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Temperature-responsive PLLA/PNIPAM nanofibers for switchable release
R. Elashnikov, P. Slepička, S. Rimpelova, P. Ulbrich, V. Švorčík, O. Lyutakov,
Language English Country Netherlands
Document type Journal Article
Grant support
NV15-33459A
MZ0
CEP Register
- MeSH
- Acrylic Resins chemistry MeSH
- Anti-Infective Agents, Local chemistry metabolism pharmacology MeSH
- Escherichia coli drug effects MeSH
- Gentian Violet chemistry metabolism pharmacology MeSH
- Microscopy, Atomic Force MeSH
- Microscopy, Electron, Scanning MeSH
- Nanofibers chemistry MeSH
- Drug Carriers chemistry MeSH
- Polyesters chemistry MeSH
- Wettability MeSH
- Spectroscopy, Fourier Transform Infrared MeSH
- Staphylococcus epidermidis drug effects MeSH
- Temperature MeSH
- Drug Liberation MeSH
- Phase Transition MeSH
- Publication type
- Journal Article MeSH
Smart antimicrobial materials with on-demand drug release are highly desired for biomedical applications. Herein, we report about temperature-responsive poly(N-isopropylacrylamide) (PNIPAM) nanospheres doped with crystal violet (CV) and incorporated into the poly-l-lactide (PLLA) nanofibers. The nanofibers were prepared by electrospinning, using different initial polymers ratios. The morphology of the nanofibers and polymers distribution in the nanofibers were characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM). The interaction between PNIPAM and PLLA in the nanofibers was studied by Fourier transform infrared spectroscopy (FTIR) and its effect on the PNIPAM phase transition was also investigated. It was shown that by the changing of the environmental temperature across the lower critical solution temperature (LCST) of PNIPAM, the switchable wettability and controlled CV release can be achieved. The temperature-dependent release kinetics of CV from polymer nanofibers was investigated by ultraviolet-visible spectroscopy (UV-Vis). The temperature-responsive release of antibacterial CV was also tested for triggering of antibacterial activity, which was examined on Staphylococcus epidermidis (S. epidermidis) and Escherichia coli (E. coli). Thus, the proposed material is promising value for controllable drug-release.
References provided by Crossref.org
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- $a Smart antimicrobial materials with on-demand drug release are highly desired for biomedical applications. Herein, we report about temperature-responsive poly(N-isopropylacrylamide) (PNIPAM) nanospheres doped with crystal violet (CV) and incorporated into the poly-l-lactide (PLLA) nanofibers. The nanofibers were prepared by electrospinning, using different initial polymers ratios. The morphology of the nanofibers and polymers distribution in the nanofibers were characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM). The interaction between PNIPAM and PLLA in the nanofibers was studied by Fourier transform infrared spectroscopy (FTIR) and its effect on the PNIPAM phase transition was also investigated. It was shown that by the changing of the environmental temperature across the lower critical solution temperature (LCST) of PNIPAM, the switchable wettability and controlled CV release can be achieved. The temperature-dependent release kinetics of CV from polymer nanofibers was investigated by ultraviolet-visible spectroscopy (UV-Vis). The temperature-responsive release of antibacterial CV was also tested for triggering of antibacterial activity, which was examined on Staphylococcus epidermidis (S. epidermidis) and Escherichia coli (E. coli). Thus, the proposed material is promising value for controllable drug-release.
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