Cargando…

Development of bone seeker–functionalised microspheres as a targeted local antibiotic delivery system for bone infections

OBJECTIVE: Bone infections are challenging to treat because of limited capability of systemic antibiotics to accumulate at the bone site. To enhance therapeutic action, systemic treatments are commonly combined with local antibiotic-loaded materials. Nevertheless, available drug carriers have undesi...

Descripción completa

Detalles Bibliográficos
Autores principales: Rotman, Stijn G., Thompson, Keith, Grijpma, Dirk W., Richards, Robert G., Moriarty, Thomas F., Eglin, David, Guillaume, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Speaking Orthopaedic Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7152806/
https://www.ncbi.nlm.nih.gov/pubmed/32309139
http://dx.doi.org/10.1016/j.jot.2019.07.006
_version_ 1783521551816065024
author Rotman, Stijn G.
Thompson, Keith
Grijpma, Dirk W.
Richards, Robert G.
Moriarty, Thomas F.
Eglin, David
Guillaume, Olivier
author_facet Rotman, Stijn G.
Thompson, Keith
Grijpma, Dirk W.
Richards, Robert G.
Moriarty, Thomas F.
Eglin, David
Guillaume, Olivier
author_sort Rotman, Stijn G.
collection PubMed
description OBJECTIVE: Bone infections are challenging to treat because of limited capability of systemic antibiotics to accumulate at the bone site. To enhance therapeutic action, systemic treatments are commonly combined with local antibiotic-loaded materials. Nevertheless, available drug carriers have undesirable properties, including inappropriate antibiotic release profiles and nonbiodegradability. To alleviate such limitations, we aim to develop a drug delivery system (DDS) for local administration that can interact strongly with bone mineral, releasing antibiotics at the infected bone site. METHODS: Biodegradable polyesters (poly (ε-caprolactone) or poly (D,l-lactic acid)) were selected to fabricate antibiotic-loaded microspheres by oil in water emulsion. Antibiotic release and antimicrobial effects on Staphylococcus aureus were assessed by zone of inhibition measurements. Microsphere bone affinity was increased by functionalising the bisphosphonate drug alendronate to the microsphere surface using carbodiimide chemistry. Effect of bone targeting microspheres on bone homeostasis was tested by looking at the resorption potential of osteoclasts exposed to the developed microspheres. RESULTS: In vitro, the antibiotic release profile from the microspheres was shown to be dependent on the polymer used and the microsphere preparation method. Mineral binding assays revealed that microsphere surface modification with alendronate significantly enhanced interaction with bone-like materials. Additionally, alendronate functionalised microspheres did not differentially affect osteoclast mineral resorption in vitro, compared with nonfunctionalised microspheres. CONCLUSION: We report the development and characterisation of a DDS which can release antibiotics in a sustained manner. Surface-grafted alendronate groups enhanced bone affinity of the microsphere construct, resulting in a bone targeting DDS. THE TRANSLATIONAL POTENTIAL OF THIS ARTICLE: The DDS presented can be loaded with hydrophobic antibiotics, representing a potential, versatile and biodegradable candidate to locally treat bone infection.
format Online
Article
Text
id pubmed-7152806
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Chinese Speaking Orthopaedic Society
record_format MEDLINE/PubMed
spelling pubmed-71528062020-04-17 Development of bone seeker–functionalised microspheres as a targeted local antibiotic delivery system for bone infections Rotman, Stijn G. Thompson, Keith Grijpma, Dirk W. Richards, Robert G. Moriarty, Thomas F. Eglin, David Guillaume, Olivier J Orthop Translat Original Article OBJECTIVE: Bone infections are challenging to treat because of limited capability of systemic antibiotics to accumulate at the bone site. To enhance therapeutic action, systemic treatments are commonly combined with local antibiotic-loaded materials. Nevertheless, available drug carriers have undesirable properties, including