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dc.contributor.authorShen, Wenjiang
dc.contributor.authorGrover, William H.
dc.contributor.authorHecht, Vivian Chaya
dc.contributor.authorPayer, Kristofor Robert
dc.contributor.authorBryan, Andrea Kristine
dc.contributor.authorManalis, Scott R
dc.date.accessioned2015-10-29T14:55:25Z
dc.date.available2015-10-29T14:55:25Z
dc.date.issued2013-12
dc.date.submitted2013-09
dc.identifier.issn1473-0197
dc.identifier.issn1473-0189
dc.identifier.urihttp://hdl.handle.net/1721.1/99500
dc.description.abstractCell size, measured as either volume or mass, is a fundamental indicator of cell state. Far more tightly regulated than size is density, the ratio between mass and volume, which can be used to distinguish between cell populations even when volume and mass appear to remain constant. Here we expand upon a previous method for measuring cell density involving a suspended microchannel resonator (SMR). We introduce a new device, the dual SMR, as a high-precision instrument for measuring single-cell mass, volume, and density using two resonators connected by a serpentine fluidic channel. The dual SMR designs considered herein demonstrate the critical role of channel geometry in ensuring proper mixing and damping of pressure fluctuations in microfluidic systems designed for precision measurement. We use the dual SMR to compare the physical properties of two well-known cancer cell lines: human lung cancer cell H1650 and mouse lymphoblastic leukemia cell line L1210.en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (Koch Institute Support (Core) Grant P30-CA14051)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.). Physical Sciences Oncology Center (U54CA143874)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.). Cell Decision Process Center (P50GM68762)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Contract R01GM085457)en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/c3lc51022ken_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleMeasuring single cell mass, volume, and density with dual suspended microchannel resonatorsen_US
dc.typeArticleen_US
dc.identifier.citationBryan, Andrea K., Vivian C. Hecht, Wenjiang Shen, Kristofor Payer, William H. Grover, and Scott R. Manalis. “Measuring Single Cell Mass, Volume, and Density with Dual Suspended Microchannel Resonators.” Lab Chip 14, no. 3 (2014): 569–576.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Microsystems Technology Laboratoriesen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorBryan, Andrea K.en_US
dc.contributor.mitauthorHecht, Vivian Chayaen_US
dc.contributor.mitauthorPayer, Kristofor Roberten_US
dc.contributor.mitauthorGrover, William H.en_US
dc.contributor.mitauthorManalis, Scott R.en_US
dc.relation.journalLab on a Chipen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsBryan, Andrea K.; Hecht, Vivian C.; Shen, Wenjiang; Payer, Kristofor; Grover, William H.; Manalis, Scott R.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5223-9433
dc.identifier.orcidhttps://orcid.org/0000-0003-4110-1388
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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