Microfluidics - CPR-1000 Current Probe Reader manufacturer - china CRI-1001 Tester

Microscale behavior of fluids Silicone rubber and glasscorridors (indicated here as Ji,j) into a 1D lattice. The
microfluidic devices. Top: a photograph of theecosystem service (of habitat renewal) to each MHP
devices. Bottom: DIC micrographs of a serpentinerepresented here as i (red arrows). Each MHP can
channel ~15 m wide. The behavior of fluids at thealso hold different carrying capacity Ki for its
microscale can differ from 'macrofluidic' behavior insupporting local population of bacterial cells (depicted
that factors such as surface tension, energyin green). By combining microfluidics with landscape
dissipation, and fluidic resistance start to dominate theecology and nanofluidics, a nano/micro fabricated
system. Microfluidics studies how these behaviorsfluidic landscape can be constructed by building local
change, and how they can be worked around, orpatches of bacterial habitat and connecting them by
exploited for new uses. At small scales (channeldispersal corridors. The resulting landscapes can be
diameters of around 100 nanometers to severalused as physical implementations of an adaptive
hundred micrometers) some interesting andlandscape , by generating a spatial mosaic of patches
sometimes unintuitive properties appear. In particular,of opportunity distributed in space and time. The
the Reynolds number (which compares the effect ofpatchy nature of these fluidic landscapes allows for
momentum of a fluid to the effect of viscosity) canthe study of adapting bacterial cells in a
become very low. A key consequence of this is thatmetapopulation system. The evolutionary ecology of
fluids, when side-by-side, do not necessarily mix inthese bacterial systems in these synthetic
the traditional sense; molecular transport betweenecosystems allows for using biophysics to address
them must often be through diffusion. High specificityquestions in evolutionary biology. Cellular biophysics By
of chemical and physical properties (concentration,rectifying the motion of individual swimming bacteria ,
pH, temperature, shear force, etc.) can also bemicrofluidic structures can be use to extract
ensured resulting in more uniform reaction conditionsmechanical motion from a population of motile
and higher grade products in single and multi-stepbacterial cells . This way, bacteria-powered rotors can
reactions. Effects of micro domain laminar flowbe built. Optics Tuneable Microlens Array Acoustic
surface tension electrowetting fast thermal relaxationdroplet ejection (ADE) Acoustic droplet ejection uses
electrical surface charges diffusion Key applicationa pulse of ultrasound to move low volumes of fluids
areas Microfluidic structures include micropneumatic(typically nanoliters or picoliters) without any physical
systems, i.e. microsystems for the handling ofcontact. This technology focuses acoustic energy into
off-chip fluids (liquid pumps, gas valves, etc), anda fluid sample in order to eject droplets as small as a
microfluidic structures for the on-chip handling ofmillionth of a millionth of a liter (picoliter = 10-12 liter).
nano- and picolitre volumes. To date, the mostADE technology is a very gentle process, and it can
successful commercial application of microfluidics isbe used to transfer proteins, high molecular weight
the inkjet printhead. Significant research has beenDNA and live cells without damage or loss of viability.
applied to the application of microfluidics for theThis feature makes the technology suitable for a
production of industrially relevant quantities ofwide variety of applications including proteomics and
material. Advances in microfluidics technology arecell-based assays. Fuel cells For more details on this
revolutionizing molecular biology procedures fortopic, see Electroosmotic pump. Microfluidic fuel cells
enzymatic analysis (e.g., glucose and lactate assays),can use laminar flow to separate the fuel and its
DNA analysis (e.g., polymerase chain reaction andoxidant to control the interaction of the two fluids
high-throughput sequencing), and proteomics. Thewithout a physical barrier as would be required in
basic idea of microfluidic biochips is to integrate assayconventional fuel cells. See also Fluidics Nanofluidics
operations such as detection, as well as sampleList of microfluidics research groups Lab on a chip
pre-treatment and sample preparation on one chip.Digital microfluidics Fluids@Home References ^ Kirby,
An emerging application area for biochips is clinicalB.J. (2010). Micro- and Nanoscale Fluid Mechanics:
pathology, especially the immediate point-of-careTransport in Microfluidic Devices. Cambridge University
diagnosis of diseases. In addition, microfluidics-basedPress. ^ Karniadakis, G.M., Beskok, A., Aluru, N. (2005).
