Evidence map›Paper›PMID 40644523›Full record

ArticlePloS one2025

An ingestible device for automated sampling and location tracing in gastrointestinal tract.

Tao Li, Jeremy Felton, Johnathan Lewis, Qisen Cheng, Ryan Meredith, Hsueh-Tsung Lu, Alexander Benken, Partha P Dutta, Jinhui Liao, Xiangyu D Zhao and 10 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

20 authors.

Tao LiCenter for Wireless Integrated MicroSensing and Systems (WIMS2), University of Michigan, Ann Arbor, Michigan, United States of America.ORCID https://orcid.org/0000-0001-7296-822X
Jeremy FeltonDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, Ann Arbor, Michigan, United States of America.
Johnathan LewisCenter for Wireless Integrated MicroSensing and Systems (WIMS2), University of Michigan, Ann Arbor, Michigan, United States of America.
Qisen ChengCenter for Wireless Integrated MicroSensing and Systems (WIMS2), University of Michigan, Ann Arbor, Michigan, United States of America.ORCID https://orcid.org/0000-0001-8675-6666
Ryan MeredithCenter for Wireless Integrated MicroSensing and Systems (WIMS2), University of Michigan, Ann Arbor, Michigan, United States of America.
Hsueh-Tsung LuCenter for Wireless Integrated MicroSensing and Systems (WIMS2), University of Michigan, Ann Arbor, Michigan, United States of America.
Alexander BenkenCenter for Wireless Integrated MicroSensing and Systems (WIMS2), University of Michigan, Ann Arbor, Michigan, United States of America.
Partha P DuttaCenter for Wireless Integrated MicroSensing and Systems (WIMS2), University of Michigan, Ann Arbor, Michigan, United States of America.
Jinhui LiaoDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, Ann Arbor, Michigan, United States of America.
Xiangyu D ZhaoCenter for Wireless Integrated MicroSensing and Systems (WIMS2), University of Michigan, Ann Arbor, Michigan, United States of America.ORCID https://orcid.org/0000-0002-3525-9747
Aleksas MatvekasDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, Ann Arbor, Michigan, United States of America.
Jason BakerDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, United States of America.
William L HaslerDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, United States of America.
Andrew BabiskinOffice of Research and Standards, Office of Generic Drugs, FDA, Silver Spring, Maryland, United States of America.
Ross WalengaOffice of Research and Standards, Office of Generic Drugs, FDA, Silver Spring, Maryland, United States of America.
Lanyan Lucy FangOffice of Research and Standards, Office of Generic Drugs, FDA, Silver Spring, Maryland, United States of America.
Robert LionbergerOffice of Research and Standards, Office of Generic Drugs, FDA, Silver Spring, Maryland, United States of America.
Manjunath P PaiDepartment of Clinical Pharmacy, College of Pharmacy, University of Michigan, Ann Arbor, Michigan, United States of America.
Duxin SunDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, Ann Arbor, Michigan, United States of America.
Yogesh B GianchandaniCenter for Wireless Integrated MicroSensing and Systems (WIMS2), University of Michigan, Ann Arbor, Michigan, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluids sampled from the gastrointestinal (GI) tract are of interest for evaluating the bioequivalence of oral medications, and more generally for evaluating GI-related diseases, and for profiling the individual gut microbiome. Existing options for capturing multiple fluid samples from specific locations in the GI tract are limited and invasive, particularly for the small intestine. Here, we report the development of an ingestible capsule for the collection of multiple fluid samples along the GI tract; we additionally report the use of data from sensors within the capsule to determine the sampling regions. The capsule has an ingestible size of Φ14 × 42 mm3. Within this volume, it includes three separate cartridges that capture and retain samples within capillaries; a stepper motor for positioning the sampling cartridges at a sampling port; a 3-axis accelerometer that enables a new method of correlating sample location; a microcontroller with wireless communication and sensor data storage capabilities; and batteries to power the device. We describe in vitro characterization and in vivo tests performed with canine models that have successfully verified the capabilities of the capsule. Fluid samples from the stomach, small intestine, and colon regions of the GI tract are identified by inertial measurements taken within the capsule, and correlated to measurements of the concentration of mesalamine (a drug used for testing) and the bile salt profile in each region, respectively.

Indexed as

Gastrointestinal TractAnimalsDogs

Identifiers

PMID40644523
PMCPMC12250150

What OpenQuestion holds

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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.