Microfluidic Channel Research Articles

Rolling Stone Gathers Moss: Rolling Microneedles Generate Meta Microfluidic Microneedles (MMM)

AbstractMicrofluidic chips play crucial roles while lack satisfactory controllability and comprehensive functionality. Inspired by biological systems, this study proposes a method utilizing rolling microneedles (RMNs) to generate muti‐structured templates, realizing photonic crystal membrane (PC) based meta microfluidic microneedle chip (MMM) for efficient wound management. This approach offers advantages in terms of speed and cost‐effectiveness, achieving dual‐sided permeation and patterned design by directly RMNs at desired locations, serving as both template tools for microneedle fabrication. The integration of RMNs with a PC membrane results in the design of 3D multilayer microfluidic channels, effectively addressing issues related to spontaneous fluid flow. As fluid reaches the PC membrane, it generates distinctive structural colors and exhibits fluorescence enhancement, enabling the monitoring of inflammatory factors in mouse wounds and facilitating efficient wound management. In summary, this preparation method involving RMNs paves the way for the design and fluid control of microfluidic chips. This bioinspired patch holds significant potential not only for wound management but also for areas such as clinical drug delivery and point‐of‐care testing (POCT).

Vortex random lasing with tunable wavelength and orbital angular momentum

Random lasing with special structured light field has broad application prospects in various fields. However, the complex spatial modes of random lasing increase the difficulty of light field regulation and limit its practical application. Here, a vortex random lasing with dynamically tunable wavelength and orbital angular momentum is proposed based on the microfluidic channel. Different color random lasers are integrated into the same microfluidic channel for coarse control of the emission wavelengths from 462 to 685 nm by dynamically controlling the liquid flow. A special-shape cavity with a variable size of a gain region is further constructed to finely manipulate the emission wavelengths. Moreover, the vortex random lasing with tunable orbital angular momentum mode from −50 to 50 is realized. The results provide an outstanding strategy for generating the partially coherent vortex beams and may promote the practical applications of random lasers in the fields of sensing, imaging, and communication.

Analysis of sperm cell motion in high viscosity Newtonian and non-Newtonian fluids using a microfluidic channel

Analysis of sperm cell motion in high viscosity Newtonian and non-Newtonian fluids using a microfluidic channel

Great enhancement of sensitivity for SARS-CoV-2 detection by integrated graphene FET biosensor using ζ potential modulator

By modulating a ζ potential of graphene FET (G-EFT), the sensitivity of G-FET could be enhanced than that without modulation. Therefore, 1 × 107 FFU ml−1 SARS-CoV-2 was detected using G-FET modified with the ζ potential modulator which is the cation polymer with the positive charge. This method is based on the relationship between the surface charge and the sensitivity, in which the highest sensitivity is obtained when the ζ potential is 0 and/or the surface charge is almost 0. In this study, the microfluidic channel was installed on G-FET to get the precise result because it could wash away the free-floating virus and the physical adsorbed virus. 32 G-FETs including the reference FETs were integrated on the silicon substrate and the precise results were obtained by subtracting the noise terms.

An All‐Colloidal and Eco‐Friendly Quantum‐Dot Laser

AbstractColloidal zinc‐chalcogenide quantum dots (QDs) are emerging as the promising heavy‐metal‐free light–emitters, however, the development of light amplification and lasing therein remains challenging. Here, corroborated by comprehensive in situ and transient spectroscopy, it is unraveled that the ultrafast photooxidization‐induced trapping process (≈2 ps) and the sub‐bandgap photoinduced absorption under intense excitation are the main hindrances to light amplification in ZnSeTe QDs. Upon tackling the hurdle by heterostructure engineering, this study demonstrates that the ZnSeTe QDs exhibit intrinsically superior gain performance, including the high gain cross‐section (5.6 × 10−16 cm2), long gain lifetime (615 ps), low pump threshold (≈25.9 µJ cm−2) and high fatigue resistance. On this basis, a microfluidic channel is designed to mass‐produce the micellar cavities whose surfaces are treated to combine with the ZnSeTe QDs. The active QD‐micelle hybrids show state‐of‐the‐art lasing performance and allow the fiber‐based micro‐manipulation toward the single‐mode lasers. These findings not only provide essential knowledge on the gain physics in ZnSeTe QDs, but also open a new avenue to develop high‐performance eco‐friendly lasers.

