Aperiodic and periodic components of oscillatory brain activity in relation to cognition and symptoms in pediatric ADHD.

Children with attention-deficit/hyperactivity disorder show deficits in processing speed, as well as aberrant neural oscillations, including both periodic (oscillatory) and aperiodic (1/f-like) activity, reflecting the pattern of power across frequencies. Both components were suggested as underlying neural mechanisms of cognitive dysfunctions in attention-deficit/hyperactivity disorder. Here, we examined differences in processing speed and resting-state-Electroencephalogram neural oscillations and their associations between 6- and 12-year-old children with (n = 33) and without (n = 33) attention-deficit/hyperactivity disorder. Spectral analyses of the resting-state EEG signal using fast Fourier transform revealed increased power in fronto-central theta and beta oscillations for the attention-deficit/hyperactivity disorder group, but no differences in the theta/beta ratio. Using the parameterization method, we found a higher aperiodic exponent, which has been suggested to reflect lower neuronal excitation-inhibition, in the attention-deficit/hyperactivity disorder group. While fast Fourier transform-based theta power correlated with clinical symptoms for the attention-deficit/hyperactivity disorder group only, the aperiodic exponent was negatively correlated with processing speed across the entire sample. Finally, the aperiodic exponent was correlated with fast Fourier transform-based beta power. These results highlight the different and complementary contribution of periodic and aperiodic components of the neural spectrum as metrics for evaluation of processing speed in attention-deficit/hyperactivity disorder. Future studies should further clarify the roles of periodic and aperiodic components in additional cognitive functions and in relation to clinical status.

Silica-Supported Nitrogen-Enriched Porous Benzimidazole-Linked and Triazine-Based Polymers for the Adsorption of CO2.

Two crystalline and five amorphous benzimidazole polymers (BINP) were synthesized and conjugated to porous silica via amine and aldehyde-based materials by a simple reflux procedure. The resulting polymers were subject to thermal analysis for monitoring and quantification of the adsorption and desorption of CO2. All the polymers were capable of adsorbing CO2 from a flowing stream of only 80 mL/min at 25 °C. The adsorbed CO2 onto the polymers were effectively desorbed at room temperature, illustrating the potential application of such polymers for repeated adsorption/desorption of CO2. The CO2 adsorption capacities of these polymers were dependent upon their nitrogen content, specific surface area, and pore size. The available nitrogen atoms for binding to the carbon of CO2 via tetrel bonds also plays an important role in the capture of this gas. Minimal and much lower CO2 adsorption was also noted with two crystalline polymers, compared to the five amorphous counterparts. Intermolecular hydrogen bonding and π-π interaction effectively prevented the polymer N sites of the crystalline polymers from interacting with polarized CO2 molecules.

Carboxylic acid decorated self-assembled monolayer films: new acid synthesis chemistry and reaction chemistry including bridged diacyl peroxide preparation.

Interfacial chemical transformations are an important way to control the physical and chemical properties of surfaces. Organic molecules that self-assemble into monolayers are a proven, effective tool for surface modification, and the ability to do controlled chemical transformations on the exposed surface of the self-assembled monolayer (SAM) adds significant diversity to this capability. Given the importance of carboxylic acid groups in applications ranging from controlling surface ionization to anchoring biological molecules, we have studied alternative ways to install acid groups on a surface and have probed the factors that control their chemistry. The work reported herein describes a new way to install carboxylic acid groups on surfaces and explores the intermolecular chemistry between acid groups on adjacent monolayer-forming molecules both on flat interfaces and on nanoparticles. It addresses the interplay of molecular flexibility and chain packing in controlling processes that bridge neighboring molecules. Finally, the creation of bridged diacyl peroxides from neighboring acid groups provides useful surface bound polymerization initiators that can effectively and conformally cover both flat surfaces and particles with ultrathin polymer films.

Controlled formation of thiol and disulfide interfaces.

The work reported herein describes the controlled creation of uniform thiol-functionalized siloxane-anchored self-assembled monolayers (SAMs) and their selective transformation into intramonolayer (bridging) disulfides. These disulfides provide for the efficient immobilization of (bio)molecules bearing pendant thiols or disulfides, with no need for added oxidant. The unambiguous development of this surface chemistry required analytical methods that distinguish thiol and disulfide moieties on a surface. Physical properties such as wetting and monolayer thickness do not suffice nor do routine spectroscopic techniques (e.g., XPS, IR). Therefore, a method for distinguishing and quantifying thiol and disulfide surface functionality on a monolayer array based on the reaction with 2,4-dinitrofluorobenzene (DNFB, Sanger's reagent) is reported. DNFB readily reacts with thiol-SAMs (but not with disulfides) to form stable derivatives with distinctive IR, UV, and XPS signatures. Finally, the thiol-disulfide chemistry is applied to thiol-functionalized hybrid silica nanoparticles. These high-surface-area nanoparticles provide solid supports heavily loaded with thiol groups whose chemistry is also reported herein.

