Frontiers in Bioengineering and Biotechnology (Jul 2020)

Automation, Monitoring, and Standardization of Cell Product Manufacturing

  • Meletios-Nikolaos Doulgkeroglou,
  • Meletios-Nikolaos Doulgkeroglou,
  • Alessia Di Nubila,
  • Alessia Di Nubila,
  • Bastian Niessing,
  • Niels König,
  • Robert H. Schmitt,
  • Jackie Damen,
  • Stephen J. Szilvassy,
  • Wing Chang,
  • Lynn Csontos,
  • Sharon Louis,
  • Patrick Kugelmeier,
  • Vincent Ronfard,
  • Vincent Ronfard,
  • Vincent Ronfard,
  • Yves Bayon,
  • Dimitrios I. Zeugolis,
  • Dimitrios I. Zeugolis

DOI
https://doi.org/10.3389/fbioe.2020.00811
Journal volume & issue
Vol. 8

Abstract

Read online

Although regenerative medicine products are at the forefront of scientific research, technological innovation, and clinical translation, their reproducibility and large-scale production are compromised by automation, monitoring, and standardization issues. To overcome these limitations, new technologies at software (e.g., algorithms and artificial intelligence models, combined with imaging software and machine learning techniques) and hardware (e.g., automated liquid handling, automated cell expansion bioreactor systems, automated colony-forming unit counting and characterization units, and scalable cell culture plates) level are under intense investigation. Automation, monitoring and standardization should be considered at the early stages of the developmental cycle of cell products to deliver more robust and effective therapies and treatment plans to the bedside, reducing healthcare expenditure and improving services and patient care.

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