Kajsa Uvdal

Structure of 3-aminopropyl triethoxy silane on silicon oxide

Abstract 3-Aminopropyl triethoxy silane (APTES) was deposited onto silicon oxide surfaces under various conditions of solvent, heat, and time, and then exposed to different curing environments, including air, heat, and ethanol. The macro- and micromolecular structure of APTES was probed on different levels using different techniques. The thickness of APTES layers was measured by ellipsometry, macromolecular structures were identified using microscopic methods (scanning electron microscopy and atomic force microscopy), and chemical form was investigated using angle-resolved X-ray photoelectron spectroscopy and also reflection infrared spectroscopy of APTES on gold and aluminum oxide surfaces. Coverage equivalent to one monolayer was achieved using very mild reaction and curing conditions (reaction in dry toluene for 15 min at room temperature, curing in air, or 15 min in 200°C oven), whereas thick layers were made by increasing reaction and curing times. APTES initially adsorbed to the surface, and curing was necessary to complete covalent binding between APTES and the surface. Deposition of APTES from water gave thin layers, probably electrostatically bound to silicon.

Polyethylene glycol-covered ultra-small Gd2O3 nanoparticles for positive contrast at 1.5 T magnetic resonance clinical scanning

The size distribution and magnetic properties of ultra-small gadolinium oxide crystals (US-Gd2O3) were studied, and the impact of polyethylene glycol capping on the relaxivity constants (r1, r2) an ...

Synthesis and Characterization of PEGylated Gd2O3 Nanoparticles for MRI Contrast Enhancement

Recently, much attention has been given to the development of biofunctionalized nanoparticles with magnetic properties for novel biomedical imaging. Guided, smart, targeting nanoparticulate magnetic resonance imaging (MRI) contrast agents inducing high MRI signal will be valuable tools for future tissue specific imaging and investigation of molecular and cellular events. In this study, we report a new design of functionalized ultrasmall rare earth based nanoparticles to be used as a positive contrast agent in MRI. The relaxivity is compared to commercially available Gd based chelates. The synthesis, PEGylation, and dialysis of small (3-5 nm) gadolinium oxide (DEG-Gd(2)O(3)) nanoparticles are presented. The chemical and physical properties of the nanomaterial were investigated with Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, and dynamic light scattering. Neutrophil activation after exposure to this nanomaterial was studied by means of fluorescence microscopy. The proton relaxation times as a function of dialysis time and functionalization were measured at 1.5 T. A capping procedure introducing stabilizing properties was designed and verified, and the dialysis effects were evaluated. A higher proton relaxivity was obtained for as-synthesized diethylene glycol (DEG)-Gd(2)O(3) nanoparticles compared to commercial Gd-DTPA. A slight decrease of the relaxivity for as-synthesized DEG-Gd(2)O(3) nanoparticles as a function of dialysis time was observed. The results for functionalized nanoparticles showed a considerable relaxivity increase for particles dialyzed extensively with r(1) and r(2) values approximately 4 times the corresponding values for Gd-DTPA. The microscopy study showed that PEGylated nanoparticles do not activate neutrophils in contrast to uncapped Gd(2)O(3). Finally, the nanoparticles are equipped with Rhodamine to show that our PEGylated nanoparticles are available for further coupling chemistry, and thus prepared for targeting purposes. The long term goal is to design a powerful, directed contrast agent for MRI examinations with specific targeting possibilities and with properties inducing local contrast, that is, an extremely high MR signal at the cellular and molecular level.

