Recent advances in computing technology have highlighted deficiencies with electrical interconnections at the motherboard and card-to-backplane levels. The CPU speeds of computing systems are drastically increasing with on-chip local clock speeds expected to approach 6 GHz by 2010. Yet, card-to-backplane communication speeds have been unable to maintain the same pace. At speeds beyond a few gigahertz the implementation of electronic interconnects gets increasingly complex, thus, alternative optical interconnection techniques are being extensively researched to relieve the expected CPU to data bus bottleneck. Despite the advantages afforded by optical interconnects there are still demands for improved packaging, enhanced signal tapping, and reduced cost expenditures. In this dissertation, we present a novel array waveguide evanescent coupling (AWEC) technology for card-to-backplane applications. The interconnection scheme is based on waveguide directional coupling between a backplane waveguide and a flexible waveguide connected to the access card or daughter board. To gain access to the shared bus media, coupling of evanescent waves is exploited to tap optical signals from the backplane waveguide to the corresponding card waveguide. The approach results in the elimination of micro-mirror out of plane deflectors and local waveguide termination obstacles present in other reported optical interconnect schemes. Most importantly, the AWEC method can yield efficient multi-drop bus architectures, not possible through free-space, fiber, or traditional guided wave approaches, that only achieve point-to-point topologies. The AWEC concept for optical interconnection was introduced through coupled mode theory, numerical simulations and BeamPROP aided CAD models. Subsequent experimental waveguide analysis was performed and shown to reasonably agree with the simulation results. Likewise, a high-resolution, cost-effective, and rapid prototyping approach for AWEC fabrication has been formulated. Significantly, when compared to other soft lithographic methods, the novel vacuum assisted microfluidic (VAM) technique results in improved waveguide structures, polymer background residue elimination and lower propagation losses. Moreover, experimental results show that our evanescent coupling approach facilitates high-speed coupling between card and backplane waveguides at speeds of 10 Gbps per channel; currently limited only by our testing electronics. In addition, satisfactory eye diagram performance comparable to that of a conventional fiber link, was also observed for the AWEC, alluding to possible aggregate speeds of 100 Gbps. Similarly, we implemented an elementary AWEC shared bus architecture and demonstrate a microprocessor-to-memory interconnect prototype through the proposed AWEC link. Notably, we expect that the AWEC scheme will be significant for high-speed optical interconnects in advanced computing systems.

AC Electrokinetics (ACEK) has attracted much research interest for microfluidic manipulation for the last few years. It shows great potential for functions such as micropumping, mixing and concentrating particles. Most of current ACEK research focuses on AC electroosmosis (ACEO), which is limited to solutions with conductivity less than 0.02 S/m, excluding most biofluidic applications. To solve for this problem, this dissertation seeks to apply AC electrothermal (ACET) effect to manipulate conductive fluids and particles within, and it is among the first demonstration of ACET devices, a particle trap and an ACET micropump. The experiments used fluids at a conductivity of 0.224 S/m that is common in bio-applications. Pumping and trapping were demonstrated at low voltages, reaching ~100 um/s for no more than 8 Vrms at 200 kHz. The flow velocity was measured to follow a quadratic relationship with applied voltage which is in accordance with theory. This research also studies ACET effect on low ionic strength microfluidics, since Joule heating is ubiquitous in electrokinetic devices. One contribution is that our study suggested ACET as one possible reason of flow reversal, which has intrigued the researchers in ACEK field. Electrically, a microfluidic cell can be viewed as an impedance network of capacitances and resistors. Heat dissipation in those elements varies with AC frequency and fluid properties, so changes the relative importance of heat generation at the electrode/electrolyte interface and in the resistive fluid bulk, which could change the temperature gradient in the device, hence changing the flow direction. Another contribution of this dissertation is the reaction enhanced ACET micropumping. A dramatic improvement in flow rate over conventional ac micropumps is achieved by introducing a thin fluid layer of high ionic density near the electrodes. Such an ionic layer is produced by superimposing a DC offset on AC signal that induces Faradaic reaction. The velocity improvement, in some cases, is over an order of magnitude, reaching a linear velocity of up to 2.5 mm/s with only 5.4Vrms. This discovery presents an exciting opportunity of utilizing ACET effect in microfluidic applications.

Thesis (Ph. D.)--Ohio State University, 2006. / Title from first page of PDF file. Includes bibliographical references (p. 178-197).

