Evidence map›Paper›PMID 33237403›Full record

ReviewIn vitro cellular & developmental biology. Animal2021

Human small intestinal organotypic culture model for drug permeation, inflammation, and toxicity assays.

Jan Markus, Tim Landry, Zachary Stevens, Hailey Scott, Pierre Llanos, Michelle Debatis, Alexander Armento, Mitchell Klausner, Seyoum Ayehunie

Open access · bronzeAbstract readReview
In one paragraph

Review in In vitro cellular & developmental biology. Animal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
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

23 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
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  4. Emerging advances in intestinal models for in vitro preclinical research.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Review
  5. Article
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  7. Engineered Tissue Models to Decode Host-Microbiota Interactions.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  8. Review
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  15. Review
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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

9 authors at 2 institutions in 1 country.

Jan MarkusIn Vitro Life Science Laboratories, Bratislava, Slovak Republic.
Tim LandryMatTek Corporation, Ashland, MA, USA.
Zachary StevensMatTek Corporation, Ashland, MA, USA.
Hailey ScottMatTek Corporation, Ashland, MA, USA.
Pierre LlanosMatTek Corporation, Ashland, MA, USA.
Michelle DebatisMatTek Corporation, Ashland, MA, USA.
Alexander ArmentoMatTek Corporation, Ashland, MA, USA.
Mitchell KlausnerMatTek Corporation, Ashland, MA, USA.
Seyoum AyehunieMatTek Corporation, Ashland, MA, USA. sayehunie@mattek.com.
MatTek Corporation (United States) · USAshland (United States) · US

Funding

An In Vitro Human Small Intestine Tissue Model for Drug Permeation StudiesR44GM108164 · NIGMS · MATTEK CORPORATION · PI AYEHUNIE, SEYOUM · 2016 to 2018
$1.3M
Novel Approach for Characterizing Exposure and Response to Engineered Nanomaterials in the GutR43ES030648 · NIEHS · MATTEK CORPORATION · PI AYEHUNIE, SEYOUM · 2019 to 2019
$225k
NIEHS NIH HHS R43 ES030648NIGMS NIH HHS R44 GM108164
6 · The paper itself

Abstract

The gastrointestinal tract (GIT), in particular, the small intestine, plays a significant role in food digestion, fluid and electrolyte transport, drug absorption and metabolism, and nutrient uptake. As the longest portion of the GIT, the small intestine also plays a vital role in protecting the host against pathogenic or opportunistic microbial invasion. However, establishing polarized intestinal tissue models in vitro that reflect the architecture and physiology of the gut has been a challenge for decades and the lack of translational models that predict human responses has impeded research in the drug absorption, metabolism, and drug-induced gastrointestinal toxicity space. Often, animals fail to recapitulate human physiology and do not predict human outcomes. Also, certain human pathogens are species specific and do not infect other hosts. Concerns such as variability of results, a low throughput format, and ethical considerations further complicate the use of animals for predicting the safety and efficacy xenobiotics in humans. These limitations necessitate the development of in vitro 3D human intestinal tissue models that recapitulate in vivo-like microenvironment and provide more physiologically relevant cellular responses so that they can better predict the safety and efficacy of pharmaceuticals and toxicants. Over the past decade, much progress has been made in the development of in vitro intestinal models (organoids and 3D-organotypic tissues) using either inducible pluripotent or adult stem cells. Among the models, the MatTek's intestinal tissue model (EpiIntestinal™ Ashland, MA) has been used extensively by the pharmaceutical industry to study drug permeation, metabolism, drug-induced GI toxicity, pathogen infections, inflammation, wound healing, and as a predictive model for a clinical adverse outcome (diarrhea) to pharmaceutical drugs. In this paper, our review will focus on the potential of in vitro small intestinal tissues as preclinical research tool and as alternative to the use of animals.

Indexed as

Cell Culture TechniquesModels, BiologicalToxicity TestsAnimalsHumansInflammationIntestine, SmallPermeabilityPharmaceutical PreparationsPharmaceutical PreparationsDrug absorptionDrug-induced toxicityInflammationIntestinal tissue modelMetabolismNanotoxicityWound healing

Identifiers

PMID33237403
PMCPMC7687576
OpenAlexW3107607221

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.