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강주헌

Kang, Joo H.
Translational Multiscale Biofluidics Lab.
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dc.citation.endPage 5666 -
dc.citation.number 42 -
dc.citation.startPage 5657 -
dc.citation.title SMALL -
dc.citation.volume 11 -
dc.contributor.author Kang, Joo H. -
dc.contributor.author Um, Eujin -
dc.contributor.author Diaz, Alexande -
dc.contributor.author Driscoll, Harry -
dc.contributor.author Rodas, Melissa J -
dc.contributor.author Domansky, Karel -
dc.contributor.author Watters, Alexander L. -
dc.contributor.author Super, Michael -
dc.contributor.author Stone, Howard A. -
dc.contributor.author Ingber, Donald E. -
dc.date.accessioned 2023-12-22T00:36:59Z -
dc.date.available 2023-12-22T00:36:59Z -
dc.date.created 2016-02-23 -
dc.date.issued 2015-11 -
dc.description.abstract Magnetic nanoparticles have been employed to capture pathogens for many biological applications; however, optimal particle sizes have been determined empirically in specific capturing protocols. Here, a theoretical model that simulates capture of bacteria is described and used to calculate bacterial collision frequencies and magnetophoretic properties for a range of particle sizes. The model predicts that particles with a diameter of 460 nm should produce optimal separation of bacteria in buffer flowing at 1 L h(-1). Validating the predictive power of the model, Staphylococcus aureus is separated from buffer and blood flowing through magnetic capture devices using six different sizes of magnetic particles. Experimental magnetic separation in buffer conditions confirms that particles with a diameter closest to the predicted optimal particle size provide the most effective capture. Modeling the capturing process in plasma and blood by introducing empirical constants (c(e)), which integrate the interfering effects of biological components on the binding kinetics of magnetic beads to bacteria, smaller beads with 50 nm diameters are predicted that exhibit maximum magnetic separation of bacteria from blood and experimentally validated this trend. The predictive power of the model suggests its utility for the future design of magnetic separation for diagnostic and therapeutic applications. -
dc.identifier.bibliographicCitation SMALL, v.11, no.42, pp.5657 - 5666 -
dc.identifier.doi 10.1002/smll.201501820 -
dc.identifier.issn 1613-6810 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/18872 -
dc.identifier.url http://onlinelibrary.wiley.com/doi/10.1002/smll.201501820/abstract?systemMessage=Wiley+Online+Library+will+be+unavailable+for+up+to+3+hours+on+Saturday+19th+March+2016+from++11%3A00-14%3A00+GMT+%2F+07%3A00-10%3A00+EDT+%2F+19%3A00-22%3A00+SGT+for+essential+maintenance.++Apologies+for+the+inconvenience. -
dc.identifier.wosid 000364692700007 -
dc.language 영어 -
dc.publisher WILEY-V C H VERLAG GMBH -
dc.title Optimization of Pathogen Capture in Flowing Fluids with Magnetic Nanoparticles -
dc.type Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -

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