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Velocity measurements of blood flow in a rectangular PDMS microchannel assessed by confocal micro-PIV system

dc.contributor.authorLima, Rui A.
dc.contributor.authorWada, Shigeo
dc.contributor.authorTanaka, Shuji
dc.contributor.authorTakeda, Motohiro
dc.contributor.authorTsubota, Ken-ichi
dc.contributor.authorIshikawa, Takuji
dc.contributor.authorYamaguchi, Takami
dc.date.accessioned2010-02-19T10:50:23Z
dc.date.available2010-02-19T10:50:23Z
dc.date.issued2006
dc.description.abstractThis paper examines the ability to measure the velocity of both physiological saline (PS) and in vitro blood in a rectangular polydimethysiloxane (PDMS) microchannel by means of the confocal micro-PIV system. The PDMS microchannel, was fabricated by conventional soft lithography, had a microchannel near to a perfect rectangular shape (300μm wide, 45μm deep) and was optically transparent, which is suitable to measure both PS and in vitro blood using the confocal system. By using this latter combination, the measurements of trace particles seeded in the flow were performed for both fluids at a constant flow rate (Re=0.021). Generally, all the velocity profiles were found to be markedly blunt in the central region mainly due to the low aspect ratio (h/w=0.15) of the rectangular microchannel. Predictions by a theoretical model for the rectangular microchannel have showed fairly good correspondence with the experimental micro-PIV results for the PS fluid. Conversely, for the in vitro blood with 20% haematocrit, small fluctuations were found on velocity profiles.pt
dc.description.sponsorshipThis study was supported in part by the following grants: International Doctoral Program in Engineering from the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT), “Revolutionary Simulation Software (RSS21)” next-generation IT program of MEXT; Grants-in-Aid for Scientific Research from MEXT and JSPS Scientific Research in Priority Areas (768) “Biomechanics at Micro- and Nanoscale Levels,” Scientific Research (A) No.16200031 “Mechanism of the formation, destruction, and movement of thrombi responsible for ischemia of vital organs.” The authors also thank all members of Esashi, Ono and Tanaka Lab. for their assistance in fabricating the PDMS microchannel.
dc.identifier.citationLima, R.; Wada, S.; Tanaka, S.; Takeda, M.; Tsubota, K.; Ishikawa, T.; Yamaguchi, T. (2006). Velocity measurements of blood flow in a rectangular PDMS microchannel assessed by confocal micro-PIV system. In World Congress on Medical Physics and Biomedical Engineering. Seoul, Korea.pt
dc.identifier.urihttp://hdl.handle.net/10198/2018
dc.language.isoengpt
dc.publisherSpringerpt
dc.subjectMicrocirculationpt
dc.subjectConfocal micro-PIVpt
dc.subjectPDMS microchannelpt
dc.subjectRed blood cellspt
dc.titleVelocity measurements of blood flow in a rectangular PDMS microchannel assessed by confocal micro-PIV systempt
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceSeoul, Koreapt
oaire.citation.titleWorld Congress on Medical Physics and Biomedical Engineeringpt
person.familyNameLima
person.givenNameRui A.
person.identifier.ciencia-idEE12-C3FB-349D
person.identifier.orcid0000-0003-3428-637X
person.identifier.ridH-5157-2016
person.identifier.scopus-author-id18437397800
rcaap.rightsopenAccesspt
rcaap.typeconferenceObjectpt
relation.isAuthorOfPublication7b50c499-8095-4f4f-8b1b-fa7388e4ff62
relation.isAuthorOfPublication.latestForDiscovery7b50c499-8095-4f4f-8b1b-fa7388e4ff62

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