Готові списки джерел за темами / Microfluidic Probe Integrated Device

Добірка наукової літератури з теми "Microfluidic Probe Integrated Device"

Автор: Grafiati

Опубліковано: 10 грудня 2022

Оновлено: 28 січня 2023

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Статті в журналах з теми "Microfluidic Probe Integrated Device"

Shinha, Kenta, and Hiroshi KIMURA. "Microfluidic probe integrated device for cell-based assay." Proceedings of Mechanical Engineering Congress, Japan 2016 (2016): J0270202. http://dx.doi.org/10.1299/jsmemecj.2016.j0270202.

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Shinha, Kenta, Wataru Nihei, and Hiroshi Kimura. "A Microfluidic Probe Integrated Device for Spatiotemporal 3D Chemical Stimulation in Cells." Micromachines 11, no. 7 (July 16, 2020): 691. http://dx.doi.org/10.3390/mi11070691.

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Анотація:

Numerous in vitro studies have been conducted in conventional static cell culture systems. However, most of the results represent an average response from a population of cells regardless of their local microenvironment. A microfluidic probe is a non-contact technology that has been widely used to perform local chemical stimulation within a restricted space, providing elaborated modulation and analysis of cellular responses within the microenvironment. Although microfluidic probes developed earlier have various potential applications, the two-dimensional structure can compromise their functionality and flexibility for practical use. In this study, we developed a three-dimensional microfluidic probe integrated device equipped with vertically oriented microchannels to overcome crucial challenges and tested the potential utility of the device in biological research. We demonstrated that the device tightly regulated spatial diffusion of a fluorescent molecule, and the flow profile predicted by simulation replicated the experimental results. Additionally, the device modulated the physiological Ca2+ response of cells within the restricted area by altering the local and temporal concentrations of biomolecules such as ATP. The novel device developed in this study may provide various applications for biological studies and contribute to further understanding of molecular mechanisms underlying cellular physiology.

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Sakuma, Shinya, and Fumihito Arai. "Cellular Force Measurement Using a Nanometric-Probe-Integrated Microfluidic Chip with a Displacement Reduction Mechanism." Journal of Robotics and Mechatronics 25, no. 2 (April 20, 2013): 277–84. http://dx.doi.org/10.20965/jrm.2013.p0277.

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This paper presents noncontact nanometric positioning of a probe tip with high output force in a microfluidic chip. To measure cellular force in a microfluidic chip on the basis of cell deformation, we employed an on-chip probe with a magnetic drive method with actuation on the order of millinewtons. A reduction mechanism was proposed to realize nanometric resolution for positioning the probe tip. This mechanism utilizes a combination of springs with different stiffness levels and is driven bymagnetic force. The performance of the prototype device was examined and results indicated that, as ameasure of repetitive positioning accuracy, standard deviation of probe tip displacement was under 0.18 µm. Deformation was successfully measured for an oocyte on the order of 0.1 mN, demonstrating, as a consequence, nanometric order noncontact actuation of the on-chip probe with high output force. Using this on-chip probe, cellular force measurement was achieved for the microfluidic chip.

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Zamboni, Riccardo, Annamaria Zaltron, Elena Izzo, Gregorio Bottaro, Davide Ferraro, and Cinzia Sada. "Opto-Microfluidic System for Absorbance Measurements in Lithium Niobate Device Applied to pH Measurements." Sensors 20, no. 18 (September 19, 2020): 5366. http://dx.doi.org/10.3390/s20185366.

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The aim of Lab-on-a-chip systems is the downscaling of analytical protocols into microfluidic devices, including optical measurements. In this context, the growing interest of the scientific community in opto-microfluidic devices has fueled the development of new materials. Recently, lithium niobate has been presented as a promising material for this scope, thanks to its remarkable optical and physicochemical properties. Here, we present a novel microfluidic device realized starting from a lithium niobate crystal, combining engraved microfluidic channels with integrated and self-aligned optical waveguides. Notably, the proposed microfabrication strategy does not compromise the optical coupling between the waveguides and the microchannel, allowing one to measure the transmitted light through the liquid flowing in the channel. In addition, the device shows a high versatility in terms of the optical properties of the light source, such as wavelength and polarization. Finally, the developed opto-microfluidic system is successfully validated as a probe for real-time pH monitoring of the liquid flowing inside the microchannel, showing a high integrability and fast response.

