Fluidic Conduits Research Articles

Using parallel plates capacitor as a volumetric flow rate sensor and direction detection for microfluidic/nanofluidic and extra smaller applications

This paper shows how a single parallel plate capacitor can be used to sense volumetric flow rate in micro/nano and smaller scale fluidic conduits and how a double parallel plate capacitor can be used to sense both volumetric flow rate and direction of flow. The concept was developed based on the principles of conservation of energy with some fundamentals of electricity and electromagnetics. Furthermore, the concept was validated experimentally to be accurate. Upon validation the measurement of the sensor was found to be in good agreement with experimental measurement with more accuracy obtained as the supplied voltage for the sensor is increased. Also, the accuracy of the developed concept increases as the characteristic length of the conduit decreases which makes the developed concept even more suitable for smaller scales applications. The concept consumes extremely low power and can be used directly without calibration provided that accurate value for magnetic permittivity of fluid is available. Moreover, the concept can be used for any type of fluid of any conduit shape with easy incorporation onto lab-on-a-chip or MEMS technology. The sensitivity of the sensor is approximately 0.03 A/(m3/s) which is good compared to other sensors.

Angstrofluidics: Walking to the Limit

Angstrom-scale fluidic channels are ubiquitous in nature and play an important role in regulating cellular traffic, signaling, and responding to stimuli. Synthetic angstrom channels are now a reality with the emergence of several cutting-edge bottom-up and top-down fabrication methods. In particular, the use of atomically thin 2D materials and nanotubes as components to build fluidic conduits has pushed the limits of fabrication to the angstrom scale. Here, we provide an overview of recent developments in the fabrication methods for nano- and angstrofluidic channels while categorizing them on the basis of dimensionality (0D pores, 1D tubes, 2D slits), along with the latest advances in measurement techniques. We discuss the ion transport governed by various stimuli in these channels and the variation of ionic mobility, streaming power, and osmotic power with pore size across all the dimensionalities. Finally, we highlight unique future opportunities in the development of smart ionic devices.

Streaming potential in bio-mimetic microvessels mediated by capillary glycocalyx

Implantable medical devices and biosensors are pivotal in revolutionizing the field of medical technology by opening new dimensions in the field of disease detection and cure. These devices need to harness a biocompatible and physiologically sustainable safe power source instead of relying on external stimuli, overcoming the constraints on their applicability in-vivo. Here, by appealing to the interplay of electromechanics and hydrodynamics in physiologically relevant microvessels, we bring out the role of charged endothelial glycocalyx layer (EGL) towards establishing a streaming potential across physiological fluidic conduits. We account for the complex rheology of blood-mimicking fluid by appealing to Newtonian fluid model representing the blood plasma and a viscoelastic fluid model representing the whole blood. We model the EGL as a poroelastic layer with volumetric charge distribution. Our results reveal that for physiologically relevant micro-flows, the streaming potential induced is typically of the order of 0.1 V/mm, which may turn out to be substantial towards energizing biosensors and implantable medical devices whose power requirements are typically in the range of micro to milliwatts. We also bring out the specific implications of the relevant physiological parameters towards establishment of the streaming potential, with a vision of augmenting the same within plausible functional limits. We further unveil that the dependence of streaming potential on EGL thickness might be one of the key aspects in unlocking the mystery behind the angiogenesis pattern. Our results may open up novel bio-sensing and actuating possibilities in medical diagnostics as well as may provide a possible alternative regarding the development of physiologically safe and biocompatible power sources within the human body.

Flow and deformation characteristics of a flexible microfluidic channel with axial gradients in wall elasticity.