devices, capable of continuous sampling and real-timeMicroflows and Nanoflows. Springer Verlag.  ^ Bruus,
testing of air/water samples for biochemical toxinsH. (2007). Theoretical Microfluidics. Oxford University
and other dangerous pathogens, can serve as anPress.  ^ Tabeling, P. (2005). Introduction to
always-on "bio-smoke alarm" for early warning.Microfluidics. Oxford University Press.  ^ J
Continuous-flow microfluidics These technologies areShestopalov, J. D. Tice and R. F. Ismagilov,"Multi-step
based on the manipulation of continuous liquid flowsynthesis of nanoparticles performed on millisecond
through microfabricated channels. Actuation of liquidtime scale in a microfluidic droplet-based system" Lab
flow is implemented either by external pressureChip, 2004, 4, 316 - 321, DOI: 10.1039/b403378g. ^
sources, external mechanical pumps, integratedNguyen, N.T., Wereley, S. (2006). Fundamentals and
mechanical micropumps, or by combinations ofApplications of Microfluidics. Artech House.  ^ Wei Li,
capillary forces and electrokinetic mechanisms.Jesse Greener, Dan Voicu and Eugenia Kumacheva
Continuous-flow microfluidic operation is the"Multiple modular microfluidic (M3) reactors for the
mainstream approach because it is easy to implementsynthesis of polymer particles" Lab Chip, 2009, 9,
and less sensitive to protein fouling problems.2715 - 2721, DOI: 10.1039/b906626h. ^ Herold, KE;
Continuous-flow devices are adequate for manyRasooly, A (editor) (2009). Lab-on-a-Chip Technology:
well-defined and simple biochemical applications, andFabrication and Microfluidics. Caister Academic Press.
for certain tasks such as chemical separation, butISBN 978-1-904455-46-2.  ^ a b Herold, KE; Rasooly,
they are less suitable for tasks requiring a highA (editor) (2009). Lab-on-a-Chip Technology:
degree of flexibility or complicated fluid manipulations.Biomolecular Separation and Analysis. Caister
These closed-channel systems are inherently difficultAcademic Press. ISBN 978-1-904455-47-9.  ^ Chang,
to integrate and scale because the parameters thatH.C., Yeo, Leslie (2009). Electrokinetically Driven
govern flow field vary along the flow path makingMicrofluidics and Nanofluidics. Cambridge University
the fluid flow at any one location dependent on thePress.  ^ Fan et al. (2009). "Two-Dimensional
properties of the entire system. Permanently-etchedElectrophoresis in a Chip". Lab-on-a-Chip Technology:
microstructures also lead to limited reconfigurabilityBiomolecular Separation and Analysis. Caister
and poor fault tolerance capability. Process monitoringAcademic Press. ISBN 978-1-904455-47-9.  ^
capabilities in continuous-flow systems can beBontoux et al. (2009). "Elaborating Lab-on-a-Chips for
achieved with highly sensitive microfluidic flowSingle-cell Transcriptome Analysis". Lab-on-a-Chip
sensors based on MEMS technology which offerTechnology: Biomolecular Separation and Analysis.
resolutions down to the nanoliter range. DigitalCaister Academic Press. ISBN 978-1-904455-47-9.  ^
(droplet-based) microfluidics Alternatives to theCady, NC (2009). "Microchip-based PCR Amplification
above closed-channel continuous-flow systems includeSystems". Lab-on-a-Chip Technology: Biomolecular
novel open structures, where discrete, independentlySeparation and Analysis. Caister Academic Press. ISBN
controllable droplets are manipulated on a substrate978-1-904455-47-9.  ^ Keymer J.E., P. Galajda, C.
using electrowetting. Following the analogy of digitalMuldoon R., and R. Austin (November 2006). "Bacterial
microelectronics, this approach is referred to as digitalmetapopulations in nanofabricated landscapes". PNAS
microfluidics, which was pioneered as the "fluid103 (46): 17290-295. doi:10.1073/pnas.0607971103.  ^
transistor" by Cytonix and subsequentlyGalajda P, J.E. Keymer, P Chaikin, R. Austin
commercialized by Duke University. By using discrete(December 2007). "A Wall of Funnels Concentrates
unit-volume droplets, a microfluidic function can beSwimming Bacteria". Journal of Bacteriology 189 (23):
reduced to a set of repeated basic operations, i.e.,8704-8707. doi:10.1128/JB.01033-07.  ^ Angelani L., R.
moving one unit of fluid over one unit of distance.Di Leonardo, G. Ruocco (2009). "Self-Starting
This "digitization" method facilitates the use of aMicromotors in a Bacterial Bath". Phys. Rev. Let. 102:
hierarchical and cell-based approach for microfluidic048104. doi:10.1103/PhysRevLett.102.048104.  ^ Di
biochip design. Therefore, digital microfluidics offers aLeonardo R, L. Angelani , G. Ruocco, V. Iebba, M.P.
