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Controlled gentamicin release from multi-layered electrospun nanofibrous structures of various thicknesses
J. Sirc, S. Kubinova, R. Hobzova, D. Stranska, P. Kozlik, Z. Bosakova, D. Marekova, V. Holan, E. Sykova, J. Michalek,
Language English Country New Zealand
Document type Journal Article, Research Support, Non-U.S. Gov't
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PubMed
23071393
DOI
10.2147/ijn.s35781
Knihovny.cz E-resources
- MeSH
- Anti-Bacterial Agents administration & dosage chemistry MeSH
- Diffusion MeSH
- Electrochemistry methods MeSH
- Gentamicins administration & dosage MeSH
- Gram-Positive Bacteria drug effects physiology MeSH
- Delayed-Action Preparations administration & dosage chemistry MeSH
- Nanocapsules chemistry ultrastructure MeSH
- Rotation MeSH
- Materials Testing MeSH
- Particle Size MeSH
- Cell Survival drug effects MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Polyvinyl alcohol nanofibers incorporating the wide spectrum antibiotic gentamicin were prepared by Nanospider™ needleless technology. A polyvinyl alcohol layer, serving as a drug reservoir, was covered from both sides by polyurethane layers of various thicknesses. The multilayered structure of the nanofibers was observed using scanning electron microscopy, the porosity was characterized by mercury porosimetry, and nitrogen adsorption/desorption measurements were used to determine specific surface areas. The stability of the gentamicin released from the electrospun layers was proved by high-performance liquid chromatography (HPLC) and inhibition of bacterial growth. Drug release was investigated using in vitro experiments with HPLC/MS quantification, while the antimicrobial efficacy was evaluated on Gram-positive Staphylococcus aureus and Gram-negative Pseudomonas aeruginosa. Both experiments proved that the released gentamicin retained its activity and showed that the retention of the drug in the nanofibers was prolonged with the increasing thickness of the covering layers.
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