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Human Platelet Membrane Functionalized Microchips with Plasmonic Codes for Cancer Detection

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dc.contributor.authorSumit Kumar-
dc.contributor.authorJae-A Han-
dc.contributor.authorIssac J. Michael-
dc.contributor.authorKi D.-
dc.contributor.authorVijaya Sunkara-
dc.contributor.authorJuhee Park-
dc.contributor.authorShreedhar Gautam-
dc.contributor.authorHa H.K.-
dc.contributor.authorZhang L.-
dc.contributor.authorYoon-Kyoung Cho-
dc.date.available2019-10-11T08:09:21Z-
dc.date.created2019-08-20-
dc.date.issued2019-07-
dc.identifier.issn1616-301X-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/6303-
dc.description.abstract© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, WeinheimThe possibility of functional roles played by platelets in close alliance with cancer cells has inspired the design of new biomimetic systems that exploit platelet–cancer cell interactions. Here, the role of platelets in cancer diagnostics is leveraged to design a microfluidic platform capable of detecting cancer-derived extracellular vesicles (EVs) from ultrasmall volumes (1 µL) of human plasma samples. Further, the captured EVs are counted by direct optical coding of plasmonic nanoprobes modified with EV-specific antibodies. Owing to the inherent properties of platelets for multifaceted interaction with cancer cells, the microfluidic chip equipped with a biologically interfaced platelet membrane-cloaked surface (denoted “PLT-Chip”) can capture a significantly higher number of EVs from multiple types of cancer cell lines (prostate, lung, bladder, and breast) than the normal cell-derived EVs. Furthermore, this chip allows the monitoring of the growth of tumor spheroids (100 µm–2.5 mm) and clearly distinguishes the plasma of cancer patients from that of normal healthy controls. This robust, multifaceted, and cancer-specific binding affinity, coupled with excellent biocompatibility, is a unique feature of platelet membrane-cloaked surfaces, which therefore represent promising alternatives to antibodies for application in EVs-based cancer theranostics-
dc.description.uri1-
dc.language영어-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectcancer-
dc.subjectextracellular vesicles-
dc.subjectplasmonic coupling-
dc.subjectplatelets-
dc.titleHuman Platelet Membrane Functionalized Microchips with Plasmonic Codes for Cancer Detection-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000478612000014-
dc.identifier.scopusid2-s2.0-85069891584-
dc.identifier.rimsid69385-
dc.contributor.affiliatedAuthorSumit Kumar-
dc.contributor.affiliatedAuthorJae-A Han-
dc.contributor.affiliatedAuthorIssac J. Michael-
dc.contributor.affiliatedAuthorVijaya Sunkara-
dc.contributor.affiliatedAuthorJuhee Park-
dc.contributor.affiliatedAuthorShreedhar Gautam-
dc.contributor.affiliatedAuthorYoon-Kyoung Cho-
dc.identifier.doi10.1002/adfm.201902669-
dc.identifier.bibliographicCitationADVANCED FUNCTIONAL MATERIALS, v.29, no.30, pp.1902669-
dc.citation.titleADVANCED FUNCTIONAL MATERIALS-
dc.citation.volume29-
dc.citation.number30-
dc.citation.startPage1902669-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusEXOSOMES-
dc.subject.keywordAuthorcancer-
dc.subject.keywordAuthorextracellular vesicles-
dc.subject.keywordAuthorplasmonic coupling-
dc.subject.keywordAuthorplatelets-
Appears in Collections:
Center for Soft and Living Matter(첨단연성물질 연구단) > 1. Journal Papers (저널논문)
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