32 research outputs found
Mechanical Metamaterials with Negative Compressibility Transitions
When tensioned, ordinary materials expand along the direction of the applied
force. Here, we explore network concepts to design metamaterials exhibiting
negative compressibility transitions, during which a material undergoes
contraction when tensioned (or expansion when pressured). Continuous
contraction of a material in the same direction of an applied tension, and in
response to this tension, is inherently unstable. The conceptually similar
effect we demonstrate can be achieved, however, through destabilisations of
(meta)stable equilibria of the constituents. These destabilisations give rise
to a stress-induced solid-solid phase transition associated with a twisted
hysteresis curve for the stress-strain relationship. The strain-driven
counterpart of negative compressibility transitions is a force amplification
phenomenon, where an increase in deformation induces a discontinuous increase
in response force. We suggest that the proposed materials could be useful for
the design of actuators, force amplifiers, micro-mechanical controls, and
protective devices.Comment: Supplementary information available at
http://www.nature.com/nmat/journal/v11/n7/abs/nmat3331.htm
Photonic Analogue of Two-dimensional Topological Insulators and Helical One-Way Edge Transport in Bi-Anisotropic Metamaterials
Recent progress in understanding the topological properties of condensed
matter has led to the discovery of time-reversal invariant topological
insulators. Because of limitations imposed by nature, topologically non-trivial
electronic order seems to be uncommon except in small-band-gap semiconductors
with strong spin-orbit interactions. In this Article we show that artificial
electromagnetic structures, known as metamaterials, provide an attractive
platform for designing photonic analogues of topological insulators. We
demonstrate that a judicious choice of the metamaterial parameters can create
photonic phases that support a pair of helical edge states, and that these edge
states enable one-way photonic transport that is robust against disorder.Comment: 13 pages, 3 figure
Antigenic, Immunologic and Genetic Characterization of Rough Strains B.abortus RB51, B.melitensis B115 and B.melitensis B18
The lipopolysaccharide (LPS) is considered the major virulent factor in Brucella spp. Several genes have been identified involved in the synthesis of the three LPS components: lipid A, core and O-PS. Usually, Brucella strains devoid of O-PS (rough mutants) are less virulent than the wild type and do not induce undesirable interfering antibodies. Such of them proved to be protective against brucellosis in mice. Because of these favorable features, rough strains have been considered potential brucellosis vaccines. In this study, we evaluated the antigenic, immunologic and genetic characteristics of rough strains B.abortus RB51, B.melitensis B115 and B.melitensis B18. RB51 derived from B.abortus 2308 virulent strain and B115 is a natural rough strain in which the O-PS is present in the cytoplasm. B18 is a rough rifampin-resistan mutant isolated in our laboratory
Cisplatin-induced emesis: systematic review and meta-analysis of the ferret model and the effects of 5-HT3 receptor antagonists
PURPOSE: The ferret cisplatin emesis model has been used for ~30 years and enabled identification of clinically used anti-emetics. We provide an objective assessment of this model including efficacy of 5-HT(3) receptor antagonists to assess its translational validity. METHODS: A systematic review identified available evidence and was used to perform meta-analyses. RESULTS: Of 182 potentially relevant publications, 115 reported cisplatin-induced emesis in ferrets and 68 were included in the analysis. The majority (n = 53) used a 10 mg kg(−1) dose to induce acute emesis, which peaked after 2 h. More recent studies (n = 11) also used 5 mg kg(−1), which induced a biphasic response peaking at 12 h and 48 h. Overall, 5-HT(3) receptor antagonists reduced cisplatin (5 mg kg(−1)) emesis by 68% (45–91%) during the acute phase (day 1) and by 67% (48–86%) and 53% (38–68%, all P < 0.001), during the delayed phase (days 2, 3). In an analysis focused on the acute phase, the efficacy of ondansetron was dependent on the dosage and observation period but not on the dose of cisplatin. CONCLUSION: Our analysis enabled novel findings to be extracted from the literature including factors which may impact on the applicability of preclinical results to humans. It reveals that the efficacy of ondansetron is similar against low and high doses of cisplatin. Additionally, we showed that 5-HT(3) receptor antagonists have a similar efficacy during acute and delayed emesis, which provides a novel insight into the pharmacology of delayed emesis in the ferret
Plasmonic Luneburg and Eaton Lenses
Plasmonics is an interdisciplinary field focusing on the unique properties of
both localized and propagating surface plasmon polaritons (SPPs) -
quasiparticles in which photons are coupled to the quasi-free electrons of
metals. In particular, it allows for confining light in dimensions smaller than
the wavelength of photons in free space, and makes it possible to match the
different length scales associated with photonics and electronics in a single
nanoscale device. Broad applications of plasmonics have been realized including
biological sensing, sub-diffraction-limit imaging, focusing and lithography,
and nano optical circuitry. Plasmonics-based optical elements such as
waveguides, lenses, beam splitters and reflectors have been implemented by
structuring metal surfaces or placing dielectric structures on metals, aiming
to manipulate the two-dimensional surface plasmon waves. However, the abrupt
discontinuities in the material properties or geometries of these elements lead
to increased scattering of SPPs, which significantly reduces the efficiency of
these components. Transformation optics provides an unprecedented approach to
route light at will by spatially varying the optical properties of a material.