Surface functionalization and biomedical applications based on SiC

The search for materials and systems, capable of operating long term under physiological conditions, has been a strategy for many research groups during the past years. Silicon carbide (SiC) is a material, which can meet the demands due to its high biocompatibility, high inertness to biological tissues and to aggressive environment, and the possibility to make all types of electronic devices.This paper reviews progress in biomedical and biosensor related research on SiC. For example, less biofouling and platelet aggregation when exposed to blood is taken advantage of in a variety of medical implantable materials while the robust semiconducting properties can be explored in surface functionalized bioelectronic devices.

l-cysteine adsorbed on gold and copper: An X-ray photoelectron spectroscopy study

Abstract l -Cysteine adsorbates and multilayer films on gold and copper surfaces have been investigated by X-ray photoelectron spectroscopy. Both adsorbates, prepared by vapor deposition in UHV and prepared from solution, strongly indicate a dissociative chemisorption through the thiol group (−SH) on the metal surface. We suggest that an organized double layer is formed on gold, for the UHV-prepared layer. In the case of copper, evidence is found for the coordination of both amino and carboxyl groups to the surface, in addition to chemisorption through the thiol group. When l -cysteine is adsorbed from solution on copper, all of the thiol groups interact with copper ions, even in a 25-A-thick layer. This indicates copper ion diffusion and copper complex formation through the entire layer.

Multicolor Fluorescent Semiconducting Polymer Dots with Narrow Emissions and High Brightness

Fluorescent semiconducting polymer dots (Pdots) have attracted great interest because of their superior characteristics as fluorescent probes, such as high fluorescence brightness, fast radiative rates, and excellent photostability. However, currently available Pdots generally exhibit broad emission spectra, which significantly limit their usefulness in many biological applications involving multiplex detections. Here, we describe the design and development of multicolor narrow emissive Pdots based on different boron dipyrromethene (BODIPY) units. BODIPY-containing semiconducting polymers emitting at multiple wavelengths were synthesized and used as precursors for preparing the Pdots, where intraparticle energy transfer led to highly bright, narrow emissions. The emission full width at half-maximum of the resulting Pdots varies from 40 to 55 nm, which is 1.5-2 times narrower than those of conventional semiconducting polymer dots. BODIPY 520 Pdots were about an order of magnitude brighter than commercial Qdot 525 under identical laser excitation conditions. Fluorescence imaging and flow cytometry experiments indicate that the narrow emissions from these bright Pdots are promising for multiplexed biological detections.

Nanoscale Ln(III)-Carboxylate Coordination Polymers (Ln = Gd, Eu, Yb): Temperature-Controlled Guest Encapsulation and Light Harvesting

We report the self-assembly of stable nanoscale coordination polymers (NCPs), which exhibit temperature-controlled guest encapsulation and release, as well as an efficient light-harvesting property. NCPs are obtained by coordination-directed organization of pi-conjugated dicarboxylate (L1) and lanthanide metal ions Gd(III), Eu(III), and Yb(III) in a DMF system. Guest molecules trans-4-styryl-1-methylpyridiniumiodide (D1) and methylene blue (D2) can be encapsulated into NCPs, and the loading amounts can be controlled by changing reaction temperatures. Small angle X-ray diffraction (SAXRD) results reveal that the self-assembled discus-like NCPs exhibit long-range ordered structures, which remain unchanged after guest encapsulations. Experimental results reveal that the negatively charged local environment around the metal connector is the driving force for the encapsulation of cationic guests. The D1 molecules encapsulated in NCPs at 140 degrees C can be released gradually at room temperature in DMF. Guest-loaded NCPs exhibit efficient light harvesting with energy transfer from the framework to the guest D1 molecule, which is studied by photoluminescence and fluorescence lifetime decays. This coordination-directed encapsulation approach is general and should be extended to the fabrication of a wide range of multifunctional nanomaterials.

