AI Article Synopsis

  • Recent regulatory updates focus on using in vitro testing platforms for preclinical drug evaluations and toxicity assessments, highlighting the need for advanced tissue models that replicate liver functions.
  • Liver organoids, grown from human cells, show potential as effective tools for drug testing, but their regulatory acceptance is challenged by the absence of standardized quality evaluation methods.
  • The paper outlines proposed quality standards for liver organoids that cover aspects like cell source validation, organoid production, and functional testing to improve reliability and promote the use of organoids in drug development as alternatives to animal testing.

Article Abstract

Recent amendments to regulatory frameworks have placed a greater emphasis on the utilization of in vitro testing platforms for preclinical drug evaluations and toxicity assessments. This requires advanced tissue models capable of accurately replicating liver functions for drug efficacy and toxicity predictions. Liver organoids, derived from human cell sources, offer promise as a reliable platform for drug evaluation. However, there is a lack of standardized quality evaluation methods, which hinders their regulatory acceptance. This paper proposes comprehensive quality standards tailored for liver organoids, addressing cell source validation, organoid generation, and functional assessment. These guidelines aim to enhance reproducibility and accuracy in toxicity testing, thereby accelerating the adoption of organoids as a reliable alternative or complementary tool to animal testing in drug development. The quality standards include criteria for size, cellular composition, gene expression, and functional assays, thus ensuring a robust hepatotoxicity testing platform.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11170117PMC
http://dx.doi.org/10.15283/ijsc24044DOI Listing

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