Zeitschriftenaufsätze

A new water-soluble thermosensitive star-like copolymer, dextran-graft-poly-N-iso-propilacrylamide (D-g-PNIPAM), was created and characterized by various techniques (size-exclusion chromatography, differential scanning calorimetry, Fourier-transform infrared (FTIR) spectroscopy, and dynamic light scattering (DLS) spectroscopy). The viability of cancer cell lines (human transformed cervix epithelial cells, HeLa) as a model for cancer cells was studied using MTT and Live/Dead assays after incubation with a D-g-PNIPAM copolymer as a carrier for the drug doxorubicin (Dox) as well as a D-g-PNIPAM + Dox mixture as a function of the concentration. FTIR spectroscopy clearly indicated the complex formation of Dox with the D-g-PNIPAM copolymer. The size distribution of particles in Hank’s solution was determined by the DLS technique at different temperatures. The in vitro uptake of the studied D-g-PNIPAM + Dox nanoparticles into cancer cells was demonstrated by confocal laser scanning microscopy. It was found that D-g-PNIPAM + Dox nanoparticles in contrast to Dox alone showed higher toxicity toward cancer cells. All of the aforementioned facts indicate a possibility of further preclinical studies of the water-soluble D-g-PNIPAM particles’ behavior in animal tumor models in vivo as promising carriers of anticancer agents.

Heteroepitaxy of planar, low-defect III-V semiconductor layers on Ge(100) requires a single-domain substrate surface, where dimer rows are aligned in parallel on atomically well-ordered terraces, which are separated by steps of even numbered atomic height. The presence of Ga and As in the sample ambience crucially impacts the preparation of such Ge(100) surfaces. Ga and As are commonly omnipresent, when applying metalorganic chemical vapor deposition (MOCVD), either directly supplied by precursors, in the form of MOCVD reactor residuals, or both. We study the impact of the growth conditions on the Ge(100) surface formation in situ, in dependence on the reactor pre-conditioning, the type of As supply, and/or temperature, utilizing surface-sensitive reflection anisotropy spectroscopy. We benchmark the in situ spectra to in system X-ray photoelectron spectroscopy, low energy electron diffraction and scanning tunneling microscopy. We find that interaction of tertiarybutylarsine (TBAs) with a coating of the inner MOCVD reactor walls by GaAs residuals favors desorption of As from reactor parts resulting in As-dimers on the Ge(100) surface, which are rotated by 90˚ compared to preparation routes employing TBAs in Ga-free ambience. The optical in situ control enables precise adjustment and switching between distinct Ge(100) surface reconstructions for subsequent III-V heteroepitaxy.

An automated microfluidic system with computer-controlled syringe pumps was applied for screening a three-dimensional concentration space for the formation of binary gold-platinum metal nanorods. Leveraging the micro segmented flow technique, precise residence and reactant addition timings as well as concentration spaces were addressed. The density and thickness of quasi-isotropic platinum shells on gold nanorod cores were tuned from isolated spots to a dense arrangement of high-aspect-ratio columns. The changing optical properties of the particles in the platinum deposition were used for monitoring the reaction progress and the products by the means of a fiber based micro flow-through spectrophotometer allowing to optimize process times. From our data, we propose an electrochemical model, postulating a diode-like effect and limitations for the formation of Pt nuclei on the gold surface and the formation of nano local elements. This point of view is supported by the observed decoration effects of gold facets and to the formation of columnar structures of the platinum shell.

Fluorogenic labeling strategies have emerged as powerful tools for in vivo and in vitro imaging applications for diagnostic and theranostic purposes. Free organic chromophores (fluorescent dyes) are bright but rapidly degrade. Inorganic nanoparticles (e.g., quantum dots) are photostable but toxic to biological systems. Alternatively, dye-doped polymer particles are promising for labeling and imaging due to their properties that overcome limitations of photodegradation and toxicity. This progress report, therefore, presents various synthesis techniques for the generation of dye-doped fluorescent polymer particles. Polymer particles are relatively soft compared to inorganic nanoparticles and can be synthesized with characteristics like biocompatibility and stimuli responsiveness. Also, their ability of loading fluorophores through various interactions reveals brightness. Here, a multiscale-multicolor library of bright and soft fluorescent polymer particles is generated hierarchically. Various microfluidic supported strategies have been applied where fluorophores can be linked to polymeric networks noncovalently and covalently in the interior, and at the surface of nanoparticles (60-550 nm). Besides, microfluidic strategies for hydrophilic and hydrophobic fluorescent polymer microparticles (20-800 [my]m) have been performed for systematic tuning in size and color combination. Furthermore, soft and bright particulate assemblies are enabled through interfacial interactions at the intermediate scale (600 nm-3 [my]m) between the nanometer and micrometer lengthscale.