Silica-coated gold nanorods (AuNRs) with slica shell thickness of 20 nm exhibit the highest photothermal performance, which is beneficial for various nanophotonic applications in materials science.
Obtaining
molecular information from inside cells is an important
topic to understand the outcome of molecular interactions between
potential drug molecules and biomolecules inside cells. To envision
this goal, we investigated the surface-enhanced Raman scattering-based
single-cell spectroscopic method to monitor changes in intracellular
molecular signatures during mitochondrially mediated apoptosis in
real time. Triphenylphosphine-modified gold nanoparticles were localized
successfully to the mitochondria and greatly enhanced to obtain the
intrinsic Raman scattering spectrum of mitochondria and cytochrome
c
in the live cell. Photothermally induced apoptosis showed
a moderate decrease in the disulfide bond and a sharp increase in
β-sheet structures depending on the input-laser power, along
with morphological changes. However, chemical drug induced-apoptosis
showed more subtle changes in the disulfide bond, as well as changes
in Raman peaks corresponding to cytochrome
c
, and
the appearance of a new peak at 1420 cm
–1
, which
enabled us to study the molecular interactions within the mitochondria
in real time from a single cell, following treatment with a novel
pyruvate dehydrogenase kinase inhibitor.
Icephobic
surfaces have gained immense attention owing to their
significant roles in decreasing the energy consumption of refrigerators
and in improving safety issues by preventing the formation of ice
on them. Superhydrophobic surfaces incorporating micro- or nanoscale
roughness and hydrophobic functional groups have been shown to prevent
ice accumulation. Herein, we report a simple, low-cost, and solution-based
one-step process for the production of superhydrophobic surfaces with
three-dimensional (3D) self-assembled structures. The controlled hydrolysis
and polycondensation of n-octadecyltrichlorosilane
(OTS-Cl) in an acetone solution produced a highly uniform superhydrophobic
surface on various substrates such as glass, metals, and polymers
without the limitation of the surface curvature structure. The as-prepared
3D self-assembled surface exhibited a very high contact angle of 161.7°
and a low contact hysteresis of 1.47°. The solvent type, H2O content in acetone, and carbon chain length of the silane
compound were critical in the formation of self-assembled nanostructures.
The thickness of the superhydrophobic 3D self-assembled structure
could be varied by controlling the surface properties of the glass
substrate. In addition, a novel octadecyl silica nanosquare plate
structure was formed as an intermediate for the microlamella structure.
The water drop impact experiments on the 3D self-assembled superhydrophobic
glass substrates at low temperatures (T < −25
°C) showed that the as-prepared superhydrophobic glass possessed
a high impalement threshold for water contact, resulting in excellent
and stable icephobic properties. The preparation method proposed in
this study is scalable and can be used on a flat glass surface or
in a glass vial inside a glass tube. Moreover, it can be applied to
various substrates such as metals and polyurethane surfaces with curvature.
Therefore, the solution-based self-assembly method proposed in this
study is a promising approach to produce superhydrophobic and icephobic
surfaces on a wide range of substrates regardless of their structure
and properties.
Obtaining molecular information of cells in real time has been a critical challenge in studying the interaction between molecules of interest and intracellular components. Fluorescence-based methods have long served as...
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.