flexible and scalable system architecture as well asConte, S. Schippa, F. De Angelis, F. Mecarini, E. Di
high fault-tolerance capability. Moreover, becauseFabrizio (October 2009). "A bacterial ratchet motor".
each droplet can be controlled independently, thesearXiv:Condensed Matter.Statistical Mechanics.  ^
systems also have dynamic reconfigurability, wherebySokolova A., M.M. Apodacac, B.A. Grzybowskic, I.S.
groups of unit cells in a microfluidic array can beAransona (December 2009). "Swimming bacteria
reconfigured to change their functionality during thepower microscopic gears". PNAS 107 (3): 969-974.
concurrent execution of a set of bioassays. Althoughdoi:10.1073/pnas.0913015107.  ^ Liquid micro-lens
droplets are manipulated in confined microfluidicarray activated by selective electrowetting on lithium
channels, since the control on droplets is notniobate substrates S. Grilli, L. Miccio, V. Vespini, A.
independent, it should not be confused as "digitalFinizio, S. De Nicola, and P. Ferraro Optics Express 16,
microfluidics". One common actuation method for8084-8093 (2008). ^ P. Ferraro, L. Miccio, S. Grilli, A.
digital microfluidics is electrowetting-on-dielectricFinizio, S. De Nicola, and V. Vespini, "Manipulating Thin
(EWOD). Many lab-on-a-chip applications have beenLiquid Films for Tunable Microlens Arrays," Optics
demonstrated within the digital microfluidics paradigm& Photonics News 19, 34-34 (2008) ^ Water
using electrowetting. However, recently otherManagement in PEM Fuel Cells ^ Building a Better Fuel
techniques for droplet manipulation have also beenCell Using Microfluidics ^ Fuel Cell Initiative at MnIT
demonstrated using Surface Acoustic Waves,Microfluidics Laboratory Further reading Review
optoelectrowetting etc. DNA chips (microarrays) EarlyPapers Whitesides, G. M.; "The origins and the future
biochips were based on the concept of a DNAof microfluidics"; Nature 2006, 442, 368-373. Squires,
microarray, e.g., the GeneChip DNAarray fromT. M.; Quake, S. R.; Reviews of Modern Physics 2005,
Affymetrix, which is a piece of glass, plastic or silicon77, 977-1026. Microfluidics: Fluid physics at the
substrate on which pieces of DNA (probes) arenanoliter scale Books Herold, KE; Rasooly, A (editor)
affixed in a microscopic array. Similar to a DNA(2009). Lab-on-a-Chip Technology: Fabrication and
microarray, a protein array is a miniature array whereMicrofluidics. Caister Academic Press. ISBN
a multitude of different capture agents, most978-1-904455-46-2.  Herold, KE; Rasooly, A (editor)
frequently monoclonal antibodies, are deposited on a(2009). Lab-on-a-Chip Technology: Biomolecular
chip surface; they are used to determine theSeparation and Analysis. Caister Academic Press. ISBN
presence and/or amount of proteins in biological978-1-904455-47-9.  External links Wikibooks has a
samples, e.g., blood. A drawback of DNA and proteinbook on the topic of Microfluidics Biomicrofluidics, an
arrays is that they are neither reconfigurable noropen access, peer reviewed journal published by the
scalable after manufacture. Digital microfluidics hasAmerican Institute of Physics MEMSuniverse, a
been described as a means for carrying out DigitalVideos and animations of Microfluidic devices and their
PCR. Molecular biology In addition to microarraysapplications Supercool microfluidics - Our
biochips have been designed for two-dimensionalunderstanding of life and technology at extreme
electrophoresis, transcriptome analysis, and PCRtemperatures could become clearer thanks to a
amplification. Other applications include variousmicrofluidic device that studies ice formation reported
electrophoresis and liquid chromatography applicationsin Chemical Technology from the Royal Society of
for proteins and DNA, cell separation, in particularChemistry From microfluidic applications to nanofluidic
blood cell separation, protein analysis, cell manipulationphenomena - a Chem Soc Rev themed issue
and analysis including cell viability analysis andshowcasing the latest advances in microfluidic and
microorganism capturing. Evolutionary biology Threenanofluidic research, guest edited by Albert van den
Micro Habitat Patches MHPs connected by dispersalBerg, Harold Craighead and Peidong Yang.