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3D-Printing of Hierarchically Designed and Osteoconductive Bone Tissue Engineering Scaffolds
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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215341/ https://www.ncbi.nlm.nih.gov/pubmed/32295064 http://dx.doi.org/10.3390/ma13081836 |
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author | Söhling, Nicolas Neijhoft, Jonas Nienhaus, Vinzenz Acker, Valentin Harbig, Jana Menz, Fabian Ochs, Joachim Verboket, René D. Ritz, Ulrike Blaeser, Andreas Dörsam, Edgar Frank, Johannes Marzi, Ingo Henrich, Dirk |
author_facet | Söhling, Nicolas Neijhoft, Jonas Nienhaus, Vinzenz Acker, Valentin Harbig, Jana Menz, Fabian Ochs, Joachim Verboket, René D. Ritz, Ulrike Blaeser, Andreas Dörsam, Edgar Frank, Johannes Marzi, Ingo Henrich, Dirk |
author_sort | Söhling, Nicolas |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7215341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72153412020-05-18 3D-Printing of Hierarchically Designed and Osteoconductive Bone Tissue Engineering Scaffolds Söhling, Nicolas Neijhoft, Jonas Nienhaus, Vinzenz Acker, Valentin Harbig, Jana Menz, Fabian Ochs, Joachim Verboket, René D. Ritz, Ulrike Blaeser, Andreas Dörsam, Edgar Frank, Johannes Marzi, Ingo Henrich, Dirk Materials (Basel) Article 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. MDPI 2020-04-13 /pmc/articles/PMC7215341/ /pubmed/32295064 http://dx.doi.org/10.3390/ma13081836 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Söhling, Nicolas Neijhoft, Jonas Nienhaus, Vinzenz Acker, Valentin Harbig, Jana Menz, Fabian Ochs, Joachim Verboket, René D. Ritz, Ulrike Blaeser, Andreas Dörsam, Edgar Frank, Johannes Marzi, Ingo Henrich, Dirk 3D-Printing of Hierarchically Designed and Osteoconductive Bone Tissue Engineering Scaffolds |
title | 3D-Printing of Hierarchically Designed and Osteoconductive Bone Tissue Engineering Scaffolds |
title_full | 3D-Printing of Hierarchically Designed and Osteoconductive Bone Tissue Engineering Scaffolds |
title_fullStr | 3D-Printing of Hierarchically Designed and Osteoconductive Bone Tissue Engineering Scaffolds |
title_full_unstemmed | 3D-Printing of Hierarchically Designed and Osteoconductive Bone Tissue Engineering Scaffolds |
title_short | 3D-Printing of Hierarchically Designed and Osteoconductive Bone Tissue Engineering Scaffolds |
title_sort | 3d-printing of hierarchically designed and osteoconductive bone tissue engineering scaffolds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215341/ https://www.ncbi.nlm.nih.gov/pubmed/32295064 http://dx.doi.org/10.3390/ma13081836 |
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