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Horayama, Masayuki, Tomoki Ohkubo, Kenta Arai, Kazuya Kabayama, Teruo Fuji, and Hiroshi Kimura. "H-2-4 Cell-based assay device integrated with a microfluidic probe." Proceedings of the Conference on Information, Intelligence and Precision Equipment : IIP 2014 (2014): _H—2–4–1_—_H—2–4–2_. http://dx.doi.org/10.1299/jsmeiip.2014._h-2-4-1_.

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Horayama, Masayuki, Tomoki Okubo, Teruo Fujii, and Hiroshi Kimura. "5PM1-C-3 Cell-based assay device integrated with a microfluidic probe." Proceedings of the Symposium on Micro-Nano Science and Technology 2013.5 (2013): 29–30. http://dx.doi.org/10.1299/jsmemnm.2013.5.29.

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Caneira, Catarina R. F., Denis R. Santos, Virginia Chu, and João P. Conde. "Regenerable Bead-Based Microfluidic Device with integrated THIN-Film Photodiodes for Real Time Monitoring of DNA Detection." Proceedings 2, no. 13 (December 10, 2018): 953. http://dx.doi.org/10.3390/proceedings2130953.

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Nanoporous microbead-based microfluidic systems for biosensing applications allow enhanced sensitivities, while being low cost and amenable for miniaturization. The regeneration of the microfluidic biosensing system results in a further decrease in costs while the integration of on-chip signal transduction enhances portability. Here, we present a regenerable bead-based microfluidic device, with integrated thin-film photodiodes, for real-time monitoring of molecular recognition between a target DNA and complementary DNA (cDNA). High-sensitivity assay cycles could be performed without significant loss of probe DNA density and activity, demonstrating the potential for reusability, portability and reproducibility of the system.

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Lee, Ji Hye, June Moon Jang, Han Sang Cho, Ki Cheol Han, Tae Song Kim, Ji Yoon Kang, and Eun Gyeong Yang. "Design and Characterization of Microfluidic Analysis System for RNA-Aminoglycoside Interactions." Key Engineering Materials 277-279 (January 2005): 90–95. http://dx.doi.org/10.4028/www.scientific.net/kem.277-279.90.

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Microfluidic devices are of considerable interest, since such technology offers great promise for the development of powerful and versatile miniaturized analyzers. Accordingly, the present work describes a microfluidic screening system that is composed of a microchip, hydrodynamic pumping unit and fluorescence detectors. To develop an assay for RNA-aminoglycoside interactions, microchips are designed and fabricated on a glass substrate, then flow simulations are performed in the microchannels. After optimizing the flow control and buffer composition for fluorescence-based biochemical assays, a fluorescently labeled aminoglycoside probe and RNA are allowed to flow continuously to the main micro-channel based on hydrodynamic pumping and their interactions monitored by fluorescence quenching, which is reversed upon competition with other aminoglycosides. Consequently, the proposed device can serve as an integrated microfluidic platform for the high-throughput screening of high affinity antibiotics for RNA targets.

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Hui, Liu, Tang, Song, Madou, Xia, and Wu. "Determination of Mercury(II) on A Centrifugal Microfluidic Device Using Ionic Liquid Dispersive Liquid−Liquid Microextraction." Micromachines 10, no. 8 (August 8, 2019): 523. http://dx.doi.org/10.3390/mi10080523.

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An integrated centrifugal microfluidic device was developed to preconcentrate and detect hazardous mercury (II) in water with ionic liquid as environmentally friendly extractant. An automatically salt-controlled ionic liquid dispersive liquid–liquid microextraction on a centrifugal microfluidic device was designed, fabricated, and characterized. The entire liquid transport mixing and separation process was controlled by rotation speed, siphon valves, and capillary valves. Still frame images on the rotating device showed the process in detail, revealing the sequential steps of mixing, siphon priming, transportation between chambers, and phase separation. The preconcentration of red dye could be clearly observed with the naked eye. By combining fluorescence probe and microscopy techniques, the device was tested to determine ppb-level mercury (II) in water, and was found to exhibit good linearity and low detection limit.

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SHINHA, Kenta, and Hiroshi KIMURA. "Evaluation of cell response to spatiotemporal chemical stimulation using a microfluidic probe integrated device." Proceedings of Mechanical Engineering Congress, Japan 2018 (2018): J0220206. http://dx.doi.org/10.1299/jsmemecj.2018.j0220206.

