Evidence map›Paper›PMID 40781489›Full record

ArticleDrug delivery and translational research2026

3D-Printed core-shell tablet for effective oral delivery of AT-MSC secretome in inflammatory bowel disease therapy.

Elena Munoz-Perez, Edorta Santos-Vizcaino, Alvaro Goyanes, Abdul W Basit, Rosa Maria Hernandez

Abstract read
In one paragraph

Article in Drug delivery and translational research, 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. Article
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.

Elena Munoz-PerezNanoBioCel Research Group, Laboratory of Pharmaceutics, School of Pharmacy, University of the Basque Country (UPV/EHU), Paseo de la Universidad 7, Vitoria-Gasteiz, 01006, Spain.
Edorta Santos-VizcainoNanoBioCel Research Group, Laboratory of Pharmaceutics, School of Pharmacy, University of the Basque Country (UPV/EHU), Paseo de la Universidad 7, Vitoria-Gasteiz, 01006, Spain.
Alvaro GoyanesDepartamento de Farmacología, Farmacia y Tecnología Farmacéutica, Facultad de Farmacia, Instituto de Materiales (iMATUS) and Health Research Institute of Santiago de Compostela (IDIS), Universidade de Santiago de Compostela, Santiago de Compostela, 15782, Spain.
Abdul W BasitDepartment of Pharmaceutics, UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London, WC1N 1AX, UK. abdul.basit@pharmacy.ac.uk.
Rosa Maria HernandezNanoBioCel Research Group, Laboratory of Pharmaceutics, School of Pharmacy, University of the Basque Country (UPV/EHU), Paseo de la Universidad 7, Vitoria-Gasteiz, 01006, Spain. rosa.hernandez@ehu.eus.ORCID http://orcid.org/0000-0002-3947-409X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The complexity of inflammatory bowel disease (IBD) and its pharmacological management has driven research to explore novel treatment options for this condition. Among the emerging therapies, Mesenchymal Stromal Cells (MSCs) have proven to be effective, showing strong immunomodulatory properties. However, the efficiency of direct MSC administration has been questioned due to their short half-life and risk of rejection. As an alternative, MSCs secretome, containing the beneficial paracrine effectors of MSCs, is being explored as a promising cell-free therapeutic tool. However, the oral delivery of this secretome is complex and presents a significant technological challenge. Additionally, the personalization of secretome-based therapies is essential, as it is a costly treatment that requires dose customization for each patient. This study introduces a novel approach for the oral delivery of adipose-tissue derived MSC secretome (AT-S) using 3D-printed core-shell tablets. Remarkably, lyophilized secretome (LpAT-S) was used during the study to improve the manageability and stability of the secretome. The 3D printed system proved to be capable of protecting secretome proteins from gastric degradation, offering an unprecedented possibility for the oral administration of secretome therapies. Overall, this study shows that 3D printing offers a promising, patient-friendly solution for the oral administration of MSC secretome for the first time, aligning with precision medicine goals to provide tailored therapies for IBD.

Indexed as

Inflammatory Bowel DiseasesMesenchymal Stem CellsPrinting, Three-DimensionalSecretomeAdipose TissueAdministration, OralCells, CulturedHumansTabletsTablets

Identifiers

PMID40781489
PMCPMC13294233

What OpenQuestion holds

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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.