19 research outputs found

    QCD and strongly coupled gauge theories : challenges and perspectives

    Get PDF
    We highlight the progress, current status, and open challenges of QCD-driven physics, in theory and in experiment. We discuss how the strong interaction is intimately connected to a broad sweep of physical problems, in settings ranging from astrophysics and cosmology to strongly coupled, complex systems in particle and condensed-matter physics, as well as to searches for physics beyond the Standard Model. We also discuss how success in describing the strong interaction impacts other fields, and, in turn, how such subjects can impact studies of the strong interaction. In the course of the work we offer a perspective on the many research streams which flow into and out of QCD, as well as a vision for future developments.Peer reviewe

    Mechano-responsive polymer solutions based on CO2 supersaturation: shaking-induced phase transitions and self-assembly or dissociation of polymeric nanoparticles

    No full text
    Mechanical stimulation of supersaturated aqueous CO2 solutions is accompanied by a pH increase within seconds. In solutions of tailored homo- and AB diblock copolymers this is exploited to induce micelle formation, or, taking advantage of an aqueous upper critical solution temperature transition, nanoparticle disassembl

    Anti-metastatic effects of RAPTA-C conjugated polymeric micelles on two-dimensional (2D) breast tumor cells and three-dimensional (3D) multicellular tumor spheroids

    Full text link
    Macromolecular ruthenium (Ru) complexes are a promising avenue to better, and more selective, chemotherapeutics to treat metastatic cancers. In our previous research, amphiphilic block copolymeric micelles carrying RAPTA-C (RuCl2(p-cymene)(PTA)) were demonstrated to improve the cellular uptake and cytotoxicity of RAPTA-C (Blunden et al., 2013). However, the anti-metastatic effect of RAPTA-C conjugated polymeric micelles is yet to be established. In this work, we investigated the anti-metastatic effects of RAPTA-C conjugated micelles in both 2D and 3D in vitro breast tumor cell models in comparison with free RAPTA-C. RAPTA-C conjugated micelles showed an improved anti-metastatic effect compared with RAPTA-C for 2D cultured breast tumor cells. RAPTA-C micelles selectively targeted the metastatic tumor cells over the nontumorigenic CHO cells. 3D MCTS assays showed that RAPTA-C conjugated micelles showed a cell growth inhibition similar to that of ten times of the free drug. Further improvement of the RAPTA-C delivery vehicle may provide useful tools to harness ruthenium compounds for metastatic cancer therapy. STATEMENT OF SIGNIFICANCE: The interest in ruthenium drugs stem from their anti-metastatic effect. In contrast to other metal-based drugs that inhibit the growth of tumor cells, ruthenium drugs seem less toxic, but have a pronounce effect on the migration of cancer cells. The ruthenium drug chosen here, RAPTA-C, is capable of inhibiting migration as shown in various assays here. In this publication, we could show for the first time that this effect is enhanced when the drug is delivered using micelles. Important in particular is that the effect is more pronounced in cancerous breast cancer cells while RAPTA-C delivered in micelles does not seem to show any effect on healthy cells. We believe that the presented micelles are suitable carriers for this anti-metastatic drug. The design of the micelle would also allow the encapsulation of other drugs in future studies creating a potentially powerful bullet
    corecore