Cargando…
Calcium phosphate cement with icariin-loaded gelatin microspheres as a local drug delivery system for bone regeneration
BACKGROUND: Icariin (ICA), a main active ingredient of Herba Epimedium, could promote bone formation, inhibit bone resorption and alleviate inflammatory responses. The aim of this study was to investigate the effect of ICA on the inhibition of bacteria associated with peri-implantitis, and fabricate...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773482/ https://www.ncbi.nlm.nih.gov/pubmed/36550581 http://dx.doi.org/10.1186/s12938-022-01052-0 |
_version_ | 1784855201288552448 |
---|---|
author | Liu, Ning Huang, Shuo Guo, Fang Zhai, Shafei Wang, Danyang Li, Fang Liu, Changkui |
author_facet | Liu, Ning Huang, Shuo Guo, Fang Zhai, Shafei Wang, Danyang Li, Fang Liu, Changkui |
author_sort | Liu, Ning |
collection | PubMed |
description | BACKGROUND: Icariin (ICA), a main active ingredient of Herba Epimedium, could promote bone formation, inhibit bone resorption and alleviate inflammatory responses. The aim of this study was to investigate the effect of ICA on the inhibition of bacteria associated with peri-implantitis, and fabricate a calcium phosphate cement (CPC) with ICA-loaded gelatin microspheres (GMs) as a local drug delivery system efficiently promoting bone formation and alleviating inflammation. RESULTS: In this study, ICA exhibited antibacterial activity against P. gingivalis with a MIC value of 1 × 10(–4) mol/L. When the concentration of ICA was 0.5 mM, the encapsulation efficiency of GMs reached the maximum value of 76.26 ± 3.97%. GMs with ICA revealed a controlled release profile, 0.5 mM ICA exhibited a higher ICA release profile than the other groups during a 21 d monitoring span. The results of SEM and XRD demonstrated successful fabrication of a calcium phosphate cement with ICA-loaded GMs. ICA released from CPC/GMs (ICA) was slower than ICA released from GMs within 10 days. CPC/GMs (ICA) exhibited antibacterial activity against P. gingivalis, but the antibacterial rate of CPC/GMs (ICA) was only 17.15 ± 6.06%. In addition, CPC/GMs (ICA) promoted the proliferation of BMSCs and significantly stimulated the differentiation and maturation of BMSCs. In vivo, H&E and Masson staining experiments demonstrated that CPC/GMs (ICA) exhibited better capacity for bone regeneration than CPC/GMs and CPC, and the expression of TNF-α and IL-1β in the tissue around CPC/GMs (ICA) was significantly lower than CPC/GMs and CPC in IHC staining (P < 0.05). CONCLUSION: In this study, ICA exhibited limited antibacterial activity against bacteria associated with peri-implantitis. A composite material of calcium phosphate cement with ICA-loaded gelatin microspheres was developed, which not only promoting osteoinductivity and bone formation, but also alleviating inflammation, demonstrating its potential as a promising bone substitute material for treatment of peri-implantitis. |
format | Online Article Text |
id | pubmed-9773482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97734822022-12-23 Calcium phosphate cement with icariin-loaded gelatin microspheres as a local drug delivery system for bone regeneration Liu, Ning Huang, Shuo Guo, Fang Zhai, Shafei Wang, Danyang Li, Fang Liu, Changkui Biomed Eng Online Research BACKGROUND: Icariin (ICA), a main active ingredient of Herba Epimedium, could promote bone formation, inhibit bone resorption and alleviate inflammatory responses. The aim of this study was to investigate the effect of ICA on the inhibition of bacteria associated with peri-implantitis, and fabricate a calcium phosphate cement (CPC) with ICA-loaded gelatin microspheres (GMs) as a local drug delivery system efficiently promoting bone formation and alleviating inflammation. RESULTS: In this study, ICA exhibited antibacterial activity against P. gingivalis with a MIC value of 1 × 10(–4) mol/L. When the concentration of ICA was 0.5 mM, the encapsulation efficiency of GMs reached the maximum value of 76.26 ± 3.97%. GMs with ICA revealed a controlled release profile, 0.5 mM ICA exhibited a higher ICA release profile than the other groups during a 21 d monitoring span. The results of SEM and XRD demonstrated successful fabrication of a calcium phosphate cement with ICA-loaded GMs. ICA released from CPC/GMs (ICA) was slower than ICA released from GMs within 10 days. CPC/GMs (ICA) exhibited antibacterial activity against P. gingivalis, but the antibacterial rate of CPC/GMs (ICA) was only 17.15 ± 6.06%. In addition, CPC/GMs (ICA) promoted the proliferation of BMSCs and significantly stimulated the differentiation and maturation of BMSCs. In vivo, H&E and Masson staining experiments demonstrated that CPC/GMs (ICA) exhibited better capacity for bone regeneration than CPC/GMs and CPC, and the expression of TNF-α and IL-1β in the tissue around CPC/GMs (ICA) was significantly lower than CPC/GMs and CPC in IHC staining (P < 0.05). CONCLUSION: In this study, ICA exhibited limited antibacterial activity against bacteria associated with peri-implantitis. A composite material of calcium phosphate cement with ICA-loaded gelatin microspheres was developed, which not only promoting osteoinductivity and bone formation, but also alleviating inflammation, demonstrating its potential as a promising bone substitute material for treatment of peri-implantitis. BioMed Central 2022-12-22 /pmc/articles/PMC9773482/ /pubmed/36550581 http://dx.doi.org/10.1186/s12938-022-01052-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Liu, Ning Huang, Shuo Guo, Fang Zhai, Shafei Wang, Danyang Li, Fang Liu, Changkui Calcium phosphate cement with icariin-loaded gelatin microspheres as a local drug delivery system for bone regeneration |
title | Calcium phosphate cement with icariin-loaded gelatin microspheres as a local drug delivery system for bone regeneration |
title_full | Calcium phosphate cement with icariin-loaded gelatin microspheres as a local drug delivery system for bone regeneration |
title_fullStr | Calcium phosphate cement with icariin-loaded gelatin microspheres as a local drug delivery system for bone regeneration |
title_full_unstemmed | Calcium phosphate cement with icariin-loaded gelatin microspheres as a local drug delivery system for bone regeneration |
title_short | Calcium phosphate cement with icariin-loaded gelatin microspheres as a local drug delivery system for bone regeneration |
title_sort | calcium phosphate cement with icariin-loaded gelatin microspheres as a local drug delivery system for bone regeneration |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773482/ https://www.ncbi.nlm.nih.gov/pubmed/36550581 http://dx.doi.org/10.1186/s12938-022-01052-0 |
work_keys_str_mv | AT liuning calciumphosphatecementwithicariinloadedgelatinmicrospheresasalocaldrugdeliverysystemforboneregeneration AT huangshuo calciumphosphatecementwithicariinloadedgelatinmicrospheresasalocaldrugdeliverysystemforboneregeneration AT guofang calciumphosphatecementwithicariinloadedgelatinmicrospheresasalocaldrugdeliverysystemforboneregeneration AT zhaishafei calciumphosphatecementwithicariinloadedgelatinmicrospheresasalocaldrugdeliverysystemforboneregeneration AT wangdanyang calciumphosphatecementwithicariinloadedgelatinmicrospheresasalocaldrugdeliverysystemforboneregeneration AT lifang calciumphosphatecementwithicariinloadedgelatinmicrospheresasalocaldrugdeliverysystemforboneregeneration AT liuchangkui calciumphosphatecementwithicariinloadedgelatinmicrospheresasalocaldrugdeliverysystemforboneregeneration |