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Precision cell-free DNA extraction for liquid biopsy by integrated microfluidics

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dc.contributor.authorLee, Hoyoon-
dc.contributor.authorPark, Chanhee-
dc.contributor.authorNa, Wonhwi-
dc.contributor.authorPark, Kyong Hwa-
dc.contributor.authorShin, Sehyun-
dc.date.accessioned2021-08-31T09:36:39Z-
dc.date.available2021-08-31T09:36:39Z-
dc.date.created2021-06-18-
dc.date.issued2020-02-24-
dc.identifier.issn2397-768X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/57609-
dc.description.abstractCell-free DNA (cfDNA) has been implicated as an important biomarker in cancer management. Thus, efficient techniques for cfDNA extraction are necessary for precision medicine. We developed a centrifugation-free cfDNA extraction microfluidic chip capable of extracting cfDNA from plasma samples through microfluidic circuits within 15 min under vacuum pressure using an immiscible solvent. The microfluidic chip had excellent performance that was comparable to the most widely used commercial product (QIAamp kit) in terms of extraction efficiency, purity, and quality of DNA samples. The microfluidic chip was validated for the continuous monitoring of HER-2 type breast cancer and was able to successfully detect a point mutation in phosphatidylinositol-4,5-bisphosphate 3-kinase (PIK3CA) during severe liver metastasis. The chip effectively eliminates the repetitive centrifugation processes and dramatically shortened the sample preparation time. The proposed platform could facilitate the development of a sample-to-answer system for use in liquid biopsy of cancers.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherNATURE PUBLISHING GROUP-
dc.subjectCIRCULATING DNA-
dc.subjectNUCLEIC-ACIDS-
dc.subjectSOLID-PHASE-
dc.subjectPLASMA DNA-
dc.subjectCANCER-
dc.subjectPURIFICATION-
dc.subjectHETEROGENEITY-
dc.subjectBIOMARKERS-
dc.subjectMUTATIONS-
dc.subjectSILICA-
dc.titlePrecision cell-free DNA extraction for liquid biopsy by integrated microfluidics-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Kyong Hwa-
dc.contributor.affiliatedAuthorShin, Sehyun-
dc.identifier.doi10.1038/s41698-019-0107-0-
dc.identifier.wosid000520512300001-
dc.identifier.bibliographicCitationNPJ PRECISION ONCOLOGY, v.4, no.1-
dc.relation.isPartOfNPJ PRECISION ONCOLOGY-
dc.citation.titleNPJ PRECISION ONCOLOGY-
dc.citation.volume4-
dc.citation.number1-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusCIRCULATING DNA-
dc.subject.keywordPlusNUCLEIC-ACIDS-
dc.subject.keywordPlusSOLID-PHASE-
dc.subject.keywordPlusPLASMA DNA-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusPURIFICATION-
dc.subject.keywordPlusHETEROGENEITY-
dc.subject.keywordPlusBIOMARKERS-
dc.subject.keywordPlusMUTATIONS-
dc.subject.keywordPlusSILICA-
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