Evidence map›Paper›PMID 41297178›Full record

ReviewDrug metabolism and disposition: the biological fate of chemicals2025

Microphysiological systems as an emerging in vitro approach for the evaluation of drug absorption, distribution, metabolism, and excretion and toxicity.

Shivangi Shrimali, Dongying Li, Bridgett Knox, Weida Tong, Baitang Ning

Abstract readReview
In one paragraph

Review in Drug metabolism and disposition: the biological fate of chemicals, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. New Personalized Medicine Model for Medication Management.Journal of personalized medicine · 2026
    Review
  5. Review
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Shivangi ShrimaliDivision of Bioinformatics and Biostatistics, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, Arkansas.
Dongying LiDivision of Bioinformatics and Biostatistics, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, Arkansas. Electronic address: dongying.li@fda.hhs.gov.
Bridgett KnoxDivision of Bioinformatics and Biostatistics, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, Arkansas.
Weida TongDivision of Bioinformatics and Biostatistics, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, Arkansas.
Baitang NingDivision of Bioinformatics and Biostatistics, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, Arkansas. Electronic address: baitang.ning@fda.hhs.gov.

Funding

Intramural FDA HHS FD999999
6 · The paper itself

Abstract

Microphysiological systems (MPSs) are emerging in vitro technologies designed to recapitulate human physiology for applications in drug development and safety assessment. Compared with conventional in vitro systems, MPSs may contain multiple types of cells and display dynamic and mechanical features of organ microenvironments. As part of new approach methodologies, MPSs are expected to contribute to reducing reliance on animal testing by providing human-relevant models that align with the principles of replacement, reduction, and refinement. This review discusses the advantages of MPSs over conventional in vitro systems for drug absorption, distribution, metabolism, and excretion and toxicity evaluation. We then systematically examines organ-specific MPS platforms used in absorption, distribution, metabolism, and excretion and toxicity studies. Next, we briefly evaluated the reproducibility of MPSs across different systems. Finally, we provide our perspectives and considerations on employing MPSs in regulatory applications. SIGNIFICANCE STATEMENT: This minireview provides an overview of the current trends in the field of microphysiological systems within the framework of new approach methodologies. This review will give readers insights into key differences between microphysiological systems and other in vitro methods in drug absorption, distribution, metabolism, and excretion, followed by recent advances in several organ chips for drug evaluation.

Indexed as

Microphysiological SystemsPharmaceutical PreparationsAnimalsDrug DevelopmentDrug Evaluation, PreclinicalHumansTissue DistributionToxicity TestsPharmaceutical PreparationsDistributionDrug absorptionDrug evaluationDrug toxicityMetabolism and excretionMicrophysiological systems

Identifiers

PMID41297178
PMCPMC12697006

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.