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This text focuses on the physics of fluid transport in micro- and nanofabricated liquid-phase systems, with consideration of gas bubbles, solid particles, and macromolecules. This text was designed with the goal of bringing together several areas that are often taught separately - namely, fluid mechanics, electrodynamics, and interfacial chemistry and electrochemistry - with a focused goal of preparing the modern microfluidics researcher to analyse and model continuum fluid mechanical systems encountered when working with micro- and nanofabricated devices. This text serves as a useful reference for practising researchers but is designed primarily for classroom instruction. Worked sample problems are included throughout to assist the student, and exercises at the end of each chapter help facilitate class learning.
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Microfluidic devices --- Dispositifs microfluidiques --- Microfluidics --- Microfluidique
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This book is the second edition of the one originally published in 2016, which focused on state-of-the-art microfluidic research in medical and biological applications. Similar to the first edition, beginners in the field —undergraduates, engineers, biologists, medical and pharmaceutical researchers—will easily learn to understand microfluidic-based medical and biological applications. Because a wide range of topics is summarized here, it also helps experts to learn more about fields outside their own specialties. In this second edition, significant revisions have been made to chapters covering technologies that have seen major advancements, such as acoustofluidics, protein crystallography, organ-on-a-chip systems, nanopore sensing, and paper-based microfluidics. In addition, the chapters on cancer diagnosis using exosomes and single-cell sequencing using droplet microfluidics, which are attracting attention as new technologies, have been newly added. Readers will be convinced that microfluidic devices have great potential for medical and biological applications.
Microfluidic devices. --- Microfluidics. --- Labs on a chip.
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This book focuses on state-of-the-art microfluidic research in medical and biological applications. The top-level researchers in this research field explain carefully and clearly what can be done by using microfluidic devices. Beginners in the field —undergraduates, engineers, biologists, medical researchers—will easily learn to understand microfluidic-based medical and biological applications. Because a wide range of topics is summarized here, it also helps experts to learn more about fields outside their own specialties. The book covers many interesting subjects, including cell separation, protein crystallization, single-cell analysis, cell diagnosis, point-of-care testing, immunoassay, embyos/worms on a chip and organ-on-a-chip. Readers will be convinced that microfluidic devices have great potential for medical and biological applications.
Analytical chemistry. --- Microarrays. --- Biomedical engineering. --- Regenerative medicine. --- Tissue engineering. --- Analytical Chemistry. --- Biomedical Engineering and Bioengineering. --- Regenerative Medicine/Tissue Engineering. --- Biomedical engineering --- Regenerative medicine --- Tissue culture --- Medicine --- Regeneration (Biology) --- Clinical engineering --- Medical engineering --- Bioengineering --- Biophysics --- Engineering --- Analysis, Chemical --- Analytical chemistry --- Chemical analysis --- Metallurgical analysis --- Mineralogy, Determinative --- Microfluidics --- Microfluidics. --- Microfluidic Analytical Techniques. --- Lab-On-A-Chip Devices. --- Microchip Analytical Devices --- Microfluidic Devices --- Microfluidic Lab-On-A-Chip --- Microfluidic Microchips --- Nanochip Analytical Devices --- Analytical Device, Microchip --- Analytical Device, Nanochip --- Analytical Devices, Microchip --- Analytical Devices, Nanochip --- Device, Lab-On-A-Chip --- Device, Microchip Analytical --- Device, Microfluidic --- Device, Nanochip Analytical --- Devices, Lab-On-A-Chip --- Devices, Microchip Analytical --- Devices, Microfluidic --- Devices, Nanochip Analytical --- Lab On A Chip Devices --- Lab-On-A-Chip Device --- Lab-On-A-Chip, Microfluidic --- Lab-On-A-Chips, Microfluidic --- Microchip Analytical Device --- Microchip, Microfluidic --- Microchips, Microfluidic --- Microfluidic Device --- Microfluidic Lab On A Chip --- Microfluidic Lab-On-A-Chips --- Microfluidic Microchip --- Nanochip Analytical Device --- Microchip Analytical Procedures --- Microfluidic Analysis --- Analyses, Microfluidic --- Analysis, Microfluidic --- Analytical Technique, Microfluidic --- Analytical Techniques, Microfluidic --- Microfluidic Analyses --- Microfluidic Analytical Technique --- Technique, Microfluidic Analytical --- Techniques, Microfluidic Analytical --- Microfluidic --- Rheology --- Microfluidic Analytical Techniques --- Fluidics --- Nanofluids --- instrumentation --- Analytic chemistry --- Chemistry, Analytic --- Chemistry
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Microfluidic devices. --- Biomedical materials. --- Bioartificial materials --- Biocompatible materials --- Biomaterials (Biomedical materials) --- Hemocompatible materials --- Medical materials --- Medicine --- Biomedical engineering --- Materials --- Biocompatibility --- Prosthesis --- Fluidic devices --- Microtechnology --- Microfluidic Analytical Techniques.
