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Robotic fluidic coupling and interrogation of multiple vascularized organ chips

Novak, R. (author)
Ingram, M. (author)
Marquez, S. (author)
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Das, D. (author)
Delahanty, A. (author)
Herland, Anna (author)
Karolinska Institutet,KTH,Mikro- och nanosystemteknik
Maoz, B. M. (author)
Jeanty, S. S. F. (author)
Somayaji, M. R. (author)
Burt, M. (author)
Calamari, E. (author)
Chalkiadaki, A. (author)
Cho, A. (author)
Choe, Y. (author)
Chou, D. B. (author)
Cronce, M. (author)
Dauth, S. (author)
Divic, T. (author)
Fernandez-Alcon, J. (author)
Ferrante, T. (author)
Ferrier, J. (author)
FitzGerald, E. A. (author)
Fleming, R. (author)
Jalili-Firoozinezhad, S. (author)
Grevesse, T. (author)
Goss, J. A. (author)
Hamkins-Indik, T. (author)
Henry, O. (author)
Hinojosa, C. (author)
Huffstater, T. (author)
Jang, K. -J (author)
Kujala, V. (author)
Leng, L. (author)
Mannix, R. (author)
Milton, Y. (author)
Nawroth, J. (author)
Nestor, B. A. (author)
Ng, C. F. (author)
O’Connor, B. (author)
Park, T. -E (author)
Sanchez, H. (author)
Sliz, J. (author)
Sontheimer-Phelps, A. (author)
Swenor, B. (author)
Thompson, G. , I I (author)
Touloumes, G. J. (author)
Tranchemontagne, Z. (author)
Wen, N. (author)
Yadid, M. (author)
Bahinski, A. (author)
Hamilton, G. A. (author)
Levner, D. (author)
Levy, O. (author)
Przekwas, A. (author)
Prantil-Baun, R. (author)
Parker, K. K. (author)
Ingber, D. E. (author)
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 (creator_code:org_t)
2020-01-27
2020
English.
In: Nature Biomedical Engineering. - : Nature Research. - 2157-846X.
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Organ chips can recapitulate organ-level (patho)physiology, yet pharmacokinetic and pharmacodynamic analyses require multi-organ systems linked by vascular perfusion. Here, we describe an ‘interrogator’ that employs liquid-handling robotics, custom software and an integrated mobile microscope for the automated culture, perfusion, medium addition, fluidic linking, sample collection and in situ microscopy imaging of up to ten organ chips inside a standard tissue-culture incubator. The robotic interrogator maintained the viability and organ-specific functions of eight vascularized, two-channel organ chips (intestine, liver, kidney, heart, lung, skin, blood–brain barrier and brain) for 3 weeks in culture when intermittently fluidically coupled via a common blood substitute through their reservoirs of medium and endothelium-lined vascular channels. We used the robotic interrogator and a physiological multicompartmental reduced-order model of the experimental system to quantitatively predict the distribution of an inulin tracer perfused through the multi-organ human-body-on-chips. The automated culture system enables the imaging of cells in the organ chips and the repeated sampling of both the vascular and interstitial compartments without compromising fluidic coupling.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)

Keyword

Blood
Physiological models
Tissue culture
Culture systems
Experimental system
In-situ microscopies
Liquid handling
Organ systems
Reduced order models
Sample collection
Vascular perfusion
Robotics

Publication and Content Type

ref (subject category)
art (subject category)

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