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A Modified Murine Calvarial Osteolysis Model Exposed to Ti Particles in Aseptic Loosening
AIM: To investigate the different effects on osteolysis between commercial pure Ti particles and TiAl6V4 particles obtained from prosthesis of patients with aseptic loosening. METHOD: Scanning electron microscope, energy dispersive X-ray spectrometry, and X-ray diffraction were used for the size tes...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468620/ https://www.ncbi.nlm.nih.gov/pubmed/32908884 http://dx.doi.org/10.1155/2020/3403489 |
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author | Deng, Zhantao Wang, Shuai Li, Mengyuan Fu, Guangtao Liu, Chang Li, Shuxian Jin, Jiewen Lyu, Feng-Juan Ma, Yuanchen Zheng, Qiujian |
author_facet | Deng, Zhantao Wang, Shuai Li, Mengyuan Fu, Guangtao Liu, Chang Li, Shuxian Jin, Jiewen Lyu, Feng-Juan Ma, Yuanchen Zheng, Qiujian |
author_sort | Deng, Zhantao |
collection | PubMed |
description | AIM: To investigate the different effects on osteolysis between commercial pure Ti particles and TiAl6V4 particles obtained from prosthesis of patients with aseptic loosening. METHOD: Scanning electron microscope, energy dispersive X-ray spectrometry, and X-ray diffraction were used for the size test, chemical composition test, and phase analysis of two kinds of Ti particles. Microcomputed tomography (micro-CT) and 3-dimensional reconstruction analysis were applied to analyze the bone loss quantitatively and radiologically. Hematoxylin-eosin (HE) staining and tartrate-resistant acid phosphatase (TRAP) staining were used to assess the histologic difference. RESULT: TiAl6V4 particles were constituted by FeO, Al(45)V(7), and Al(3)Ti while pure Ti particles were constituted by Ti, Ti(3)O, and C(4)H(7)NO(3). Similar particle size of nanoscale was detected of two Ti particles. A TiAl6V4 osteolysis model had more severe bone loss when scanned with micro-CT and assessed by quantitative analysis. TiAl6V4 also presented deeper and wider calvarial bone loss in HE staining and more activated osteoclasts in TRAP staining. CONCLUSION: A mouse calvarial model is the most effective animal model for the primary in vivo research of aseptic loosening. Compared with commercial Ti particles, TiAl6V4 particles derived from prosthesis of an aseptic loosening patient had more severe bone loss and more activated osteoclast, which was more consistent with pathogenesis of aseptic loosening in vivo, had high success rate of establishment of a model, and was more desired in animal modeling. |
format | Online Article Text |
id | pubmed-7468620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-74686202020-09-08 A Modified Murine Calvarial Osteolysis Model Exposed to Ti Particles in Aseptic Loosening Deng, Zhantao Wang, Shuai Li, Mengyuan Fu, Guangtao Liu, Chang Li, Shuxian Jin, Jiewen Lyu, Feng-Juan Ma, Yuanchen Zheng, Qiujian Biomed Res Int Research Article AIM: To investigate the different effects on osteolysis between commercial pure Ti particles and TiAl6V4 particles obtained from prosthesis of patients with aseptic loosening. METHOD: Scanning electron microscope, energy dispersive X-ray spectrometry, and X-ray diffraction were used for the size test, chemical composition test, and phase analysis of two kinds of Ti particles. Microcomputed tomography (micro-CT) and 3-dimensional reconstruction analysis were applied to analyze the bone loss quantitatively and radiologically. Hematoxylin-eosin (HE) staining and tartrate-resistant acid phosphatase (TRAP) staining were used to assess the histologic difference. RESULT: TiAl6V4 particles were constituted by FeO, Al(45)V(7), and Al(3)Ti while pure Ti particles were constituted by Ti, Ti(3)O, and C(4)H(7)NO(3). Similar particle size of nanoscale was detected of two Ti particles. A TiAl6V4 osteolysis model had more severe bone loss when scanned with micro-CT and assessed by quantitative analysis. TiAl6V4 also presented deeper and wider calvarial bone loss in HE staining and more activated osteoclasts in TRAP staining. CONCLUSION: A mouse calvarial model is the most effective animal model for the primary in vivo research of aseptic loosening. Compared with commercial Ti particles, TiAl6V4 particles derived from prosthesis of an aseptic loosening patient had more severe bone loss and more activated osteoclast, which was more consistent with pathogenesis of aseptic loosening in vivo, had high success rate of establishment of a model, and was more desired in animal modeling. Hindawi 2020-08-25 /pmc/articles/PMC7468620/ /pubmed/32908884 http://dx.doi.org/10.1155/2020/3403489 Text en Copyright © 2020 Zhantao Deng et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Deng, Zhantao Wang, Shuai Li, Mengyuan Fu, Guangtao Liu, Chang Li, Shuxian Jin, Jiewen Lyu, Feng-Juan Ma, Yuanchen Zheng, Qiujian A Modified Murine Calvarial Osteolysis Model Exposed to Ti Particles in Aseptic Loosening |
title | A Modified Murine Calvarial Osteolysis Model Exposed to Ti Particles in Aseptic Loosening |
title_full | A Modified Murine Calvarial Osteolysis Model Exposed to Ti Particles in Aseptic Loosening |
title_fullStr | A Modified Murine Calvarial Osteolysis Model Exposed to Ti Particles in Aseptic Loosening |
title_full_unstemmed | A Modified Murine Calvarial Osteolysis Model Exposed to Ti Particles in Aseptic Loosening |
title_short | A Modified Murine Calvarial Osteolysis Model Exposed to Ti Particles in Aseptic Loosening |
title_sort | modified murine calvarial osteolysis model exposed to ti particles in aseptic loosening |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468620/ https://www.ncbi.nlm.nih.gov/pubmed/32908884 http://dx.doi.org/10.1155/2020/3403489 |
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