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Article ? AI-assigned paper type based on the abstract. Classification may not be perfect — flag errors using the feedback button. Tier 2 ? Original research — experimental, observational, or case-control study. Direct primary evidence. Detection Methods Gut & Microbiome Human Health Effects Remediation Sign in to save

Gut-on-a-Chip Research for Drug Development: Implications of Chip Design on Preclinical Oral Bioavailability or Intestinal Disease Studies

Biomimetics 2023 15 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 55 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Joanne M. Donkers, Joanne M. Donkers, Joanne M. Donkers, Evita van de Steeg, Evita van de Steeg Jamie I. van der Vaart, Jamie I. van der Vaart, Evita van de Steeg Evita van de Steeg, Evita van de Steeg, Evita van de Steeg Evita van de Steeg Evita van de Steeg, Evita van de Steeg, Evita van de Steeg Evita van de Steeg, Evita van de Steeg

Summary

This review examines how gut-on-a-chip laboratory devices are designed and used to study drug absorption and intestinal diseases outside the body. Researchers highlight four key design factors that influence how well these miniature gut models replicate real biological conditions. The study suggests these systems offer more realistic insights than traditional cell culture methods for understanding how drugs and food components interact with the intestinal lining.

Study Type In vitro

The gut plays a key role in drug absorption and metabolism of orally ingested drugs. Additionally, the characterization of intestinal disease processes is increasingly gaining more attention, as gut health is an important contributor to our overall health. The most recent innovation to study intestinal processes in vitro is the development of gut-on-a-chip (GOC) systems. Compared to conventional in vitro models, they offer more translational value, and many different GOC models have been presented over the past years. Herein, we reflect on the almost unlimited choices in designing and selecting a GOC for preclinical drug (or food) development research. Four components that largely influence the GOC design are highlighted, namely (1) the biological research questions, (2) chip fabrication and materials, (3) tissue engineering, and (4) the environmental and biochemical cues to add or measure in the GOC. Examples of GOC studies in the two major areas of preclinical intestinal research are presented: (1) intestinal absorption and metabolism to study the oral bioavailability of compounds, and (2) treatment-orientated research for intestinal diseases. The last section of this review presents an outlook on the limitations to overcome in order to accelerate preclinical GOC research.

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