In this thesis, we discuss some physical phenomena related to the manipulation of droplets, and their possible use as alternatives for digital microfluidics. In a first part, the behavior of droplets in the vicinity of another liquid interface is explored. We have shown that droplets can be kept bouncing onto a liquid interface, provided this latter is vertically vibrated. The bouncing mechanisms are investigated in several configurations. Bouncing droplets may also experience self-propulsion and partial coalescence. The second part of this thesis is dedicated to the study of droplets sliding down fibers. The basic microfluidic operations are advantageously implemented with simple fiber networks. Dans cette thèse, nous discutons plusieurs phénomènes physiques liés à la manipulation des gouttes et à leur application possible en temps qu'alternatives à la microfluidique digitale actuelle. La première partie est consacrée au comportement de gouttes au voisinage d'une autre interface liquide. Nous avons prouvé qu'une goutte peut rebondir indéfiniment sur une interface liquide vibrée verticalement. Les mécanismes du rebond sont analysés en détail pour plusieurs configurations. Sous certaines conditions, les gouttes rebondissantes peuvent également s'auto-propulser ou coalescer partiellement. Dans une seconde partie, nous étudions le glissement des gouttes sur des fibres. Les opérations microfluidiques de base sont avantageusement réalisées sur de simples réseaux de fibres.

Imagine if you could combine the power and capabilities ofan entire laboratory in the palm of your hand. Advances inmicrofluidic chip technology promise to integrate andminiaturize multiple lab processes into a single palm-sizeddevice. The advantages of these lab-on-a-chip devices,sometimes also referred to as micro total analysis systems(µTAS), compared with conventional bench-scale systems arenumerous and wide ranging and include: less reagentconsumption, low manufacturing costs, increased performance,faster analysis, high sample throughput, integration andautomation possibilities, and disposability. However,microfluidic devices also present challenges such as theinterfacing to the macro world and detection limits. In this thesis the focus has been to develop novel discretemicrofluidic components for biotechnology and organic chemicalapplications with the goal to integrate them to formlab-on-chips. A flow-through filter-chamber device has beendesigned, manufactured and evaluated for chemical analysis onbeads. Passive liquid handling has been integrated on the chipin the form of hydrophobic valves at the inlet channels. Anarray format has also been developed to allow parallel analysisof multiple samples. The filter-chamber functions well forsingle nucleotide analysis using pyrosequencing. Initialevaluations on catalyst screening in the filter-chamber devicehas been performed. The suitability of valve-less micropumps for biochemicalapplications is presented. Fluids encountered in variousbiochemical methods, including living cells, that areproblematic for other micropumps have been pumped with goodperformance. This thesis also introduces expandablemicrospheres as a novel component in microfluidics includingapplications such as one-shot valves, micropositioning andsurface enlargement. A novel technique for bead immobilization in microfluidicdevices based on surface chemistry is presented in this thesis.Beads for both biochemical assays and organic chemistry havebeen self-sorted and self-assembled in line patterns as narrowas 5 µm on both structured and unstructured substrates.This method will greatly facilitate the generation of screeningplatforms, for example. To develop a microfluidic device for catalysis-on-chip,ligands for asymmetric catalysis have successfully beenimmobilized in silicon channels by consecutive microcontactprinting, which is a novel technique presented in thisthesis. <b>Keywords:</b>microfluidics, beads, microspheres, silicon,filter-chamber, flow-through, bead trapping, DRIE, passivevalves, fluorocarbon, microfluidic array, adhesive bonding,valve-less micropump, microcontact printing, PDMS,self-assembly, self-sorting, DNA, SNP, pyrosequencing,allele-specific extension, expandable microspheres, catalysis,chiral ligand, monolayer, miniaturization, lab-on-a-chip,µTAS.

Digital microfluidics is a new technology that permits manipulation of liquid droplets on an array of electrodes. Using this technology, nanoliter to microliter size droplets of different samples and reagents can be dispensed from reservoirs, moved, split, and merged together. Digital microfluidics is poised to become an important and useful tool for biomedical applications because of its capacity to precisely and automatically carry out sequential chemical reactions. In this thesis, a set of tools is presented to accelerate the integration of digital microfluidics into Lab-on-a-Chip platforms for a wide range of applications. An important contribution in this thesis is the development of three rapid prototyping techniques, including the use of laser printing to pattern flexible printed circuit board (PCB) substrates, to make the technology accessible and less expensive. Using these techniques, both digital and channel microfluidic devices can be produced in less than 30 minutes at a minimal cost. These rapid prototyping techniques led to a new method for manipulating liquid droplets on non-planar surfaces. The method, called All Terrain Droplet Actuation (ATDA), was used for several applications, including DNA enrichment by liquid-liquid extraction. ATDA has great potential for the integration of different physico-chemical environments on Lab-on-a-Chip devices. A second important contribution described herein is the development of a new microfluidic format, hybrid microfluidics, which combines digital and channel microfluidics on the same platform. The new hybrid device architecture was used to perform biological sample processing (e.g. enzymatic digestion and fluorescent labeling) followed by electrophoretic separation of the analytes. This new format will facilitate complete automation of Lab-on-a-Chip devices and will eliminate the need for extensive manual sample processing (e.g. pipetting) or expensive robotic stations. Finally, numerical modeling of droplet actuation on single-plate digital microfluidic devices, using electrodynamics, was used to evaluate the droplet actuation forces. Modeling results were verified experimentally using an innovative technique that estimates actuation forces based on resistive forces against droplet motion. The results suggested a list of design tips to produce better devices. It is hoped that the work presented in this thesis will help introduce digital microfluidics to many of the existing Lab-on-a-Chip applications and inspire the development of new ones.

