Microsystems for biomimetic stimulation of cardiac cells

The heart is a complex integrated system that leverages mechanoelectrical signals to synchronize cardiomyocyte contraction and push blood throughout the body. The correct magnitude, timing, and distribution of these signals is critical for proper functioning of the heart; aberrant signals can lead to acute incidents, long-term pathologies, and even death. Due to the heart's limited regenerative capacity and the wide variety of pathologies, heart disease is often studied in vitro. However, it is difficult to accurately replicate the cardiac environment outside of the body. Studying the biophysiology of the heart in vitro typically consists of studying single cells in a tightly controlled static environment or whole tissues in a complex dynamic environment. Micro-electromechanical systems (MEMS) allow us to bridge these two extremes by providing increasing complexity for cell culture without having to use a whole tissue. Here, we carefully describe the electromechanical environment of the heart and discuss MEMS specifically designed to replicate these stimulation modes. Strengths, limitations and future directions of various designs are discussed for a variety of applications.     

A stochastic interactive model for the diffusion of information

Two important generalizations of information diffusion models are the presence of stochastic effects and the possibility of arbitrary patterns of influence among individuals. A Markov random fields model includes both of these features. Under very weak assumptions, there is a unique equilibrium distribution of information patterns for given stochastic (local) interactions among a finite population. This has implications for policies to influence the transmission of information. The dynamic behavior of a special and simple case of the model tends to approximate the standard (logistic) diffusion curve. For an infinite population, uniqueness of equilibrium distributions may fail; some sufficient conditions to ensure uniqueness are given.     

Families of completely positive maps associated with monotone metrics

An operator convex function on (0,∞)$(0,\infty )$ which satisfies the symmetry condition k(x⁻¹)=xk(x)$k(x^{-1})=xk(x)$ can be used to define a type of non-commutative multiplication by a positive definite matrix (or its inverse) using the primitive concepts of left and right multiplication and the functional calculus. The operators for the inverse can be used to define quadratic forms associated with Riemannian metrics which contract under the action of completely positive trace-preserving maps.     

Quantitation of melatonin and n-acetylserotonin in human plasma by nanoflow LC-MS/MS and electrospray LC-MS/MS

Melatonin (MEL) and its chemical precursor N-acetylserotonin (NAS) are believed to be potential biomarkers for sleep-related disorders. Measurement of these compounds, however, has proven to be difficult due to their low circulating levels, especially that of NAS. Few methods offer the sensitivity, specificity and dynamic range needed to monitor MEL and its precursors and metabolites in small blood samples, such as those obtained from pediatric patients. In support of our ongoing study to determine the safety, tolerability and PK dosing strategies for MEL in treating insomnia in children with autism spectrum disorder, two highly sensitive LC-MS/MS assays were developed for the quantitation of MEL and precursor NAS at pg/mL levels in small volumes of human plasma. A validated electrospray ionization (ESI) method was used to quantitate high levels of MEL in PK studies, and a validated nanospray (nESI) method was developed for quantitation of MEL and NAS at endogenous levels. In both assays, plasma samples were processed by centrifugal membrane dialysis after addition of stable isotopic internal standards, and the components were separated by either conventional LC using a Waters SymmetryShield RP18 column (2.1?×?100 mm, 3.5?μm) or on a polyimide-coated, fused-silica capillary self-packed with 17?cm AquaC18 (3?μm, 125??). Quantitation was done using the SRM transitions m/z 233?→?174 and m/z 219?→?160 for MEL and NAS, respectively. The analytical response ratio versus concentration curves were linear for MEL (nanoflow LC: 11.7-1165 pg/mL, LC: 1165-116,500 pg/mL) and for NAS (nanoflow LC: 11.0-1095 pg/mL).     

Solid state proton spin–lattice relaxation in four structurally related organic molecules

We report and interpret the temperature dependence of the proton spin–lattice relaxation rate at 8.50 and 22.5 MHz in four polycrystalline solids composed of structurally related molecules: 2-ethylanthracene, 2-t-butylanthracene, 2-ethylanthraquinone, and 2-t-butylanthraquinone. We have been unable to grow single crystals and therefore do not know the crystal structures. Hence, we use the NMR relaxometry data to make predictions about the solid state structures. As expected, we are able to conclude that the ethyl groups do not reorient in the solid state but that the t-butyl groups do. The anthraquinones have a “simpler” structure than the anthracenes. The best dynamical models suggest that there is a unique crystallographic site for the t-butyl groups in 2-t-butylanthraquinone and two sites, each with half the molecules, for the ethyl groups in 2-ethylanthraquinone. There are also two sites in 2-ethylanthracene, but with unequal weights, suggesting four sites in the unit cell with lower symmetry than the two anthraquinones. Finally, the observed relaxation rate data in 2-t-butylanthracene is very complex and its interpretation demonstrates the uniqueness problem that arises in interpreting relaxometry data without the knowledge of the crystal structure.     

Effects of humidity,imidization history,and thickness on water sorption behavior of poly(p-phenylene biphenyltetracarboximide) films

Poly(p-phenylene biphenyltetracarboximide) films with various thicknesses were prepared from the poly(amic acid) precursor by thermal imidization at 230–400°C for 1–10 h under a nitrogen atmosphere. The water sorption in the films was measured at 25°C over 22–100% relative humidity using a Cahn microbalance as a function of film thickness and thermal imidization history. The water diffusion in all the films followed nearly Fickian process despite the morphological heterogeneity due to the ordered and less ordered phases. The diffusion coefficient and water uptake varied in 0.85 × 10^?10 ? 7.50 × 10^?10 cm²/s and 0.12–2.4 wt %, respectively, depending upon humidity, film thickness, and imidization history. Both diffusion coefficient and water uptake increased with increasing humidity, but decreased as imidization temperature and time increased. With increasing film thickness, the diffusion coefficient increased whereas the water uptake decreased. The water sorption behavior was interpreted with the consideration of morphological variations, such as polymer chain order, in-plane orientation, and intermolecular packing order due to the film thickness and imidization history. © 1995 John Wiley & Sons, Inc.     

High resolution spin labeled fatty acid: synthesis and EPR spectral characteristics

Stearic acid spin label substituted with deuterium in all positions and¹⁵N in the paramagnetic group has been synthesized and was found to display a 5.5 fold gain in sensitivity in the EPR spectrum and a 60% decrease in linewidth compared to the unmodified analog.     

Shear-induced phase separation in solutions of wormlike micelles

Polymer solutions in the vicinity of the theta-point are known to undergo shear-induced turbidity or phase separation. The present study shows that a similar phenomenon also occurs for certain wormlike micellar solutions. Wormlike micelles are the self-assembled counterparts of polymers and are characterized by their ability to reversibly break and recombine. In the system of interest, the micelles are formed by the cationic surfactant erucyl bis(hydroxyethyl)methylammonium chloride (EHAC), in conjunction with a salt such as sodium chloride (NaCl) or sodium salicylate (NaSal). Micellar samples that become turbid under shear show evidence of critical concentration fluctuations and may contain predominantly branched micelles. The shear-induced turbidity in these samples correlates with the appearance of flow-dichroism in rheooptic experiments and with an increase in low-q scattering in small-angle light scattering under flow (flow-SALS) experiments. The characteristic "butterfly" pattern, with enhanced scattering in the flow direction and a dark streak perpendicular to the flow direction, is typically observed in flow-SALS. The results suggest that the turbidity is due to a shear-induced growth of concentration fluctuations, which in turn manifests as large anisotropic domains, typically oriented along the vorticity axis.