# Synergistic Combination of Additive One‐ and Two‐Photon Polymerization Printing Methods to Fabricate 3D Microstructured Perfusable Angiogenesis–on–a–Chip Systems

**Authors:** Daria Sokoliuk, Rizlene Bouhaya, Peter Haeger, Kathrin Godthardt, Daniel Fetting, Lenard Spiecker, Heinrich Spiecker, Alexander Rockenbach, Holger Rothe, Klaus Liefeith, Doris Heinrich

PMC · DOI: 10.1002/elsc.70059 · 2026-01-27

## TL;DR

This paper introduces a new 3D printing method to create microfluidic chips that support blood vessel growth, offering a promising tool for drug testing and tissue research.

## Contribution

The paper presents a novel two-step fabrication method combining one- and two-photon polymerization for creating perfusable angiogenesis-on-a-chip systems.

## Key findings

- The developed chip successfully induces endothelial cell sprouting in response to angiogenic factors.
- The fabrication method allows for leak-free bonding and enables EC migration into an extracellular matrix.
- The platform is versatile and can be customized for various biological applications.

## Abstract

Tissue engineering, and in particular the development of organ‐on‐a‐chip (OOC) models, holds significant promise for advancing personalized medicine and reducing the use of animal models. The integration of microfluidics and advanced biomaterials in OOC systems provides controlled microenvironments and fosters the creation of physiologically relevant tissue models. A critical aspect of OOC models is the fabrication of perfusable chips to create vascular networks that are essential for sustaining long‐term 3D cultures. Here we show a two‐step fabrication approach that combines one‐ and two‐photon polymerization (2PP) to create a microfluidic chip capable of supporting endothelial cell (EC) angiogenesis. The chip features a 2PP‐printed sealing contour to ensure leak‐free bonding of chip parts, and an array of channel‐separating‐pillars that enable EC migration from the parent vessel into an extracellular matrix. Our results demonstrate that the developed angiogenesis‐on‐a‐chip model successfully induces EC sprouting in response to angiogenic factors. This work significantly contributes to the field by providing a versatile platform for vascular studies, highlighting the potential for its application in drug screening. The flexibility and precision of our fabrication method also allows for customizing OOC devices for various biological applications, thereby enhancing the relevance of these systems in investigation of complex tissue interactions.

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12836039/full.md

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Source: https://tomesphere.com/paper/PMC12836039