Antibacterial efficacy of core-shell nanostructures encapsulating gentamicin against an in vivo intracellular Salmonella model
dc.contributor.author | Ranjan, Ashish | en |
dc.contributor.author | Pothayee, Nikorn | en |
dc.contributor.author | Seleem, Mohamed N. | en |
dc.contributor.author | Tyler, Ronald D. | en |
dc.contributor.author | Brenseke, Bonnie | en |
dc.contributor.author | Sriranganathan, Nammalwar | en |
dc.contributor.author | Riffle, Judy S. | en |
dc.contributor.author | Kasimanickam, Ramanathan K. | en |
dc.date.accessioned | 2020-09-21T16:18:24Z | en |
dc.date.available | 2020-09-21T16:18:24Z | en |
dc.date.issued | 2009-01-01 | en |
dc.date.updated | 2020-09-21T16:18:21Z | en |
dc.description.abstract | Pluronic based core-shell nanostructures encapsulating gentamicin were designed in this study. Block copolymers of (PAA(+/-)Na-b-(PEO-b-PPO-b-PEO)-b-PAA(+/-)Na) were blended with PAA(-) Na(+) and complexed with the polycationic antibiotic gentamicin to form nanostructures. Synthesized nanostructures had a hydrodynamic diameter of 210 nm, zeta potentials of -0.7 (+/-0.2), and incorporated approximately 20% by weight of gentamicin. Nanostructures upon co-incubation with J774A.1 macrophage cells showed no adverse toxicity in vitro. Nanostructures administered in vivo either at multiple dosage of 5 microg g(-1) or single dosage of 15 microg g(-1) in AJ-646 mice infected with Salmonella resulted in significant reduction of viable bacteria in the liver and spleen. Histopathological evaluation for concentration-dependent toxicity at a dosage of 15 microg g(-1) revealed mineralized deposits in 50% kidney tissues of free gentamicin-treated mice which in contrast was absent in nanostructure-treated mice. Thus, encapsulation of gentamicin in nanostructures may reduce toxicity and improve in vivo bacterial clearance. | en |
dc.description.version | Published version | en |
dc.format.extent | Pages 289-297 | en |
dc.format.extent | 9 page(s) | en |
dc.format.medium | Print-Electronic | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.doi | https://doi.org/10.2147/ijn.s7137 | en |
dc.identifier.eissn | 1178-2013 | en |
dc.identifier.issn | 1178-2013 | en |
dc.identifier.orcid | Sriranganathan, Nammalwar [0000-0002-9232-2888] | en |
dc.identifier.orcid | Seleem, Mohamed [0000-0003-0939-0458] | en |
dc.identifier.pmid | 20054433 (pubmed) | en |
dc.identifier.uri | http://hdl.handle.net/10919/100047 | en |
dc.identifier.volume | 4 | en |
dc.language.iso | en | en |
dc.publisher | Dove Medical Press | en |
dc.rights | Creative Commons Attribution-NonCommercial 4.0 International | en |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ | en |
dc.subject | Life Sciences & Biomedicine | en |
dc.subject | Nanoscience & Nanotechnology | en |
dc.subject | Pharmacology & Pharmacy | en |
dc.subject | Science & Technology - Other Topics | en |
dc.subject | gentamicin | en |
dc.subject | core-shell nanostructures | en |
dc.subject | Salmonella | en |
dc.subject | PLURONIC(R) BLOCK-COPOLYMERS | en |
dc.subject | INDUCED NEPHROTOXICITY | en |
dc.subject | DRUG-DELIVERY | en |
dc.subject | LIPOSOMES | en |
dc.subject | NANOPARTICLES | en |
dc.subject | NANOCARRIERS | en |
dc.subject | RELEASE | en |
dc.subject | 0601 Biochemistry and Cell Biology | en |
dc.subject | 1007 Nanotechnology | en |
dc.subject | 1115 Pharmacology and Pharmaceutical Sciences | en |
dc.subject | Nanoscience & Nanotechnology | en |
dc.subject.mesh | Animals | en |
dc.subject.mesh | Mice | en |
dc.subject.mesh | Salmonella | en |
dc.subject.mesh | Salmonella Infections | en |
dc.subject.mesh | Gentamicins | en |
dc.subject.mesh | Coated Materials, Biocompatible | en |
dc.subject.mesh | Drug Carriers | en |
dc.subject.mesh | Anti-Bacterial Agents | en |
dc.subject.mesh | Crystallization | en |
dc.subject.mesh | Materials Testing | en |
dc.subject.mesh | Drug Compounding | en |
dc.subject.mesh | Diffusion | en |
dc.subject.mesh | Dose-Response Relationship, Drug | en |
dc.subject.mesh | Particle Size | en |
dc.subject.mesh | Surface Properties | en |
dc.subject.mesh | Nanostructures | en |
dc.subject.mesh | Nanomedicine | en |
dc.title | Antibacterial efficacy of core-shell nanostructures encapsulating gentamicin against an in vivo intracellular Salmonella model | en |
dc.title.serial | International Journal of Nanomedicine | en |
dc.type | Article - Refereed | en |
dc.type.dcmitype | Text | en |
dc.type.other | Article | en |
dc.type.other | Journal | en |
pubs.organisational-group | /Virginia Tech/Veterinary Medicine | en |
pubs.organisational-group | /Virginia Tech/Faculty of Health Sciences | en |
pubs.organisational-group | /Virginia Tech/All T&R Faculty | en |
pubs.organisational-group | /Virginia Tech/Veterinary Medicine/Biomedical Sciences and Pathobiology | en |
pubs.organisational-group | /Virginia Tech/Veterinary Medicine/CVM T&R Faculty | en |
pubs.organisational-group | /Virginia Tech/University Research Institutes/Fralin Life Sciences/Durelle Scott | en |
pubs.organisational-group | /Virginia Tech | en |
pubs.organisational-group | /Virginia Tech/University Research Institutes/Fralin Life Sciences | en |
pubs.organisational-group | /Virginia Tech/University Research Institutes | en |
pubs.organisational-group | /Virginia Tech/Science | en |
pubs.organisational-group | /Virginia Tech/Science/Chemistry | en |
pubs.organisational-group | /Virginia Tech/Science/COS T&R Faculty | en |
pubs.organisational-group | /Virginia Tech/Veterinary Medicine/Large Animal Clinical Sciences | en |
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