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An Antibiotic-Releasing Bone Void Filling (ABVF) Putty for the Treatment of Osteomyelitis

The number of total joint replacements (TJR) is on the rise with a corresponding increase in the number of infected TJR, which necessitates revision surgeries. Current treatments with either non-biodegradable, antibiotic-releasing polymethylmethacrylate (PMMA) based bone cement, or systemic antibiot...

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Autores principales: Hasan, Raquib, Wohlers, Abbey, Shreffler, Jacob, Mulinti, Pranothi, Ostlie, Hunter, Schaper, Codi, Brooks, Benjamin, Brooks, Amanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698155/
https://www.ncbi.nlm.nih.gov/pubmed/33187199
http://dx.doi.org/10.3390/ma13225080
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author Hasan, Raquib
Wohlers, Abbey
Shreffler, Jacob
Mulinti, Pranothi
Ostlie, Hunter
Schaper, Codi
Brooks, Benjamin
Brooks, Amanda
author_facet Hasan, Raquib
Wohlers, Abbey
Shreffler, Jacob
Mulinti, Pranothi
Ostlie, Hunter
Schaper, Codi
Brooks, Benjamin
Brooks, Amanda
author_sort Hasan, Raquib
collection PubMed
description The number of total joint replacements (TJR) is on the rise with a corresponding increase in the number of infected TJR, which necessitates revision surgeries. Current treatments with either non-biodegradable, antibiotic-releasing polymethylmethacrylate (PMMA) based bone cement, or systemic antibiotic after surgical debridement do not provide effective treatment due to fluctuating antibiotic levels at the site of infection. Here, we report a biodegradable, easy-to-use “press-fitting” antibiotic-releasing bone void filling (ABVF) putty that not only provides efficient antibiotic release kinetics at the site of infection but also allows efficient osseointegration. The ABVF formulation was prepared using poly (d,l-lactide-co-glycolide) (PLGA), polyethylene glycol (PEG), and polycaprolactone (PCL) as the polymer matrix, antibiotic vancomycin, and osseointegrating synthetic bone PRO OSTEON for bone-growth support. ABVF was homogenous, had a porous structure, was moldable, and showed putty-like mechanical properties. The ABVF putty released vancomycin for 6 weeks at therapeutic level. Furthermore, the released vancomycin showed in vitro antibacterial activity against Staphylococcus aureus for 6 weeks. Vancomycin was not toxic to osteoblasts. Finally, ABVF was biodegradable in vivo and showed an effective infection control with the treatment group showing significantly higher bone growth (p < 0.001) compared to the control group. The potential of infection treatment and osseointegration makes the ABVF putty a promising treatment option for osteomyelitis after TJR.
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spelling pubmed-76981552020-11-29 An Antibiotic-Releasing Bone Void Filling (ABVF) Putty for the Treatment of Osteomyelitis Hasan, Raquib Wohlers, Abbey Shreffler, Jacob Mulinti, Pranothi Ostlie, Hunter Schaper, Codi Brooks, Benjamin Brooks, Amanda Materials (Basel) Article The number of total joint replacements (TJR) is on the rise with a corresponding increase in the number of infected TJR, which necessitates revision surgeries. Current treatments with either non-biodegradable, antibiotic-releasing polymethylmethacrylate (PMMA) based bone cement, or systemic antibiotic after surgical debridement do not provide effective treatment due to fluctuating antibiotic levels at the site of infection. Here, we report a biodegradable, easy-to-use “press-fitting” antibiotic-releasing bone void filling (ABVF) putty that not only provides efficient antibiotic release kinetics at the site of infection but also allows efficient osseointegration. The ABVF formulation was prepared using poly (d,l-lactide-co-glycolide) (PLGA), polyethylene glycol (PEG), and polycaprolactone (PCL) as the polymer matrix, antibiotic vancomycin, and osseointegrating synthetic bone PRO OSTEON for bone-growth support. ABVF was homogenous, had a porous structure, was moldable, and showed putty-like mechanical properties. The ABVF putty released vancomycin for 6 weeks at therapeutic level. Furthermore, the released vancomycin showed in vitro antibacterial activity against Staphylococcus aureus for 6 weeks. Vancomycin was not toxic to osteoblasts. Finally, ABVF was biodegradable in vivo and showed an effective infection control with the treatment group showing significantly higher bone growth (p < 0.001) compared to the control group. The potential of infection treatment and osseointegration makes the ABVF putty a promising treatment option for osteomyelitis after TJR. MDPI 2020-11-11 /pmc/articles/PMC7698155/ /pubmed/33187199 http://dx.doi.org/10.3390/ma13225080 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hasan, Raquib
Wohlers, Abbey
Shreffler, Jacob
Mulinti, Pranothi
Ostlie, Hunter
Schaper, Codi
Brooks, Benjamin
Brooks, Amanda
An Antibiotic-Releasing Bone Void Filling (ABVF) Putty for the Treatment of Osteomyelitis
title An Antibiotic-Releasing Bone Void Filling (ABVF) Putty for the Treatment of Osteomyelitis
title_full An Antibiotic-Releasing Bone Void Filling (ABVF) Putty for the Treatment of Osteomyelitis
title_fullStr An Antibiotic-Releasing Bone Void Filling (ABVF) Putty for the Treatment of Osteomyelitis
title_full_unstemmed An Antibiotic-Releasing Bone Void Filling (ABVF) Putty for the Treatment of Osteomyelitis
title_short An Antibiotic-Releasing Bone Void Filling (ABVF) Putty for the Treatment of Osteomyelitis
title_sort antibiotic-releasing bone void filling (abvf) putty for the treatment of osteomyelitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698155/
https://www.ncbi.nlm.nih.gov/pubmed/33187199
http://dx.doi.org/10.3390/ma13225080
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