作者
Richard Novák,M. Ingram,Susan Marquez,Debarun Das,Aaron Delahanty,Anna Herland,Ben M. Maoz,Sauveur S. F. Jeanty,Mahadevabharath R. Somayaji,Morgan A. Burt,Elizabeth Calamari,Angeliki Chalkiadaki,Alexander Cho,Youngjae Choe,David B. Chou,Michael J. Cronce,Stephanie Dauth,Toni Divic,Jose Fernandez-Alcon,Thomas C. Ferrante,John P. Ferrier,Edward A. Fitzgerald,Rachel C. Fleming,Sasan Jalili‐Firoozinezhad,Thomas Grevesse,Josue A. Goss,Tiama Hamkins-Indik,Olivier Henry,Chris Hinojosa,Tessa Huffstater,Kyung‐Jin Jang,Ville Kujala,Lian Leng,Robert Mannix,Yuka Milton,Janna Nawroth,Bret Nestor,Carlos F. Ng,Blakely B. O’Connor,Tae‐Eun Park,Henry Sanchez,Josiah Sliz,Alexandra Sontheimer-Phelps,Ben Swenor,G. W. Thompson,George J. Touloumes,Zachary Tranchemontagne,Norman Wen,Moran Yadid,Anthony Bahinski,Kyung‐Jin Jang,Daniel Levner,Oren Levy,Andrzej Przekwas,Rachelle Prantil‐Baun,Kevin Kit Parker,Donald E. Ingber
摘要
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.