<p>A digital microfluidic biochip (DMFB) is a device that digitizes fluidic samples into tiny droplets and operates chemical processes on a single chip. Movement control of droplets can be realized by using electrowetting-on-dielectric (EWOD) technology. DMFBs have high configurability, high sensitivity, low cost and reduced human error as well as a promising future in the applications of point-of-care medical diagnostic, and DNA sequencing. As the demands of scalability, configurability and portability increase, a new DMFB architecture called Microelectrode Dot Array (MEDA) has been introduced recently to allow configurable electrodes shape and more precise control of droplets.</p> <p>The objective of this work is to investigate a routing algorithm which can not only handle the routing problem for traditional DMFBs, but also be able to route different sizes of droplets and incorporate diagonal movements for MEDA. The proposed droplet routing algorithm is based on 3D-A* search algorithm. The simulation results show that the proposed algorithm can reduce the maximum latest arrival time, average latest arrival time and total number of used cells. By enabling channel-based routing in MEDA, the equivalent total number of used cells can be significantly reduced. Compared to all existing algorithms, the proposed algorithm can achieve so far the least average latest arrival time.</p>

Isolation of selected populations from heterogeneous cell mixtures and retrieval of the captured population of interest for regenerative medicine and diagnostics applications is one of the challenges that may be addressed by microfluidics. An affinity adhesion strategy was tested using the tetrapeptides RGDS (arg-gly-asp-ser), REDV (arg-glu-asp-val) and VAPG (val-ala-pro-gly) to modify an alginate hydrogel surface layer to selectively adhere fibroblast (FB), endothelial (EC) and smooth muscle cell (SMC) populations, respectively, of the non-myocyte cardiac cell fraction. Incorporation of peptides into sodium alginate gel surface coatings demonstrated a preferential, seeding density-dependent adhesion relationship on alginate-RGDS when tested with a cardiomyocyte-depleted cell suspension in both static culture and in microfluidic devices. Seeding density-dependent attachment was seen with close to 100% release of viable cells from coated surfaces upon application of ethylenediaminetetraacetic acid (EDTA). Further work will optimize the system with REDV and VAPG to capture ECs and SMCs.

In this thesis, I present a microfluidic platform that enables automated image-based assessment of biological structure and function. My work focuses on assessing intact resistance arteries from the mouse cerebral vascular bed with a diameter of approximately 120µm in vitro. The experimental platform consists of a microfluidic device and a world-to-chip fluidic interconnect that minimizes unwanted dead volumes and eliminates the need for any liquid-filled peripheral equipment. The integrated platform is computer controlled and capable of fully automated operation once a small blood vessel segment is loaded onto the chip. Robust operation of the platform was demonstrated through a series of case studies that assessed small artery function and changes therein induced by incubation with the drug nifedipine, a dihydropyridine calcium channel blocker. In addition artery segments were stained for L-type calcium channels, F-actin and nuclei, from which structural information about cell alignment and shape was quantified.

In this thesis, I present a microfluidic platform that enables automated image-based assessment of biological structure and function. My work focuses on assessing intact resistance arteries from the mouse cerebral vascular bed with a diameter of approximately 120µm in vitro. The experimental platform consists of a microfluidic device and a world-to-chip fluidic interconnect that minimizes unwanted dead volumes and eliminates the need for any liquid-filled peripheral equipment. The integrated platform is computer controlled and capable of fully automated operation once a small blood vessel segment is loaded onto the chip. Robust operation of the platform was demonstrated through a series of case studies that assessed small artery function and changes therein induced by incubation with the drug nifedipine, a dihydropyridine calcium channel blocker. In addition artery segments were stained for L-type calcium channels, F-actin and nuclei, from which structural information about cell alignment and shape was quantified.