4.7 Article

Beyond the on/off chip trade-off: A reversibly sealed microfluidic platform for 3D tumor microtissue analysis

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 274, 期 -, 页码 393-401

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2018.07.166

关键词

Microfluidics; Tumor microtissue; SEM analysis; Fluorescence; Modular chip; Spheroid

资金

  1. Ministere de l'Enseignement Superieur et de la Recherche
  2. Universite Paris-Descartes
  3. Centre National de la Recherche Scientifique (CNRS)
  4. Institut National de la Sante et de la Recherche Medicale (INSERM)
  5. Institut National du Cancer (INCA)
  6. canceropole Ile-de-France [2016-1-EMERG-54-UP 5-1]
  7. SIRIC CARPEM
  8. Fondation de la Recherche Medicale [SPF20160936257]
  9. ligue nationale contre le cancer (LNCC, Program Equipe labelisee LIGUE) [EL2016.LNCC/VaT]
  10. HTE Program-HetColi network
  11. INSERM Physicancer program [PC201423]
  12. CAMPUS FRANCE [39525QJ]
  13. Universita Italo-Francese [G18_208]
  14. Pierre-Gilles de Gennes Institute equipment (Investissements d'Avenir program) [ANR 10-NANO 0207]

向作者/读者索取更多资源

Nowadays, microfluidic 3D cell culture is widely used to mimic complex microtissue and dynamic environment, performing more realistic in vitro assays for drug testing. Herein, we developed a novel microfluidic platform for tumor microtissue culture, drug response analysis and versatile microscopic characterization. By reversibly bonding the chip, we go beyond the on/off chip tradeoff, which allows us to perform both fluorescence and SEM characterization of tumor microtissues on a simple platform. The microfluidic chip consists of spherical microwells connected via microchannels, bonded through a magnetic system. Colorectal cancer HT-29 cells were cultured as spherical microtissues on chip and their growth kinetics monitored. The cytotoxic activity of Camptothecin was evaluated by in situ live/dead fluorescence staining and quantification of morphology parameters. Finally, we demonstrated the possibility to collect the 3D tumor microtissues and characterize their surface damaged by the drug using scanning electron microscopy. This reversibly sealed microfluidic platform thus enables to grow sets of 3D tumor microtissues in a controlled dynamic microenvinroment, and subsequently to retrieve the 3D tumor microtissues after chemotherapeutic treatment for in- depth analysis.

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