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Clinically relevant preclinical animal models for testing novel cranio‐maxillofacial bone 3D‐printed biomaterials

Bone tissue engineering is a rapidly developing field with potential for the regeneration of craniomaxillofacial (CMF) bones, with 3D printing being a suitable fabrication tool for patient‐specific implants. The CMF region includes a variety of different bones with distinct functions. The clinical i...

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Autores principales: Hatt, Luan P., Thompson, Keith, Helms, Jill A., Stoddart, Martin J., Armiento, Angela R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847734/
https://www.ncbi.nlm.nih.gov/pubmed/35170248
http://dx.doi.org/10.1002/ctm2.690
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author Hatt, Luan P.
Thompson, Keith
Helms, Jill A.
Stoddart, Martin J.
Armiento, Angela R.
author_facet Hatt, Luan P.
Thompson, Keith
Helms, Jill A.
Stoddart, Martin J.
Armiento, Angela R.
author_sort Hatt, Luan P.
collection PubMed
description Bone tissue engineering is a rapidly developing field with potential for the regeneration of craniomaxillofacial (CMF) bones, with 3D printing being a suitable fabrication tool for patient‐specific implants. The CMF region includes a variety of different bones with distinct functions. The clinical implementation of tissue engineering concepts is currently poor, likely due to multiple reasons including the complexity of the CMF anatomy and biology, and the limited relevance of the currently used preclinical models. The ‘recapitulation of a human disease’ is a core requisite of preclinical animal models, but this aspect is often neglected, with a vast majority of studies failing to identify the specific clinical indication they are targeting and/or the rationale for choosing one animal model over another. Currently, there are no suitable guidelines that propose the most appropriate animal model to address a specific CMF pathology and no standards are established to test the efficacy of biomaterials or tissue engineered constructs in the CMF field. This review reports the current clinical scenario of CMF reconstruction, then discusses the numerous limitations of currently used preclinical animal models employed for validating 3D‐printed tissue engineered constructs and the need to reduce animal work that does not address a specific clinical question. We will highlight critical research aspects to consider, to pave a clinically driven path for the development of new tissue engineered materials for CMF reconstruction.
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spelling pubmed-88477342022-02-25 Clinically relevant preclinical animal models for testing novel cranio‐maxillofacial bone 3D‐printed biomaterials Hatt, Luan P. Thompson, Keith Helms, Jill A. Stoddart, Martin J. Armiento, Angela R. Clin Transl Med Reviews Bone tissue engineering is a rapidly developing field with potential for the regeneration of craniomaxillofacial (CMF) bones, with 3D printing being a suitable fabrication tool for patient‐specific implants. The CMF region includes a variety of different bones with distinct functions. The clinical implementation of tissue engineering concepts is currently poor, likely due to multiple reasons including the complexity of the CMF anatomy and biology, and the limited relevance of the currently used preclinical models. The ‘recapitulation of a human disease’ is a core requisite of preclinical animal models, but this aspect is often neglected, with a vast majority of studies failing to identify the specific clinical indication they are targeting and/or the rationale for choosing one animal model over another. Currently, there are no suitable guidelines that propose the most appropriate animal model to address a specific CMF pathology and no standards are established to test the efficacy of biomaterials or tissue engineered constructs in the CMF field. This review reports the current clinical scenario of CMF reconstruction, then discusses the numerous limitations of currently used preclinical animal models employed for validating 3D‐printed tissue engineered constructs and the need to reduce animal work that does not address a specific clinical question. We will highlight critical research aspects to consider, to pave a clinically driven path for the development of new tissue engineered materials for CMF reconstruction. John Wiley and Sons Inc. 2022-02-15 /pmc/articles/PMC8847734/ /pubmed/35170248 http://dx.doi.org/10.1002/ctm2.690 Text en © 2022 The Authors. Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Hatt, Luan P.
Thompson, Keith
Helms, Jill A.
Stoddart, Martin J.
Armiento, Angela R.
Clinically relevant preclinical animal models for testing novel cranio‐maxillofacial bone 3D‐printed biomaterials
title Clinically relevant preclinical animal models for testing novel cranio‐maxillofacial bone 3D‐printed biomaterials
title_full Clinically relevant preclinical animal models for testing novel cranio‐maxillofacial bone 3D‐printed biomaterials
title_fullStr Clinically relevant preclinical animal models for testing novel cranio‐maxillofacial bone 3D‐printed biomaterials
title_full_unstemmed Clinically relevant preclinical animal models for testing novel cranio‐maxillofacial bone 3D‐printed biomaterials
title_short Clinically relevant preclinical animal models for testing novel cranio‐maxillofacial bone 3D‐printed biomaterials
title_sort clinically relevant preclinical animal models for testing novel cranio‐maxillofacial bone 3d‐printed biomaterials
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847734/
https://www.ncbi.nlm.nih.gov/pubmed/35170248
http://dx.doi.org/10.1002/ctm2.690
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