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Organoids are emerging as a powerful tool to investigate complex biological structures in vitro. Vascularization of organoids is crucial to recapitulate the morphology and function of the represented human organ, especially in the case of the kidney, whose primary function of blood filtration is closely associated with blood circulation. Current in vitro microfluidic approaches have only provided initial vascularization of kidney organoids, whereas in vivo transplantation to animal models is problematic due to ethical problems, with the exception of xenotransplantation onto a chicken chorioallantoic membrane (CAM). Although CAM can serve as a good environment for vascularization, it can only be used for a fixed length of time, limited by development of the embryo. Here, we propose a novel lab on a chip design that allows organoids of different origin to be cultured and vascularized on a CAM, as well as to be transferred to in vitro conditions when required. Mouse embryonic kidneys cultured on the CAM showed enhanced vascularization by intrinsic endothelial cells, and made connections with the chicken vasculature, as evidenced by blood flowing through them. After the chips were transferred to in vitro conditions, the vasculature inside the organoids was successfully maintained. To our knowledge, this is the first demonstration of the combination of in vivo and in vitro approaches applied to microfluidic chip design. [ABSTRACT FROM AUTHOR]

Particle cross-stream migration in electrohydrodynamic microfluidic systems exhibits intriguing behaviors, which makes it interesting when viewed from a fundamental perspective and promising for nanoparticle focusing and separation applications. So far, particle behavior in such systems has been explained with the slip-induced lift force model (Saffman model), which predicts particle central or side focusing based on the direction of electric field and fluid flow. However, in our previous work, we observed particle migration patterns that did not adhere to the prediction of the Saffman model. In this work, we further studied this novel particle lateral migration behavior, which we termed the "anti-Saffman" behavior. We experimentally investigated how changing the conductivity of the suspending medium influences particle behavior and quantitatively measured the net lateral force experienced by the particles. Then, we compared this net force with the prediction of the relevant lift force models in the literature. We concluded that the anti-Saffman behavior is positively correlated with medium conductivity and shear rate (∝ γ ̇ 2 ). Furthermore, the comparison with the existing force models revealed that none of them can predict the experimentally observed particle lift. The net lift predicted by hydrodynamic lift models indicated that the underlying mechanism behind our experiments also potentially has a hydrodynamic origin. We believe this phenomenon offers the possibility of manipulating and separating nanoparticles suspended in standard aqueous electrolyte solutions, which makes it applicable to various biological samples. [ABSTRACT FROM AUTHOR]

Transfusion of red blood cells (RBCs) is one of the most valuable and widespread treatments in modern medicine. Lifesaving RBC transfusions are facilitated by the cold storage of RBC units in blood banks worldwide. Currently, RBC storage and subsequent transfusion practices are performed using simplistic workflows. More specifically, most blood banks follow the "first-in-first-out" principle to avoid wastage, whereas most healthcare providers prefer the "last-in-first-out" approach simply favoring chronologically younger RBCs. Neither approach addresses recent advances through -omics showing that stored RBC quality is highly variable depending on donor-, time-, and processing-specific factors. Thus, it is time to rethink our workflows in transfusion medicine taking advantage of novel technologies to perform RBC quality assessment. We imagine a future where lab-on-a-chip technologies utilize novel predictive markers of RBC quality identified by -omics and machine learning to usher in a new era of safer and precise transfusion medicine. [ABSTRACT FROM AUTHOR]

Targeted, on‐demand delivery has been of interest using materials responsive to environmental stimuli. A delivery technique based on precise release of aqueous microdroplets from a liquid crystal (LC) medium with contactless stimulation is presented. A nematic LC is doped with a photothermal dye that produces heat under near IR light exposure. The heat is used to overcome the elastic strains in the LC phase, promoting the release of initially entrapped water droplets to the neighboring aqueous solution. Designing the geometry of LC‐based emulsions and tuning the light intensity and position allows for manipulation of the release in two distinct modes defined as pulsated and continuous. In the pulsated mode, water droplets are released transiently from the casted water‐in‐LC emulsion layer based on sweeping by the moving isotropic‐nematic phase boundary controlled by light. In the continuous mode, water droplets are ejected continuously from a droplet‐shaped water‐in‐LC emulsion, due to a heating‐induced internal flow controlled by light. The droplet release by contactless stimulation is used for the on‐demand dosing of dopamine and its oxidizing reagent from isolated reservoirs to obtain an in situ reaction signal for a hydrogen peroxide assay. A new dual‐mode release system developed with photothermal LCs holds potential in drug release, controlled mixing, and photothermal therapy. [ABSTRACT FROM AUTHOR]

