Vasopressin for refractory persistent pulmonary hypertension of the newborn in preterm neonates - a case series.

OBJECTIVE: To describe the clinical outcomes following treatment with vasopressin for a sub-cohort of critically ill preterm neonates who have refractory persistent pulmonary hypertension of the newborn (PPHN). DESIGN: Case series. SETTING: Tertiary neonatal intensive care unit, Toronto, Canada. POPULATION: Neonates born <37 weeks gestational age (GA) who received vasopressin for refractory PPHN (lack of response to inhaled nitric oxide) over a 4-year period. MEASUREMENTS: Changes in physiological indices of cardio-pulmonary stability during vasopressin therapy were analyzed using one-way repeated measures ANOVA, compared to pretreatment values. Data regarding survival to discharge and neurodevelopmental outcomes at 18-24 months were described. MAIN RESULTS: Thirteen neonates with a mean GA of 31.4 ± 3.3 weeks were included. Vasopressin was initiated at 28.5 ± 4.5 h of age. Overall, oxygenation and hemodynamic variables improved significantly following vasopressin therapy (p < .05 at 24 h vs. pretreatment). Oxygenation failure resolved in 8 cases, of which 7 patients survived (6 without disability). Among the 5 cases where oxygenation failure persisted despite vasopressin, 4 died while one survived with disability. CONCLUSIONS: Vasopressin offers promise as a therapy for preterm neonates with refractory PPHN and hemodynamic instability, but prospective investigation is needed.

Microwave enhanced sorption of methylene blue dye onto bio-synthesized iron oxide nanoparticles: kinetics, isotherms, and thermodynamics studies.

To adequately address the grave human health risks and environmental damage caused by the uncontrolled utilization of organic dyes, we greenly synthesized iron oxide nanoparticles (IONPs) using Spirulina platensis micro-algae for sequestration of cationic methylene blue (MB) dye from an aqueous solution. The nano-engineered sorbent was thoroughly scrutinized by different spectral analyses of; FT-IR, SEM, EDX, BET surface area, TEM, VSM, UV/Vis spectroscopy, and PHPZC measurement. The adsorption of MB was methodically carried out in a batch process to investigate the effects of initial pH (2.2-10.4), adsorbent concentration (0.5-5.0 g L-1), initial dye concentration (10-1000 mg L-1), contact time (0-230 min), and adsorption temperature (298 K, 308 K, 318 K, and 328 K). The outlined results inferred that the maximum adsorption capacity of MB dye by IONPs (surface area of 134.003 m2/g, a total pore volume of 0.3715 cc/g, and average pore size of 5.54 nm) was 312.5 mg g-1 under the optimized pH value (i.e., pH = 10.4). Collectively, the adsorption kinetics profile showed that the experimental data were in good agreement with the PSORE model, and the equilibrium adsorption isotherm data were quantitatively dominated by the Langmuir model. The thermodynamic findings conformed to the endothermic nature of the adsorption process. Interestingly, the proposed microwave scenario enhanced the adsorption rate and the equilibrium was attained in a very short time (only 1 min), compared with the normal sorption conditions (∼70 min). Repeatability of the spent sorbent was successfully emphasized for 5 times of adsorption/desorption cycles using 0.5 M of HCl. The productive adsorbent admirably sequestered MB dye from spiked real specimens (>83%). These results demonstrated that IONPs can be considered as a cost-efficient adsorbent in practical applications such as wastewater purification.

Green synthesis of recyclable iron oxide nanoparticles using Spirulina platensis microalgae for adsorptive removal of cationic and anionic dyes.

Globally, organic dyes are major constituents in wastewater effluents due to their large-scale industrial applications. These persistent pollutants adversely impact the public health of different living entities. Thus, wastewater remediation has become an indispensable necessity. Herein, we greenly synthesized iron oxide nanoparticles (SP-IONPs) using Spirulina platensis microalgae to remove cationic crystal violet (CV) and anionic methyl orange (MO) dyes from their aqueous solution. The engineered sorbent was thoroughly scrutinized by different characterization techniques of FT-IR, BET surface area, SEM, EDX, TEM, VSM, UV/Vis spectroscopy, and pHPZC measurement. The proficiency of SP-IONPs was methodically appraised for its sorptive performance towards the target CV and MO dyes under variable technological parameters (batch scenario). Collectively, the outlined results inferred an amazing efficacy characterized to the SP-IONPs sorbent for the expulsion of relevant dyes from the aqueous media. Regarding the dynamic static sorption data, the kinetics profile was ascribed to the pseudo-second order model, whereas sorption isotherm was quantitatively dominated by the Langmuir theory with maximum sorption capacities of 256.4 mg g-1 and 270.2 mg g-1 for CV and MO, respectively. Thermodynamics findings conformed the endothermic nature of sorption process. Repeatability of the spent sorbent was successfully emphasized for 5 times of sorption/desorption cycles. The productive sorbent admirably sequestered CV and MO dyes from  spiked tap water. The potency of SP-IONPs as color collecting material from real dyeing effluents was achieved.

