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A multiscale optimisation method for bone growth scaffolds based on triply periodic minimal surfaces
Tissue engineered bone scaffolds are potential alternatives to bone allografts and autografts. Porous scaffolds based on triply periodic minimal surfaces (TPMS) are good candidates for tissue growth because they offer high surface-to-volume ratio, have tailorable stiffness, and can be easily fabrica...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595174/ https://www.ncbi.nlm.nih.gov/pubmed/34318358 http://dx.doi.org/10.1007/s10237-021-01496-8 |
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author | Lehder, E. F. Ashcroft, I. A. Wildman, R. D. Ruiz-Cantu, L. A. Maskery, I. |
author_facet | Lehder, E. F. Ashcroft, I. A. Wildman, R. D. Ruiz-Cantu, L. A. Maskery, I. |
author_sort | Lehder, E. F. |
collection | PubMed |
description | Tissue engineered bone scaffolds are potential alternatives to bone allografts and autografts. Porous scaffolds based on triply periodic minimal surfaces (TPMS) are good candidates for tissue growth because they offer high surface-to-volume ratio, have tailorable stiffness, and can be easily fabricated by additive manufacturing. However, the range of TPMS scaffold types is extensive, and it is not yet clear which type provides the fastest cell or tissue growth while being sufficiently stiff to act as a bone graft. Nor is there currently an established methodology for TPMS bone scaffold design which can be quickly adopted by medical designers or biologists designing implants. In this study, we examine six TPMS scaffold types for use as tissue growth scaffolds and propose a general methodology to optimise their geometry. At the macro-scale, the optimisation routine ensures a scaffold stiffness within suitable limits for bone, while at the micro-scale it maximises the cell growth rate. The optimisation procedure also ensures the scaffold pores are of sufficient diameter to allow oxygen and nutrient delivery via capillaries. Of the examined TPMS structures, the Lidinoid and Split P cell types provide the greatest cell growth rates and are therefore the best candidates for bone scaffolds. |
format | Online Article Text |
id | pubmed-8595174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-85951742021-11-24 A multiscale optimisation method for bone growth scaffolds based on triply periodic minimal surfaces Lehder, E. F. Ashcroft, I. A. Wildman, R. D. Ruiz-Cantu, L. A. Maskery, I. Biomech Model Mechanobiol Original Paper Tissue engineered bone scaffolds are potential alternatives to bone allografts and autografts. Porous scaffolds based on triply periodic minimal surfaces (TPMS) are good candidates for tissue growth because they offer high surface-to-volume ratio, have tailorable stiffness, and can be easily fabricated by additive manufacturing. However, the range of TPMS scaffold types is extensive, and it is not yet clear which type provides the fastest cell or tissue growth while being sufficiently stiff to act as a bone graft. Nor is there currently an established methodology for TPMS bone scaffold design which can be quickly adopted by medical designers or biologists designing implants. In this study, we examine six TPMS scaffold types for use as tissue growth scaffolds and propose a general methodology to optimise their geometry. At the macro-scale, the optimisation routine ensures a scaffold stiffness within suitable limits for bone, while at the micro-scale it maximises the cell growth rate. The optimisation procedure also ensures the scaffold pores are of sufficient diameter to allow oxygen and nutrient delivery via capillaries. Of the examined TPMS structures, the Lidinoid and Split P cell types provide the greatest cell growth rates and are therefore the best candidates for bone scaffolds. Springer Berlin Heidelberg 2021-07-27 2021 /pmc/articles/PMC8595174/ /pubmed/34318358 http://dx.doi.org/10.1007/s10237-021-01496-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Lehder, E. F. Ashcroft, I. A. Wildman, R. D. Ruiz-Cantu, L. A. Maskery, I. A multiscale optimisation method for bone growth scaffolds based on triply periodic minimal surfaces |
title | A multiscale optimisation method for bone growth scaffolds based on triply periodic minimal surfaces |
title_full | A multiscale optimisation method for bone growth scaffolds based on triply periodic minimal surfaces |
title_fullStr | A multiscale optimisation method for bone growth scaffolds based on triply periodic minimal surfaces |
title_full_unstemmed | A multiscale optimisation method for bone growth scaffolds based on triply periodic minimal surfaces |
title_short | A multiscale optimisation method for bone growth scaffolds based on triply periodic minimal surfaces |
title_sort | multiscale optimisation method for bone growth scaffolds based on triply periodic minimal surfaces |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595174/ https://www.ncbi.nlm.nih.gov/pubmed/34318358 http://dx.doi.org/10.1007/s10237-021-01496-8 |
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