Related Experiment Video
Updated: Aug 5, 2026

Artificial Lung Device Priming for In Situ Fiber Bundle Surface Grafting
Published on: March 28, 2025
From Fiber Bundles to Architected Membranes: Triply Periodic Minimal Surface Architectures for Biohybrid Artificial
Michael Pflaum1,2,3, Kai P Barbian4, Florian Neuhaus5
1Department of Cardiothoracic, Transplantation, and Vascular Surgery, Hannover Medical School, Hannover, Germany.
Abstract:
Artificial lung systems rely almost exclusively on hollow fiber membrane (HFM) bundles, where gas exchange is constrained by heterogeneous flow distribution and thrombogenic blood-material interfaces. Here, we introduce an architecture-driven design framework for artificial lungs based on additively manufactured triply periodic minimal surface (TPMS) membranes. In contrast to discrete fiber bundles, TPMS membranes form continuous three-dimensional architectures that simultaneously regulate perfusion pathways, diffusion interfaces, and blood-material interactions. Computational fluid dynamics and multiphysics transport simulations reveal that membrane architecture governs gas exchange through coupled effects of membrane thickness, unit cell size, and three-dimensional flow topology. Optimized TPMS architectures achieved on average up to ∼88% higher oxygen transfer rates across the investigated flow regime compared to conventional HFM while enabling substantially more homogeneous flow fields and reduced stagnation zones. Experimental screening identifies polydimethylsiloxane-based printable elastomers compatible with thin gas-permeable membranes and endothelial functionalization. The biohybrid endothelial interface mitigates thrombogenic interactions, while maintaining gas transport. Computed tomography-derived implant geometries demonstrate the feasibility of translating architected membrane systems into anatomically integrated artificial lungs. Together, these results establish a new design paradigm for artificial lungs, in which membrane architecture becomes the primary determinant of gas transport, flow distribution, and hemocompatibility.