This paper presents modeling and analysis of eddy-current damping that is formed by a conductive plate placed below the levitating object in order to suppress vibrations and ensure stability. It is demonstrated that vibrations should be damped to preserve stability and precision especially for stepwise motion. The levitated object is a small permanent magnet in our experiments. A magnetic drive unit is used for vertical motion of the magnet. Eddy-current distribution in the plate is calculated by solving diffusion equation for vector magnetic potential. The eddy force applied to the object is derived by a coil model representation. It is shown that if a 20 mm radius, 9 mm thick aluminum circular plate is used for eddy-current damping, the levitated object can closely follow a step input with a steady-state precision varying between 0.04 and 0.07 mm depending on the plate object distance. Eddy-current damping is a key technique that improves levitation performance to increase the diversity of applications of magnetic levitation systems in micromanipulation and microelectronic fabrication. Index Terms--Eddy current, eddy-current damping, magnetic levitation, mechatronics, modeling.

Extracellular nanovesicles, particularly exosomes, can deliver their diverse bioactive biomolecular content, including miRNAs, proteins, and lipids, thus providing a context for investigating the capability of exosomes to induce stem cells toward lineage‐specific cells and tissue regeneration. In this study, it is demonstrated that rat subventricular zone neural stem cell‐derived exosomes (rSVZ‐NSCExo) can control neural‐lineage specification of human mesenchymal stem cells (hMSCs). Microarray analysis shows that the miRNA content of rSVZ‐NSCExo is a faithful representation of rSVZ tissue. Through immunocytochemistry, gene expression, and multi‐omics analyses, the capability to use rSVZ‐NSCExo to induce hMSCs into a neuroglial or neural stem cell phenotype and genotype in a temporal and dose‐dependent manner via multiple signaling pathways is demonstrated. The current study presents a new and innovative strategy to modulate hMSCs fate by harnessing the molecular content of exosomes, thus suggesting future opportunities for rSVZ‐NSCExo in nerve tissue regeneration. [ABSTRACT FROM AUTHOR]

Pazopanib (PAZ), a tyrosine kinase inhibitor, is used to treat advanced renal cell carcinoma (RCC) and advanced soft tissue sarcoma (STS). The FDA approved PAZ for RCC in 2009 and for STS in 2012. The antitumor activity of pazopanib, according to the degree of inhibition, shows different results depending on the dose. Renal cell carcinoma is the most sensitive carcinoma to pazopanib, with 77% inhibition at the 10 mg/kg dose. Clinical studies have shown 53% to 65% inhibition in carcinomas such as breast carcinoma, prostate carcinoma, and melanoma. Plasma proteins such as human serum albumin (HSA) have a critical role in transporting and storing bioactive components. This feature of HSA is very important for the development of cancer therapy. Here, we investigated the interaction between PAZ and HSA to evaluate their binding strength, binding types, and conformational change in HSA. We used spectroscopic methods to assess the drug–protein interaction. Fluorescence measurements revealed that the interaction of PAZ with HSA occurred via the static quenching mechanism. The calculated binding number and binding constants were 1.041 and 1.436 × 106 M−1, respectively, at 298.15 K based on fluorescence screening. The high binding constant and calculated Gibbs free energy at different temperatures showed spontaneous and strong binding. Circular dichroism measurements showed that the α-helix structure of HSA was retained as the secondary structure, with a slight reduction in its percentage after adding PAZ. Furthermore, molecular modeling studies suggested that the docking score of PAZ is higher than those of bicalutamide and ibuprofen, the drugs that were chosen as model competitors against PAZ. Accordingly, PAZ was found to replace bicalutamide and ibuprofen on the HSA binding site, which was also confirmed by UV absorption spectroscopy. [ABSTRACT FROM AUTHOR]

The article discusses the need for objective tools to assess the quality of stored red blood cells (RBCs) for transfusion medicine. The authors highlight the potential of lab-on-a-chip (LOC) technologies to quantitatively evaluate RBC quality using multidimensional metrics. They acknowledge the development of a point-of-care device called Erysense, which assesses the flow properties and morphological abnormalities of stored RBCs. However, they also mention limitations and challenges that need to be addressed, such as the need for extensive validation, automation of the workflow, and addressing storage lesions. The authors suggest that while scalable strategies for in vitro erythropoiesis are promising, other steps can be taken to address blood shortages and improve transfusion practices. [Extracted from the article]

The flow behavior of blood is determined mainly by red blood cell (RBC) deformation and aggregation as well as blood viscoelasticity. These intricately interdependent parameters should be monitored by healthcare providers to understand all aspects of circulatory flow dynamics under numerous cases including cardiovascular and infectious diseases. Current medical instruments and microfluidic systems lack the ability to quantify these parameters all at once and in physiologically relevant flow conditions. This work presents a handheld platform and a measurement method for quantitative analysis of multiple of these parameters from 50 μl undiluted blood inside a miniaturized channel. The assay is based on an optical transmission analysis of collective RBC deformation and aggregation under near-infrared illumination during a 1 s damped oscillatory flow and at stasis, respectively. Measurements with blood of different hemo-rheological properties demonstrate that the presented approach holds a potential for initiating simultaneous and routine on-chip blood flow analysis even in resource-poor settings. [ABSTRACT FROM AUTHOR]

