Yoonsun Jang

Enhanced Antibacterial Activity of Silver/Polyrhodanine-Composite-Decorated Silica Nanoparticles

This work describes the synthesis of silver/polyrhodanine-composite-decorated silica nanoparticles and their antibacterial activity. Polymerization of polyrhodanine proceeded preferentially on the surface of the silica nanoparticles where Ag(+) ions were located. In addition, the embedded Ag(+) ions were reduced to form metallic Ag nanoparticles; consequently, silver/polyrhodanine-composite nanoparticles (approximately 7 nm in diameter) were formed on the surface of the silica nanoparticles. The resulting nanostructure was investigated using electron microscopy, Fourier-transform infrared spectroscopy, ultraviolet-visible spectroscopy, and X-ray photoelectron spectroscopy. The silver/polyrhodanine-nanocomposite-decorated silica nanoparticles exhibited excellent antimicrobial activity toward gram-negative Escherichia coli and gram-positive Staphylococcus aureus because of the antibacterial effects of the silver nanoparticles and the polyrhodanine. The silver/polyrhodanine-composite nanoparticles may therefore have potential for use as a long-term antibacterial agent.

Highly Fluorescent Amidine/Schiff Base Dual-Modified Polyacrylonitrile Nanoparticles for Selective and Sensitive Detection of Copper Ions in Living Cells

Highly fluorescent surface modified polyacrylonitrile nanoparticles (PAN NPs) of 50 nm diameter were fabricated for selective Cu(2+) sensing. After surface modification, the PAN NPs were converted to amidine/Schiff base dual-modified PAN nanoparticles (tPAN NPs) with a Cu(2+) sensing property and high QY (0.19). The selectivity of tPAN NPs for Cu(2+) is much higher than that of other metal ions due to the fact that amidine group on the surface of tPAN NPs has a higher binding affinity with Cu(2+). The effect of other metal ions on the fluorescence intensity of the tPAN NPs was also studied, and other metal ions showed a low interference response in the detection of Cu(2+). Furthermore, as a metal ion chelator, ethylenediaminetetraacetate can competitively interact with Cu(2+) to recover the quenched fluorescence of tPAN NPs. The tPAN NPs are easily introduced into cells and exhibit low toxicity, enabling their use as a fluorescence sensor for Cu(2+) in living cells. The tPAN NPs provide a new direction for the development of copper ion sensors in living cells.

Fabrication of a silica/titania hollow nanorod and its electroresponsive activity

In this study, a 1D oriented hollow SiO2/TiO2 (HST) rod-like material was successfully fabricated via a sequential combination of sol–gel use, TiO2 incorporation, and a sonication-mediated etching and redeposition method. This carefully manipulated new material has numerous advantageous physical and intrinsic properties, such as increased surface area, pore volume, interfacial polarization, and dielectric properties introduced from each synthetic step. The synthesized HST rod was adopted as an electrorheological (ER) material for practical examination of these characteristics. The HST rod materials exhibited 1.5- and 3-fold higher ER performance than a non-metal SiO2 rod and a non-hollow SiO2/TiO2 core/shell (ST/CS) rod, which are interim synthetic steps. Moreover, the HST rod exhibited remarkable 6-fold increased ER efficiency relative to a sphere-shaped hollow SiO2/TiO2 particle synthesized using a similar experimental method. These notable enhancements in ER performance are attributed to incorporation of the experimentally designed characteristics of the HST rod: 1D structure, metal oxide incorporation, and creation of a hollow cavity. For future study, we expect that these versatile HST rod materials can be applied in a range of fields including drug delivery, photo-catalysis, and as building blocks.

Fabrication of barium- and strontium-doped silica/titania hollow nanoparticles and their synergetic effects on promoting neuronal differentiation by activating ERK and p38 pathways.

