Cargando…
Bone infection site targeting nanoparticle-antibiotics delivery vehicle to enhance treatment efficacy of orthopedic implant related infection
Orthopedic implants account for 99% of orthopedic surgeries, however, orthopedic implant-related infection is one of the most serious complications owing to the potential for limb-threatening sequelae and mortality. Current antibiotic treatments still lack the capacity to target bone infection sites...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958424/ https://www.ncbi.nlm.nih.gov/pubmed/35386313 http://dx.doi.org/10.1016/j.bioactmat.2022.02.003 |
_version_ | 1784676939906154496 |
---|---|
author | Nie, Bin'en Huo, Shicheng Qu, Xinhua Guo, Jingjing Liu, Xi Hong, Qimin Wang, You Yang, Jianping Yue, Bing |
author_facet | Nie, Bin'en Huo, Shicheng Qu, Xinhua Guo, Jingjing Liu, Xi Hong, Qimin Wang, You Yang, Jianping Yue, Bing |
author_sort | Nie, Bin'en |
collection | PubMed |
description | Orthopedic implants account for 99% of orthopedic surgeries, however, orthopedic implant-related infection is one of the most serious complications owing to the potential for limb-threatening sequelae and mortality. Current antibiotic treatments still lack the capacity to target bone infection sites, thereby resulting in unsatisfactory therapeutic effects. Here, the bone infection site targeting efficacy of D6 and UBI(29-41) peptides was investigated, and bone-and-bacteria dual-targeted nanoparticles (NPs) with D6 and UBI(29-41) peptides were first fabricated to target bone infection site and control the release of vancomycin in bone infection site. The results of this study demonstrated that the bone-and-bacteria dual-targeted mesoporous silica NPs exhibit excellent bone and bacteria targeting efficacy, excellent biocompatibility and effective antibacterial properties in vitro. Furthermore, in a rat model of orthopedic implant-related infection with methicillin-resistant Staphylococcus aureus, the growth of bacteria was evidently inhibited without cytotoxicity, thus realizing the early treatment of implant-related infection. Hence, the bone-and-bacteria dual-targeted molecule-modified NPs may target bacteria-infected bone sites and act as ideal candidates for the therapy of orthopedic implant-related infections. |
format | Online Article Text |
id | pubmed-8958424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | KeAi Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-89584242022-04-05 Bone infection site targeting nanoparticle-antibiotics delivery vehicle to enhance treatment efficacy of orthopedic implant related infection Nie, Bin'en Huo, Shicheng Qu, Xinhua Guo, Jingjing Liu, Xi Hong, Qimin Wang, You Yang, Jianping Yue, Bing Bioact Mater Article Orthopedic implants account for 99% of orthopedic surgeries, however, orthopedic implant-related infection is one of the most serious complications owing to the potential for limb-threatening sequelae and mortality. Current antibiotic treatments still lack the capacity to target bone infection sites, thereby resulting in unsatisfactory therapeutic effects. Here, the bone infection site targeting efficacy of D6 and UBI(29-41) peptides was investigated, and bone-and-bacteria dual-targeted nanoparticles (NPs) with D6 and UBI(29-41) peptides were first fabricated to target bone infection site and control the release of vancomycin in bone infection site. The results of this study demonstrated that the bone-and-bacteria dual-targeted mesoporous silica NPs exhibit excellent bone and bacteria targeting efficacy, excellent biocompatibility and effective antibacterial properties in vitro. Furthermore, in a rat model of orthopedic implant-related infection with methicillin-resistant Staphylococcus aureus, the growth of bacteria was evidently inhibited without cytotoxicity, thus realizing the early treatment of implant-related infection. Hence, the bone-and-bacteria dual-targeted molecule-modified NPs may target bacteria-infected bone sites and act as ideal candidates for the therapy of orthopedic implant-related infections. KeAi Publishing 2022-02-12 /pmc/articles/PMC8958424/ /pubmed/35386313 http://dx.doi.org/10.1016/j.bioactmat.2022.02.003 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Nie, Bin'en Huo, Shicheng Qu, Xinhua Guo, Jingjing Liu, Xi Hong, Qimin Wang, You Yang, Jianping Yue, Bing Bone infection site targeting nanoparticle-antibiotics delivery vehicle to enhance treatment efficacy of orthopedic implant related infection |
title | Bone infection site targeting nanoparticle-antibiotics delivery vehicle to enhance treatment efficacy of orthopedic implant related infection |
title_full | Bone infection site targeting nanoparticle-antibiotics delivery vehicle to enhance treatment efficacy of orthopedic implant related infection |
title_fullStr | Bone infection site targeting nanoparticle-antibiotics delivery vehicle to enhance treatment efficacy of orthopedic implant related infection |
title_full_unstemmed | Bone infection site targeting nanoparticle-antibiotics delivery vehicle to enhance treatment efficacy of orthopedic implant related infection |
title_short | Bone infection site targeting nanoparticle-antibiotics delivery vehicle to enhance treatment efficacy of orthopedic implant related infection |
title_sort | bone infection site targeting nanoparticle-antibiotics delivery vehicle to enhance treatment efficacy of orthopedic implant related infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958424/ https://www.ncbi.nlm.nih.gov/pubmed/35386313 http://dx.doi.org/10.1016/j.bioactmat.2022.02.003 |
work_keys_str_mv | AT niebinen boneinfectionsitetargetingnanoparticleantibioticsdeliveryvehicletoenhancetreatmentefficacyoforthopedicimplantrelatedinfection AT huoshicheng boneinfectionsitetargetingnanoparticleantibioticsdeliveryvehicletoenhancetreatmentefficacyoforthopedicimplantrelatedinfection AT quxinhua boneinfectionsitetargetingnanoparticleantibioticsdeliveryvehicletoenhancetreatmentefficacyoforthopedicimplantrelatedinfection AT guojingjing boneinfectionsitetargetingnanoparticleantibioticsdeliveryvehicletoenhancetreatmentefficacyoforthopedicimplantrelatedinfection AT liuxi boneinfectionsitetargetingnanoparticleantibioticsdeliveryvehicletoenhancetreatmentefficacyoforthopedicimplantrelatedinfection AT hongqimin boneinfectionsitetargetingnanoparticleantibioticsdeliveryvehicletoenhancetreatmentefficacyoforthopedicimplantrelatedinfection AT wangyou boneinfectionsitetargetingnanoparticleantibioticsdeliveryvehicletoenhancetreatmentefficacyoforthopedicimplantrelatedinfection AT yangjianping boneinfectionsitetargetingnanoparticleantibioticsdeliveryvehicletoenhancetreatmentefficacyoforthopedicimplantrelatedinfection AT yuebing boneinfectionsitetargetingnanoparticleantibioticsdeliveryvehicletoenhancetreatmentefficacyoforthopedicimplantrelatedinfection |