Enhancing fabrication of hybrid microfluidic devices through silane‐based bonding: A focus on polydimethylsiloxane‐cyclic olefin copolymer and PDMS‐lithium niobate

AbstractEffective manipulation and control of fluids in microfluidic channels requires robust bonding between the different components. Polydimethylsiloxane (PDMS) is widely employed in microchannel fabrication due to its affordability, biocompatibility, and straightforward fabrication process. However, PDMS's low surface energy poses challenges in bonding with many organic and inorganic substrates, hindering the development of hybrid microfluidic devices. In this study, a simple and versatile three step process is presented for bonding PDMS microchannels with organic (cyclic olefin copolymer (COC)) and inorganic substrates (lithium niobate (LiNbO3)) using plasma activation and a silane coupling agent. Initially, the PDMS surface undergoes oxygen/argon plasma activation, followed by functionalization with (3‐aminopropyl) triethoxysilane (APTES). Subsequently, the COC or LiNbO3 is plasma activated and brought into contact with PDMS under a load at a specific temperature. Characterization by Fourier transform infrared, scanning electron microscopy, atomic force microscopy, and contact angle measurements confirmed the successful treatment of the substrates. In addition, bonding strength of the fabricated hybrid devices was assessed through leakage and tensile tests. Under optimized conditions (100°C and 4% v/v APTES), PDMS‐COC hybrid microchannels achieved a flow rate of 600 mL/h without leakage and a tensile strength of 562 kPa. Conversely, the PDMS‐ LiNbO3 assembly demonstrated a flow rate of 216 mL/h before leakage, with a tensile strength of 334 kPa. This bonding method exhibits significant potential and versatility for various materials in microfluidic applications, ranging from biomedical research to enhanced oil recovery.

Electrohydrodynamic (In)Stability of Microfluidic Channel Flows: Analytical Expressions in the Limit of Small Reynolds Number

We study electrohydrodynamic (EHD) linear (in)stability of microfluidic channel flows, i.e., the stability of interface between two shearing viscous (perfect) dielectrics exposed to an electric field in large aspect ratio microchannels. We then apply our results to particular microfluidic systems known as two-liquid electroosmotic (EO) pumps. Our novel results are detailed analytical expressions for the growth rate of two-dimensional EHD modes in Couette–Poiseuille flows in the limit of small Reynolds number (R); the expansions to both zeroth and first order in R are considered. The growth rates are complicated functions of viscosity-, height-, density-, and dielectric-constant ratio, as well as of wavenumbers and voltages. To make the results useful to experimentalists, e.g., for voltage-control EO pump operations, we also derive equations for the impending voltages of the neutral stability curves that divide stable from unstable regions in voltage–wavenumber stability diagrams. The voltage equations and the stability diagrams are given for all wavenumbers. We finally outline the flow regimes in which our first-order-R voltage corrections could potentially be experimentally measured. Our work gives insight into the coupling mechanism between electric field and shear flow in parallel-planes channel flows, correcting an analogous EHD expansion to small R from the literature. We also revisit the case of pure shear instability, when the first-order-R voltage correction equals zero, and replace the renowned instability mechanism due to viscosity stratification at small R with the mechanism due to discontinuity in the slope of the unperturbed velocity profile.

The effect of 3D printed microfluidic array designs on the preparation of liposome nanoparticles

In this study Digital Light Processing (DLP) was used to manufacture microfluidic arrays with complex geometries for the fabrication of stable liposome nanoparticles. For the purposes of the study three different microfluidic array designs were 3D printed featuring herringbone structures.The effect of the herringbone numbers and the length of the microfluidic channels on the formation of liposomes was investigated by varying the Total Flow Rate (TFR) and the Flow Rate Ratio (FRR). Laser diffraction analysis showed the production of liposomes with reproducible particle sizes and narrow polydispersity index. The obtained particle size was affected by the TFR (3, 5 and 10 ml/min) and FRR (8:2 and 6:4) varying from 40 to 90 nm. However, the number of herringbone structures in the printed microfluidic arrays demonstrated no significant variations on the liposome particle sizes. Stability studies of the formed nanoparticles showed no changes for the 8:2 FRR and small increase of 8–10 nm for the 6:4 respectively. Overall, the study demonstrated the 3D printing capabilities for the printing of complex microfluidic arrays and the successful engineering of liposomes.