Pristine, barium-doped, and strontium-doped hollow nanoparticles (p-HNPs, Ba-HNP, and Sr-HNP; HNPs) are prepared by sonication-mediated etching and redeposition (SMER) method and alkali-earth-metal hydroxide solution treatment. The HNPs are investigated to facilitate synergetic neuronal differentiation through alkali-earth-metal doping and in conjunction with nerve growth factor (NGF). PC12 cells are used as model cells for neuronal differentiation. The differentiation efficiency is improved in the presence of the HNPs+NGF, and the neurite length is in the order of Sr-HNP+NGF > Ba-HNP+NGF > p-HNP+NGF > NGF. Silica/titania have increasing effect on both differentiation efficiency and neurite length, and doped barium/strontium influences additional elongation of the average neurite length. Take advantage of hollow structure, NGF is encapsulated into HNPs, and they are further applied for directly inducing differentiation. The maximum differentiation efficiency is 67% in presence of the NGF-encapsulated Sr-HNP, which was 1.3 times higher than previous research. Furthermore, the neurite length is also 2.7 times higher than MnO2 decorated poly(3,4-ethylenedioxythiophene) nanoellipsoids. Ba- and Sr-HNP may offer a possibility for novel application of metal-hybrid nanomaterials for cell differentiation, and can be expanded to other cellular applications.

Smart Fluid System Dually Responsive to Light and Electric Fields: An Electrophotorheological Fluid

Electrophotorheological (EPR) fluids, whose rheological activity is dually responsive to light and electric fields (E fields), is formulated by mixing photosensitive spiropyran-decorated silica (SP-sSiO2) nanoparticles with zwitterionic lecithin and mineral oil. A reversible photorheological (PR) activity of the EPR fluid is developed via the binding and releasing mechanism of lecithin and merocyanine (MC, a photoisomerized form of SP) under ultraviolet (UV) and visible (VIS) light applications. Moreover, the EPR fluid exhibits an 8-fold higher electrorheological (ER) performance compared to the SP-sSiO2 nanoparticle-based ER fluid (without lecithin) under an E field, which is attributed to the enhanced dielectric properties facilitated by the binding of the lecithin and SP molecules. Upon dual application of UV light and an E field, the EPR fluid exhibits high EPR performance (ca. 115.3 Pa) that far exceeds its separate PR (ca. 0.8 Pa) and ER (ca. 57.5 Pa) activities, because of the synergistic contributions of the PR and ER effects through rigid and fully connected fibril-like structures. Consequently, this study offers a strategy on formulation of dual-stimuli responsive smart fluid systems.

Enhanced Electrorheological Performance of Mixed Silica Nanomaterial Geometry

The mixed geometrical effect on the electrorheological (ER) activity of bimodal ER fluids was investigated by mixing SiO2 spheres and rods of different dimensions. To gain an in-depth understanding of the mixed geometrical effect, 12 bimodal ER fluids were prepared from 4 sizes of SiO2 spheres (50, 100, 150, and 350 nm) and 3 types of SiO2 rods with different aspect ratios (L/D = 2, 3, and 5). Five concentrations of SiO2 spheres and rods were created for each bimodal ER fluid, resulting in a total of 60 sets of comprehensive ER measurements. Some bimodal ER fluids exhibited enhanced ER performance, as high as 23.0%, compared to single SiO2 rod-based ER fluids to reveal the mixed geometrical effect of bimodal ER fluids. This interesting experimental result is based on the structural reinforcement provided by spheres to fibrillated rod materials, demonstrating the mixed geometrical effect on ER activity.

Dual electric and magnetic responsivity of multilayered magnetite-embedded core/shell silica/titania nanoparticles with outermost silica shell

Multilayered magnetite-embedded core/shell silica/titania (SiO2/TiO2) nanoparticles with an outermost silica shell (SiO2/TiO2@Fe3O4/SiO2) were synthesized and used to develop stimuli-responsive smart fluids. Benefiting from the incorporation of the various materials, these smart fluids demonstrated electrorheological (ER) and magnetorheological (MR) activities under applied external electric (E) and magnetic (H) fields, respectively, and electromagnetorheological (EMR) characteristics with the simultaneous application of E and H fields. The inner SiO2/TiO2 core nanoparticles, embedded Fe3O4 nanoparticles and the outer SiO2 shell served as electroresponsive, magnetoresponsive and preventative materials toward corrosion, sedimentation and aggregation. The EMR performance of these fluids depended on the direction of the applied E and H fields. Notably, a 6.6-fold enhancement in EMR activity was observed with parallel application of E and H fields compared to perpendicular direction. This study demonstrates an effective approach to precisely and spatially control the rheological/mechanical properties of dual-responsive smart fluids via both field-induced and directional control of external fields.