Re-imagining human cell culture media: Challenges, innovations, and future directions.

Journal: Biotechnology advances
Published Date:

Abstract

The development of optimized culture media is pivotal to advancements in human cell culture, underpinning progress in regenerative medicine, cell therapies, and personalized medicine. While foundational formulations like Eagle's Minimum Essential Medium (MEM) and Dulbecco's Modified Eagle Medium (DMEM) have historically enabled significant biological research, these media were primarily designed for non-human cells and do not adequately address the unique metabolic and functional requirements of human cells. This review examines the evolution of cell culture media, identifying persistent challenges in reproducibility, scalability, and ethical concerns, particularly regarding the reliance on animal-derived components such as fetal bovine serum (FBS). We highlight innovations in serum-free and chemically defined media that offer promising alternatives by enhancing consistency, aligning with Good Manufacturing Practices, and addressing ethical concerns. Emerging approaches, including omics-based profiling, high-throughput screening, and artificial intelligence (AI)-driven media design, are reshaping media optimization by enabling precise tailoring to the needs of specific human cell types and patient-derived cells. Furthermore, we discuss economic and regulatory challenges, emphasizing the need for cost-effective and scalable solutions to facilitate clinical translation. Looking forward, integrating advanced biotechnological tools such as 3D bioprinting, organ-on-a-chip systems, and personalized media formulations presents a transformative opportunity for human cell culture. These innovations, aligned with ethical and clinical standards, can drive the development of human-specific media systems that ensure reproducibility, scalability, and enhanced therapeutic potential, thereby advancing both research and clinical applications.

Authors

  • Akila Wijerathna-Yapa
    Department of Process Engineering and Applied Science, Faculty of Engineering, Dalhousie University, PO Box 15000, Halifax, Nova Scotia B3H 4R2, Canada.
  • Kathy Sharon Isaac
    Department of Process Engineering and Applied Science, Faculty of Engineering, Dalhousie University, PO Box 15000, Halifax, Nova Scotia B3H 4R2, Canada.
  • Michelle Combe
    Department of Process Engineering and Applied Science, Faculty of Engineering, Dalhousie University, PO Box 15000, Halifax, Nova Scotia B3H 4R2, Canada.
  • Samuel Hume
    Medical Sciences Division, University of Oxford, Oxford OX3 9DU, UK.
  • Stanislav Sokolenko
    Department of Process Engineering and Applied Science, Faculty of Engineering, Dalhousie University, PO Box 15000, Halifax, Nova Scotia B3H 4R2, Canada. Electronic address: Stanislav.Sokolenko@dal.ca.