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Scalable Fabrication of Stretchable, Dual Channel, Microfluidic Organ Chips.
Novak, Richard; Didier, Meredyth; Calamari, Elizabeth; Ng, Carlos F; Choe, Youngjae; Clauson, Susan L; Nestor, Bret A; Puerta, Jefferson; Fleming, Rachel; Firoozinezhad, Sasan J; Ingber, Donald E.
Affiliation
  • Novak R; Wyss Institute for Biologically Inspired Engineering, Harvard University; richard.novak@wyss.harvard.edu.
  • Didier M; Wyss Institute for Biologically Inspired Engineering, Harvard University; Apple, Inc.
  • Calamari E; Wyss Institute for Biologically Inspired Engineering, Harvard University.
  • Ng CF; Wyss Institute for Biologically Inspired Engineering, Harvard University.
  • Choe Y; Wyss Institute for Biologically Inspired Engineering, Harvard University.
  • Clauson SL; Wyss Institute for Biologically Inspired Engineering, Harvard University.
  • Nestor BA; Wyss Institute for Biologically Inspired Engineering, Harvard University.
  • Puerta J; Wyss Institute for Biologically Inspired Engineering, Harvard University.
  • Fleming R; Wyss Institute for Biologically Inspired Engineering, Harvard University.
  • Firoozinezhad SJ; Wyss Institute for Biologically Inspired Engineering, Harvard University.
  • Ingber DE; Wyss Institute for Biologically Inspired Engineering, Harvard University; Harvard John A. Paulson School of Engineering and Applied Sciences, Harvard University; Vascular Biology Program and Department of Surgery, Boston Children's Hospital and Harvard Medical School.
J Vis Exp ; (140)2018 10 20.
Article in En | MEDLINE | ID: mdl-30394380
ABSTRACT
A significant number of lead compounds fail in the pharmaceutical pipeline because animal studies often fail to predict clinical responses in human patients. Human Organ-on-a-Chip (Organ Chip) microfluidic cell culture devices, which provide an experimental in vitro platform to assess efficacy, toxicity, and pharmacokinetic (PK) profiles in humans, may be better predictors of therapeutic efficacy and safety in the clinic compared to animal studies. These devices may be used to model the function of virtually any organ type and can be fluidically linked through common endothelium-lined microchannels to perform in vitro studies on human organ-level and whole body-level physiology without having to conduct experiments on people. These Organ Chips consist of two perfused microfluidic channels separated by a permeable elastomeric membrane with organ-specific parenchymal cells on one side and microvascular endothelium on the other, which can be cyclically stretched to provide organ-specific mechanical cues (e.g., breathing motions in lung). This protocol details the fabrication of flexible, dual channel, Organ Chips through casting of parts using 3D printed molds, enabling combination of multiple casting and post-processing steps. Porous poly (dimethyl siloxane) (PDMS) membranes are cast with micrometer sized through-holes using silicon pillar arrays under compression. Fabrication and assembly of Organ Chips involves equipment and steps that can be implemented outside of a traditional cleanroom. This protocol provides researchers with access to Organ Chip technology for in vitro organ- and body-level studies in drug discovery, safety and efficacy testing, as well as mechanistic studies of fundamental biological processes.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Culture Techniques / Microfluidics Type of study: Guideline / Prognostic_studies Limits: Animals / Humans Language: En Journal: J Vis Exp Year: 2018 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Culture Techniques / Microfluidics Type of study: Guideline / Prognostic_studies Limits: Animals / Humans Language: En Journal: J Vis Exp Year: 2018 Document type: Article