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dc.contributor.authorSutton, N.
dc.contributor.authorTracey, M.C.
dc.contributor.authorJohnston, I.D.
dc.contributor.authorGreenaway, R.
dc.contributor.authorRampling, M.W.
dc.date.accessioned2009-12-07T09:49:48Z
dc.date.available2009-12-07T09:49:48Z
dc.date.issued1997
dc.identifier.citationSutton , N , Tracey , M C , Johnston , I D , Greenaway , R & Rampling , M W 1997 , ' A Novel Instrument for Studying the Flow Behaviour of Erythrocytes through Microchannels Simulating Human ' , Microvascular Research , vol. 53 , no. 3 , pp. 272-281 . https://doi.org/10.1006/mvre.1997.2014
dc.identifier.issn0026-2862
dc.identifier.otherPURE: 111380
dc.identifier.otherPURE UUID: e3683be4-c1ce-4f47-9ccf-a113dc3b8c34
dc.identifier.otherdspace: 2299/4062
dc.identifier.otherScopus: 0031149740
dc.identifier.otherORCID: /0000-0001-9696-3191/work/62748183
dc.identifier.otherORCID: /0000-0002-0073-8684/work/69424237
dc.identifier.urihttp://hdl.handle.net/2299/4062
dc.descriptionOriginal article can be found at: http://www.sciencedirect.com/science/journal/00262862 Copyright Elsevier Inc. DOI: 10.1006/mvre.1997.2014 [Full text of this article is not available in the UHRA]
dc.description.abstractA novel instrument has been developed to study the microrheology of erythrocytes as they flow through channels of dimensions similar to human blood capillaries. The channels are produced in silicon substrates using microengineering technology. Accurately defined, physiological driving pressures and temperatures are employed whilst precise, real-time image processing allows individual cells to be monitored continuously during their transit. The instrument characterises each cell in a sample of ca. 1000 in terms of its volume and flow velocity profile during its transit through a channel. The unique representation of the data in volume/velocity space provides new insights into the microrheological behaviour of blood. The image processing and subsequent data analysis enable the system to reject anomalous events such as multiple cell transits, thereby ensuring integrity of the resulting data. By employing an array of microfluidic flow channels we can integrate a number of different but precise and highly reproducible channel sizes and geometries within one array, thereby allowing multiple, concurrent, isobaric measurements on one sample. As an illustration of the performance of the system, volume/velocity data sets recorded in a microfluidic device incorporating multiple channels of 100 μm length and individual widths ranging between 3.0 and 4.0 μm are presented.en
dc.language.isoeng
dc.relation.ispartofMicrovascular Research
dc.titleA Novel Instrument for Studying the Flow Behaviour of Erythrocytes through Microchannels Simulating Humanen
dc.contributor.institutionSchool of Engineering and Technology
dc.contributor.institutionCentre for Engineering Research
dc.contributor.institutionMicrofluidics and Microengineering
dc.contributor.institutionExtracellular Vesicle Research Unit
dc.contributor.institutionCentre for Research in Biodetection Technologies
dc.contributor.institutionCentre for Hazard Detection and Protection Research
dc.contributor.institutionSchool of Physics, Engineering & Computer Science
dc.contributor.institutionDepartment of Engineering and Technology
dc.contributor.institutionBioEngineering
dc.contributor.institutionMicro Electro-Mechanical Systems
dc.contributor.institutionParticle Instruments and diagnostics
dc.contributor.institutionCentre for Climate Change Research (C3R)
dc.description.statusPeer reviewed
rioxxterms.versionofrecordhttps://doi.org/10.1006/mvre.1997.2014
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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