Axial gradients in wall elasticity may have significant implications in the deformation and flow characteristics of a narrow fluidic conduit, bearing far-reaching consequences in physiology and bio-engineering. Here, we present a theoretical and experimental framework for fluid-structure interactions in microfluidic channels with axial gradients in wall elasticity, in an effort to arrive at a potential conceptual foundation for in vitro study of mirovascular physiology. Towards this, we bring out the static deformation and steady flow characteristics of a circular microchannel made of polydimethylsiloxane (PDMS) bulk, considering imposed gradients in the substrate elasticity. In particular, we study two kinds of elasticity variations - a uniformly soft (or hard) channel with a central strip that is hard (or soft), and, increasing elasticity along the length of the channel. The former kind yields a centrally constricted (or expanded) deformed profile in response to the flow. The latter kind leads to increasingly bulged channel radius from inlet to outlet in response to flow. We also formulate an analytical model capturing the essential physics of the underlying elastohydrodynamic interactions. The theoretical predictions match favourably with the experimental observations and are also in line with reported results on stenosis in mice. The present framework, thus, holds the potential for acting as a fundamental design basis towards developing in vitro models for micro-circulation, capable of capturing exclusive artefacts of healthy and diseased conditions.

Mass Flow Monitoring by Distributed Fiber Optical Temperature Sensing.

We developed a novel method to monitor mass flow based on distributed fiber optical temperature sensing. Examination of the temporal and spatial temperature distribution along the entire length of a locally heated fluidic conduit reveals heat flow under forced convection. Our experimental results are in good agreement with two-dimensional finite element analysis that couples fluid dynamic and heat transfer equations. Through analysis of the temperature distribution bidirectional flow rates can be measured over three orders of magnitude. The technique is not flow intrusive, works in harsh conditions, including high-temperatures, high pressures, corrosive media, and strong electromagnetic environments. We demonstrate a first experimental implementation on a short fluidic system with a length of one meter. This range covers many applications such as low volume drug delivery, diagnostics, as well as process and automation technology. Yet, the technique can, without restrictions, be applied to long range installations. Existing fiber optics infrastructures, for instance on oil pipelines or down hole installations, would only require the addition of a heat source to enable reliable flow monitoring capability.

A Microfluidic SPLITT Device for Fractionating Low-Molecular Weight Samples

In this article, we report the design of a microfluidic split flow thin cell (SPLITT) fractionation device with internal electrodes placed across the width of its analysis channel for assaying low-molecular weight samples. The reported device allows the realization of lateral electric fields and separation distances of the orders of 100 V/cm and 500 μm, respectively, that are suitable for fractionating such mixtures with high resolution. Our experiments show that a key challenge to realizing electrophoretic fractionations using the current design is to minimize the electroosmotically driven fluid circulations in its SPLITT channel that tend to hydrodynamically mix the liquid streams flowing through this duct. The present work addresses this challenge by chemically modifying the surface of our fluidic conduits with a new coating medium, N-(2-triethoxysilylpropyl) formamide, which has been shown to diminish electroosmotic flow in glass microchannels by over 5 orders of magnitude. Finally, we describe the integration of the reported microfluidic fractionation device to a mass spectrometer via the electrospray ionization interface to allow inline label-free detection of analytes in our assay. Product purity greater than 95% has been accomplished using the SPLITT system presented here for a sample of peptides having the same electrical polarity.

Hand-held syringe as a portable plastic pump for on-chip continuous-flow PCR: miniaturization of sample injection device

On-chip continuous-flow polymerase chain reactions (PCRs) generally require peripheral apparatus such as a pump for injecting a sample liquid into the fluidic channel. This makes the overall instrumentation bulky, limiting integration. In this study, we propose a new scheme for injecting a sample employing a hand-held syringe as a portable plastic pump, and apply it to an on-chip continuous-flow PCR. In the proposed injection scheme, sample actuation was realized inside a highly gas-permeable and blunt-ended fluidic conduit connected to a hand-held plastic syringe filled with compressed air. In this system, the degree of air diffusion via the walls of the gas-permeable conduit becomes greater in the anterior (closer to the outlet) end of the sample plug than the posterior (closer to the inlet) end, because a relatively larger quantity of air is retained inside the syringe at the posterior end of the sample plug. This creates a pressure gradient at the inlet and outlet of the fluidic conduit and propels the sample forward toward the outlet. Preliminary experiments were performed for the quantitative analyses and evaluation of the proposed sample injection scheme using gas-permeable silicone tubes. As practical applications, a 230 bp gene fragment from a plasmid vector and the first 282 bp of the interferon-beta (IFN-β) promoter from a human genomic DNA were successfully amplified on a microdevice coupled with a hand-held syringe as a portable sample actuation device, greatly enhancing device portability for on-site analyses.