inappropriate antibiotic release profiles and nonbiodegradability. To alleviate such limitations, we aim to develop a drug delivery system (DDS) for local administration that can interact strongly with bone mineral, releasing antibiotics at the infected bone site. METHODS: Biodegradable polyesters (poly (ε-caprolactone) or poly (D,l-lactic acid)) were selected to fabricate antibiotic-loaded microspheres by oil in water emulsion. Antibiotic release and antimicrobial effects on Staphylococcus aureus were assessed by zone of inhibition measurements. Microsphere bone affinity was increased by functionalising the bisphosphonate drug alendronate to the microsphere surface using carbodiimide chemistry. Effect of bone targeting microspheres on bone homeostasis was tested by looking at the resorption potential of osteoclasts exposed to the developed microspheres. RESULTS: In vitro, the antibiotic release profile from the microspheres was shown to be dependent on the polymer used and the microsphere preparation method. Mineral binding assays revealed that microsphere surface modification with alendronate significantly enhanced interaction with bone-like materials. Additionally, alendronate functionalised microspheres did not differentially affect osteoclast mineral resorption in vitro, compared with nonfunctionalised microspheres. CONCLUSION: We report the development and characterisation of a DDS which can release antibiotics in a sustained manner. Surface-grafted alendronate groups enhanced bone affinity of the microsphere construct, resulting in a bone targeting DDS. THE TRANSLATIONAL POTENTIAL OF THIS ARTICLE: The DDS presented can be loaded with hydrophobic antibiotics, representing a potential, versatile and biodegradable candidate to locally treat bone infection. Chinese Speaking Orthopaedic Society 2019-08-30 /pmc/articles/PMC7152806/ /pubmed/32309139 http://dx.doi.org/10.1016/j.jot.2019.07.006 Text en © 2019 The Authors http://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 Original Article
Rotman, Stijn G.
Thompson, Keith
Grijpma, Dirk W.
Richards, Robert G.
Moriarty, Thomas F.
Eglin, David
Guillaume, Olivier
Development of bone seeker–functionalised microspheres as a targeted local antibiotic delivery system for bone infections
title Development of bone seeker–functionalised microspheres as a targeted local antibiotic delivery system for bone infections
title_full Development of bone seeker–functionalised microspheres as a targeted local antibiotic delivery system for bone infections
title_fullStr Development of bone seeker–functionalised microspheres as a targeted local antibiotic delivery system for bone infections
title_full_unstemmed Development of bone seeker–functionalised microspheres as a targeted local antibiotic delivery system for bone infections
title_short Development of bone seeker–functionalised microspheres as a targeted local antibiotic delivery system for bone infections
title_sort development of bone seeker–functionalised microspheres as a targeted local antibiotic delivery system for bone infections
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7152806/
https://www.ncbi.nlm.nih.gov/pubmed/32309139
http://dx.doi.org/10.1016/j.jot.2019.07.006
work_keys_str_mv AT rotmanstijng developmentofboneseekerfunctionalisedmicrospheresasatargetedlocalantibioticdeliverysystemforboneinfections
AT thompsonkeith developmentofboneseekerfunctionalisedmicrospheresasatargetedlocalantibioticdeliverysystemforboneinfections
AT grijpmadirkw developmentofboneseekerfunctionalisedmicrospheresasatargetedlocalantibioticdeliverysystemforboneinfections
AT richardsrobertg developmentofboneseekerfunctionalisedmicrospheresasatargetedlocalantibioticdeliverysystemforboneinfections
AT moriartythomasf developmentofboneseekerfunctionalisedmicrospheresasatargetedlocalantibioticdeliverysystemforboneinfections
AT eglindavid developmentofboneseekerfunctionalisedmicrospheresasatargetedlocalantibioticdeliverysystemforboneinfections
AT guillaumeolivier developmentofboneseekerfunctionalisedmicrospheresasatargetedlocalantibioticdeliverysystemforboneinfections