5 research outputs found
Uptake of TiO<sub>2</sub> Nanoparticles into C. elegans Neurons Negatively Affects Axonal Growth and Worm Locomotion Behavior
We
employ model organism Caenorhabditis elegans to effectively study the toxicology of anatase and rutile phase
titanium dioxide (TiO<sub>2</sub>) nanoparticles (NPs). The experimental
results show that nematode C. elegans can take up fluorescein isothiocyanate-labeled TiO<sub>2</sub> NPs
and that both anatase and rutile TiO<sub>2</sub> NPs can be detected
in the cytoplasm of cultured primary neurons imaged by transmission
electron microscopy. After TiO<sub>2</sub> NP exposure, these neurons
also grow shorter axons, which may be related to the detected impeded
worm locomotion behavior. Furthermore, anatase TiO<sub>2</sub> NPs
did not affect the worm’s body length; however, we determined
that a concentration of 500 μg/mL of anatase TiO<sub>2</sub> NPs reduced the worm population by 50% within 72 h. Notably, rutile
TiO<sub>2</sub> NPs negatively affect both the body size and worm
population. Worms unable to enter the L4 larval stage explain a severe
reduction in the worm population at TiO<sub>2</sub> NPs LC<sub>50</sub>/3d. To obtain a better understanding of the cellular mechanisms
involved in TiO<sub>2</sub> NP intoxication, DNA microarray assays
were employed to determine changes in gene expression in the presence
or absence of TiO<sub>2</sub> NP exposure. Our data reveal that three
genes (with significant changes in expression levels) were related
to metal binding or metal detoxification (mtl-2, C45B2.2, and nhr-247),
six genes were involved in fertility and reproduction (mtl-2, F26F2.3,
ZK970.7, clec-70, K08C9.7, and C38C3.7), four genes were involved
in worm growth and body morphogenesis (mtl-2, F26F2.3, C38C3.7, and
nhr-247), and five genes were involved in neuronal function (C41G6.13,
C45B2.2, srr-6, K08C9.7, and C38C3.7)
SPR setups and experimental procedures.
<p>(A) Schematic illustration of the SPR device: The He-Ne laser penetrated through a polarizer and a beam splitter, which split the beam 50/50. One was detected by a photodiode and the other one was coupled by a prism to generate Surface Plasmon Wave on the Au chip in which the angle shift was detected by a photodiode. (B) The OB-cadherin expressing cells flowing into the chamber were captured by the Au chip pre-coated with OB-cadherin antibodies, which changed the angle of the reflected laser beam. (C) A typical graphical data from SPR measurements.</p
Molecular biology detection of MSC-osteoblast differentiation.
<p>(A) Real-time PCR of OB-cadherin expression. (B) Western blot of OB-cadherin expression during osteogenic induction of MSCs. SaOS2 served as positive control. (C) The OB-cadherin expression level intensity analyzed by semi-quantitative method and was normalized to the intensity of SaOS2. (D) Alkaline phosphatase (AP) staining and von kossa (VK) staining.</p
HNO<sub>3</sub>‑Assisted Polyol Synthesis of Ultralarge Single-Crystalline Ag Microplates and Their Far Propagation Length of Surface Plasmon Polariton
We
developed a HNO<sub>3</sub>-assisted polyol reduction method
to synthesize ultralarge single-crystalline Ag microplates routinely.
The edge length of the synthesized Ag microplates reaches 50 μm,
and their top facets are (111). The mechanism for dramatically enlarging
single-crystalline Ag structure stems from a series of competitive
anisotropic growths, primarily governed by carefully tuning the adsorption
of Ag<sup>0</sup> by ethylene glycol and the desorption of Ag<sup>0</sup> by a cyanide ion on Ag(100). Finally, we measured the propagation
length of surface plasmon polaritons along the air/Ag interface under
534 nm laser excitation. Our single-crystalline Ag microplate exhibited
a propagation length (11.22 μm) considerably greater than that
of the conventional E-gun deposited Ag thin film (5.27 μm)
Surfactant-Directed Fabrication of Supercrystals from the Assembly of Polyhedral Au–Pd Core–Shell Nanocrystals and Their Electrical and Optical Properties
Au–Pd
core–shell nanocrystals with cubic, truncated
cubic, cuboctahedral, truncated octahedral, and octahedral structures
have been employed to form micrometer-sized polyhedral supercrystals
by both the droplet evaporation method and novel surfactant diffusion
methods. Observation of cross-sectional samples indicates shape preservation
of interior nanocrystals within a supercrystal. Low-angle X-ray diffraction
techniques and electron microscopy have been used to confirm the presence
of surfactant between contacting nanocrystals. By diluting the nanocrystal
concentration or increasing the solution temperature, supercrystal
size can be tuned gradually to well below 1 μm using the surfactant
diffusion method. Rectangular supercrystal microbars were obtained
by increasing the amounts of cubic nanocrystals and surfactant used.
Au–Ag core–shell cubes and PbS cubes with sizes of 30–40
nm have also been fabricated into supercrystals, showing the generality
of the surfactant diffusion approach to form supercrystals with diverse
composition. Electrical conductivity measurements on single Au–Pd
supercrystals reveal loss of metallic conductivity due to the presence
of insulating surfactant. Cubic Au–Pd supercrystals show infrared
absorption at 3.2 μm due to extensive plasmon coupling. Mie-type
resonances centered at 9.8 μm for the Au–Pd supercrystals
disappear once the Pd shells are converted into PdH after hydrogen
absorption