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Nanoparticles in an antibiotic-loaded nanomesh for drug delivery

Antibiotic loaded nanomeshes were fabricated by electrospinning polycaprolactone, a biocompatible polymer, with 12.5% w/w Colistin, 1.4% w/w Vancomycin and either cationic or anionic gold nanoparticles in varying combinations. The resulting nanomeshes had different antibiotic release profiles, with...

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Autores principales: Fuller, Melanie A., Carey, Ashley, Whiley, Harriet, Kurimoto, Rio, Ebara, Mitsuhiro, Köper, Ingo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072143/
https://www.ncbi.nlm.nih.gov/pubmed/35530227
http://dx.doi.org/10.1039/c9ra06398f
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author Fuller, Melanie A.
Carey, Ashley
Whiley, Harriet
Kurimoto, Rio
Ebara, Mitsuhiro
Köper, Ingo
author_facet Fuller, Melanie A.
Carey, Ashley
Whiley, Harriet
Kurimoto, Rio
Ebara, Mitsuhiro
Köper, Ingo
author_sort Fuller, Melanie A.
collection PubMed
description Antibiotic loaded nanomeshes were fabricated by electrospinning polycaprolactone, a biocompatible polymer, with 12.5% w/w Colistin, 1.4% w/w Vancomycin and either cationic or anionic gold nanoparticles in varying combinations. The resulting nanomeshes had different antibiotic release profiles, with citrate capped gold nanoparticles combined with Colistin having the highest sustained release over 14 days for a 4 mg, 1.5 cm(2) nanomesh. The electrospinning parameters were optimised to ensure the spinning of a homogenous mesh and the addition of antibiotics was confirmed through (1)H NMR and ATR-FTIR. This research, as a proof of concept, suggests an opportunity for fabricating nanomeshes which contain gold nanoparticles as a drug release mechanism for antibiotics.
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spelling pubmed-90721432022-05-06 Nanoparticles in an antibiotic-loaded nanomesh for drug delivery Fuller, Melanie A. Carey, Ashley Whiley, Harriet Kurimoto, Rio Ebara, Mitsuhiro Köper, Ingo RSC Adv Chemistry Antibiotic loaded nanomeshes were fabricated by electrospinning polycaprolactone, a biocompatible polymer, with 12.5% w/w Colistin, 1.4% w/w Vancomycin and either cationic or anionic gold nanoparticles in varying combinations. The resulting nanomeshes had different antibiotic release profiles, with citrate capped gold nanoparticles combined with Colistin having the highest sustained release over 14 days for a 4 mg, 1.5 cm(2) nanomesh. The electrospinning parameters were optimised to ensure the spinning of a homogenous mesh and the addition of antibiotics was confirmed through (1)H NMR and ATR-FTIR. This research, as a proof of concept, suggests an opportunity for fabricating nanomeshes which contain gold nanoparticles as a drug release mechanism for antibiotics. The Royal Society of Chemistry 2019-09-24 /pmc/articles/PMC9072143/ /pubmed/35530227 http://dx.doi.org/10.1039/c9ra06398f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Fuller, Melanie A.
Carey, Ashley
Whiley, Harriet
Kurimoto, Rio
Ebara, Mitsuhiro
Köper, Ingo
Nanoparticles in an antibiotic-loaded nanomesh for drug delivery
title Nanoparticles in an antibiotic-loaded nanomesh for drug delivery
title_full Nanoparticles in an antibiotic-loaded nanomesh for drug delivery
title_fullStr Nanoparticles in an antibiotic-loaded nanomesh for drug delivery
title_full_unstemmed Nanoparticles in an antibiotic-loaded nanomesh for drug delivery
title_short Nanoparticles in an antibiotic-loaded nanomesh for drug delivery
title_sort nanoparticles in an antibiotic-loaded nanomesh for drug delivery
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072143/
https://www.ncbi.nlm.nih.gov/pubmed/35530227
http://dx.doi.org/10.1039/c9ra06398f
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