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Дисертації з теми "Microfluidic Probe Integrated Device"

Shaw, Kirsty Jane. "Integrated DNA extraction and amplification on a microfluidic device." Thesis, University of Hull, 2009. http://hydra.hull.ac.uk/resources/hull:2414.

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An evaluation of DNA extraction and amplification performed in microfluidic systems was carried out, with the aim of integrating the two processes in a single microfluidic device. This integrated device will then be incorporated upstream of capillary gel electrophoresis and fluorescence-based detection for development of a completely integrated genetic analysis system. DNA extraction was performed using a silica substrate with both hydrodynamic and electro-osmotic pumping (EOP), resulting in maximum DNA extraction efficiencies of 82% and 52% respectively under optimised conditions. While the DNA extraction efficiency was lower using EOP, this method eliminates the need for external pumps and ensures easier mechanical connection to the microfluidic device. The use of thermally activated silica monoliths as the solid-phase resulted in superior DNA extraction efficiencies compared to when photo-initiated monoliths and silica beads were used. DNA amplification of up to nine forensically relevant loci was successfully achieved on the microfluidic device in volumes as low as 1.1 microlitres using Peltier heating. A combination of silanisation and dynamic passivation was required to prevent PCR inhibition resulting from DNA polymerase adsorption. A custom-built microwave heating system was also evaluated, which was capable of heating and cooling rates of 65degC/second and 58degC/second, respectively. EOP was used in the generation of an integrated microfluidic device, for DNA extraction and amplification. The silica monolith used as the solid-phase for DNA extraction also acted as a pump for electrokinetic movement. All necessary reagents for carrying out both DNA extraction and amplification were encapsulated in agarose gel and pre-loaded onto the microfluidic device creating a self-contained, ready-to-use system. Following addition of the biological sample to the microfluidic device, all electrokinetic movement and thermal cycling was controlled using a custom-built operating system.

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Rivas, Cardona Juan Alberto. "Development of a microfluidic device for patterning multiple species by scanning probe lithography." [College Station, Tex. : Texas A&M University, 2006. http://hdl.handle.net/1969.1/ETD-TAMU-1823.

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Dhopeshwarkar, Rahul Rajesh. "Electrokinetic concentration enrichment within a microfluidic device integrated with a hydrogel microplug." [College Station, Tex. : Texas A&M University, 2007. http://hdl.handle.net/1969.1/ETD-TAMU-1442.

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Sánchez, Daniela [Verfasser], and A. [Akademischer Betreuer] Guber. "Automated Integrated Microfluidic Device for DNA Cloning / Daniela Sánchez ; Betreuer: A. Guber." Karlsruhe : KIT-Bibliothek, 2019. http://d-nb.info/1184990085/34.

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Hui, Lawrence Kwan Yeung. "Integrated microfluidic device for single-cell high throughput screening in dynamic gene expression analysis." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 2008. http://wwwlib.umi.com/cr/ucsd/fullcit?p1457283.

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Анотація:

Thesis (M.S.)--University of California, San Diego, 2008.
Title from first page of PDF file (viewed November 13, 2008). Available via ProQuest Digital Dissertations. Includes bibliographical references (p. 58-60).

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Epshteyn, Alla. "Design and Fabrication of a Membrane Integrated Microfluidic Cell Culture Device Suitable for High-Resolution Imaging." Scholar Commons, 2010. http://scholarcommons.usf.edu/etd/3517.

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Malaria remains a serious concern for people living and traveling to warm climates in Africa, Asia, and some parts of America. Understanding the mechanism of the malaria parasite in the liver phase could lead to important discoveries for preventative and treatment therapeutics before the disease develops into the blood stage. While in vitro liver cell culture models have been explored, a device that mimics the liver cell architecture with the capability of high-resolution imaging has never been created. In this research, a cell culture microfluidic device was designed and fabricated with a membrane integrated design to mimic the architecture of a liver, cell chamber dimensions affable for high-resolution imaging, and fluidic port design for optical access to both sides of the membrane for the study of malaria parasite invasion.

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Dimopoulos, Georges. "Etude, caractérisation et modélisation des micromagnétodiodes à grille en silicium sur saphir." Grenoble INPG, 1989. http://www.theses.fr/1989INPG0015.

