Evidence map›Paper›PMID 41793548›Full record

ArticleBiomedical microdevices2026

Ingestible active capsule for gastrointestinal microbiome sampling.

Mohammed Hadi Shahadha, Andreas Voigt, Denise Gruner, Uwe Marschner, Maxime Le Floch, Jochen Hampe, Frank Brauer, Sebastian Schostek, Marco Luniak, Karlheinz Bock and 1 more

Abstract read
In one paragraph

Article in Biomedical microdevices, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Mohammed Hadi ShahadhaInstitute for Semiconductors and Microsystems, Dresden University of Technology, Dresden, Germany. mohammed.shahadha@tu-dresden.de.
Andreas VoigtInstitute for Semiconductors and Microsystems, Dresden University of Technology, Dresden, Germany.
Denise GrunerInstitute for Semiconductors and Microsystems, Dresden University of Technology, Dresden, Germany.
Uwe MarschnerInstitute for Semiconductors and Microsystems, Dresden University of Technology, Dresden, Germany.
Maxime Le FlochUniversity Hospital Dresden, Medical Clinic 1, Dresden, Germany.
Jochen HampeUniversity Hospital Dresden, Medical Clinic 1, Dresden, Germany.
Frank BrauerOvesco Endoscopy AG, Tübingen, Germany.
Sebastian SchostekOvesco Endoscopy AG, Tübingen, Germany.
Marco LuniakInstitute of Electronic Packaging Technology and Centre for Microtechnical Manufacturing, Dresden University of Technology, Dresden, Germany.
Karlheinz BockInstitute of Electronic Packaging Technology and Centre for Microtechnical Manufacturing, Dresden University of Technology, Dresden, Germany.
Andreas RichterInstitute for Semiconductors and Microsystems, Dresden University of Technology, Dresden, Germany. andreas.richter7@tu-dresden.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Various gastrointestinal disorders have been linked to gut microbiome dysbiosis, as it plays a critical role in immune regulation, metabolism, nutrient digestion, and pathogen suppression. However, the microbiome’s spatial variability across gastrointestinal segments and its intra- and interindividual differences complicate its study and clinical interpretation. While fecal DNA analysis is commonly used, stool samples only capture an accumulated signal and miss the spatial dynamics of microbial populations. To address this, we propose a modular sampling capsule capable of wirelessly collecting liquid. The capsule consists of two main modules: (i) an actuator module integrating a polymer-based microfluidic system with meltable wax-based opening valve, screen-printed microheater, cellulose membrane-based closing valve, evacuated sampling chamber with dried sample preservative material, filter membrane (size exclusion 150 μm), and sample extraction channel; and (ii) a control electronic module with communication, localization, and power supply units. The actuator module was validated in vitro using a diluted stool simulant (330 mg/mL) and an uncleaned porcine intestine. The opening valve activated within 3.6 ± 0.5 s at 120 ± 10 mA and 0.8 V. The sample was then filtered and aspirated into the sampling chamber within 1–2 s, and the closing valve sealed the inlet completely within 10 min. We overcame design, material, and fabrication challenges to construct an actuator module that functions effectively in liquids with variable physicochemical conditions (pH, chemical composition, viscosity, and particle size). These results demonstrate the feasibility of a controlled, segment-specific intestinal sampling capsule, representing a step towards precise and accurate microbiome profiling.

Indexed as

Gastrointestinal MicrobiomeAnimalsCapsulesEquipment DesignFecesHumansSwineCapsulesGut liquid biopsyGut microbiome diagnosticIngestible capsuleLiquid sampling capsuleMedical robotics

Identifiers

PMID41793548
PMCPMC12967682

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.