35 research outputs found
RGDS-functionalized polyethylene glycol hydrogel-coated magnetic iron oxide nanoparticles enhance specific intracellular uptake by HeLa cells
The objective of this study was to develop thin, biocompatible, and biofunctional hydrogel-coated small-sized nanoparticles that exhibit favorable stability, viability, and specific cellular uptake. This article reports the coating of magnetic iron oxide nanoparticles (MIONPs) with covalently cross-linked biofunctional polyethylene glycol (PEG) hydrogel. Silanized MIONPs were derivatized with eosin Y, and the covalently cross-linked biofunctional PEG hydrogel coating was achieved via surface-initiated photopolymerization of PEG diacrylate in aqueous solution. The thickness of the PEG hydrogel coating, between 23 and 126 nm, was tuned with laser exposure time. PEG hydrogel-coated MIONPs were further functionalized with the fibronectin-derived arginine-glycine-aspartic acid-serine (RGDS) sequence, in order to achieve a biofunctional PEG hydrogel layer around the nanoparticles. RGDS-bound PEG hydrogel-coated MIONPs showed a 17-fold higher uptake by the human cervical cancer HeLa cell line than that of amine-coated MIONPs. This novel method allows for the coating of MIONPs with nano-thin biofunctional hydrogel layers that may prevent undesirable cell and protein adhesion and may allow for cellular uptake in target tissues in a specific manner. These findings indicate that the further biofunctional PEG hydrogel coating of MIONPs is a promising platform for enhanced specific cell targeting in biomedical imaging and cancer therapy
Anti-icing Properties on Surfaces through a Functional Composite: Effect of Ionic Salts
This study reports the potential
of a unique functional composite
for anti-icing applications. To date, various ionic salt formulations
have been applied to prevent ice accumulation on surfaces. However,
salt can be removed by external factors and large amounts must be
used to attain anti-icing properties. Incorporating hydrophilic salts
into hydrophobic mediums and controlled release of specific agents
can provide effective solution to reduce ice accumulation on surfaces.
Here, we developed functional polymer composites with salt pockets
of altered ionic salts consisting of potassium formate (KCOOH), sodium
chloride (NaCl), or magnesium chloride (MgCl<sub>2</sub>). We dissolved
ionic salts in hydrophilic gel domains and dispersed in a hydrophobic
styrene–butadiene–styrene polymer matrix. Na<sup>+</sup> and Cl<sup>–</sup> ions delayed ice formation by 42.6 min
at −2 °C compared to that for unmodified surfaces. Functional
composites prepared with the NaCl ionic salt exhibited better anti-icing
behavior at −2 °C because of their high concentration
compared to that of the composites prepared with KCOOH and MgCl<sub>2</sub> ionic salts. We also characterized the release of ionic salts
from composite-modified hydrophobic medium separately up to 118 days.
Furthermore, we monitored freezing of water on composite-incorporated
or composite-coated hydrophobic surfaces in a camera-integrated cold
chamber with a uniform temperature (−2 °C). The results
demonstrated significant increases in the delay of freezing on composite-incorporated
or composite-coated surfaces compared to that on controls. We observed
altered effects of each ionic salt on the mechanical, morphological,
and functional properties of the composite-incorporated or composite-coated
hydrophobic surfaces. Our results suggested that the efficiency of
a polymer composite to promote anti-icing behavior on a surface is
directly related to the type and concentration of the particular ionic
salt incorporation into the composite. This approach is promising
and demonstrates significant potential of the ionic salt embedded
within polymer composite-modified hydrophobic surfaces to attain delayed
icing function
Correction: Investigation of Real-Time Photorepair Activity on DNA via Surface Plasmon Resonance
Correction: Investigation of Real-Time Photorepair Activity on DNA via Surface Plasmon Resonance.