Fabrication and Characterization of Hydrogen Peroxide and Thymol-Loaded PVA/PVP Hydrogel Coatings as a Novel Anti-Mold Surface for Hay Protection.

Animal food source production is increasing due to the growing world population. Many sources (e.g., hay) are prone to mold development, resulting in food degradation. This study proposes an environmentally friendly anti-mold fungicide comprising hydrogen peroxide (HP) and thymol entrapped in a polyvinyl alcohol/pyrrolidone (PVA/PVP) hydrogel (PVA is biodegradable and PVP is water soluble and non-toxic) coated on a polyethylene (PE) films for preservative hay packaging. The hydrogels improved the thermal stability of the entrapped HP and thymol, resulting in a prolonged release into the hay and thereby increasing anti-mold activity. The hydrogel composition and morphology, thymol and HP thermal stability, and release rates through indirect (gas phase) contact were investigated. Fungicidal capabilities were tested, indicating wide-range efficiency against mold growth on hay with a clear advantage for the thymol-loaded hydrogels. No visual side effects were observed on hay exposed to the released fumes of HP and/or thymol. These results demonstrate the potential of thymol-loaded hydrogels as effective and safe post-harvest preservatives.

Ultra Short Heart Rate Variability Predicts Clinical Outcomes in Patients with a Clinical Presentation Consistent with Myocarditis: A Derivation Cohort Analysis.

Myocarditis prognosis varies substantially, hence identification of novel prognostic factors is crucial. The prognostic role of ultra-short heart-rate variability (HRV) in myocarditis remains unknown. In a retrospective study, adult patients admitted to a tertiary hospital due to clinically suspected myocarditis were included. Clinical, laboratory and HRV parameters were assessed as predictors of severe short term complications (heart failure (HF), dilated cardiomyopathy­DCM, ventricular arrhythmia­VA and death), utilizing logistic regression (LR). Accuracy was evaluated with receiver operating characteristic (ROC) curve area under the curve (AUC). HRV indices included standard deviation of normal beat intervals (SDNN) and root mean square of successive differences (RMSSD). 115 patients, aged 34 (±13) years old, were examined. Six patients (5%) developed severe HFrEF. RMSSD was included in a multivariate LR model (RMSSD < 10.72 ms adjusted odds ratio (AOR) 14.056, p-value 0.024). Model classification accuracy was very good, with an AUC of 86%. Eight patients (7%) developed DCM. RMSSD < 10.72 ms was included in a multivariate classification model (AOR 8.826, p-value 0.013); model classification AUC of 82%. HRV did not predict development of VA or death. SDNN and especially RMSSD may be prognostic indicators in myocarditis.

Three dimension optical imaging in a high throughput layered expression system.

Layered peptide array (LPA) system enables multiplex screening of biomarkers [1-3]. One of the main problems of the LPA system is the screening of the layered-membranes stack. Nowadays, each membrane is imaged separately using conventional fluorescent imaging. This process is time consuming and requires extensive manual interaction. This paper describes a general solution for optical imaging of a layered grid medium using photogrammetric methods. The suggested method enables visualization of the LPA membranes stack by using only two images of the stack. This study is a proof of concept of the suggested solution using MATLAB simulation and phantom experiments.

Amino acid-based ionic liquids as precursors for the synthesis of chiral nanoporous carbons.

The synthesis of chiral nanoporous carbons based on chiral ionic liquids (CILs) of amino acids as precursors is described. Such unique precursors for the carbonization of CILs yield chiral carbonaceous materials with high surface area (≈620 m2 g-1). The enantioselectivities of the porous carbons are examined by advanced techniques such as selective adsorption of enantiomers using cyclic voltammetry, isothermal titration calorimetry, and mass spectrometry. These techniques demonstrate the chiral nature and high enantioselectivity of the chiral carbon materials. Overall, we believe that the novel approach presented here can contribute significantly to the development of new chiral carbon materials that will find important applications in chiral chemistry, such as in chiral catalysis and separation and in chiral sensors. From a scientific point of view, the approach and results reported here can significantly deepen our understanding of chirality at the nanoscale and of the structure and nature of chiral nonporous materials and surfaces.