Show simple item record

dc.contributor.authorLi, Peng
dc.contributor.authorMao, Zhangming
dc.contributor.authorPeng, Zhangli
dc.contributor.authorZhou, Lanlan
dc.contributor.authorChen, Yuchao
dc.contributor.authorHuang, Po-Hsun
dc.contributor.authorTruica, Cristina I.
dc.contributor.authorDrabick, Joseph J.
dc.contributor.authorEl-Deiry, Wafik S.
dc.contributor.authorDao, Ming
dc.contributor.authorSuresh, Subra
dc.contributor.authorHuang, Tony Jun
dc.date.accessioned2015-11-02T18:37:59Z
dc.date.available2015-11-02T18:37:59Z
dc.date.issued2015-04
dc.date.submitted2015-02
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/99656
dc.description.abstractCirculating tumor cells (CTCs) are important targets for cancer biology studies. To further elucidate the role of CTCs in cancer metastasis and prognosis, effective methods for isolating extremely rare tumor cells from peripheral blood must be developed. Acoustic-based methods, which are known to preserve the integrity, functionality, and viability of biological cells using label-free and contact-free sorting, have thus far not been successfully developed to isolate rare CTCs using clinical samples from cancer patients owing to technical constraints, insufficient throughput, and lack of long-term device stability. In this work, we demonstrate the development of an acoustic-based microfluidic device that is capable of high-throughput separation of CTCs from peripheral blood samples obtained from cancer patients. Our method uses tilted-angle standing surface acoustic waves. Parametric numerical simulations were performed to design optimum device geometry, tilt angle, and cell throughput that is more than 20 times higher than previously possible for such devices. We first validated the capability of this device by successfully separating low concentrations (~100 cells/mL) of a variety of cancer cells from cell culture lines from WBCs with a recovery rate better than 83%. We then demonstrated the isolation of CTCs in blood samples obtained from patients with breast cancer. Our acoustic-based separation method thus offers the potential to serve as an invaluable supplemental tool in cancer research, diagnostics, drug efficacy assessment, and therapeutics owing to its excellent biocompatibility, simple design, and label-free automated operation while offering the capability to isolate rare CTCs in a viable state.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 1 R01 GM112048-01A1)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 1R33EB019785-01)en_US
dc.description.sponsorshipNational Science Foundation (U.S.)en_US
dc.description.sponsorshipPenn State Center for Nanoscale Science (Materials Research Science and Engineering Center Grant DMR-0820404)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant U01HL114476)en_US
dc.language.isoen_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.1504484112en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceNational Academy of Sciences (U.S.)en_US
dc.titleAcoustic separation of circulating tumor cellsen_US
dc.typeArticleen_US
dc.identifier.citationLi, Peng, Zhangming Mao, Zhangli Peng, Lanlan Zhou, Yuchao Chen, Po-Hsun Huang, Cristina I. Truica, et al. “Acoustic Separation of Circulating Tumor Cells.” Proc Natl Acad Sci USA 112, no. 16 (April 6, 2015): 4970–4975.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.contributor.mitauthorPeng, Zhanglien_US
dc.contributor.mitauthorDao, Mingen_US
dc.relation.journalProceedings of the National Academy of Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsLi, Peng; Mao, Zhangming; Peng, Zhangli; Zhou, Lanlan; Chen, Yuchao; Huang, Po-Hsun; Truica, Cristina I.; Drabick, Joseph J.; El-Deiry, Wafik S.; Dao, Ming; Suresh, Subra; Huang, Tony Junen_US
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record