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dc.contributor.authorKo, Jihoon-
dc.contributor.authorSong, Jiyoung-
dc.contributor.authorChoi, Nakwon-
dc.contributor.authorKim, Hong Nam-
dc.date.accessioned2024-01-19T08:04:09Z-
dc.date.available2024-01-19T08:04:09Z-
dc.date.created2023-12-28-
dc.date.issued2024-03-
dc.identifier.issn2192-2640-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/113082-
dc.description.abstractPatient-derived microphysiological systems (P-MPS) have emerged as powerful tools in precision medicine that provide valuable insight into individual patient characteristics. This review discusses the development of P-MPS as an integration of patient-derived samples, including patient-derived cells, organoids, and induced pluripotent stem cells, into well-defined MPSs. Emphasizing the necessity of P-MPS development, its significance as a nonclinical assessment approach that bridges the gap between traditional in vitro models and clinical outcomes is highlighted. Additionally, guidance is provided for engineering approaches to develop microfluidic devices and high-content analysis for P-MPSs, enabling high biological relevance and high-throughput experimentation. The practical implications of the P-MPS are further examined by exploring the clinically relevant outcomes obtained from various types of patient-derived samples. The construction and analysis of these diverse samples within the P-MPS have resulted in physiologically relevant data, paving the way for the development of personalized treatment strategies. This study describes the significance of the P-MPS in precision medicine, as well as its unique capacity to offer valuable insights into individual patient characteristics. Microphysiological systems now integrate patient-derived samples, functioning as physiologically relevant avatars for high-throughput assays. This evolution addresses an unmet clinical need for a patient-centered nonclinical assessment platform, steering toward more precise and personalized approaches in medical research and drug development.image-
dc.languageEnglish-
dc.publisherWiley-Blackwell-
dc.titlePatient-Derived Microphysiological Systems for Precision Medicine-
dc.typeArticle-
dc.identifier.doi10.1002/adhm.202303161-
dc.description.journalClass1-
dc.identifier.bibliographicCitationAdvanced Healthcare Materials, v.13, no.7-
dc.citation.titleAdvanced Healthcare Materials-
dc.citation.volume13-
dc.citation.number7-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid001118467900001-
dc.identifier.scopusid2-s2.0-85179359261-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeReview-
dc.subject.keywordPlusON-A-CHIP-
dc.subject.keywordPlusPLURIPOTENT STEM-CELLS-
dc.subject.keywordPlusCIRCULATING TUMOR-CELLS-
dc.subject.keywordPlusLUNG-CANCER ORGANOIDS-
dc.subject.keywordPlusMICROFLUIDIC DEVICES-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusAUTOIMMUNE-DISEASES-
dc.subject.keywordPlusPANCREATIC-CANCER-
dc.subject.keywordPlusENDOTHELIAL-CELLS-
dc.subject.keywordPlusTHERAPY RESPONSE-
dc.subject.keywordAuthormicrophysiological system-
dc.subject.keywordAuthorpatient-derived-
dc.subject.keywordAuthorphysiologically-relevant-
dc.subject.keywordAuthorprecision medicine-
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