Microfluidic–nanophotonic sensor for on-chip analysis of complex refractive index

Photonic biosensors based on photonic integrated circuits (PICs) and microfluidic channels (MFCs) have become the subject of intensive research for point-of-care (POC) device applications. In the presented work, we demonstrate the possibility of identifying the complex refractive index (RI) of analyzed liquids through the optimization of the geometry configuration of MFCs under PICs by experimental and numerical approaches. Our results suggest that the real and imaginary parts of the RI for analytes under study can be determined from spectrum of devices with optimized MFCs width. This work paves the way for promising opportunities to identify the presence and concentration of biological markers by using RI sensors for in situ POC applications.

Electro-Optical Multiclassification Platform for Minimizing Occasional Inaccuracy in Point-of-Care Biomarker Detection.

On-site diagnostic tests that accurately identify disease biomarkers lay the foundation for self-healthcare applications. However, these tests routinely rely on single-mode signals and suffer from insufficient accuracy, especially for multiplexed point-of-care tests (POCTs) within a few minutes. Here, this work develops a dual-mode multiclassification diagnostic platform that integrates an electrochemiluminescence sensor and a field-effect transistor sensor in a microfluidic chip. The microfluidic channel guides the testing samples to flow across electro-optical sensor units, which produce dual-mode readouts by detecting infectious biomarkers of tuberculosis (TB), human rhinovirus (HRV), and group B streptococcus (GBS). Then, machine-learning classifiers generate three-dimensional (3D) hyperplanes to diagnose different diseases. Dual-mode readouts derived from distinct mechanisms enhance the anti-interference ability physically, and machine-learning-aided diagnosis in high-dimensional space reduces the occasional inaccuracy mathematically. Clinical validation studies with 501 unprocessed samples indicate that the platform has an accuracy approaching 99%, higher than the 77%-93% accuracy of rapid point-of-care testing technologies at 100% statistical power (>150 clinical tests). Moreover, the diagnosis time is 5min without a trade-off of accuracy. This work solves the occasional inaccuracy issue of rapid on-site diagnosis, endowing POCT systems with the same accuracy as laboratory tests and holding unique prospects for complicated scenes of personalized healthcare.

Air-Breathing Silicon PV Module Enabled by Internal Microfluidic Channels for Direct Cooling Application: A Validated Design Concept

Air-Breathing Silicon PV Module Enabled by Internal Microfluidic Channels for Direct Cooling Application: A Validated Design Concept

Capillarity Enabled Large-Array Liquid Metal Electrodes for Compact and High-Throughput Dielectrophoretic Microfluidics.

Dielectrophoresis (DEP) particle separation has label-free, well-controllable, and low-damage merits. Sidewall microelectrodes made of liquid metal alloy (LMA) inherits the additional advantage of thick electrodes to generate impactful DEP force. However, existing LMA electrode-based devices lack the ability to integrate large-array electrodes in a compact footprint, severely limiting flow rate and thus throughput. Herein, a facile and versatile method is proposed to integrate high-density thick LMA electrodes in microfluidic devices, taking advantage of the passive control ability of capillary burst valves (CBVs). CBVs with carefully designed burst pressures are co-designed in microfluidic channels, allowing self-assembly of LMA electrode array through simple hand-push injection. The arrayed electrode configuration brings the accumulative DEP deflection effect. Specifically, The fabricated 5000 pairs of sidewall electrodes in a compact chip are demonstrted to achieve ten times higher throughput in DEP deflection. The 5000-electrode-pair device is applied to successfully separate four mixed samples, including human peripheral blood mononuclear cells and A549 cellswith the flow rate of 70 µL min-1. It is envisioned that this work can greatly facilitate LMA electrode array fabrication and offer a robust and versatile platform for DEP separation applications.

