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Biocompatibility of artificial bone based on vancomycin loaded mesoporous silica nanoparticles and calcium sulfate composites

The aim of this study was to evaluate the in vitro and in vivo biocompatibility of artificial bone based on vancomycin loaded mesoporous silica nanoparticles and calcium sulfate composites. In vitro cytotoxicity tests by cholecystokinin octapeptide (CCK-8) assay showed that the 5 %Van-MSN-CaSO(4) an...

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Autores principales: Gu, Jisheng, Wang, Teng, Fan, Guoxin, Ma, Junhua, Hu, Wei, Cai, Xiaobing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756035/
https://www.ncbi.nlm.nih.gov/pubmed/26883948
http://dx.doi.org/10.1007/s10856-016-5671-z
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author Gu, Jisheng
Wang, Teng
Fan, Guoxin
Ma, Junhua
Hu, Wei
Cai, Xiaobing
author_facet Gu, Jisheng
Wang, Teng
Fan, Guoxin
Ma, Junhua
Hu, Wei
Cai, Xiaobing
author_sort Gu, Jisheng
collection PubMed
description The aim of this study was to evaluate the in vitro and in vivo biocompatibility of artificial bone based on vancomycin loaded mesoporous silica nanoparticles and calcium sulfate composites. In vitro cytotoxicity tests by cholecystokinin octapeptide (CCK-8) assay showed that the 5 %Van-MSN-CaSO(4) and Van-CaSO(4) bone cements were cytocompatible for mouse osteoblastic cell line MC3T3-E1. The microscopic observation confirmed that MC3T3-E1cells incubated with Van-CaSO(4) group and 5 %Van-MSN-CaSO(4) group exhibited clear spindle-shaped changes, volume increase and maturation, showing that these cements supported adhesion of osteoblastic cells on their surfaces. In addition, the measurement of alkaline phosphatase activity revealed the osteoconductive property of these biomaterials. In order to assess in vivo biocompatibility, synthesized cements were implanted into the distal femur of twelve adult male and female New Zealand rabbits. After implantation in artificial defects of the distal femur, 5 %Van-MSN-CaSO(4) and Van-CaSO(4) bone cements did not damage the function of main organs of rabbits. In addition, the Van-MSN-CaSO(4) composite allowed complete repair of bone defects with new bone formation 3 months after implantation. These results show potential application of Van-MSN-CaSO(4) composites as bone graft materials for the treatment of open fracture in human due to its mechanical, osteoconductive and potential sustained drug release characteristics and the absence of adverse effects on the body.
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spelling pubmed-47560352016-02-26 Biocompatibility of artificial bone based on vancomycin loaded mesoporous silica nanoparticles and calcium sulfate composites Gu, Jisheng Wang, Teng Fan, Guoxin Ma, Junhua Hu, Wei Cai, Xiaobing J Mater Sci Mater Med Engineering and Nano-engineering Approaches for Medical Devices The aim of this study was to evaluate the in vitro and in vivo biocompatibility of artificial bone based on vancomycin loaded mesoporous silica nanoparticles and calcium sulfate composites. In vitro cytotoxicity tests by cholecystokinin octapeptide (CCK-8) assay showed that the 5 %Van-MSN-CaSO(4) and Van-CaSO(4) bone cements were cytocompatible for mouse osteoblastic cell line MC3T3-E1. The microscopic observation confirmed that MC3T3-E1cells incubated with Van-CaSO(4) group and 5 %Van-MSN-CaSO(4) group exhibited clear spindle-shaped changes, volume increase and maturation, showing that these cements supported adhesion of osteoblastic cells on their surfaces. In addition, the measurement of alkaline phosphatase activity revealed the osteoconductive property of these biomaterials. In order to assess in vivo biocompatibility, synthesized cements were implanted into the distal femur of twelve adult male and female New Zealand rabbits. After implantation in artificial defects of the distal femur, 5 %Van-MSN-CaSO(4) and Van-CaSO(4) bone cements did not damage the function of main organs of rabbits. In addition, the Van-MSN-CaSO(4) composite allowed complete repair of bone defects with new bone formation 3 months after implantation. These results show potential application of Van-MSN-CaSO(4) composites as bone graft materials for the treatment of open fracture in human due to its mechanical, osteoconductive and potential sustained drug release characteristics and the absence of adverse effects on the body. Springer US 2016-02-16 2016 /pmc/articles/PMC4756035/ /pubmed/26883948 http://dx.doi.org/10.1007/s10856-016-5671-z Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Engineering and Nano-engineering Approaches for Medical Devices
Gu, Jisheng
Wang, Teng
Fan, Guoxin
Ma, Junhua
Hu, Wei
Cai, Xiaobing
Biocompatibility of artificial bone based on vancomycin loaded mesoporous silica nanoparticles and calcium sulfate composites
title Biocompatibility of artificial bone based on vancomycin loaded mesoporous silica nanoparticles and calcium sulfate composites
title_full Biocompatibility of artificial bone based on vancomycin loaded mesoporous silica nanoparticles and calcium sulfate composites
title_fullStr Biocompatibility of artificial bone based on vancomycin loaded mesoporous silica nanoparticles and calcium sulfate composites
title_full_unstemmed Biocompatibility of artificial bone based on vancomycin loaded mesoporous silica nanoparticles and calcium sulfate composites
title_short Biocompatibility of artificial bone based on vancomycin loaded mesoporous silica nanoparticles and calcium sulfate composites
title_sort biocompatibility of artificial bone based on vancomycin loaded mesoporous silica nanoparticles and calcium sulfate composites
topic Engineering and Nano-engineering Approaches for Medical Devices
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756035/
https://www.ncbi.nlm.nih.gov/pubmed/26883948
http://dx.doi.org/10.1007/s10856-016-5671-z
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