In recent years, magnetic levitation is finding interesting applications in various fields related to microdevices. Producing inexpensive microfabricated magnetic films is of high importance to all magnetically levitated microdevices. This paper introduces a microlevitation system and presents the fabrication of Co–Ni–Mn–P films using electrodeposition. The fabrication parameters are varied such that magnetization direction of the film is varied by changing the crystal structure. The magnetic properties of the films such as coercivity, remanence, and maximum energy product demonstrate that hexagonal structure promotes out-of-plane magnetization whereas cubic structure reinforces in-plane magnetization. The performance of the Co–Ni–Mn–P films is evaluated by magnetic levitation experiments of silicon samples. Satisfactory results are obtained toward the goal of realization of a magnetically levitated microgripper. [ABSTRACT FROM AUTHOR]

Droplet-based microfluidic systems require a precise control of droplet physical properties; hence, measuring the morphological properties of droplets is critical to obtain high sensitivity analysis. The ability to perform such measurements in real-time is another demand which has not been addressed yet. In this study, we used coplanar electrodes configured in the differential measurement mode for impedimetric measurement of size and velocity. To obtain the size of the droplets, detailed 3D finite element simulations of the system were performed. The interaction of the non-uniform electric field and the droplet was investigated. Electrode geometry optimization steps were described and design guideline rules were laid out. User-friendly software was developed for real-time observation of droplet length and velocity together with in situ statistical analysis results. A comparison between impedimetric and optical measurement tools is given. Finally, to illustrate the benefit of having real-time analysis, iDM was used to synthesize particles with a predefined monodispersity limit and to study the response times of syringe pump and pressure pump driven droplet generation devices. This analysis allows one to evaluate the 'warm-up' time for a droplet generator system, after which droplets reach the desired steady-state size required by the application of interest. [ABSTRACT FROM AUTHOR]

The erythrocyte sedimentation rate (ESR) is a frequently used 30 min or 60 min clinical test for screening of several inflammatory conditions, infections, trauma, and malignant diseases, as well as non-inflammatory conditions including prostate cancer and stroke. Erythrocyte aggregation (EA) is a physiological process where erythrocytes form face-to-face linear structures, called rouleaux, at stasis or low shear rates. In this work, we proposed a method for ESR measurement from EA. We developed a microfluidic opto-electro-mechanical system, using which we experimentally showed a significant correlation (R2 = 0.86) between ESR and EA. The microfluidic system was shown to measure ESR from EA using fingerprick blood in 2 min. 40 μl of whole blood is filled in a disposable polycarbonate cartridge which is illuminated with a near infrared emitting diode. Erythrocytes were disaggregated under the effect of a mechanical shear force using a solenoid pinch valve. Following complete disaggregation, transmitted light through the cartridge was measured using a photodetector for 1.5 min. The intensity level is at its lowest at complete disaggregation and highest at complete aggregation. We calculated ESR from the transmitted signal profile. We also developed another microfluidic cartridge specifically for monitoring the EA process in real-time during ESR measurement. The presented system is suitable for ultrafast, low-cost, and low-sample volume measurement of ESR at the point-of-care. [ABSTRACT FROM AUTHOR]

Droplet-based microfluidic systems offer tremendous benefits for high throughput biochemical assays. Despite the wide use of electrical detection for microfluidic systems, application of impedimetric sensing for droplet systems is very limited. This is mainly due to the insulating oil-based continuous phase used for most aqueous samples of interest. We present modelling and experimental verification of impedimetric detection of hemagglutination in microdroplets. We have detected agglutinated red blood cells in microdroplets and screened whole blood samples for multiple antibody sera using conventional microelectrodes. We were able to form antibody and whole blood microdroplets in PDMS microchannels without any tedious chemical surface treatment. Following the injection of a blood sample into antibody droplets, we have detected the agglutination-positive and negative droplets in an automated manner. In order to understand the characteristics of impedimetric detection inside microdroplets, we have developed the lumped electrical circuit equivalent of an impedimetric droplet content detection system. The empirical lumped element values are in accordance with similar models developed for single phase electrical impedance spectroscopy systems. The presented approach is of interest for label-free, quantitative analysis of droplets. In addition, the standard electronic equipment used for detection allows miniaturized detection circuitries that can be integrated with a fluidic system for a quantitative microdroplet-based hemagglutination assay that is conventionally performed in well plates. [ABSTRACT FROM AUTHOR]

