Biomechanical properties of 3D-printed bone scaffolds are improved by treatment with CRFP
Abstract Background One of the major challenges in orthopedics is to develop implants that overcome current postoperative problems such as osteointegration, proper load bearing, and stress shielding. Current implant techniques such as allografts or endoprostheses never reach full bone integration, a...
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doaj-e8eded50cfe64574bfa3000b522140f92020-11-25T00:44:09ZengBMCJournal of Orthopaedic Surgery and Research1749-799X2017-12-011211910.1186/s13018-017-0700-2Biomechanical properties of 3D-printed bone scaffolds are improved by treatment with CRFPCarlos G. Helguero0Vamiq M. Mustahsan1Sunjit Parmar2Sahana Pentyala3John L. Pfail4Imin Kao5David E. Komatsu6Srinivas Pentyala7Department of Mechanical Engineering, Stony Brook UniversityDepartment of Mechanical Engineering, Stony Brook UniversityDepartment of Anesthesiology, Stony Brook Medical CenterDepartment of Anesthesiology, Stony Brook Medical CenterDepartment of Anesthesiology, Stony Brook Medical CenterDepartment of Mechanical Engineering, Stony Brook UniversityDepartment of Orthopedics, Stony Brook Medical CenterDepartment of Anesthesiology, Stony Brook Medical CenterAbstract Background One of the major challenges in orthopedics is to develop implants that overcome current postoperative problems such as osteointegration, proper load bearing, and stress shielding. Current implant techniques such as allografts or endoprostheses never reach full bone integration, and the risk of fracture due to stress shielding is a major concern. To overcome this, a novel technique of reverse engineering to create artificial scaffolds was designed and tested. The purpose of the study is to create a new generation of implants that are both biocompatible and biomimetic. Methods 3D-printed scaffolds based on physiological trabecular bone patterning were printed. MC3T3 cells were cultured on these scaffolds in osteogenic media, with and without the addition of Calcitonin Receptor Fragment Peptide (CRFP) in order to assess bone formation on the surfaces of the scaffolds. Integrity of these cell-seeded bone-coated scaffolds was tested for their mechanical strength. Results The results show that cellular proliferation and bone matrix formation are both supported by our 3D-printed scaffolds. The mechanical strength of the scaffolds was enhanced by trabecular patterning in the order of 20% for compression strength and 60% for compressive modulus. Furthermore, cell-seeded trabecular scaffolds modulus increased fourfold when treated with CRFP. Conclusion Upon mineralization, the cell-seeded trabecular implants treated with osteo-inductive agents and pretreated with CRFP showed a significant increase in the compressive modulus. This work will lead to creating 3D structures that can be used in the replacement of not only bone segments, but entire bones.http://link.springer.com/article/10.1186/s13018-017-0700-2 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Carlos G. Helguero Vamiq M. Mustahsan Sunjit Parmar Sahana Pentyala John L. Pfail Imin Kao David E. Komatsu Srinivas Pentyala |
spellingShingle |
Carlos G. Helguero Vamiq M. Mustahsan Sunjit Parmar Sahana Pentyala John L. Pfail Imin Kao David E. Komatsu Srinivas Pentyala Biomechanical properties of 3D-printed bone scaffolds are improved by treatment with CRFP Journal of Orthopaedic Surgery and Research |
author_facet |
Carlos G. Helguero Vamiq M. Mustahsan Sunjit Parmar Sahana Pentyala John L. Pfail Imin Kao David E. Komatsu Srinivas Pentyala |
author_sort |
Carlos G. Helguero |
title |
Biomechanical properties of 3D-printed bone scaffolds are improved by treatment with CRFP |
title_short |
Biomechanical properties of 3D-printed bone scaffolds are improved by treatment with CRFP |
title_full |
Biomechanical properties of 3D-printed bone scaffolds are improved by treatment with CRFP |
title_fullStr |
Biomechanical properties of 3D-printed bone scaffolds are improved by treatment with CRFP |
title_full_unstemmed |
Biomechanical properties of 3D-printed bone scaffolds are improved by treatment with CRFP |
title_sort |
biomechanical properties of 3d-printed bone scaffolds are improved by treatment with crfp |
publisher |
BMC |
series |
Journal of Orthopaedic Surgery and Research |
issn |
1749-799X |
publishDate |
2017-12-01 |
description |
Abstract Background One of the major challenges in orthopedics is to develop implants that overcome current postoperative problems such as osteointegration, proper load bearing, and stress shielding. Current implant techniques such as allografts or endoprostheses never reach full bone integration, and the risk of fracture due to stress shielding is a major concern. To overcome this, a novel technique of reverse engineering to create artificial scaffolds was designed and tested. The purpose of the study is to create a new generation of implants that are both biocompatible and biomimetic. Methods 3D-printed scaffolds based on physiological trabecular bone patterning were printed. MC3T3 cells were cultured on these scaffolds in osteogenic media, with and without the addition of Calcitonin Receptor Fragment Peptide (CRFP) in order to assess bone formation on the surfaces of the scaffolds. Integrity of these cell-seeded bone-coated scaffolds was tested for their mechanical strength. Results The results show that cellular proliferation and bone matrix formation are both supported by our 3D-printed scaffolds. The mechanical strength of the scaffolds was enhanced by trabecular patterning in the order of 20% for compression strength and 60% for compressive modulus. Furthermore, cell-seeded trabecular scaffolds modulus increased fourfold when treated with CRFP. Conclusion Upon mineralization, the cell-seeded trabecular implants treated with osteo-inductive agents and pretreated with CRFP showed a significant increase in the compressive modulus. This work will lead to creating 3D structures that can be used in the replacement of not only bone segments, but entire bones. |
url |
http://link.springer.com/article/10.1186/s13018-017-0700-2 |
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