Here, motivated by this approach, we use grey-scale lithography to
adiabatically tailor the topology of a dielectric layer adjacent to a metal
surface to demonstrate a plasmonic Luneburg lens that can focus SPPs. We also
realize a plasmonic Eaton lens that can bend SPPs. Since the optical properties
are changed gradually rather than abruptly in these lenses, losses due to
scattering can be significantly reduced in comparison with previously reported
plasmonic elements.Comment: Accepted for publication in Nature Nanotechnolog
Why Can't Rodents Vomit? A Comparative Behavioral, Anatomical, and Physiological Study
The vomiting (emetic) reflex is documented in numerous mammalian species, including primates and carnivores, yet laboratory rats and mice appear to lack this response. It is unclear whether these rodents do not vomit because of anatomical constraints (e.g., a relatively long abdominal esophagus) or lack of key neural circuits. Moreover, it is unknown whether laboratory rodents are representative of Rodentia with regards to this reflex. Here we conducted behavioral testing of members of all three major groups of Rodentia; mouse-related (rat, mouse, vole, beaver), Ctenohystrica (guinea pig, nutria), and squirrel-related (mountain beaver) species. Prototypical emetic agents, apomorphine (sc), veratrine (sc), and copper sulfate (ig), failed to produce either retching or vomiting in these species (although other behavioral effects, e.g., locomotion, were noted). These rodents also had anatomical constraints, which could limit the efficiency of vomiting should it be attempted, including reduced muscularity of the diaphragm and stomach geometry that is not well structured for moving contents towards the esophagus compared to species that can vomit (cat, ferret, and musk shrew). Lastly, an in situ brainstem preparation was used to make sensitive measures of mouth, esophagus, and shoulder muscular movements, and phrenic nerve activity-key features of emetic episodes. Laboratory mice and rats failed to display any of the common coordinated actions of these indices after typical emetic stimulation (resiniferatoxin and vagal afferent stimulation) compared to musk shrews. Overall the results suggest that the inability to vomit is a general property of Rodentia and that an absent brainstem neurological component is the most likely cause. The implications of these findings for the utility of rodents as models in the area of emesis research are discussed. © 2013 Horn et al
Brucellosis Vaccines: Assessment of Brucella melitensis Lipopolysaccharide Rough Mutants Defective in Core and O-Polysaccharide Synthesis and Export
Background: The brucellae are facultative intracellular bacteria that cause brucellosis, one of the major neglected zoonoses. In endemic areas, vaccination is the only effective way to control this disease. Brucella melitensis Rev 1 is a vaccine effective against the brucellosis of sheep and goat caused by B. melitensis, the commonest source of human infection. However, Rev 1 carries a smooth lipopolysaccharide with an O-polysaccharide that elicits antibodies interfering in serodiagnosis, a major problem in eradication campaigns. Because of this, rough Brucella mutants lacking the O-polysaccharide have been proposed as vaccines. Methodology/Principal Findings: To examine the possibilities of rough vaccines, we screened B. melitensis for lipopolysaccharide genes and obtained mutants representing all main rough phenotypes with regard to core oligosaccharide and O-polysaccharide synthesis and export. Using the mouse model, mutants were classified into four attenuation patterns according to their multiplication and persistence in spleens at different doses. In macrophages, mutants belonging to three of these attenuation patterns reached the Brucella characteristic intracellular niche and multiplied intracellularly, suggesting that they could be suitable vaccine candidates. Virulence patterns, intracellular behavior and lipopolysaccharide defects roughly correlated with the degree of protection afforded by the mutants upon intraperitoneal vaccination of mice. However, when vaccination was applied by the subcutaneous route, only two mutants matched the protection obtained with Rev 1 albeit at doses one thousand fold higher than this reference vaccine. These mutants, which were blocked in O-polysaccharide export and accumulated internal O-polysaccharides, stimulated weak anti-smooth lipopolysaccharide antibodies. Conclusions/Significance: The results demonstrate that no rough mutant is equal to Rev 1 in laboratory models and question the notion that rough vaccines are suitable for the control of brucellosis in endemic areas.This work was funded by the European Commission (Research Contract QLK2-CT-2002-00918) and the Ministerio de Ciencia y Tecnología of Spain
(Proyecto AGL2004-01162/GAN)