@article{a10857153bc542e0888307a7a59557a6,
title = "Enhanced Isolation and Release of Circulating Tumor Cells Using Nanoparticle Binding and Ligand Exchange in a Microfluidic Chip",
abstract = "The detection of rare circulating tumor cells (CTCs) in the blood of cancer patients has the potential to be a powerful and noninvasive method for examining metastasis, evaluating prognosis, assessing tumor sensitivity to drugs, and monitoring therapeutic outcomes. In this study, we have developed an efficient strategy to isolate CTCs from the blood of breast cancer patients using a microfluidic immune-affinity approach. Additionally, to gain further access to these rare cells for downstream characterization, our strategy allows for easy detachment of the captured CTCs from the substrate without compromising cell viability or the ability to employ next generation RNA sequencing for the identification of specific breast cancer genes. To achieve this, a chemical ligand-exchange reaction was engineered to release cells attached to a gold nanoparticle coating bound to the surface of a herringbone microfluidic chip (NP-HBCTC-Chip). Compared to the use of the unmodified HBCTC-Chip, our approach provides several advantages, including enhanced capture efficiency and recovery of isolated CTCs.",
author = "Park, {Myoung Hwan} and Eduardo Re{\'a}tegui and Wei Li and Tessier, {Shannon N.} and Wong, {Keith H.K.} and Jensen, {Anne E.} and Vishal Thapar and David Ting and Mehmet Toner and Stott, {Shannon L.} and Hammond, {Paula T.}",
note = "Funding Information: Our research was supported by Stand up to Cancer, a joint program of the Entertainment Industry Foundation (EIF) and the American Association for Cancer Research (AACR) (M.T., P.T.H.), the National Institute for Biomedical Imaging and Bioengineering (NIBIB) EB008047 (M.T.), the Koch Institute Core Grant P30-CA14051 from the NCI (P.T.H.) and NIH P41 EB002503-11 (M.T.). We acknowledge all our patients and healthy blood donors. All blood specimens were obtained with informed patient consent according to an institutional review board (IRB) protocol (05-300) at the Massachusetts General Hospital. The authors also wish to express their appreciation to the Institute for Soldier Nanotechnologies at MIT, supported by the Army Research Office under contract W911NF-13-D-0001 and the Air Force under contract W911NF-07-D-0004, whose facilities and/or equipment were used to conduct the research reported in this paper. Thanks to Aditya Bardia, Lecia V. Sequist, Libby Laura, Octavio Hurtado, and Charles Vanderburg at the Advanced Tissue Resource Core (ATRC) for expert technical support. Thanks to Nicole Vincent Jordan for providing TaqMan primers, and Cindy Agpraseuth for helping with microfluidic device preparations. Thanks to Berent Aldicakti, Eric Thai, and Kevin Duc Vo for RNA extraction and RNA library preparations. S.N.T. holds a Natural Sciences and Engineering Research Council (NSERC) of Canada Postdoctoral Fellowship. Publisher Copyright: {\textcopyright} 2017 American Chemical Society.",
year = "2017",
month = feb,
day = "22",
doi = "10.1021/jacs.6b12236",
language = "English",
volume = "139",
pages = "2741--2749",
journal = "Journal of the American Chemical Society",
issn = "0002-7863",
publisher = "American Chemical Society (ACS)",
number = "7",
}