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biotechnologie --- Biotechnology --- bioengineering --- Fluid mechanics --- Microfluidic Analytical Techniques --- Biomedical Research --- Molecular Biology --- Medical electronics --- Molecular biology --- Microfluidics --- Biotechnologie --- Electronique en médecine --- Biologie moléculaire --- Microfluidique --- Periodicals. --- Périodiques --- Microfluidic Analytical Techniques. --- Biotechnology. --- Biomedical Research. --- Molecular Biology. --- Medical electronics. --- Microfluidics. --- Molecular biology. --- Chemistry --- Chemical Engineering --- Molecular biochemistry --- Molecular biophysics --- Biomedical electronics --- Electronics in clinical medicine --- Electronics in medicine --- Biochemical Genetics --- Biology, Molecular --- Genetics, Biochemical --- Genetics, Molecular --- Molecular Genetics --- Biochemical Genetic --- Genetic, Biochemical --- Genetic, Molecular --- Molecular Genetic --- Experimental Medicine --- Investigational Medicine --- Investigative Medicine --- Research, Biomedical --- Research, Medical --- Medical Research --- Medicine, Experimental --- Medicine, Investigational --- Medicine, Investigative --- Biotechnologies --- Microfluidic Analysis --- Analyses, Microfluidic --- Analysis, Microfluidic --- Analytical Technique, Microfluidic --- Analytical Techniques, Microfluidic --- Microfluidic Analyses --- Microfluidic Analytical Technique --- Technique, Microfluidic Analytical --- Techniques, Microfluidic Analytical --- Biochemistry --- Biophysics --- Biomolecules --- Systems biology --- Fluidics --- Nanofluids --- Biomedical engineering --- Electronics --- Chemical engineering --- Genetic engineering --- Genetic Phenomena --- Animals, Laboratory --- Bioengineering
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We have developed a microfluidic two-layered channel system based on polycarbonate to investigate the transmigration of cancer cells under flow conditions and defined shear rate using live cell microscopy. The two layers are separated by a porous membrane with an endothelial monolayer on top of the membrane to mimic the blood vessel wall. To extend the measuring capabilities of our microfluidic chip, gold electrodes were structured on the membrane using optical lithography and chemical etching.
membrane --- Krebszellen --- SensorikCancer cell --- Metastasierung --- Mikrofluidik --- Blutgefäß --- sensors --- Membran --- Blood vessel --- Impedanz --- microfluidic --- Impedance
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Artificial organs. --- Organs, Artificial --- Prosthesis --- Surgery --- Artificial organs --- Microfluidic devices --- Microphysiological Systems --- Technological innovations. --- Therapeutic use.
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The intramolecular SEA ligation for the preparation of cyclic peptides of various sizes was studied under microfluidic conditions. Two type of peptides, namely POL (10 residues) and RTD-1 (18 residues) as well as difficult junctions (e.g. valine, isoleucine, and threonine) were chosen as the main targets of this research. The microfluidic setup for the intramolecular SEA ligation formally telescoped two process steps. In the first microreactor, the reversible N,S-acyl shift reaction lead to the reactive SEA thioester species in ~90% conversion for all studied peptides. The telescoping of the first step and the use of the reactive SEA thioester species in the capture step of the N- terminal cysteine mediated by an exogenous arylthiol catalyst produced a cyclic thioester intermediate which upon irreversible S,N-acyl shift gave the final cyclic product. This fully telescoped process of 64 (POL and analogs) to 75 min (RTD-1 and analogs) total residence time gave the associated desired cyclic product with conversions ranging from 60 to 96% depending on the peptide sequence and the ligation site.
SEA Ligation --- Peptides --- Cyclic Peptides --- Microfluidic --- Physique, chimie, mathématiques & sciences de la terre > Chimie
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We report herein on the valorization of glycerol, a “bio-based platform” molecule with a large availability, towards epichlorohydrin, a major building block in the production of epoxy resins. Epichlorohydrin production from glycerol has become economically viable with the rise of the bio-fuel market. Glycerol is obtained as a by-product of the biofuel industry, making it available in large quantities and at low price. Epichlorohydrin is traditionally produced from propene, a petro-based compound whose price tends to fluctuate a lot. The classical process towards epichlorhydrin suffers from several drawbacks such as a low atom economy, the use of hazardous materials and the production of toxic by-products. Our research is focused on the development of a safe and efficient continuous-flow process that allows the production of epichlorohydrin from glycerol. The first step of the synthesis involves the conversion of glycerol into monochlorohydrins and then dichlorohydrins with a chlorination agent (here aqueous HCl) catalyzed by carboxylic acids. The temperature and residence time were optimized in a microfluidic setup. Then, a catalyst screening was undertaken, highlighting the high efficiency of common lactones such as γ-butyrolactone and ε-caprolactone, as well of aliphatic dicarboxylic acids such as adipic and pimelic acids. The latter showed an exceptional catalytic activity (>99% conversion, 81% cumulated yields towards chlorohydrins) and high selectivity for 1,3-dichloro-2-propanol. The second step of the synthesis is the epoxidation of dichlohydrins towards epichlorohydrin with the help of a base such as NaOH. The epoxidation reaction was firstly studied in conventional batch reactors and then, transposed to continuous flow operation under microfluidic conditions. This step was very fast and showed >90% of conversion in less than 5 minutes at room temperature. Finally, the two steps of the reaction were concatenated into a single microfluidic system allowing the direct use “on the spot” of the toxic chlorohydrins generated in the first step. The process showed very promising results with 98% of conversion and 96% of cumulated yields towards a ca. 1:1 mixture of epichlorohydrin and glycidol, another value-added compound. Moreover, the conditions reported herein have a low environmental footprint since the reaction occurs in water, and the chlorination agent is HCl. The inherent high heat and mass transfer capacities related to microfluidic reactors coupled with the use of an excellent catalyst significantly reduced the spaceframe for this process, with total reaction times of 25 minutes under continuous flow conditions.
continuous flow --- platform molecules --- microfluidic --- biomass --- Physique, chimie, mathématiques & sciences de la terre > Chimie
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