Microfluidic SERS chip for quantitative detection of weak surficial affinity molecules

Microfluidic SERS chip has become increasingly attractive in sensitive chemical and biomolecular analysis. However, microfluidic SERS chip is substantially limited when detecting weakly adsorbed molecules in fluids, let alone achieving quantitative analysis that is vital for biochemical applications. Herein, a microfluidic SERS chip that can achieve quantitative analysis of weak affinity molecules is developed. By “direct-laser-writing”, silver aggregates inherently modified with citrate are facilely fabricated in microfluidic channel. We demonstrate that the surficial citrate can not only “detain” analytes on plasmonic surface by multi-hydrogen bonding, but also serve as a stable internal-standard, which well solves the two challenges. It shows that the relative standard deviation of melamine SERS intensity at 701 cm−1 can be effectively reduced from about 20% to less than 10% by normalization using the citrate band at 1370 cm−1. Quantification of melamine in aqueous and milk samples down to 10−7 M are achieved, respectively. And the recoveries are in the range 95%-115%. Moreover, the detection of a kind of hypoglycemic drug (rosiglitazone) is also performed. This microfluidic SERS chip capable of robust quantification of weak affinity molecules would certainly extend the application scenarios of microfluidic SERS, especially for low dose, high efficiency and real time liquid analysis.

Analyzing the effects of helical flow in blood vessels using acoustofluidic-based dynamic flow generator

The effects of helical flow in a blood vessel are investigated in a dynamic flow generator using surface acoustic wave (SAW) in the microfluidic device. The SAW, generated by an interdigital transducer (IDT), induces acoustic streaming, resulting in a stable and consistent helical flow pattern in microscale channels. This approach allows rapid development of helical flow within the channel without directly contacting the medium. The precise design of the window enables the creation of distinct unidirectional vortices, which can be controlled by adjusting the amplitude of the SAW. Within this device, optimal operational parameters of the dynamic flow generator to preserve the integrity of endothelial cells are found, and in such settings, the actin filaments within the cells are aligned to the desired state. Our findings reveal that intracellular Ca2+ concentrations vary in response to flow conditions. Specifically, comparable maximum intensity and graphical patterns were observed between low-flow rate helical flow and high-flow rate Hagen-Poiseuille flow. These suggest that the cells respond to the helical flow through mechanosensitive ion channels. Finally, adherence of monocytes is effectively reduced under helical flow conditions in an inflammatory environment, highlighting the atheroprotective role of helical flow. Statement of SignificanceHelical flow in blood vessels is well known to prevent atherosclerosis. However, despite efforts to replicate helical flow in microscale channels, there is still a lack of in vitro models which can generate helical flow for analyzing its effects on the vascular system. In this study, we developed a method for generating steady and constant helical flow in microfluidic channel using acoustofluidic techniques. By utilizing this dynamic flow generator, we were able to observe the atheroprotective aspects of helical flow in vitro, including the enhancement of calcium ion flux and reduction of monocyte adhesion. This study paves the way for an in vitro model of dynamic cell culture and offers advanced investigation into helical flow in our circulatory system.

Interindividual- and blood-correlated sweat phenylalanine multimodal analytical biochips for tracking exercise metabolism

In situ monitoring of endogenous amino acid loss through sweat can provide physiological insights into health and metabolism. However, existing amino acid biosensors are unable to quantitatively assess metabolic status during exercise and are rarely used to establish blood-sweat correlations because they only detect a single concentration indicator and disregard sweat rate. Here, we present a wearable multimodal biochip integrated with advanced electrochemical electrodes and multipurpose microfluidic channels that enables simultaneous quantification of multiple sweat indicators, including phenylalanine and chloride, as well as sweat rate. This combined measurement approach reveals a negative correlation between sweat phenylalanine levels and sweat rates among individuals, which further enables identification of individuals at high metabolic risk. By tracking phenylalanine fluctuations induced by protein intake during exercise and normalizing the concentration indicator by sweat rates to reduce interindividual variability, we demonstrate a reliable method to correlate and analyze sweat-blood phenylalanine levels for personal health monitoring.

Microfluidic organ chip of fluid–solid dynamic curved interface

Dynamic curved interfaces are fundamental and ubiquitous structures in biological systems. However, replicating the structure and function associated with these interfaces for mechanobiology and drug screening is challenging. Here, we develop a dynamic curvature-enabled microfluidic organ chip of two fluid–solid dynamic curved interfaces. One interface effectively integrates adjustable biomechanics, and the other controls drug release with open microfluidics. The fluid–solid interface sensed by the cells can modulate the residual stress, stiffness, strain of the solid phase, and the flow shear stress of the fluid phase. Using the chip, we investigate the mechanotransductive responses of endothelial and epithelial cells, including Piezo1, Ca2+, and YAP, and reveal that the response of the endothelium to combined dynamic cyclic strain and flow shear stress is different from separate stimulation and also disparate from the epithelium. Furthermore, direct and high-efficiency drug release to cells is realized by constructing the other fluid–solid interface on the back side of cells, where drugs are encapsulated within cross-linked alginate hydrogel in the open microfluidic channel. Then, we replicate object-specific and location-specific biomechanical environments within carotid bifurcation and prove the effectiveness of drug delivery. Our design exemplifies dynamic curved biological interfaces with controlled mechanical environments and holds potential for patient-specific medicine.

