Temperature-responsive PLLA/PNIPAM nanofibers for switchable release

被引:64
作者
Elashnikov, Roman [1 ]
Slepicka, Petr [1 ]
Rimpelova, Silvie [2 ]
Ulbrich, Pavel [2 ]
Svorcik, Vaclav [1 ]
Lyutakov, Oleksiy [1 ]
机构
[1] Univ Chem & Technol, Dept Solid State Engn, Prague 16628, Czech Republic
[2] Univ Chem & Technol, Dept Biochem & Microbiol, Prague 16628, Czech Republic
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2017年 / 72卷
关键词
Responsive release; Polymer blends; Electrospinning; Nanofibers; Stimuli-responsive; Switchable wettability; Antibacterial; CONTROLLED DRUG-RELEASE; SILVER NANOPARTICLES; HYDROGELS; FILMS; BEHAVIOR; PH; WETTABILITY; SURFACES; ACID); PMMA;
D O I
10.1016/j.msec.2016.11.028
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
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 forte 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. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:293 / 300
页数:8
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