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dc.contributor.authorZhang, Yu Shrike
dc.contributor.authorAleman, Julio
dc.contributor.authorShin, Su Ryon
dc.contributor.authorKilic, Tugba
dc.contributor.authorKim, Duckjin
dc.contributor.authorMousavi Shaegh, Seyed Ali
dc.contributor.authorMassa, Solange
dc.contributor.authorRiahi, Reza
dc.contributor.authorChae, Sukyoung
dc.contributor.authorHu, Ning
dc.contributor.authorAvci, Huseyin
dc.contributor.authorSilvestri, Antonia
dc.contributor.authorSanati Nezhad, Amir
dc.contributor.authorManbohi, Ahmad
dc.contributor.authorDe Ferrari, Fabio
dc.contributor.authorPolini, Alessandro
dc.contributor.authorCalzone, Giovanni
dc.contributor.authorShaikh, Noor
dc.contributor.authorAlerasool, Parissa
dc.contributor.authorBudina, Erica
dc.contributor.authorKang, Jian
dc.contributor.authorBhise, Nupura
dc.contributor.authorRibas, João
dc.contributor.authorPourmand, Adel
dc.contributor.authorSkardal, Aleksander
dc.contributor.authorShupe, Thomas
dc.contributor.authorBishop, Colin E.
dc.contributor.authorDokmeci, Mehmet Remzi
dc.contributor.authorAtala, Anthony
dc.contributor.authorZhang, Weijia
dc.contributor.authorKhademhosseini, Ali
dc.date.accessioned2017-11-17T16:52:46Z
dc.date.available2017-11-17T16:52:46Z
dc.date.issued2017-03
dc.date.submitted2016-08
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/112226
dc.description.abstractOrgan-on-a-chip systems areminiaturizedmicrofluidic 3D human tissue and organ models designed to recapitulate the important biological and physiological parameters of their in vivo counterparts. They have recently emerged as a viable platform for personalized medicine and drug screening. These in vitro models, featuring biomimetic compositions, architectures, and functions, are expected to replace the conventional planar, static cell cultures and bridge the gap between the currently used preclinical animal models and the human body. Multiple organoid models may be further connected together through the microfluidics in a similar manner in which they are arranged in vivo, providing the capability to analyze multiorgan interactions. Although a wide variety of human organ-on-a-chip models have been created, there are limited efforts on the integration of multisensor systems. However, in situ continual measuring is critical in precise assessment of the microenvironment parameters and the dynamic responses of the organs to pharmaceutical compounds over extended periods of time. In addition, automated and noninvasive capability is strongly desired for long-term monitoring. Here, we report a fully integrated modular physical, biochemical, and optical sensing platform through a fluidics-routing breadboard, which operates organ-on-a-chip units in a continual, dynamic, and automated manner.We believe that this platform technology has paved a potential avenue to promote the performance of current organ-on-a-chip models in drug screening by integrating a multitude of real-time sensors to achieve automated in situ monitoring of biophysical and biochemical parameters.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant EB012597)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant AR057837)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant DE021468)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant HL099073)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R56AI105024)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant AR068258)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant AR066193)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant EB022403)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant EB021148)en_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.1612906114en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePNASen_US
dc.titleMultisensor-integrated organs-on-chips platform for automated and continual in situ monitoring of organoid behaviorsen_US
dc.typeArticleen_US
dc.identifier.citationZhang, Yu Shrike, et al. “Multisensor-Integrated Organs-on-Chips Platform for Automated and Continual in Situ Monitoring of Organoid Behaviors.” Proceedings of the National Academy of Sciences 114, 12 (March 2017): E2293–E2302 © 2017 National Academy of Sciencesen_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorZhang, Weijia
dc.contributor.mitauthorKhademhosseini, Alireza
dc.relation.journalProceedings of the National Academy of Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2017-10-30T19:40:19Z
dspace.orderedauthorsZhang, Yu Shrike; Aleman, Julio; Shin, Su Ryon; Kilic, Tugba; Kim, Duckjin; Mousavi Shaegh, Seyed Ali; Massa, Solange; Riahi, Reza; Chae, Sukyoung; Hu, Ning; Avci, Huseyin; Zhang, Weijia; Silvestri, Antonia; Sanati Nezhad, Amir; Manbohi, Ahmad; De Ferrari, Fabio; Polini, Alessandro; Calzone, Giovanni; Shaikh, Noor; Alerasool, Parissa; Budina, Erica; Kang, Jian; Bhise, Nupura; Ribas, João; Pourmand, Adel; Skardal, Aleksander; Shupe, Thomas; Bishop, Colin E.; Dokmeci, Mehmet Remzi; Atala, Anthony; Khademhosseini, Alien_US
dspace.embargo.termsNen_US
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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