Evidence map›Paper›PMID 40181053›Full record

ArticleScientific reports2025

Robust and reproducible human intestinal organoid-derived monolayer model for analyzing drug absorption.

Kai Tanaka, Tatsuki Mochizuki, Shogo Baba, Shigeto Kawai, Kiyotaka Nakano, Tatsuhiko Tachibana, Kohsuke Uchimura, Atsuhiko Kato, Takashi Miyayama, Tomohito Yamaguchi and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 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.

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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

13 authors.

Kai TanakaTranslational Research Division, Chugai Pharmaceutical Co., Ltd, 216 Totsuka Totsuka-Ku Yokohama, Kanagawa, Japan. tanaka.kai11@chugai-pharm.co.jp.
Tatsuki MochizukiTranslational Research Division, Chugai Pharmaceutical Co., Ltd, 216 Totsuka Totsuka-Ku Yokohama, Kanagawa, Japan.
Shogo BabaDepartment of Biology and Genetics, Laboratory of Cancer Medical Science, Hokuto Hospital, 7-5 Kisen, Inadacho, Obihiro, Hokkaido, Japan.
Shigeto KawaiTranslational Research Division, Chugai Pharmaceutical Co., Ltd, 216 Totsuka Totsuka-Ku Yokohama, Kanagawa, Japan.
Kiyotaka NakanoTranslational Research Division, Chugai Pharmaceutical Co., Ltd, 216 Totsuka Totsuka-Ku Yokohama, Kanagawa, Japan.
Tatsuhiko TachibanaTranslational Research Division, Chugai Pharmaceutical Co., Ltd, 216 Totsuka Totsuka-Ku Yokohama, Kanagawa, Japan.
Kohsuke UchimuraTranslational Research Division, Chugai Pharmaceutical Co., Ltd, 216 Totsuka Totsuka-Ku Yokohama, Kanagawa, Japan.
Atsuhiko KatoTranslational Research Division, Chugai Pharmaceutical Co., Ltd, 216 Totsuka Totsuka-Ku Yokohama, Kanagawa, Japan.
Takashi MiyayamaTranslational Research Division, Chugai Pharmaceutical Co., Ltd, 216 Totsuka Totsuka-Ku Yokohama, Kanagawa, Japan.
Tomohito YamaguchiDepartment of Gastroenterology, Hokuto Hospital, 7-5 Kisen, Inadacho, Obihiro, Hokkaido, Japan.
Hiroshi NishiharaKeio Cancer Center, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-Ku, Tokyo, Japan.
Kimio TeraoTranslational Research Division, Chugai Pharmaceutical Co., Ltd, 2-1-1 Nihonbashi-Muromachi Chuo-Ku, Tokyo, Japan.
Yasutaka KatoDepartment of Biology and Genetics, Laboratory of Cancer Medical Science, Hokuto Hospital, 7-5 Kisen, Inadacho, Obihiro, Hokkaido, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Predicting the absorption of orally administered drugs is crucial to drug development. Current in vitro models lack physiological relevance, robustness, and reproducibility, thus hindering reliable predictions. In this study, we developed a reproducible and robust culture method to generate a human intestinal organoid-derived monolayer model that can be applied to study drug absorption through a step-by-step approach. Our model showed similarity to primary enterocytes in terms of the drug absorption-related gene expression profile, tight barrier function, tolerability toward artificial bile juice, drug transporter and metabolizing enzyme function, and nuclear receptor activity. This method can be applied to organoids derived from multiple donors. The permeability of launched 19 drugs in our model demonstrated a correlation with human Fa values, with an R

Indexed as

Intestinal AbsorptionIntestinal MucosaIntestinesModels, BiologicalOrganoidsHumansPharmaceutical PreparationsReproducibility of ResultsPharmaceutical PreparationsDrug absorption modelingHuman intestinal organoidsIn vitro drug screeningPharmacokinetic predictionPrecision drug development

Identifiers

PMID40181053
PMCPMC11968819

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

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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.