TY - JOUR A1 - Söhling, Nicolas A1 - Neijhoft, Jonas A1 - Nienhaus, Vinzenz A1 - Acker, Valentin A1 - Harbig, Jana A1 - Menz, Fabian A1 - Ochs, Joachim A1 - Verboket, René A1 - Ritz, Ulrike A1 - Blaeser, Andreas A1 - Dörsam, Edgar A1 - Frank, Johannes A1 - Marzi, Ingo A1 - Henrich, Dirk T1 - 3d-printing of hierarchically designed and osteoconductive bone tissue engineering scaffolds T2 - Materials N2 - In Bone Tissue Engineering (BTE), autologous bone-regenerative cells are combined with a scaffold for large bone defect treatment (LBDT). Microporous, polylactic acid (PLA) scaffolds showed good healing results in small animals. However, transfer to large animal models is not easily achieved simply by upscaling the design. Increasing diffusion distances have a negative impact on cell survival and nutrition supply, leading to cell death and ultimately implant failure. Here, a novel scaffold architecture was designed to meet all requirements for an advanced bone substitute. Biofunctional, porous subunits in a load-bearing, compression-resistant frame structure characterize this approach. An open, macro- and microporous internal architecture (100 µm–2 mm pores) optimizes conditions for oxygen and nutrient supply to the implant’s inner areas by diffusion. A prototype was 3D-printed applying Fused Filament Fabrication using PLA. After incubation with Saos-2 (Sarcoma osteogenic) cells for 14 days, cell morphology, cell distribution, cell survival (fluorescence microscopy and LDH-based cytotoxicity assay), metabolic activity (MTT test), and osteogenic gene expression were determined. The adherent cells showed colonization properties, proliferation potential, and osteogenic differentiation. The innovative design, with its porous structure, is a promising matrix for cell settlement and proliferation. The modular design allows easy upscaling and offers a solution for LBDT. Y1 - 2020 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/54344 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-543443 SN - 1996-1944 VL - 13 IS - 1836 SP - 1 EP - 18 PB - MDPI CY - Basel ER -