Release and antibacterial activity of allyl isothiocyanate/β-cyclodextrin complex encapsulated in electrospun nanofibers
buir.contributor.author | Uyar, Tamer | |
buir.contributor.orcid | Uyar, Tamer|0000-0002-3989-4481 | |
dc.citation.epage | 131 | en_US |
dc.citation.spage | 125 | en_US |
dc.citation.volumeNumber | 120 | en_US |
dc.contributor.author | Aytac Z. | en_US |
dc.contributor.author | Dogan, S.Y. | en_US |
dc.contributor.author | Tekinay, T. | en_US |
dc.contributor.author | Uyar, Tamer | en_US |
dc.date.accessioned | 2016-02-08T10:46:57Z | |
dc.date.available | 2016-02-08T10:46:57Z | |
dc.date.issued | 2014 | en_US |
dc.description.abstract | Allyl isothiocyanate (AITC) is known as an efficient antibacterial agent but it has a very high volatility. Herein, AITC and AITC/β-cyclodextrin (CD)-inclusion complex (IC) incorporated in polyvinyl alcohol (PVA) nanofibers were produced via electrospinning. SEM images elucidated that incorporation of AITC and AITC/β-CD-IC into polymer matrix did not affect the bead-free fiber morphology of PVA nanofibers. 1H-NMR and headspace GC-MS analyses revealed that very low amount of AITC was remained in PVA/AITC-NF because of the rapid evaporation of AITC during the electrospinning process. Nevertheless, much higher amount of AITC was preserved in the PVA/AITC/β-CD-IC-NF due to the CD inclusion complexation. The sustained release of AITC from nanofibers was evaluated at 30°C, 50°C and 75°C via headspace GC-MS. When compared to PVA/AITC-NF, PVA/AITC/β-CD-IC-NF has shown higher antibacterial activity against Escherichia coli and Staphylococcus aureus due to the presence of higher amount of AITC in this sample which was preserved by CD-IC. © 2014 Elsevier B.V. | en_US |
dc.description.provenance | Made available in DSpace on 2016-02-08T10:46:57Z (GMT). No. of bitstreams: 1 bilkent-research-paper.pdf: 70227 bytes, checksum: 26e812c6f5156f83f0e77b261a471b5a (MD5) Previous issue date: 2014 | en |
dc.identifier.doi | 10.1016/j.colsurfb.2014.04.006 | en_US |
dc.identifier.issn | 0927-7765 | |
dc.identifier.uri | http://hdl.handle.net/11693/25569 | |
dc.language.iso | English | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1016/j.colsurfb.2014.04.006 | en_US |
dc.source.title | Colloids and Surfaces B: Biointerfaces | en_US |
dc.subject | Allyl isothiocyanate | en_US |
dc.subject | Antibacterial activity | en_US |
dc.subject | Electrospinning | en_US |
dc.subject | Nanofibers | en_US |
dc.subject | Release | en_US |
dc.subject | β-Cyclodextrin | en_US |
dc.subject | Bacteria | en_US |
dc.subject | Cyclodextrins | en_US |
dc.subject | Electrospinning | en_US |
dc.subject | Escherichia coli | en_US |
dc.subject | Allyl isothiocyanate | en_US |
dc.subject | Anti-bacterial activity | en_US |
dc.subject | Cyclodextrin complexes | en_US |
dc.subject | Electrospinning process | en_US |
dc.subject | Electrospun nanofibers | en_US |
dc.subject | Inclusion complexation | en_US |
dc.subject | Poly (vinyl alcohol) (PVA) | en_US |
dc.subject | Release | en_US |
dc.subject | Nanofibers | en_US |
dc.subject | allyl isothiocyanate | en_US |
dc.subject | beta cyclodextrin | en_US |
dc.subject | nanofiber | en_US |
dc.subject | polyvinyl alcohol | en_US |
dc.subject | allyl isothiocyanate | en_US |
dc.subject | antiinfective agent | en_US |
dc.subject | beta cyclodextrin | en_US |
dc.subject | beta cyclodextrin derivative | en_US |
dc.subject | isothiocyanic acid derivative | en_US |
dc.subject | nanofiber | en_US |
dc.subject | solution and solubility | en_US |
dc.subject | article | en_US |
dc.subject | bactericidal activity | en_US |
dc.subject | bacterium colony | en_US |
dc.subject | complex formation | en_US |
dc.subject | concentration (parameters) | en_US |
dc.subject | controlled study | en_US |
dc.subject | crystal structure | en_US |
dc.subject | electrospinning | en_US |
dc.subject | Escherichia coli | en_US |
dc.subject | evaporation | en_US |
dc.subject | mass fragmentography | en_US |
dc.subject | nanoencapsulation | en_US |
dc.subject | nonhuman | en_US |
dc.subject | priority journal | en_US |
dc.subject | proton nuclear magnetic resonance | en_US |
dc.subject | scanning electron microscopy | en_US |
dc.subject | Staphylococcus aureus | en_US |
dc.subject | tensile strength | en_US |
dc.subject | bacterial count | en_US |
dc.subject | chemistry | en_US |
dc.subject | drug effects | en_US |
dc.subject | drug release | en_US |
dc.subject | growth, development and aging | en_US |
dc.subject | microbial sensitivity test | en_US |
dc.subject | nanotechnology | en_US |
dc.subject | procedures | en_US |
dc.subject | solution and solubility | en_US |
dc.subject | ultrastructure | en_US |
dc.subject | X ray diffraction | en_US |
dc.subject | Anti-Bacterial Agents | en_US |
dc.subject | beta-Cyclodextrins | en_US |
dc.subject | Colony Count, Microbial | en_US |
dc.subject | Drug Liberation | en_US |
dc.subject | Escherichia coli | en_US |
dc.subject | Isothiocyanates | en_US |
dc.subject | Microbial Sensitivity Tests | en_US |
dc.subject | Nanofibers | en_US |
dc.subject | Nanotechnology | en_US |
dc.subject | Proton Magnetic Resonance Spectroscopy | en_US |
dc.subject | Solutions | en_US |
dc.subject | Staphylococcus aureus | en_US |
dc.subject | X-Ray Diffraction | en_US |
dc.title | Release and antibacterial activity of allyl isothiocyanate/β-cyclodextrin complex encapsulated in electrospun nanofibers | en_US |
dc.type | Article | en_US |
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