Cargando…
Promotion of in vivo degradability, vascularization and osteogenesis of calcium sulfate-based bone cements containing nanoporous lithium doping magnesium silicate
Nanoporous lithium doping magnesium silicate (nl-MS) was introduced into calcium sulfate hemihydrate to prepare calcium sulfate composite (nl-MSC) bone cements. The introduction of nl-MS improved the in vitro degradability of nl-MSC cements, which could neutralize acidic degradable products of calci...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325137/ https://www.ncbi.nlm.nih.gov/pubmed/28260883 http://dx.doi.org/10.2147/IJN.S124965 |
_version_ | 1782510322852036608 |
---|---|
author | Cao, Liehu Weng, Weizong Chen, Xiao Zhang, Jun Zhou, Qirong Cui, Jin Zhao, Yuechao Shin, Jung-Woog Su, Jiacan |
author_facet | Cao, Liehu Weng, Weizong Chen, Xiao Zhang, Jun Zhou, Qirong Cui, Jin Zhao, Yuechao Shin, Jung-Woog Su, Jiacan |
author_sort | Cao, Liehu |
collection | PubMed |
description | Nanoporous lithium doping magnesium silicate (nl-MS) was introduced into calcium sulfate hemihydrate to prepare calcium sulfate composite (nl-MSC) bone cements. The introduction of nl-MS improved the in vitro degradability of nl-MSC cements, which could neutralize acidic degradable products of calcium sulfate and prevented the pH from dropping. The cements were implanted into the bone defects of femur bone of rabbits, and the results of histological and immunohistochemical analysis revealed that massive new bone tissue formed in the defects while the cements were degradable, indicating that the osteogenesis and degradability of the nl-MSC cements were much better than the control calcium sulfate dihydrate (CSD) cements. Furthermore, the positive expression of vascular endothelial growth factor and collagen type I for nl-MSC cements was higher than CSD, indicating that addition of nl-MS into the cements enhanced vascularization and osteogenic differentiation. The results suggested that the nl-MSC cements with good biocompatibility and degradability could promote vascularization and osteogenesis, and had great potential to treat bone defects. |
format | Online Article Text |
id | pubmed-5325137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53251372017-03-03 Promotion of in vivo degradability, vascularization and osteogenesis of calcium sulfate-based bone cements containing nanoporous lithium doping magnesium silicate Cao, Liehu Weng, Weizong Chen, Xiao Zhang, Jun Zhou, Qirong Cui, Jin Zhao, Yuechao Shin, Jung-Woog Su, Jiacan Int J Nanomedicine Original Research Nanoporous lithium doping magnesium silicate (nl-MS) was introduced into calcium sulfate hemihydrate to prepare calcium sulfate composite (nl-MSC) bone cements. The introduction of nl-MS improved the in vitro degradability of nl-MSC cements, which could neutralize acidic degradable products of calcium sulfate and prevented the pH from dropping. The cements were implanted into the bone defects of femur bone of rabbits, and the results of histological and immunohistochemical analysis revealed that massive new bone tissue formed in the defects while the cements were degradable, indicating that the osteogenesis and degradability of the nl-MSC cements were much better than the control calcium sulfate dihydrate (CSD) cements. Furthermore, the positive expression of vascular endothelial growth factor and collagen type I for nl-MSC cements was higher than CSD, indicating that addition of nl-MS into the cements enhanced vascularization and osteogenic differentiation. The results suggested that the nl-MSC cements with good biocompatibility and degradability could promote vascularization and osteogenesis, and had great potential to treat bone defects. Dove Medical Press 2017-02-17 /pmc/articles/PMC5325137/ /pubmed/28260883 http://dx.doi.org/10.2147/IJN.S124965 Text en © 2017 Cao et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Cao, Liehu Weng, Weizong Chen, Xiao Zhang, Jun Zhou, Qirong Cui, Jin Zhao, Yuechao Shin, Jung-Woog Su, Jiacan Promotion of in vivo degradability, vascularization and osteogenesis of calcium sulfate-based bone cements containing nanoporous lithium doping magnesium silicate |
title | Promotion of in vivo degradability, vascularization and osteogenesis of calcium sulfate-based bone cements containing nanoporous lithium doping magnesium silicate |
title_full | Promotion of in vivo degradability, vascularization and osteogenesis of calcium sulfate-based bone cements containing nanoporous lithium doping magnesium silicate |
title_fullStr | Promotion of in vivo degradability, vascularization and osteogenesis of calcium sulfate-based bone cements containing nanoporous lithium doping magnesium silicate |
title_full_unstemmed | Promotion of in vivo degradability, vascularization and osteogenesis of calcium sulfate-based bone cements containing nanoporous lithium doping magnesium silicate |
title_short | Promotion of in vivo degradability, vascularization and osteogenesis of calcium sulfate-based bone cements containing nanoporous lithium doping magnesium silicate |
title_sort | promotion of in vivo degradability, vascularization and osteogenesis of calcium sulfate-based bone cements containing nanoporous lithium doping magnesium silicate |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325137/ https://www.ncbi.nlm.nih.gov/pubmed/28260883 http://dx.doi.org/10.2147/IJN.S124965 |
work_keys_str_mv | AT caoliehu promotionofinvivodegradabilityvascularizationandosteogenesisofcalciumsulfatebasedbonecementscontainingnanoporouslithiumdopingmagnesiumsilicate AT wengweizong promotionofinvivodegradabilityvascularizationandosteogenesisofcalciumsulfatebasedbonecementscontainingnanoporouslithiumdopingmagnesiumsilicate AT chenxiao promotionofinvivodegradabilityvascularizationandosteogenesisofcalciumsulfatebasedbonecementscontainingnanoporouslithiumdopingmagnesiumsilicate AT zhangjun promotionofinvivodegradabilityvascularizationandosteogenesisofcalciumsulfatebasedbonecementscontainingnanoporouslithiumdopingmagnesiumsilicate AT zhouqirong promotionofinvivodegradabilityvascularizationandosteogenesisofcalciumsulfatebasedbonecementscontainingnanoporouslithiumdopingmagnesiumsilicate AT cuijin promotionofinvivodegradabilityvascularizationandosteogenesisofcalciumsulfatebasedbonecementscontainingnanoporouslithiumdopingmagnesiumsilicate AT zhaoyuechao promotionofinvivodegradabilityvascularizationandosteogenesisofcalciumsulfatebasedbonecementscontainingnanoporouslithiumdopingmagnesiumsilicate AT shinjungwoog promotionofinvivodegradabilityvascularizationandosteogenesisofcalciumsulfatebasedbonecementscontainingnanoporouslithiumdopingmagnesiumsilicate AT sujiacan promotionofinvivodegradabilityvascularizationandosteogenesisofcalciumsulfatebasedbonecementscontainingnanoporouslithiumdopingmagnesiumsilicate |