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Apres avoir presente une revue des divers capteurs de champ magnetique a semiconducteur integrables, nous rappelons le principe de l'effet magnetodiode et en verifions experimentalement les lois theoriques relatives aux caracteristiques courant-tension, aux dimensions des dispositifs et a leurs sensibilites au champ magnetique pour des micromagnetodiodes a grille en silicium sur saphir (sos). Nous etudions ensuite l'influence de la grille; nous donnons une interpretation qualitative des resultats, et comparons les performances obtenues pour differentes micromagnetodiodes sur sos, mais aussi pour les premieres magnetodiodes sur simox. Nous effectuons une modelisation de l'influence de la grille a partir d'une simulation a une dimension qui permet de comprendre et de decrire correctement le fonctionnement des macromagnetodiodes a grille; nous presentons aussi differents modeles (l'un analytique et l'autre numerique) de la sensibilite magnetique de nos dispositifs. Enfin des mesures de bruit permettent de completer la caracterisation de ces capteurs, de confirmer l'origine volumique du bruit en 1/f dans les magnetodiodes et d'obtenir les lois reliant le niveau de bruit aux polarisations

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Alexander, Stewart Parks. "An integrated microoptical microfluidic device for agglutination detection and blood typing." 2007. http://www.lib.ncsu.edu/theses/available/etd-01082007-035319/unrestricted/etd.pdf.

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Ya-ChunChuang and 莊雅鈞. "Affinity Biosensor of HbA1c Integrated with Microfluidic Device Based on Impedance Measurement." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/26650499095019854030.

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Tung, Chen-Kuo, and 董震國. "In Vitro Lobule Mimic Microfluidic Device Integrated with Dielectrophoresis Patterning and Gelatin Methacrylate Hydrogels." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/pyavcw.

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碩士
國立清華大學
動力機械工程學系
102
This thesis reports a lobule-mimicking chip, which was dedicated to reconstruct lobule tissue in vitro. In order to maintain the pattern of heterogeneous cells, the biocompatible material, Gelatin methacrylate (GelMA) hydrogels, was used. GelMA is a photocrosslinkable material which could be photocrosslinked under UV light. The chip design was divided into two parts: the first part includes the GelMA concentration generator, and the second part is composed of the cell patterning and the GelMA covering chamber. The GelMA concentration generator could generate three kinds of GelMA concentration: 5%, 10%, and 15%. In the cell culture chamber, 17 sets of hexagonal electrodes were located inside of it. Each set of hexagonal electrodes was used to attract and pattern 3T3 cells and C3A cells. After two kinds of cells were patterned and attracted to the defined location, different concentration of GelMA was loaded into the cell culture chamber. In order to understand the influence between different concentration of GelMA and cells, the tests of viability and urea had been performed. The viability of cells under 5% of GelMA can maintain 95% after72-hrs culture. By increasing the concentration of GelMA, the cell viability would decrease down to 78%. The urea assay showed that cells covered by GelMA can still maintain their activity. The results also showed that patterned cells covered by GelMA modules can maintain their pattern after 3-days culture. Compared with the patterned cells without covering GelMA modules, 3T3 cells grow faster than C3A cells and migrate above C3A cells.

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Частини книг з теми "Microfluidic Probe Integrated Device"

Prabhakar, Priyanka, Raj Kumar Sen, Neeraj Dwivedi, Raju Khan, Pratima R. Solanki, Satanand Mishra, Avanish Kumar Srivastava, and Chetna Dhand. "3D-Printed Microfluidic Device with Integrated Biosensors for Biomedical Applications." In Advanced Microfluidics-Based Point-of-Care Diagnostics, 147–66. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003033479-6.

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Liu, Robin H., and Piotr Grodzinski. "Fully Integrated Microfluidic Device for Direct Sample-to-Answer Genetic Analysis." In Microarrays, 37–65. New York, NY: Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-72719-6_3.

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Killeen, Kevin, Hongfeng Yin, Sharmila Udiavar, Reid Brennen, Mark Juanitas, Elaine Poon, Dan Sobek, and Tom van de Goor. "Chip-MS: A Polymeric Microfluidic Device with Integrated Mass-Spectrometer Interface." In Micro Total Analysis Systems 2001, 331–32. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-1015-3_141.

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Wei, Huibin. "Microfluidic Device with Integrated Porous Membrane for Cell Sorting and Separation." In Springer Theses, 61–82. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-32359-1_4.

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Ono, Yasunari, Shusaku Daikoku, Yasuko Hasegawa, Toshiyuki Sato, Mariko Kobayashi, Katsuhiko Suzuki, and Osamu Kanie. "Towards Developing a Golgi Simulator: Microfluidic Device Enabling Synthesis of a Tetrasaccharide." In Molecular Imaging for Integrated Medical Therapy and Drug Development, 288–93. Tokyo: Springer Japan, 2010. http://dx.doi.org/10.1007/978-4-431-98074-2_28.

