161 research outputs found
Induced Anticlinic Ordering and Nanophase Segregation of Bow-Shaped Molecules in a Smectic Solvent
Recent experiments indicate that doping low concentrations of bent-core
molecules into calamitic smectic solvents can induce anticlinic and biaxial
smectic phases. We have carried out Monte Carlo (MC) simulations of mixtures of
rodlike molecules (hard spherocylinders with length/breadth ratio ) and bow- or banana-shaped molecules (hard spherocylinder dimers
with length/breadth ratio or 2.5 and opening angle ) to
probe the molecular-scale organization and phase behavior of rod/banana
mixtures. We find that a low concentration (3%) of dimers
induces anticlinic (SmC) ordering in an untilted smectic (SmA) phase for
. For smaller , half of each bow-shaped
molecule is nanophase segregated between smectic layers, and the smectic layers
are untilted. For , no tilted phases are induced. However,
with decreasing we observe a sharp transition from {\sl intralamellar}
nanophase segregation (bow-shaped molecules segregated within smectic layers)
to {\sl interlamellar} nanophase segregation (bow-shaped molecules concentrated
between smectic layers) near . These results demonstrate that
purely entropic effects can lead to surprisingly complex behavior in rod/banana
mixtures.Comment: 5 pages Revtex, 7 postscript figure
The double-hit protocol induces HFpEF and impairs myocardial ubiquitin-proteasome system performance in FVB/N mice
Heart failure with preserved ejection fraction (HFpEF) is a leading cause of death and disability, with its prevalence surpassing that of heart failure with reduced ejection fraction. Obesity and hypertension are often associated with HFpEF. HFpEF can be modeled through simultaneous metabolic and hypertensive stresses in male C57BL/6N mice provoked by a combination treatment of a high-fat diet (HFD) and constitutive nitric oxide synthase inhibition by Nω-nitro-L-arginine methyl-ester (L-NAME). Ubiquitin-proteasome system (UPS) dysfunction was detected in many forms of cardiomyopathy, but whether it occurs in HFpEF remains unknown. We report successful modeling of HFpEF in male FVB/N mice and, by taking advantage of a transgenic UPS reporter mouse, we have detected myocardial UPS functioning impairment during HFpEF, suggesting a pathogenic role for impaired protein degradation in the development and progression of HFpEF
Symmetries and Elasticity of Nematic Gels
A nematic liquid-crystal gel is a macroscopically homogeneous elastic medium
with the rotational symmetry of a nematic liquid crystal. In this paper, we
develop a general approach to the study of these gels that incorporates all
underlying symmetries. After reviewing traditional elasticity and clarifying
the role of broken rotational symmetries in both the reference space of points
in the undistorted medium and the target space into which these points are
mapped, we explore the unusual properties of nematic gels from a number of
perspectives. We show how symmetries of nematic gels formed via spontaneous
symmetry breaking from an isotropic gel enforce soft elastic response
characterized by the vanishing of a shear modulus and the vanishing of stress
up to a critical value of strain along certain directions. We also study the
phase transition from isotropic to nematic gels. In addition to being fully
consistent with approaches to nematic gels based on rubber elasticity, our
description has the important advantages of being independent of a microscopic
model, of emphasizing and clarifying the role of broken symmetries in
determining elastic response, and of permitting easy incorporation of spatial
variations, thermal fluctuations, and gel heterogeneity, thereby allowing a
full statistical-mechanical treatment of these novel materials.Comment: 21 pages, 4 eps figure
Identification of the methyltransferase targeting C2499 in Deinococcus radiodurans 23S ribosomal RNA
Activity of topical antimicrobial agents against multidrug-resistant bacteria recovered from burn patients
Background:
Topical antimicrobials are employed for prophylaxis and treatment of burnwound infections despite no established susceptibility breakpoints, which are becoming vital in an era of multidrug-resistant (MDR) bacteria. We compared two methods of determining topical antimicrobial susceptibilities.
Methods:
Isolates of Pseudomonas aeruginosa, methicillin-resistant Staphylococcus aureus (MRSA), extended spectrum beta-lactamase (ESBL) producing Klebsiella pneumoniae, and Acinetobacter baumanii-calcoaceticus (ABC) from burn patients were tested using broth microdilution and agar well diffusion to determine minimum inhibitory concentrations (MICs) and zones of inhibition (ZI). Isolates had systemic antibiotic resistance and clonality determined. MDR included resistance to antibiotics in three or more classes.
Results:
We assessed 22 ESBL-producing K. pneumoniae, 20 ABC (75% MDR), 20 P. aeruginosa (45% MDR), and 20 MRSA isolates. The most active agents were mupirocin for MRSA and mafenide acetate for the gram-negatives with moderate MICs/ZI found with silver sulfadiazene, silver nitrate, and honey. MDR and non-MDR isolates had similar topical resistance. There was no clonality associated with resistance patterns.
Conclusion:
Despite several methods to test bacteria for topical susceptibility, no defined breakpoints exist and standards need to be established. We recommend continuing to use silver products for prophylaxis against gram-negatives and mafenide acetate for treatment, and mupirocin for MRSA
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