Browsing by Subject "microfluidic"
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Item Development of High-Throughput Microfluidic Impedance Spectroscopy Platform for Analyzing Microdroplets in Droplet Microfluidic System(2014-07-22) Sobahi, Nebras MohammedKamal A.This thesis presents the development of a high-throughput microfluidic impedance spectroscopy platform for electrically detecting analyzing impedance measurements of non-contact and label free microdroplets. This microfluidic impedance spectroscopy platform gives valuable information of the size and contents of the microdroplets in general and particularly of cells encapsulated within droplets. Impedance spectroscopy is a common method for analyzing dielectric properties of particles with respect to the stimulating frequency. Microfluidic based impedance spectroscopy can analyze up to micro size particles. However, droplets based microfluidic impedance spectroscopy systems for analyzing cells encapsulated within droplets have been rarely developed. However, to develop a high-throughput system, a novel sensitive high-throughput droplets based microfluidic impedance spectroscopy platform for analyzing cells encapsulated with droplets at different levels concentrations at throughput of 140 Hz which has not been reported in the literature yet. The device sensitivity was demonstrated using chlamydomonas reinhardtii cells. Two throughputs (17 and 140 droplets/s) for four level of cells concentrations were discriminating and compared. The maximum deviation in the acquired data for both cases was 6.9%. At 10% difference of cells encapsulated within droplets, the device was capable of discriminating and distinguishing different between the encapsulated microdroplets.Item Integration of functional components into microfluidic chemical systems: bioimmobilization and electrochemiluminescent detection on-chip(Texas A&M University, 2005-08-29) Zhan, WeiWe have investigated and implemented several general strategies in the development of microfluidics-based chemical/biochemical sensing systems. The research in this dissertation covers the immobilization of biological reagents inside microfluidic channels using polystyrene (PS) microbeads and photopolymerizable hydrogel, electrochemical sensing via electrochemiluminescence (ECL) reporting with bipolar and two-electrode configurations, and integration of these general functions to realize multiplexing and networking on-chip. Photopolymerizable hydrogel based on Poly(ethylene glycol) (PEG) and streptavidin-coated polystyrene (PS) microbeads were employed as building blocks as well as functional components in microfluidic system. PEG hydrogels can be used to define local microenvironments at different locations in the same microchannel, which enables the introduction of multiple sensing events on the same device. Monitoring of DNA hybridization and enzyme/substrate interaction were realized thereafter by using either fluorescence or electrochemistry as the detection method. Electrogenerated chemiluminescence based on Ru(bpy)32+ (bpy = 2,2??-bipyridine) and tripropylamine (TPA) was used to photonically report various redox events in microfluidic systems. By using microfluidic electrochemical cells based on either two-electrode or bipolar electrode (one-electrode), electroactive species that undergo reduction can be electrically linked to this anodic ECL process and thus be reported by the latter. This ECL sensing scheme essentially broadens the spectrum of redox compounds that can be detected by ECL since the analytes are not required to directly participate into the light-generating processes. Microfluidics offers some unique technical advantages of performing electrochemistry over conventional methods. In particular, laminar flow allows multiple analyte streams to be brought together in parallel with little mixing. Moreover, electrochemical signals can be generally utilized as a convenient means to link individual microchannels together hence to realize microfluidic networking and cross-communication. Electrochemical microfluidic devices can be used to mimic general functions of microelectronic devices such as diodes, transistors, and logic gates. These novel functions rendered by electrochemistry are believed to bring us closer to the final goals of micro total analysis systems and lab-on-a-chip.Item Microdisk fabrication by emulsion evaporation(Texas A&M University, 2007-09-17) Wong, Susanna Wing ManColloidal suspensions of disk-like particles have been of interest in both colloidal and liquid crystal studies because they exhibit unique liquid crystalline phases different from those of rod-like molecules. Disk-like particles, such as asphaltenes in heavy oil industry, clay particles in agriculture, and red blood cells in biology, are of great interest in a variety of industries and scientific areas. However, to fabricate monodisperse microdisks, uniform in structure or composition with precise control of particle size and shape has not yet succeeded. In this thesis, we show an experimental strategy of using microfluidic technique to fabricate homogeneous ????-eicosene microemulsions with chloroform in an aqueous solution of sodium dedecyl sulfate (SDS). The monodisperse chloroform emulsions, generated by the glass-based microfluidic devices, ensure the precise control on microdisk particle size and shape. A systematic investigation was performed to study the relation between the resulted microdisk size and the initial concentration of ????-eicosene in chloroform before evaporation. The smectic liquid crystalline phase inside the wax particles controls the coin-like disk shape below the melting temperature of wax??????s rotator phase. The kinetics of the disk formation is observed using a polarized light microscope. Dynamic light scattering is used to characterize the Brownian motion of the microdisks, and the rotational diffusion is estimated from the image sequences taken by the charge-coupled device (CCD) camera. Effort has been put into collecting a large quantity of microdisks to investigate the discotic liquid crystalline phases, which can be readily probed by light scattering and microscope. In comparison, X-ray and neutron have to be used for the atomic liquid crystalline phase investigation.Item Microfluidic Systems for Investigating Bacterial Chemotaxis and Colonization(2011-02-22) Englert, Derek LynnThe overall goal of this work was to develop and utilize microfluidic models for investigating bacterial chemotaxis and biofilm formation - phenotypes that play key roles in bacterial infections. Classical methods for investigating chemotaxis and biofilm formation have many limitations and drawbacks. These include being unsuitable for investigating the effect of chemorepellents, non-quantitative readouts, and not accounting for interaction between hydrodynamics and biofilm formation. The novel microfluidic model systems for chemotaxis and biofilm formation developed in this study addresses these drawbacks. Chemotaxis model system development was done in three stages. We first developed two static chemotaxis model systems - the two fluorophore chemotaxis agarose plug assay and the mu Plug assay - for rapidly determining the extent of chemotaxis in a qualitative manner. A key feature of these model systems was the incorporation of dead cells and differential labeling with green and red fluorescent proteins for partitioning the effects of movement due to fluid flow from chemotaxis. The static systems were used to rapidly screen a wide range of conditions for use in the flow-based mu Flow chemotaxis model system. The effect of four major variables - cell preparation method, gradient strength, flow rate in the device, and imaging position - that influence the chemotactic response in the mu Flow was characterized using the repellent taxis from Ni^2 gradients as the model chemoeffector. Using the mu Flow chemotaxis device, we investigated the chemotaxis of Escherichia coli RP437 to different signals that are present in the human gastrointestinal tract and are likely to be mediators of infection through their effect on chemotaxis. Our data show that the bacterial signal indole is a repellent, while the signals autoinducer-2 (AI-2) and isatin are attractants for E. coli RP437. However, cells exposed to a competing gradient of indole and either AI-2 or isatin, attracts E. coli. The ?Flow device was also used to refute a long-standing view on how the repellent Ni2 is sensed in E. coli. Our data show that only the Tar chemoreceptor is needed for sensing Ni^2 and the nickel binding protein, NikA, and the Ni^2 transport system proteins, NikB and NikC, are not required for repellent taxis from nickel. A microfluidic biofilm model was also developed in this study and used in conjunction with a mathematical model to investigate biofilm formation and quorum sensing in closed systems (where biofilm growth and hydrodynamics are interdependent). The mathematical model predictions were experimentally validated using Pseudomonas aeruginosa PA14 in a microfluidic biofilm system at various flow rates.