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Zhu, Zhen, Yangye Geng, and Yingying Wang. "Monitoring Single S. cerevisiae Cells with Multifrequency Electrical Impedance Spectroscopy in an Electrode-Integrated Microfluidic Device." In Methods in Molecular Biology, 105–18. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0822-7_9.

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Sung, Wang-Chou, Pao-Chi Liao, Pang-Wei Chen, Gwo-Bin Lee, Mong-Kuan Chou, and Shu-Hui Chen. "Microfluidic Device with Integrated Protein Digestion, Peptide Separation and Nanospray Interface on Poly (Dimethylsiloxane) PDMS Substrate." In Micro Total Analysis Systems 2002, 509–11. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0295-0_170.

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Liang, Li-Guo, Ye-Feng Sheng, Sherry Zhou, Fatih Inci, Lanjuan Li, Utkan Demirci, and ShuQi Wang. "An Integrated Double-Filtration Microfluidic Device for Detection of Extracellular Vesicles from Urine for Bladder Cancer Diagnosis." In Methods in Molecular Biology, 355–64. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7253-1_29.

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Chien, Yu Sheng, Che Hsin Lin, Fu Jen Kao, and Cheng Wen Ko. "A Fully Integrated System for Cell/Particle Sorting in a Microfluidic Device Utilizing an Optical Tweezing and DIP Recognition Approach." In Materials Science Forum, 643–48. Stafa: Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/0-87849-990-3.643.

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"Detecting Optically Inactive Analyte: MC-CE Device Integrated with QDs/LIF Detection for Determination of Acrylamide in Food." In Microfluidic Chip-Capillary Electrophoresis Devices, 186–205. CRC Press, 2015. http://dx.doi.org/10.1201/b18846-13.

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Тези доповідей конференцій з теми "Microfluidic Probe Integrated Device"

Shinha, Kenta, and Hiroshi Kimura. "Spatiotemporal Control of Cell Culture Microenvironment by Microfluidic Probe Integrated Device." In 2018 International Symposium on Micro-NanoMechatronics and Human Science (MHS). IEEE, 2018. http://dx.doi.org/10.1109/mhs.2018.8886939.

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Strohm, Eric M., Michael C. Kolios, Dae Kun Hwang, Byeong-Ui Moon, and Scott S. H. Tsai. "Development of a microfluidic device with integrated high frequency ultrasound probe for particle characterization." In 2014 IEEE International Ultrasonics Symposium (IUS). IEEE, 2014. http://dx.doi.org/10.1109/ultsym.2014.0487.

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Maktabi, Sepehr, Jeffrey W. Schertzer, and Paul R. Chiarot. "Microfluidic-Based Fabrication and Dielectrophoretic Manipulation of Microcapsules." In ASME 2019 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/imece2019-11903.

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Abstract To probe the complexity of biological systems, large numbers of independent experiments are needed to gather statistically reliable information. A platform that performs these experiments at high-throughput demands precise control over the formation and delivery of microcapsules. Microfluidics enables passive and active modes of droplet formation, manipulation, and mixing. Aqueous- and organic-based emulsions serve as well-defined compartments that encapsulate target materials (e.g., cells, reagents, nucleic acid, and nanoparticles) in femto- to picoliter volumes surrounded by an immiscible fluid. In this work, we demonstrate a high-throughput PDMS-based microfluidic device for fabrication and control of uniform micron-size water-in-oil and oil-in-water emulsions. Passive and active modes of droplet generation (i.e., hydrodynamic flow focusing and electrospray, respectively) are utilized to form droplets in the size range of 1 to 100 μm. We also leverage dielectrophoretic forces to steer the microemulsions across flows of organic or inorganic phases. The dielectrophoretic force provides high-speed separation with no moving elements and does not require droplet charging. Two electrode designs of AC- and DC-based circuits incorporated into the PDMS block are proposed. We investigate the effect of frequency and voltage on the degree of deflection and separation efficiency of the emulsions. We show that the fabricated microcapsules can be used as templates to build synthetic lipid bilayer model membranes that more accurately mimic physiological conditions. In addition, our microfluidic-based device integrated with on-board electronics can be used as an essential component in high-speed screening bioassays.