Origin of the enhanced photocatalytic activity of (Ni, Se, and B) mono- and co-doped anatase TiO2 materials under visible light: a hybrid DFT study.

The characteristic properties of TiO2 (anatase) make doping necessary to enhance its photocatalytic activity. Herein, a density functional theory (DFT) study using the Heyd-Scuseria-Ernzerhof (HSE) hybrid functional was performed to precisely investigate the effect of mono- and co-doping (Ni, Se and B) on the structural, electronic and optical properties of anatase TiO2. Notably, the origin of the enhanced photocatalytic activity of the modified systems was determined. The response to visible light was enhanced for all the mono- and co-doped materials except for Bint, and the highest absorption coefficient was observed for Se4+ mono-doping and Se/Bint+sub and Ni/Bsub co-doping. The decrease in bandgap is associated with a red shift in the absorption edges with the smallest bandgap calculated for Ni/Bsub (2.49 eV). Additionally, the Ni, Se4+ and Se2- mono-doped systems and Ni/Se4+ co-doped systems are proposed as promising photocatalysts for water splitting applications and further experimental validation. Moreover, the Ni/Bint+sub and Se/Bint+sub co-doped materials can also be valuable photocatalysts for other energy applications due to their enhanced visible light activity and the prolonged lifetime of their produced charge carriers.

Stability studies of double-base propellants with centralite and malonanilide stabilizers using MO calculations in comparison to thermal studies.

Propellants containing nitrate esters need stabilizers to avoid early decomposition or even explosion during storage. Newly prepared malonanilides M1-M5 were tested in stabilizing double-base propellants (DBPs). Their stabilization was compared with the effect of classical stabilizer N,N'-diethyldiphenyl urea (C1) using both practical thermal stability tests (qualitative and quantitative tests) and theoretical molecular orbital calculations. This research shows that the new stabilizers (malonanilides) have good stabilizing effects. Some of malonanilides e.g. (M5) and (M2) have higher stability effects. Different mechanisms were suggested to explain the role of different stabilizers. Molecular orbital calculations using the semi-empirical program AM1 are performed on the new and classical stabilizers. Correlation was made between the volume (ml) of NO(x), weight loss (wt%), other thermal analyses data, calculated thermodynamic parameters like activation energy (E(a), kJ mol(-1)) of the decomposed propellant samples containing different stabilizers and some of their calculated properties such as HOMO, LUMO energies, the charge distribution and the pi-bond order. The stabilization effect decreases with the increase in HOMO energy. The correlation between the net charge and parameters measured for the stabilization effect shows good accordance. Comparison of the results obtained show that the high electron charge on N atom of the stabilizers and on its benzene ring is the most important factor, but not the only factor governing the stabilization effect of the stabilizers.

The electronic absorption spectra of some acyl azides molecular orbital treatment.

The electronic absorption spectra of benzoyl azide and its derivatives: p-methyl, p-methoxy, p-chloro and p-nitrobenzoyl azide were investigated in different solvents. The observed spectra differ basically from the electronic spectra of aryl azides or alkyl azides. Four intense pi-pi* transitions were observed in the accessible UV region of the spectrum of each of the studied compounds. The contribution of charge transfer configurations to the observed transitions is rather weak. Shift of band maximum with solvent polarity is minute. On the other hand, band intensity is highly dependent on the solvent used. The observed transitions are delocalized rather than localized ones as in the case with aryl and alkyl azides. The attachment of the CO group to the azide group in acyl azides has a significant effect on the electronic structure of the molecule. The arrangements as well as energies of the molecular orbitals are different in acyl azides from those in aryl azides. The first electronic transition in phenyl azide is at 276 nm, whereas that of bezoyle azide is at 251 nm. Ab initio molecular orbital calculations using both RHF/6-311G* and B3LYP/6-31+G* levels were carried out on the ground states of the studied compounds. The wave functions of the excited states were calculated using the CIS and the AM1-CI procedures.