Artificial organs, such as extracorporeal membrane oxygenators, dialyzers, and hemoadsorber cartridges, face persistent challenges related to the flow distribution within the cartridge. This uneven flow distribution leads to clot formation and inefficient mass transfer over the device's functional surface. In this work, a comprehensive methodology is presented for precisely integrating triply periodic minimal surfaces (TPMS) into module housings and question whether the internal surface topology determining the flow distribution affects blood coagulation. Three module types are compared with different internal topologies: tubular, isometric, and anisometric TPMS. First, this study includes a computational fluid dynamics (CFD) simulation of the internal hemodynamics, validated through experimental residence time distributions (RTD). Blood tests using human whole blood and subsequent visualization of blood clots by computed tomography, allow the quantification of structure-induced blood clotting. The results indicate that TPMS topologies, particularly anisometric ones, serve as effective flow distributors and significantly reduce and delay blood clotting compared to conventional tubular geometries. For these novel TPMS modules, the inner surfaces can be activated chemically or functionalized to function as a selective adsorption site or biocatalytic surface or made of a permeable material to facilitate mass transfer.
Enhanced Hemodynamics of Anisometric TPMS Topology Reduce Blood Clotting in 3D Printed Blood Contactors.
各向异性TPMS拓扑结构的增强血液动力学可减少3D打印血液接触器中的血液凝固
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作者:Hirschwald Lukas T, Hagemann Franziska, Biermann Maik, HanÃen Paul, Hoffmann Patrick, Höhs Tim, Neuhaus Florian, Tillmann Maerthe Theresa, Peric Petar, Wattenberg Maximilian, Stille Maik, Fechter Tamara, TheiÃen Alexander, Winnersbach Patrick, Barbian Kai P, Jansen Sebastian V, Steinseifer Ulrich, Wiegmann Bettina, Rossaint Rolf, Wessling Matthias, Bleilevens Christian, Linkhorst John
| 期刊: | Advanced Healthcare Materials | 影响因子: | 9.600 |
| 时间: | 2025 | 起止号: | 2025 Jan;14(2):e2403111 |
| doi: | 10.1002/adhm.202403111 | ||
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