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Wang, Chih-Hung, Chia-Jung Chang, Jiunn-Jong Wu, and Gwo-Bin Lee. "A new pathogen detection system by utlizing nanogold modified specific probe and vancomycin coated magnetic beads on an integrated microfluidic device." In 2013 IEEE 26th International Conference on Micro Electro Mechanical Systems (MEMS). IEEE, 2013. http://dx.doi.org/10.1109/memsys.2013.6474185.

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Emery, Travis S., Anna Jensen, Koby Kubrin, and Michael G. Schrlau. "Facilitating Fluid Flow Through Carbon Nanotube Arrays Using 3D Printing." In ASME 2017 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/imece2017-71656.

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Three-dimensional (3D) printing is a novel technology whose versatility allows it to be implemented in a multitude of applications. Common fabrication techniques implemented to create microfluidic devices, such as photolithography, wet etching, etc., can often times be time consuming, costly, and make it difficult to integrate external components. 3D printing provides a quick and low-cost technique that can be used to fabricate microfluidic devices in a range of intricate geometries. External components, such as nanoporous membranes, can additionally be easily integrated with minimal impact to the component. Here in, low-cost 3D printing has been implemented to create a microfluidic device to enhance understanding of flow through carbon nanotube (CNT) arrays manufactured for gene transfection applications. CNTs are an essential component of nanofluidic research due to their unique mechanical and physical properties. CNT arrays allow for parallel processing however, they are difficult to construct and highly prone to fracture. As a means of aiding in the nanotube arrays’ resilience to fracture and facilitating its integration into fluidic systems, a 3D printed microfluidic device has been constructed around these arrays. Doing so greatly enhances the robustness of the system and additionally allows for the nanotube array to be implemented for a variety of purposes. To broaden their range of application, the devices were designed to allow for multiple isolated inlet flows to the arrays. Utilizing this multiple inlet design permits distinct fluids to enter the array disjointedly. These 3D printed devices were in turn implemented to visualize flow through nanotube arrays. The focus of this report though, is on the design and fabrication of the 3D printed devices. SEM imaging of the completed device shows that the nanotube array remains intact after the printing process and the nanotubes, even those within close proximity to the printing material, remain unobstructed. Printing on top of the nanotube arrays displayed effective adhesion to the surface thus preventing leakage at these interfaces.

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Sofela, Samuel, Alla Saleh, and Mohammad A. Qasaimeh. "Integrated Microfluidic Probe for Single Cell Manipulation ^*." In 2022 International Conference on Manipulation, Automation and Robotics at Small Scales (MARSS). IEEE, 2022. http://dx.doi.org/10.1109/marss55884.2022.9870475.

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Dawoud, Abdulilah A., and Ryszard Jankowiak. "Fully Integrated Microfluidic Device with Carbon Sensing Electrode." In 2007 IEEE Sensors. IEEE, 2007. http://dx.doi.org/10.1109/icsens.2007.4388395.

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Lyu, Yingkai, Jianan Yin, Yuanshuai Zhu, Yuchen Fu, Andrew Glidle, Hitoshi Furusho, Tianxin Yang, and Huabing Yin. "An integrated opto-microfluidic device for microflow cytometry." In Integrated Sensors for Biological and Neural Sensing, edited by Hooman Mohseni. SPIE, 2021. http://dx.doi.org/10.1117/12.2575500.

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Mappes, Timo, Jürgen Mohr, Kristin Mandisloh, Mauno Schelb, and Benjamin Ross. "A compound microfluidic device with integrated optical waveguides." In Photonics Europe, edited by Hugo Thienpont, Peter Van Daele, Jürgen Mohr, and Mohammad R. Taghizadeh. SPIE, 2008. http://dx.doi.org/10.1117/12.781820.

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Wu, Qingjun, J. Z. Jiang, wang hao, zhang dongxian, Hao Jia, and Cheng Jiang. "Refractive index detection by using an integrated microfluidic device." In Sixth International Conference on Optical and Photonic Engineering, edited by Yingjie Yu, Chao Zuo, and Kemao Qian. SPIE, 2018. http://dx.doi.org/10.1117/12.2326821.

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Звіти організацій з теми "Microfluidic Probe Integrated Device"

Nguyen, Thanh Phong. Integrated Microfluidic Device for Real-Time: Reservoir Fluid Analysis. Office of Scientific and Technical Information (OSTI), July 2018. http://dx.doi.org/10.2172/1459859.

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