Dual-Material 3D-Printed Intestinal Model Devices with Integrated Villi-like Scaffolds.

ACS Appl Mater Interfaces

Center for Intestinal Absorption and Transport of Biopharmaceuticals, Department of Health Technology, Technical University of Denmark, DK-2800 Kgs. Lyngby, Denmark.

Published: December 2021

AI Article Synopsis

  • This study focuses on creating small intestinal models that replicate the structure and function of natural intestinal tissue, specifically the villi architecture, which is essential for developing effective oral pharmaceuticals.
  • The researchers used 3D printing technology to manufacture hydrogel-based scaffolds with villi-like micropillars that promote long-term culture of intestinal cells (Caco-2), mimicking the natural intestinal environment.
  • The innovative design includes a reservoir system that allows for controlled compound transport, enabling detailed analysis of cell barrier properties and responses, which can advance drug screening processes.

Article Abstract

small intestinal models aim to mimic the intestinal function and structure, including the villi architecture of the native tissue. Accurate models in a scalable format are in great demand to advance, for example, the development of orally administered pharmaceutical products. Widely used planar intestinal cell monolayers for compound screening applications fail to recapitulate the three-dimensional (3D) microstructural characteristics of the intestinal villi arrays. This study employs stereolithographic 3D printing to manufacture biocompatible hydrogel-based scaffolds with villi-like micropillar arrays of tunable dimensions in poly(ethylene glycol) diacrylates (PEGDAs). The resulting 3D-printed microstructures are demonstrated to support a month-long culture and induce apicobasal polarization of Caco-2 epithelial cell layers along the villus axis, similar to the native intestinal microenvironment. Transport analysis requires confinement of compound transport to the epithelial cell layer within a compound diffusion-closed reservoir compartment. We meet this challenge by sequential printing of PEGDAs of different molecular weights into a monolithic device, where a diffusion-open villus-structured hydrogel bottom supports the cell culture and mass transport within the confines of a diffusion-closed solid wall. As a functional demonstrator of this scalable dual-material 3D micromanufacturing technology, we show that Caco-2 cells seeded in villi-wells form a tight epithelial barrier covering the villi-like micropillars and that compound-induced challenges to the barrier integrity can be monitored by standard high-throughput analysis tools (fluorescent tracer diffusion and transepithelial electrical resistance).

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Source
http://dx.doi.org/10.1021/acsami.1c22185DOI Listing

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