1,557 research outputs found

    Digital microfluidics with pressure-based actuation

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    One of the key issues in biosensors is the time it takes for biomolecules in a solution to reach and bind to the sensor surface (particularly in low-concentration analytes). We present a novel flow scheme without microfluidic channels for label-free biosensors to decrease the delivery time of biomolecules. Through designing the biosensor in such a way that it becomes a membrane with holes, we can apply a droplet on it and push or pull it through the membrane by means of a pressure difference. Contrary to traditional microfluidics for, e.g., flow cells where the analyte flows over the sensor, the flow is now directed through the sensor. We have implemented this scheme in silicon-on-insulator biosensors and have demonstrated in a first proof-of-principle experiment, an improvement in delivery time of at least a factor of three

    Digitális mikrofluidika = Digital Microfluidics

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    A projekt során létrehoztunk felül nyitott és zárt digitális mikrofluidikai eszközöket (NYÁK lapokat), melyekhez az elektromosan változtatható nedvesítés elvét, mint a folyadékcsepp mozgatásának alapelvét felhasználva, vezérlő áramkört és szoftvert illesztettünk. A fejlesztéshez szükség volt az elektródrendszer többszöri átdolgozására, valamint a felület speciális vékonyréteges kezelésére, szigetelőként PDMS elasztomer, hidrofób felületként Teflon polimer felhasználásával. A fejlesztéssel párhuzamosan új mikrofluidikai csatornákban olyan kémiai és biológiai vizsgálatokat végeztünk el, amelyek ellenőrző, illetve elővizsgálatok lehetnek egy digitális mikrofluidikai rendszerben való megvalósításhoz. A projekt elején beszerzett sztereomikroszkóp és kamera felhasználásával olyan rendszert alakítottunk ki, amellyel valós időben lehet vizsgálni a chipen végbemenő változásokat, valamint több detektálási módszert is implementáltunk. Egy gyors kameraszámítógép felhasználásával áramlási citometriás mikrofluidikai eszközt hoztunk létre, amely eredményeinket 2 konferenciakiadványban publikáltunk. A projekt keretében megvásárolt COMSOL Multiphysics szoftverrel numerikus modellszámításokkal alátámasztottuk és igazoltuk mind a digitális mikrofluidikai cseppmozgatást és dinamikákat, mind a párhuzamosan végzett elővizsgálatokhoz szükséges mikrocsatornák optimális elrendezését és működését. | During the project years we have developed open and closed digital microfluidic devices (on PCB substrates). These devices are providing fluid droplet transports using the electrowetting on dielectric phenomenon as the droplet actuation effect. This has been achieved by developing appropriate driving circuitry and software. The development included several design improvement cycles of the electrode matrix and application of different thin films to the electrodes. The final surface treatment is a thin layer of PDMS elastomer as the dielectric and another thin layer of Teflon polymer as the hydrophobic surface. New microfluidic channel systems have been designed parallel to these developments where experimental chemical and biological analyses have been conducted. These experiments were preliminary tests to their application in digital microfluidic devices. The stereomicroscope and the camera purchased at the beginning have been combined and further developed into a real-time chip monitoring system and different detection schemes were implemented. A high-fps camera computer was combined with this device to produce a novel flow cytomety device in a microfluidic environment. These results have been published in 2 conference proceedings. A numerical simulation software (COMSOL Multiphysics) have been used to confirm droplet movements and wetting dynamics, furthermore it has been utilized to characterize and optimize microfluidic channel geometry of the preliminary test devices

    Yield Enhancement of Digital Microfluidics-Based Biochips Using Space Redundancy and Local Reconfiguration

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    As microfluidics-based biochips become more complex, manufacturing yield will have significant influence on production volume and product cost. We propose an interstitial redundancy approach to enhance the yield of biochips that are based on droplet-based microfluidics. In this design method, spare cells are placed in the interstitial sites within the microfluidic array, and they replace neighboring faulty cells via local reconfiguration. The proposed design method is evaluated using a set of concurrent real-life bioassays.Comment: Submitted on behalf of EDAA (http://www.edaa.com/

    Digital microfluidics on paper

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    This thesis is one of the first reports of digital microfluidics on paper and the first in which the chip’s circuit was screen printed unto the paper. The use of the screen printing technique, being a low cost and fast method for electrodes deposition, makes the all chip processing much more aligned with the low cost choice of paper as a substrate. Functioning chips were developed that were capable of working at as low as 50 V, performing all the digital microfluidics operations: movement, dispensing, merging and splitting of the droplets. Silver ink electrodes were screen printed unto paper substrates, covered by Parylene-C (through vapor deposition) as dielectric and Teflon AF 1600 (through spin coating) as hydrophobic layer. The morphology of different paper substrates, silver inks (with different annealing conditions) and Parylene deposition conditions were studied by optical microscopy, AFM, SEM and 3D profilometry. Resolution tests for the printing process and electrical characterization of the silver electrodes were also made. As a showcase of the applications potential of these chips as a biosensing device, a colorimetric peroxidase detection test was successfully done on chip, using 200 nL to 350 nL droplets dispensed from 1 μL drops

    Testing microelectronic biofluidic systems

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    According to the 2005 International Technology Roadmap for Semiconductors, the integration of emerging nondigital CMOS technologies will require radically different test methods, posing a major challenge for designers and test engineers. One such technology is microelectronic fluidic (MEF) arrays, which have rapidly gained importance in many biological, pharmaceutical, and industrial applications. The advantages of these systems, such as operation speed, use of very small amounts of liquid, on-board droplet detection, signal conditioning, and vast digital signal processing, make them very promising. However, testable design of these devices in a mass-production environment is still in its infancy, hampering their low-cost introduction to the market. This article describes analog and digital MEF design and testing method
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