This is the first part of a two-part study on the generation of droplets at a microfluidic T-junction operating in the transition regime where confinement of the droplet creates a large squeezing pressure that influences droplet formation. In this regime, the operation of the T-junction depends on the geometry of the intersection (height-to-width ratio, inlet width ratio), capillary number, flow ratio, and viscosity ratio of the two phases. Here in paper I we presented our experimental observations through the analysis of high-speed videos of the droplet formation process. Various parameters are tracked during the formation cycle such as the shape of the droplet (penetration depth and neck), interdroplet spacing, production rate, and flow of both phases across several T-junction designs and flow conditions. Generally, the formation process is defined by a two-stage model consisting of an initial filling stage followed by a necking stage. However, video evidence suggests the inclusion of a third stage, which we term the lag stage, at the beginning of the formation process that accounts for the retraction of the interface back into the injection channel after detachment. Based on the observations made in this paper, a model is developed to describe the formation process in paper II, which can be used to understand the design and operation of T-junction generators in the transition regime. [ABSTRACT FROM AUTHOR]

This is the second part of a two-part study on the generation of droplets at a microfluidic T-junction operating in the transition regime. In the preceding paper [Phys. Rev. E 85, 016322 (2012)], we presented our experimental observations of droplet formation and decomposed the process into three sequential stages defined as the lag, filling, and necking stages. Here we develop a model that describes the performance of microfluidic T-junction generators working in the squeezing to transition regimes where confinement of the droplet dominates the formation process. The model incorporates a detailed geometric description of the drop shape during the formation process combined with a force balance and necking criteria to define the droplet size, production rate, and spacing. The model inherently captures the influence of the intersection geometry, including the channel width ratio and height-to-width ratio, capillary number, and flow ratio, on the performance of the generator. The model is validated by comparing it to speed videos of the formation process for several T-junction geometries across a range of capillary numbers and viscosity ratios. [ABSTRACT FROM AUTHOR]

Spectrally selective thermal emission is in high demand for thermophotovoltaics, radiative cooling, and infrared sensing applications. Spectral control of the emissivity is historically achieved by choosing the material with suitable infrared properties. The recent advancements in nanofabrication techniques that lead to enhanced light–matter interactions enable optical properties like infrared emissivity that are not naturally available. In this study, thermal emitters based on nanometer‐thick dielectrics on field‐enhancement surfaces as optical security features are proposed. Such a function is achieved by generating patterns by ultrathin dielectrics that are transparent in the visible and exhibit strong infrared absorption in the spectral range of thermal cameras. The invisible patterns are then revealed by thermal imaging. The field‐enhancement surfaces enhance the emissivity of the patterns, in turn reduce the minimum temperature to detect the thermal emission down to ≈30 °C from >150 °C to exploit ubiquitous heat sources like the human body. The study provides a framework for the use of thermal emitters as optical security features and demonstrates applications on rigid and flexible substrates. Nanometer‐thick SiO2 patterns are encrypted in the visible wavelength regime to be decrypted in the infrared. This study provides a framework for the use of thermal emitters as optical security features and demonstrates applications on rigid and flexible substrates. [ABSTRACT FROM AUTHOR]

Droplet microfluidic systems have evolved as fluidic platforms that use much less sample volume and provide high throughput for biochemical analysis compared to conventional microfluidic devices. The variety of droplet fluidic applications triggered several detection techniques to be applied for analysis of droplets. In this review, we focus on label-free droplet detection techniques that were adapted to various droplet microfluidic platforms. We provide a classification of most commonly used droplet platform technologies. Then we discuss the examples of various label-free droplet detection schemes implemented for these platforms. While providing the research landscape for label-free droplet detection methods, we aim to highlight the strengths and shortcomings of each droplet platform so that a more targeted approach can be taken by researchers when selecting a droplet platform and a detection scheme for any given application. [ABSTRACT FROM AUTHOR]

We demonstrate a surface plasmon resonance imaging platform integrated with a smartphone to be used in the field with high-throughput biodetection. Inexpensive and disposable SPR substrates are produced by metal coating of commercial Blu-ray discs. A compact imaging apparatus is fabricated using a 3D printer which allows taking SPR measurements from more than 20.000 individual pixels. Real-time bulk refractive index change measurements yield noise equivalent refractive index changes as low as 4.12 × 10 −5 RIU which is comparable with the detection performance of commercial instruments. As a demonstration of a biological assay, we have shown capture of mouse IgG antibodies by immobilized layer of rabbit anti-mouse (RAM) IgG antibody with nanomolar level limit of detection. Our approach in miniaturization of SPR biosensing in a cost-effective manner could enable realization of portable SPR measurement systems and kits for point-of-care applications. [ABSTRACT FROM AUTHOR]