Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect
Abstract We previously reported the development of an osteogenic bone filler scaffold consisting of degradable polyurethane, hydroxyapatite, and decellularized bovine bone particles. The current study was aimed at evaluating the use of this scaffold as a means of local antibiotic delivery to prevent...
Main Authors: | , , , , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Publishing Group
2021-05-01
|
Series: | Scientific Reports |
Online Access: | https://doi.org/10.1038/s41598-021-89830-z |
id |
doaj-499612545c514ba09349c6d9e0ce2907 |
---|---|
record_format |
Article |
spelling |
doaj-499612545c514ba09349c6d9e0ce29072021-05-16T11:25:19ZengNature Publishing GroupScientific Reports2045-23222021-05-0111111010.1038/s41598-021-89830-zEvaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defectKaren E. Beenken0Mara J. Campbell1Aura M. Ramirez2Karrar Alghazali3Christopher M. Walker4Bailey Jackson5Christopher Griffin6William King7Shawn E. Bourdo8Rebecca Rifkin9Silke Hecht10Daniel G. Meeker11David E. Anderson12Alexandru S. Biris13Mark S. Smeltzer14Department of Microbiology and Immunology, University of Arkansas for Medical SciencesDepartment of Microbiology and Immunology, University of Arkansas for Medical SciencesDepartment of Microbiology and Immunology, University of Arkansas for Medical SciencesCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little RockDepartment of Microbiology and Immunology, University of Arkansas for Medical SciencesCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little RockCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little RockCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little RockCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little RockDepartment of Large Animal Clinical Sciences, University of Tennessee College of Veterinary MedicineDepartment of Small Animal Clinical Sciences, University of Tennessee College of Veterinary MedicineDepartment of Microbiology and Immunology, University of Arkansas for Medical SciencesDepartment of Large Animal Clinical Sciences, University of Tennessee College of Veterinary MedicineCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little RockDepartment of Microbiology and Immunology, University of Arkansas for Medical SciencesAbstract We previously reported the development of an osteogenic bone filler scaffold consisting of degradable polyurethane, hydroxyapatite, and decellularized bovine bone particles. The current study was aimed at evaluating the use of this scaffold as a means of local antibiotic delivery to prevent infection in a bone defect contaminated with Staphylococcus aureus. We evaluated two scaffold formulations with the same component ratios but differing overall porosity and surface area. Studies with vancomycin, daptomycin, and gentamicin confirmed that antibiotic uptake was concentration dependent and that increased porosity correlated with increased uptake and prolonged antibiotic release. We also demonstrate that vancomycin can be passively loaded into either formulation in sufficient concentration to prevent infection in a rabbit model of a contaminated segmental bone defect. Moreover, even in those few cases in which complete eradication was not achieved, the number of viable bacteria in the bone was significantly reduced by treatment and there was no radiographic evidence of osteomyelitis. Radiographs and microcomputed tomography (µCT) analysis from the in vivo studies also suggested that the addition of vancomycin did not have any significant effect on the scaffold itself. These results demonstrate the potential utility of our bone regeneration scaffold for local antibiotic delivery to prevent infection in contaminated bone defects.https://doi.org/10.1038/s41598-021-89830-z |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Karen E. Beenken Mara J. Campbell Aura M. Ramirez Karrar Alghazali Christopher M. Walker Bailey Jackson Christopher Griffin William King Shawn E. Bourdo Rebecca Rifkin Silke Hecht Daniel G. Meeker David E. Anderson Alexandru S. Biris Mark S. Smeltzer |
spellingShingle |
Karen E. Beenken Mara J. Campbell Aura M. Ramirez Karrar Alghazali Christopher M. Walker Bailey Jackson Christopher Griffin William King Shawn E. Bourdo Rebecca Rifkin Silke Hecht Daniel G. Meeker David E. Anderson Alexandru S. Biris Mark S. Smeltzer Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect Scientific Reports |
author_facet |
Karen E. Beenken Mara J. Campbell Aura M. Ramirez Karrar Alghazali Christopher M. Walker Bailey Jackson Christopher Griffin William King Shawn E. Bourdo Rebecca Rifkin Silke Hecht Daniel G. Meeker David E. Anderson Alexandru S. Biris Mark S. Smeltzer |
author_sort |
Karen E. Beenken |
title |
Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect |
title_short |
Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect |
title_full |
Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect |
title_fullStr |
Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect |
title_full_unstemmed |
Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect |
title_sort |
evaluation of a bone filler scaffold for local antibiotic delivery to prevent staphylococcus aureus infection in a contaminated bone defect |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-05-01 |
description |
Abstract We previously reported the development of an osteogenic bone filler scaffold consisting of degradable polyurethane, hydroxyapatite, and decellularized bovine bone particles. The current study was aimed at evaluating the use of this scaffold as a means of local antibiotic delivery to prevent infection in a bone defect contaminated with Staphylococcus aureus. We evaluated two scaffold formulations with the same component ratios but differing overall porosity and surface area. Studies with vancomycin, daptomycin, and gentamicin confirmed that antibiotic uptake was concentration dependent and that increased porosity correlated with increased uptake and prolonged antibiotic release. We also demonstrate that vancomycin can be passively loaded into either formulation in sufficient concentration to prevent infection in a rabbit model of a contaminated segmental bone defect. Moreover, even in those few cases in which complete eradication was not achieved, the number of viable bacteria in the bone was significantly reduced by treatment and there was no radiographic evidence of osteomyelitis. Radiographs and microcomputed tomography (µCT) analysis from the in vivo studies also suggested that the addition of vancomycin did not have any significant effect on the scaffold itself. These results demonstrate the potential utility of our bone regeneration scaffold for local antibiotic delivery to prevent infection in contaminated bone defects. |
url |
https://doi.org/10.1038/s41598-021-89830-z |
work_keys_str_mv |
AT karenebeenken evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT marajcampbell evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT auramramirez evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT karraralghazali evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT christophermwalker evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT baileyjackson evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT christophergriffin evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT williamking evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT shawnebourdo evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT rebeccarifkin evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT silkehecht evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT danielgmeeker evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT davideanderson evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT alexandrusbiris evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect AT markssmeltzer evaluationofabonefillerscaffoldforlocalantibioticdeliverytopreventstaphylococcusaureusinfectioninacontaminatedbonedefect |
_version_ |
1721439468786810880 |