Evidence map›Paper›PMID 38789470›Full record

ArticleScientific reports2024

A miniaturised semi-dynamic in-vitro model of human digestion.

Victor Calero, Patrícia M Rodrigues, Tiago Dias, Alar Ainla, Adriana Vilaça, Lorenzo Pastrana, Miguel Xavier, Catarina Gonçalves

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Designing Protein Gels for Nutrient Delivery: From Formulation to Digestion.Comprehensive reviews in food science and food safety · 2026
    Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Biomimic models forFood chemistry: X · 2025
    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

8 authors.

Victor Calero *International Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga, S/N, 4715-330, Braga, Portugal.
Patrícia M Rodrigues *International Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga, S/N, 4715-330, Braga, Portugal.
Tiago DiasInternational Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga, S/N, 4715-330, Braga, Portugal.
Alar AinlaInternational Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga, S/N, 4715-330, Braga, Portugal. alar.ainla@inl.int.
Adriana VilaçaInternational Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga, S/N, 4715-330, Braga, Portugal.
Lorenzo PastranaInternational Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga, S/N, 4715-330, Braga, Portugal.
Miguel XavierInternational Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga, S/N, 4715-330, Braga, Portugal. miguel.xavier@inl.int.
Catarina GonçalvesInternational Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga, S/N, 4715-330, Braga, Portugal. catarina.goncalves@inl.int.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reliable in-vitro digestion models that are able to successfully replicate the conditions found in the human gastrointestinal tract are key to assess the fate and efficiency of new formulations aimed for oral consumption. However, current in-vitro models either lack the capability to replicate crucial dynamics of digestion or require large volumes of sample/reagents, which can be scarce when working with nanomaterials under development. Here, we propose a miniaturised digestion system, a digestion-chip, based on incubation chambers integrated on a polymethylmethacrylate device. The digestion-chip incorporates key dynamic features of human digestion, such as gradual acidification and gradual addition of enzymes and simulated fluids in the gastric phase, and controlled gastric emptying, while maintaining low complexity and using small volumes of sample and reagents. In addition, the new approach integrates real-time automated closed-loop control of two key parameters, pH and temperature, during the two main phases of digestion (gastric and intestinal) with an accuracy down to ± 0.1 °C and ± 0.2 pH points. The experimental results demonstrate that the digestion-chip successfully replicates the gold standard static digestion INFOGEST protocol and that the semi-dynamic digestion kinetics can be reliably fitted to a first kinetic order model. These devices can be easily adapted to dynamic features in an automated, sensorised, and inexpensive platform and will enable reliable, low-cost and efficient assessment of the bioaccessibility of new and expensive drugs, bioactive ingredients or nanoengineered materials aimed for oral consumption, thereby avoiding unnecessary animal testing.

Indexed as

DigestionModels, BiologicalGastrointestinal TractHumansHydrogen-Ion ConcentrationKineticsLab-On-A-Chip DevicesMiniaturizationTemperature

Identifiers

PMID38789470
PMCPMC11126663

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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.