Infrared and photoelectron spectroscopy of amino acids on copper: Glycine, l-alanine and β-alanine

Abstract Infrared reflection-absorption spectroscopy and X-ray photoelectron spectroscopy (XPS) are used to characterize adsorbed layers of amino acids on evaporated copper surfaces. Thin layers of glycine, l -alanine, and β-alanine are formed by adsorption from 5 m M aqueous solutions at pH values near their isoelectric points. Glycine is most thoroughly studied, and much attention is paid to a comparison with synthesized complexes of cis -Cu(II)(Gly) 2 ·H 2 O and trans -Cu(II)(Gly) 2 ·2H 2 O. A very good agreement is obtained between calculated reflection—absorption spectra based on these model substances and observed spectra of adsorbed glycine on copper. This observation suggests that both the carboxylate oxygens and the amino nitrogens are involved in the bonding to copper and that an ionic lattice (≈10 A) consisting of Cu ions and glycine is formed on the surface. Further support for an ionic structure is obtained from a preliminary XPS study where differently prepared glycine layers on copper are compared with the cis -Cu(II)(Gly) 2 ·H 2 O complex. The composition of the ionic lattice is found to vary with the microstructure of the copper surface and with film orientation in particular. Our infrared data indicate that the cis form is more pronounced on copper films with preferred (111) orientation, whereas the trans form appears to dominate on “polycrystalline” copper. l -Alanine and β-alanine also react with copper via the carboxylate-oxygen and amino-nitrogen atoms. However, the layer thicknesses for l - and β-alanine appear to be smaller than those obtained for glycine.

One-step synthesis of water-dispersible ultra-small Fe3O4 nanoparticles as contrast agents for T1 and T2 magnetic resonance imaging

Uniform, highly water-dispersible and ultra-small Fe3O4 nanoparticles were synthesized via a modified one-step coprecipitation approach. The prepared Fe3O4 nanoparticles not only show good magnetic properties, long-term stability in a biological environment, but also exhibit good biocompatibility in cell viability and hemolysis assay. Due to the ultra-small sized and highly water-dispersibility, they exhibit excellent relaxivity properties, the 1.7 nm sized Fe3O4 nanoparticles reveal a low r2/r1 ratio of 2.03 (r1 = 8.20 mM(-1) s(-1), r2 = 16.67 mM(-1) s(-1)); and the 2.2 nm sized Fe3O4 nanoparticles also appear to have a low r2/r1 ratio of 4.65 (r1 = 6.15 mM(-1) s(-1), r2 = 28.62 mM(-1) s(-1)). This demonstrates that the proposed ultra-small Fe3O4 nanoparticles have great potential as a new type of T1 magnetic resonance imaging contrast agents. Especially, the 2.2 nm sized Fe3O4 nanoparticles, have a competitive r1 value and r2 value compared to commercial contrasting agents such as Gd-DTPA (r1 = 4.8 mM(-1) s (-1)), and SHU-555C (r2 = 69 mM(-1) s(-1)). In vitro and in vivo imaging experiments, show that the 2.2 nm sized Fe3O4 nanoparticles exhibit great contrast enhancement, long-term circulation, and low toxicity, which enable these ultra-small sized Fe3O4 nanoparticles to be promising as T1 and T2 dual contrast agents in clinical settings.

Positive MRI Enhancement in THP-1 Cells with Gd2O3 Nanoparticles

There is a demand for more efficient and tissue-specific MRI contrast agents and recent developments involve the design of substances useful as molecular markers and magnetic tracers. In this study, nanoparticles of gadolinium oxide (Gd2O3) have been investigated for cell labeling and capacity to generate a positive contrast. THP-1, a monocytic cell line that is phagocytic, was used and results were compared with relaxivity of particles in cell culture medium (RPMI 1640). The results showed that Gd2O3-labeled cells have shorter T1 and T2 relaxation times compared with untreated cells. A prominent difference in signal intensity was observed, indicating that Gd2O3 nanoparticles can be used as a positive contrast agent for cell labeling. The r1 for cell samples was 4.1 and 3.6 s(-1) mm(-1) for cell culture medium. The r2 was 17.4 and 12.9 s(-1) mm(-1), respectively. For r1, there was no significant difference in relaxivity between particles in cells compared to particles in cell culture medium, (p(r1) = 0.36), but r2 was significantly different for the two different series (p(r2) = 0.02). Viability results indicate that THP-1 cells endure treatment with Gd2O3 nanoparticles for an extended period of time and it is therefore concluded that results in this study are based on viable cells.