16 research outputs found
Silver-nanoparticles with defined morphology - Synthesis, properties and biological impact
Im Rahmen dieser Dissertation wurden verschiedene Methoden zur Darstellung von Silber-Nanopartikeln mit unterschiedlicher Morphologie, aber vergleichbarer Größe, Ladung und Funktionalisierung erarbeitet. Primäres Ziel war die Anwendung im biologischen System, woraus sich besondere Anforderungen an die Reinheit, Konzentration und Stabilität der Partikel ergaben. Es wurden im Wesentlichen fünf verschiedene Partikelsysteme synthetisiert und mit verschiedenen analytischen Methoden charakterisiert. Weiterhin wurde die Auflösungskinetik und die biologische Wirkung gegenüber eukaryotischen und prokaryotischen Zellen bestimmt.In this work, silver nanoparticles with different shapes but comparable size and identical surface functionalization were prepared. The primary objective was the application in biological media, resulting in specific requirements concerning the purity, concentration and stability of the particles. Mainly, five different particle systems were synthesized and characterized by different analytical methods. Furthermore, dissolution kinetics were determined and the biological effect towards eukaryotic and prokaryotic cells was examined
A multi-center study of their physicochemical characteristics, cell culture and in vivo experiments
PVP-capped silver nanoparticles with a diameter of the metallic core of 70 nm,
a hydrodynamic diameter of 120 nm and a zeta potential of −20 mV were prepared
and investigated with regard to their biological activity. This review
summarizes the physicochemical properties (dissolution, protein adsorption,
dispersability) of these nanoparticles and the cellular consequences of the
exposure of a broad range of biological test systems to this defined type of
silver nanoparticles. Silver nanoparticles dissolve in water in the presence
of oxygen. In addition, in biological media (i.e., in the presence of
proteins) the surface of silver nanoparticles is rapidly coated by a protein
corona that influences their physicochemical and biological properties
including cellular uptake. Silver nanoparticles are taken up by cell-type
specific endocytosis pathways as demonstrated for hMSC, primary T-cells,
primary monocytes, and astrocytes. A visualization of particles inside cells
is possible by X-ray microscopy, fluorescence microscopy, and combined FIB/SEM
analysis. By staining organelles, their localization inside the cell can be
additionally determined. While primary brain astrocytes are shown to be fairly
tolerant toward silver nanoparticles, silver nanoparticles induce the
formation of DNA double-strand-breaks (DSB) and lead to chromosomal
aberrations and sister-chromatid exchanges in Chinese hamster fibroblast cell
lines (CHO9, K1, V79B). An exposure of rats to silver nanoparticles in vivo
induced a moderate pulmonary toxicity, however, only at rather high
concentrations. The same was found in precision-cut lung slices of rats in
which silver nanoparticles remained mainly at the tissue surface. In a human
3D triple-cell culture model consisting of three cell types (alveolar
epithelial cells, macrophages, and dendritic cells), adverse effects were also
only found at high silver concentrations. The silver ions that are released
from silver nanoparticles may be harmful to skin with disrupted barrier (e.g.,
wounds) and induce oxidative stress in skin cells (HaCaT). In conclusion, the
data obtained on the effects of this well-defined type of silver nanoparticles
on various biological systems clearly demonstrate that cell-type specific
properties as well as experimental conditions determine the biocompatibility
of and the cellular responses to an exposure with silver nanoparticles
A rapid, high-yield and large-scale synthesis of uniform spherical silver nanoparticles by a microwave-assisted polyol process
Silver nanoparticles are often employed in medical devices and consumer products due to their antibacterial action. For this, reliable syntheses with quantitative yield are required. Uniform spherical silver nanoparticles with a diameter of about 180 nm were synthesized by carrying out the polyol synthesis in a microwave. Silver nitrate was dissolved in ethylene glycol and poly(N-vinyl pyrrolidone) (PVP) was added as capping agent. The particles were characterized by SEM, HRTEM, XRD, and DLS. The results are compared with the classical method where silver nitrate is reduced by glucose in aqueous solution, heated with an oil-bath. The microwave-assisted synthesis leads to an almost quantitative yield of uniform silver nanoparticles after 20 min reaction time and gives exclusively spherical particles without other shapes like triangles, rods or prisms. Diethylene glycol as solvent gave a more homogeneous particle size distribution than ethylene glycol. For both kinds of particles, dissolution in ultrapure water was examined over a period of 29 days in the presence of oxygen. The dissolution was comparable in both cases (about 50% after 4 weeks), indicating the same antibacterial action for particles from the microwave and from the glucose synthesis
On the Crystallography of Silver Nanoparticles with Different Shapes
The crystallographic properties of silver nanoparticles with different morphologies (two different kinds of spheres, cubes, platelets, and rods) were derived from X-ray powder diffraction and electron microscopy. The size of the metallic particle core was determined by scanning electron microscopy, and the colloidal stability and the hydrodynamic particle diameter were analyzed by dynamic light scattering. The preferred crystallographic orientation (texture) as obtained by X-ray powder diffraction, including pole figure analysis, and high resolution transmission electron microscopy showed the crystallographic nature of the spheres (almost no texture), the cubes (terminated by {100} faces), the platelets (terminated by {111} faces), and the rods (grown from pentagonal twins along [110] and terminated by {100} faces). The crystallite size was determined by Rietveld refinement of X-ray powder diffraction data and agreed well with the transmission electron microscopic data