Chemical Locking in Molecular Tunneling Junctions Enables Nonvolatile Memory with Large On–Off Ratios

This paper describes the reversible chemical locking of sypiropyran switches bound to metallic surfaces to enable the encoding of nonvolatile information. Data are encoded spatially by selectively locking the spiropyran moieties in their merocyanine form using a combination of exposure to acid and UV light. Without exposure to acid, the merocyanine form spontaneously converts back to the spiropyran form. Bits are resolved by defining the regions of the monolayer that are exposed to acid, using a “soft punchcard” fabricated from a silicone elastomer. Information is read by measuring the tunneling charge–transport through the monolayer using eutectic Ga–In top‐contacts. The merocyanine form is more than three orders of magnitude more conductive than the spiropyran form, allowing the differentiation of bits. Photoelectron spectroscopy shows that the monolayers are undamaged by exposure to light, acid, base, and applied bias, enabling proof‐of‐concept devices in which an 8‐bit ASCII encoded six‐character string is written, erased, and rewritten.     

Phase transition in space: how far does a symmetry bend before it breaks?

We extend the theory of symmetry-breaking dynamics in non-equilibrium second-order phase transitions known as the Kibble-Zurek mechanism (KZM) to transitions where the change of phase occurs not in time but in space. This can be due to a time-independent spatial variation of a field that imposes a phase with one symmetry to the left of where it attains critical value, while allowing spontaneous symmetry breaking to the right of that critical borderline. Topological defects need not form in such a situation. We show, however, that the size, in space, of the 'scar' over which the order parameter adjusts as it 'bends' interpolating between the phases with different symmetries follows from a KZM-like approach. As we illustrate on the example of a transverse quantum Ising model, in quantum phase transitions this spatial scale--the size of the scar--is directly reflected in the energy spectrum of the system: in particular, it determines the size of the energy gap.     

Zn(1-x)MnxTe diluted magnetic semiconductor nanowires grown by molecular beam epitaxy

It is shown that the growth of II-VI diluted magnetic semiconductor nanowires is possible by the catalytically enhanced molecular beam epitaxy (MBE). Zn(1-x)MnxTe NWs with manganese content up to x=0.60 were produced by this method. X-ray diffraction, Raman spectroscopy, and temperature dependent photoluminescence measurements confirm the incorporation of Mn(2+) ions in the cation substitutional sites of the ZnTe matrix of the NWs.     

The role of vacancies and local distortions in the design of new phase-change materials

Phase-change materials are of tremendous technological importance ranging from optical data storage to electronic memories. Despite this interest, many fundamental properties of phase-change materials, such as the role of vacancies, remain poorly understood. 'GeSbTe'-based phase-change materials contain vacancy concentrations around 10% in their metastable crystalline structure. By using density-functional theory, the origin of these vacancies has been clarified and we show that the most stable crystalline phases with rocksalt-like structures are characterized by large vacancy concentrations and local distortions. The ease by which vacancies are formed is explained by the need to annihilate energetically unfavourable antibonding Ge-Te and Sb-Te interactions in the highest occupied bands. Understanding how the interplay between vacancies and local distortions lowers the total energy helps to design novel phase-change materials as evidenced by new experimental data.     

Nanostructuring with a crosslinkable discotic material

A high-yielding synthesis afforded a hexa-peri-hexabenzocoronene carrying acrylate units at the end of six attached alkyl spacers. The polymerization of these acrylate moieties could be initiated with thermal energy and through direct photoactivation without the addition of a photoinitiator. This allowed the organization of the liquid-crystalline material to be fixed in either the crystalline state or the mesophase, which preserved the organization in the respective phase. The use of a focused synchrotron beam permitted selected regions of a thin film to be rendered insoluble. After "developing" the film in this lithographic process by dissolving the soluble, unpolymerized material, defined nano-objects remained on the substrate. In addition, the pronounced aromatic pi stacking of the novel material allows an organization in mesoporous membranes that could be fixed by thermal crosslinking. After the removal of the inorganic template, mechanically stable nanotubes were obtained, which were characterized by different microscopy techniques.     

