumor site, considering its irregular vascularization and heat dissipation for effective destruction. [ABSTRACT FROM AUTHOR]

Lipid nanoparticles (LNPs) have recently been used as nanocarriers in drug delivery systems for nucleic acid drugs. Their practical applications are currently primarily limited to the liver and specific organs. However, altering the type and composition ratio of phospholipids improves their distribution in organs other than the liver, such as the spleen and lungs. This study aimed to elucidate the effects of LNP components and particle size on in vivo distribution through systemic circulation to pancreatic islets to achieve better targeting of islets, which are a fundamental therapeutic target for diabetes. Fluorescence-labeled LNPs were prepared using three phospholipids: 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC), and 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), with particle sizes of 30–160 nm (diameter) using a microfluidic device. Baffled-structured iLiNP devices with adjusted flow-rate ratios and total flow rates were used. After the intravenous administration of LNPs to C57BL/6 J mice, the distribution of each LNP type to the major organs, including the pancreas and pancreatic islets, was compared using ex vivo fluorescence imaging and observation of pancreatic tissue sections. DSPC-LNPs- and DOPE-LNPs showed the highest distribution in the spleen and liver, respectively. In contrast, the DOPC-LNPs showed the highest distribution in the pancreas and the lowest distribution in the liver and spleen. In addition, smaller particles showed better distribution throughout the pancreas. The most significant LNP distribution in the islets was observed for DOPC-LNPs with a particle size of 160 nm. Furthermore, larger LNPs tended to be distributed in the islets, whereas smaller LNPs tended to be distributed in the exocrine glands. DOPC-LNPs were distributed in the islets at all cholesterol concentrations, with a high distribution observed at >40% cholesterol and > 3% PEG and the distribution was higher at 24 h than at 4 h. Thus, LNP composition and particle size significantly affected islet distribution characteristics, indicating that DOPC-LNPs may be a drug delivery system for effectively targeting the pancreas and islets. [Display omitted] • DOPC-LNP showed higher distribution in the pancreas. • Larger particle size showed higher distribution in islets. • Higher cholesterol content showed higher distribution in islets. • Higher DSG-PEG content showed higher distribution in islets. • Larger PEG-modified DOPC-LNPs are suitable drug delivery carriers to islets. [ABSTRACT FROM AUTHOR]