Gelation-Stabilized Functional Composite-Modified Bitumen for Anti-icing Purposes
Ionic
salts as anti-icing agents have been extensively used to
eliminate accumulation of ice on asphalt surfaces. However, salt can
be easily removed by rain or automobiles and requires frequent application
on roads. Besides this economic consideration, anti-icing agents compromise
the mechanical properties of asphalt and have a negative impact on
living organisms and the environment when used in large amounts. Incorporation
of hydrophilic salts into bitumen, a hydrophobic asphalt binder, and
controlled release of specific molecules from this hydrophobic medium
can provide an effective solution for reducing ice formation on pavements.
Bitumen has previously been modified by various polymers, including
styrene-butadiene-styrene (SBS) for improved strength and thermomechanical
properties. However, an anti-icing function was not considered in
those previous designs. In a previous study, we developed a functional
polymer composite consisting of potassium formate (HCOOK) salt pockets
dissolved in a hydrophilic gel medium and dispersed in a hydrophobic
SBS polymer matrix. Here, we developed an innovative method to obtain
polymer composite-modified bitumen and investigated further the anti-icing
properties of the functional bitumen. We improved incorporation of
this polymer composite into bitumen and demonstrated proper distribution
of the composite within bitumen through morphological and rheological
analysis. We characterized the anti-icing properties of modified bitumen
surfaces and demonstrated significant increases in freezing delay
of composite-modified bitumen compared to base bitumen in a temperature-
and humidity-controlled chamber. In addition, we characterized the
release of HCOOK salt from polymer composite-modified bitumen and
observed salt release within the range of 1.07–10.8% (w/w)
in 67 days, depending on the composite content. The results demonstrate
the potential of this polymer composite-modified bitumen for anti-icing
functionality and for industrially relevant applications
Nanoparticle and Gelation Stabilized Functional Composites of an Ionic Salt in a Hydrophobic Polymer Matrix
<div><p>Polymer composites consisted of small hydrophilic pockets homogeneously dispersed in a hydrophobic polymer matrix are important in many applications where controlled release of the functional agent from the hydrophilic phase is needed. As an example, a release of biomolecules or drugs from therapeutic formulations or release of salt in anti-icing application can be mentioned. Here, we report a method for preparation of such a composite material consisted of small KCOOH salt pockets distributed in the styrene-butadiene-styrene (SBS) polymer matrix and demonstrate its effectiveness in anti-icing coatings. The mixtures of the aqueous KCOOH and SBS-cyclohexane solutions were firstly stabilized by adding silica nanoparticles to the emulsions and, even more, by gelation of the aqueous phase by agarose. The emulsions were observed in optical microscope to check its stability in time and characterized by rheological measurements. The dry composite materials were obtained via casting the emulsions onto the glass substrates and evaporations of the organic solvent. Composite polymer films were characterized by water contact angle (WCA) measurements. The release of KCOOH salt into water and the freezing delay experiments of water droplets on dry composite films demonstrated their anti-icing properties. It has been concluded that hydrophobic and thermoplastic SBS polymer allows incorporation of the hydrophilic pockets/phases through our technique that opens the possibility for controlled delivering of anti-icing agents from the composite.</p></div
Optical microscope images of wet emulsions with internal volume fraction φ = 25% (v/v) prepared by different stabilization methods for immediately after and 3 minutes after preparation of emulsions.
<p>(a) Wet emulsions without stabilizing agent, (b) wet emulsions prepared with SDS surfactant as the stabilizing agent, (c) wet emulsions prepared by nanoparticle stabilization. Scale bar is 500 µm.</p
Viscosity versus shear rate profiles for emulsions with (a) no gelation of the internal phase, (b) gelation of the internal phase.
<p>Viscosity versus shear rate profile for homogeneous SBS solution has been included for comparison. Data indicates the average of at least three observations with corresponding standard deviations.</p
Optical microscope images of wet and dry emulsions prepared with internal volume fraction Φ = 0.33, and nanoparticle concentration of 0.7% (w/w).
<p>(a) Wet emulsions prepared without agar gel in the dispersed phase, (b) wet emulsions prepared with agar gel in the dispersed phase, (c) dry emulsions prepared without agar gel in the dispersed phase, (d) dry emulsions prepared with agar gel in the dispersed phase. Scale bar is 200 µm.</p