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dc.contributor.authorHe, Mei
dc.contributor.authorZeng, Yong
dc.date.accessioned2017-09-15T15:38:51Z
dc.date.available2017-09-15T15:38:51Z
dc.date.issued2016-08
dc.identifier.citationHe, M., & Zeng, Y. (2016). Microfluidic Exosome Analysis toward Liquid Biopsy for Cancer. Journal of Laboratory Automation, 21(4), 599–608. http://doi.org/10.1177/2211068216651035en_US
dc.identifier.urihttp://hdl.handle.net/1808/24962
dc.description.abstractAssessment of a tumor’s molecular makeup using biofluid samples, known as liquid biopsy, is a prominent research topic in precision medicine for cancer, due to its noninvasive property allowing repeat sampling for monitoring molecular changes of tumors over time. Circulating exosomes recently have been recognized as promising tumor surrogates because they deliver enriched biomarkers, such as proteins, RNAs, and DNA. However, purification and characterization of these exosomes are technically challenging. Microfluidic lab-on-a-chip technology effectively addresses these challenges owing to its inherent advantages in integration and automation of multiple functional modules, enhancing sensing performance, and expediting analysis processes. In this article, we review the state-of-the-art development of microfluidic technologies for exosome isolation and molecular characterization with emphasis on their applications toward liquid biopsy–based analysis of cancer. Finally, we share our perspectives on current challenges and future directions of microfluidic exosome analysis.en_US
dc.publisherSageen_US
dc.rights© Sage Publishing 2016en_US
dc.subjectMicrofluidic lab-on-a-chip technologyen_US
dc.subjectExosomesen_US
dc.subjectLiquid biopsyen_US
dc.subjectCanceren_US
dc.subjectPrecision medicineen_US
dc.titleMicrofluidic Exosome Analysis toward Liquid Biopsy for Canceren_US
dc.typeArticleen_US
kusw.kuauthorZeng, Yong
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1177/2211068216651035en_US
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC5556932en_US
dc.rights.accessrightsopenAccess


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