Three-dimensional on-chip continuous-flow polymerase chain reaction employing a single heater

Multi-step temperature control in a polymerase chain reaction (PCR) is a limiting factor in device miniaturization and portability. In this study, we propose the fabrication of a three-dimensional (3D) microdevice employing a single heater to minimize temperature control required for an on-chip continuous-flow PCR as well as the overall footprint by stacking the device in multi-layers. Two poly(dimethylsiloxane) (PDMS) layers with differing thicknesses are vertically stacked with their microchannel-engraved sides facing down. Through-holes are made in the thicker PDMS layer, which is sandwiched between a glass substrate at the bottom and the thinner PDMS layer at the top. In this way, a fluidic conduit is realized in a 3D configuration. The assembled 3D microdevice is then placed onto a heater glass-side down. The interface of the two PDMS layers displays a relatively lower temperature than that of the PDMS and glass layers due to the low thermal conductivity of the PDMS and its physical distance from the heater. The denaturation temperature can be controlled by adjusting the temperature of the heater, while the annealing/extension temperature can be controlled automatically by molding the thicker bottom PDMS layer into the appropriate thickness calculated using a numerical derivation proposed in this study. In this way, a cumbersome temperature measurement step is eliminated. DNA amplification was successfully carried out using the proposed 3D fluidic microdevice, and the intensity of the resulting amplicon was comparable to that obtained using a thermal cycler. This novel concept of adopting a single heating source greatly simplifies the temperature control issue present in an on-chip continuous-flow PCR. It also allows the use of a commercialized hot plate as a potential heat source, paving the way for device miniaturization and portability in a highly cost-effective manner. In this study, a simple and facile technique to make arrays of through-holes for the fluidic interconnection inside a 3D channel configuration is also addressed.

Three-dimensional opto-fluidic devices fabricated by ultrashort laser pulses for high throughput single cell detection and processing

Three-dimensional flow-through microchannels were fabricated inside bulk fused silica glass via ultrashort pulsed laser direct writing. The device fabrication sequence takes advantage of the nonlinear volumetric absorption in glass and the subsequent preferential chemical etching process. Optical waveguides were also written into the glass specimen and integrated with the fluidic conduits. Flow tests using both fluorescent particles and red blood cells (RBCs) were conducted on various three-dimensional channel configurations. Experiments showed the possibility for laser-induced cell processing inside the microchannels. To evaluate cytometer functionality, RBCs were detected inside the manufactured microchannel via both transmission and fluorescence probing.

Fluidic conduits for highly efficient purification of target species in EWOD-driven droplet microfluidics

Due to the lack of continuous flows that would wash unwanted specifies and impurities off from a target location, droplet microfluidics commonly employs a long serial dilution process to purify target species. In this work, we achieve high-purity separation for the case of electrowetting-on-dielectric (EWOD) based droplet microfluidics by introducing a "fluidic conduit" between a sample droplet and a buffer droplet. The long and slender fluidic path minimizes the diffusion and fluidic mixing between the two droplets (thus eliminating non-specific transport) but provides a conduit between them for actively transported particles (thus allowing the specific transport). The conduit is purely fluidic, stabilized chemically (e.g. using surfactants) and controlled by EWOD. The effectiveness of the technique is demonstrated by eliminating approximately 97% non-magnetic beads in just one purification step, while maintaining high collection efficiency (>99%) of magnetic beads.