Employing electrochemically derived pH gradients for Lab-on-PCB protein preconcentration devices

Protein preconcentration is an essential sample preparation step for analysis in which the targeted proteins exist in low concentrations, such as bodily fluids, water, or wastewater. Nonetheless, very few practical implementations of miniaturized protein preconcentration devices have been demonstrated in practice, and even fewer have been integrated with other microanalytical steps. Existing approaches rely heavily on additional chemicals and reagents and introduce complexity to the overall assay. In this paper, we propose a novel miniaturized isoelectric focusing-based protein preconcentration screening device based on electrochemically derived pH gradients rather than existing chemical reagent approaches. In this way, we reduce the need for additional chemical reagents to zero while enabling device incorporation in a seamlessly integrated full protein analysis microsystem via Lab-on-PCB technology. We apply our previously presented Lab-on-PCB approach to quantitatively control the pH of a solution in the vicinity of planar electrodes using electrochemical acid generation through redox-active self-assembled monolayers. The presented device comprises a printed circuit board with an array of gold electrodes that were functionalized with 4-aminothiophenol; this formed a self-assembled monolayer that was electropolymerized to improve its electrochemical reversibility. Protein preconcentration was performed in two configurations. The first was open and needed the use of a holder to suspend a well of fluid above the electrodes; the second used microfluidic channels to enclose small volumes of fluid. Reported here are the resulting data for protein preconcentration in both these forms, with a quantitative concentration factor shown for the open form and qualitative proof shown for the microfluidic.

Comparison of Faradaic and Non-Faradaic Impedance Biosensors Using 2-Electrode and 3-Electrode Configurations for the Determination of Bovine Serum Albumin (BSA)

This paper presents a study on the impedance spectroscopy methods applied to 2-electrode and 3-electrode biosensors. While 3-electrode electrochemical biosensors have been extensively studied and applied in various applications, the 2-electrode configuration of electrochemical biosensors still lacks comprehensive investigation for real-world applications. In particular, the miniaturization of the 3-electrode configuration for integration into microfluidic devices has been explored due to the relatively limited number of previous studies. A commercial screen-printed gold electrode was employed to develop immunosensors for bovine serum albumin (BSA) detection. The comparisons were performed on non-Faradaic and Faradic immunosensors corresponding to 2-electrode and 3-electrode configurations through impedance measurements. The results show the performance of both types of sensors in detecting BSA protein. While the 2-electrode configuration-based sensor can detect the BSA protein with a sensitivity of 12 Ω/µM, the 3-electrode configuration-based sensor shows superior results with a sensitivity of 7.2 kΩ/µM. Besides, the results also indicate that the 2-electrode configuration-based sensor can easily be miniaturized to integrate into a microfluidic channel to develop lab-on-a-chip systems. Although the 3-electrode configuration demonstrates advancements compared to the 2-electrode configuration, the 2-electrode system based on non-Faradaic processes still shows high potential for future applications.

Do it yourself- circular cross-section microfluidic channel

Do it yourself- circular cross-section microfluidic channel

Droplet pair breakup in microfluidic expansion channel

Previous studies on droplet splitting mainly focus on monodisperse droplets, and the understanding of the breakup of polydisperse droplet systems is still lacking. In this work, we experimentally study the breakup of droplet pairs in the expansion region of microfluidic channel. The results show that with the increase in the size ratio of the droplets in the droplet pair, the breakup mode of droplet pairs changes from rear droplet breakup to front droplet breakup, and then to front droplet alternate breakup. The expansion angle can affect the critical size ratio of the splitting mode transition, but it cannot change the transition trend. The expansion angle plays a major role in the splitting time and distance of the droplet pair. When the expansion angle is increased, the splitting time of the droplet pair is reduced and the splitting distance is shorter. Our study extends the understanding of the breakup of non-monodisperse droplet systems and provides a feasible approach for the selective and controllable splitting of droplets, which is important for laboratory-on-a-chip droplet volume manipulation and has potential applications.