From Primary MSC Culture of Adipose Tissue to Immortalized Cell Line Producing Cytokines for Potential Use in Regenerative Medicine Therapy or Immunotherapy

For twenty-five years, attempts have been made to use MSCs in the treatment of various diseases due to their regenerative and immunomodulatory properties. However, the results are not satisfactory. Assuming that MSCs can be replaced in some therapies by the active factors they produce, the immortalized MSCs line was established from human adipose tissue (HATMSC1) to produce conditioned media and test its regenerative potential in vitro in terms of possible clinical application. The production of biologically active factors by primary MSCs was lower compared to the HATMSC1 cell line and several factors were produced only by the cell line. It has been shown that an HATMSC1-conditioned medium increases the proliferation of various cell types, augments the adhesion of cells and improves endothelial cell function. It was found that hypoxia during culture resulted in an augmentation in the pro-angiogenic factors production, such as VEGF, IL-8, Angiogenin and MCP-1. The immunomodulatory factors caused an increase in the production of GM-CSF, IL-5, IL-6, MCP-1, RANTES and IL-8. These data suggest that these factors, produced under different culture conditions, could be used for different medical conditions, such as in regenerative medicine, when an increased concentration of pro-angiogenic factors may be beneficial, or in inflammatory diseases with conditioned media with a high concentration of immunomodulatory factors.     

Investigation of Shape Transformations of Vesicles,Induced by Their Adhesion to Flat Substrates Characterized by Different Adhesion Strength

The adhesion of lipid vesicles to a rigid flat surface is investigated. We examine the influence of the membrane spontaneous curvature, adhesion strength, and the reduced volume on the stability and shape transformations of adhered vesicles. The minimal strength of the adhesion necessary to stabilize the shapes of adhered vesicles belonging to different shape classes is determined. It is shown that the budding of an adhered vesicle may be induced by the change of the adhesion strength. The importance of the free vesicle shape for its susceptibility to adhesion is discussed.     

Biotin Transport-Targeting Polysaccharide-Modified PAMAM G3 Dendrimer as System Delivering α-Mangostin into Cancer Cells and C. elegans Worms

The natural xanthone α-mangostin (αM) exhibits a wide range of pharmacological activities, including antineoplastic and anti-nematode properties, but low water solubility and poor selectivity of the drug prevent its potential clinical use. Therefore, the targeted third-generation poly(amidoamine) dendrimer (PAMAM G3) delivery system was proposed, based on hyperbranched polymer showing good solubility, high biocompatibility and low immunogenicity. A multifunctional nanocarrier was prepared by attaching αM to the surface amine groups of dendrimer via amide bond in the ratio 5 (G3^2B12gh5M) or 17 (G3^2B10gh17M) residues per one dendrimer molecule. Twelve or ten remaining amine groups were modified by conjugation with D-glucoheptono-1,4-lactone (gh) to block the amine groups, and two biotin (B) residues as targeting moieties. The biological activity of the obtained conjugates was studied in vitro on glioma U-118 MG and squamous cell carcinoma SCC-15 cancer cells compared to normal fibroblasts (BJ), and in vivo on a model organism Caenorhabditis elegans. Dendrimer vehicle G3^2B12gh at concentrations up to 20 µM showed no anti-proliferative effect against tested cell lines, with a feeble cytotoxicity of the highest concentration seen only with SCC-15 cells. The attachment of αM to the vehicle significantly increased cytotoxic effect of the drug, even by 4- and 25-fold for G3^2B12gh5M and G3^2B10gh17M, respectively. A stronger inhibition of cells viability and influence on other metabolic parameters (proliferation, adhesion, ATP level and Caspase-3/7 activity) was observed for G3^2B10gh17M than for G3^2B12gh5M. Both bioconjugates were internalized efficiently into the cells. Similarly, the attachment of αM to the dendrimer vehicle increased its toxicity for C. elegans. Thus, the proposed α-mangostin delivery system allowed the drug to be more effective in the dendrimer-bound as compared to free state against both cultured the cancer cells and model organism, suggesting that this treatment is promising for anticancer as well as anti-nematode chemotherapy.