EMD273316 & EMD95833, type 4 phosphodiesterase inhibitors, stimulate fibroblastic-colony formation by bone marrow cells via direct inhibition of PDE4 and the induction of endogenous prostaglandin synthesis

BACKGROUND: Type 4 phosphodiesterase (PDE4) inhibitors have been shown to stimulate bone formation in vivo and to stimulate osteoblastic differentiation in vitro. As one possible mechanism for the stimulation of bone formation is the recruitment of osteoprogenitor cells from the bone marrow, we have investigated the effect of the PDE4 inhibitors EMD273316, EMD95833, EMD249615 and EMD 219906 on fibroblastic colony formation by whole bone marrow cells and on the ability of these colonies to adopt an osteoblastic phenotype. RESULTS: All four agents stimulated colony formation in a concentration dependent manner, however, in the case of EMD273316 & EMD95833, the effect was evident at lower concentrations and the addition of prostaglandin E2 (PGE2) was not necessary for maximal stimulation. It was subsequently found that co-incubation with indomethacin reduced the stimulatory effects of EMD273316 & EMD95833 but had no effect on the actions of EMD249615 and EMD 219906 and that EMD273316 & EMD95833 stimulated the synthesis of endogenous PGE2 by whole bone marrow cells whereas EMD249615 and EMD 219906 had no significant effect. CONCLUSIONS: These data suggest that EMD249615, EMD 219906, EMD273316 & EMD95833 can promote the recruitment of bone marrow osteoprogenitor cells leading to a stimulation of bone formation via their direct inhibitory effects on PDE4. The actions of EMD273316 & EMD95833 however, are augmented by their ability to stimulate endogenous prostanoids synthesis which acts synergistically with their direct effects on PDE4

The Rotationally-Resolved Absorption Spectrum of Formaldehyde from 6547 to 7051 cm−1

We report new experimental data on the rotationally resolved room temperature absorption spectrum of CH2O in the near infrared (NIR) region between 6804 and 7051 cm–1 (1470–1418 nm). Data have been obtained by cavity enhanced absorption spectroscopy and complement the spectrum in the wavelength range 6547–6804 cm–1, obtained using virtually the same experimental set-up and already published in an earlier publication (Staak et al., J. Mol. Spectrosc. 229 (2005) 115–121). Several vibrational combination bands occur in this region and give rise to a congested spectrum and over 4500 lines with cross- sections over 5 · 10–23 cm2 were observed. Recent experimental studies using NIR absorption spectroscopy for quantifying CH2O in different chemical systems indicate that the absorption cross-sections obtained by Staak et al. may have been overestimated. The results of these experiments are reviewed here and a recommendation for absolute absorption cross sections of CH2O in the NIR range will be given. Absolute absorption cross-sections stated here are corrected by the recommended factor

Reactivity of 3-hydroxy-3-methyl-2-butanone: Photolysis and \OH\ reaction kinetics

International audienceHydroxycarbonyl compounds are important secondary reaction products in the oxidation of Volatile Organic Compounds (VOCs) in the atmosphere. The atmospheric fate of these oxygenated \VOCs\ is however poorly understood, especially the relevance of the photolytic pathway. In this work, a combined investigation of the photolysis and temperature-dependent \OH\ radical reaction of 3-hydroxy-3-methyl-2-butanone (3H3M2B) is presented. A photolysis lifetime of about 4-5 days was estimated with a global quantum yield of 0.10. The \OH\ reaction rate coefficient follows the Arrhenius trend (298-356 K) and could be modelled through the following expression: k3H3M2B(T) = (5.12 ± 0.07) × 10−12 exp(−563 ± 119/T) in cm3 molecule−1 s−1. A 3H3M2B atmospheric lifetime of 15 days towards the \OH\ radical was evaluated. Our results showed that the photolysis pathway is the major degradation channel for 3H3M2B. Photolysis products were identified and quantified in the present work with a carbon balance of around 80% enabling a reaction mechanism to be proposed. The present work underlines the need for further studies on the atmospheric chemistry of oxygenated VOCs

Social Class

Discussion of class structure in fifth-century Athens, historical constitution of theater audiences, and the changes in the comic representation of class antagonism from Aristophanes to Menander

Impact of system factors on the water saving efficiency of household grey water recycling

Copyright © 2010 Taylor & Francis. This is an Author's Accepted Manuscript of an article published in Desalination and Water Treatment Volume 24, Issue 1-3 (2010), available online at: http://www.tandfonline.com/10.5004/dwt.2010.1542A general concern when considering the implementation of domestic grey water recycling is to understand the impacts of system factors on water saving efficiency. Key factors include household occupancy, storage volumes, treatment capacity and operating mode. Earlier investigations of the impacts of these key factors were based on a one-tank system only. This paper presents the results of an investigation into the effect of these factors on the performance of a more realistic ‘two tank’ system with treatment using an object based household water cycle model. A Monte-Carlo simulation technique was adopted to generate domestic water appliance usage data which allows long-term prediction of the system's performance to be made. Model results reveal the constraints of treatment capacity, storage tank sizes and operating mode on percentage of potable water saved. A treatment capacity threshold has been discovered at which water saving efficiency is maximised for a given pair of grey and treated grey water tank. Results from the analysis suggest that the previous one-tank model significantly underestimates the tank volumes required for a given target water saving efficiency

Investigation on vanadium chemistry in basic-oxygen-furnace (BOF) slags: a first approach

Basic oxygen furnace (BOF) slag accounts for the majority of all residual materials produced during steelmaking and may typically contain certain transition metals. Vanadium, in particular, came into focus in recent years because of its potential environmental toxicity as well as its economic value. This study addresses the vanadium chemistry in BOF slags to better understand its recovery and save handling of the waste stream. The experimental results from the electron probe microanalysis (EPMA) study show that vanadium is preferably incorporated in calcium orthosilicate-like compounds (COS), with two variations occurring, a low vanadium COS (COS-Si) (approx. 1 wt.%), and a high vanadium COS (COS-V) (up to 18 wt.%). Additionally, vanadium is incorporated in dicalcium ferrite-like compounds (DFS) with an average amount of 3 wt.%. Using powder x-ray diffraction analysis (PXRD), EPMA, and virtual component models, stoichiometric formulas of the main vanadium-bearing phases were postulated. The stoichiometries give an estimate of the oxidation states of vanadium in the respective hosts. According to these results, trivalent vanadium is incorporated on the Fe-position in dicalcium ferrite solid solution (DFS), and V4+ and V5+ are incorporated on the Si-position of the COS

The Thermo-Oxidative Degradation of Polyurethane Open-Cell Soft Foam Investigated Through Gas Chromatography and Mass Spectrometry of Volatile Organic Compounds

Polyurethane (PUR) soft foams release malodorous and potentially toxic compounds when exposed to oxidative conditions. Current chamber test methods cannot distinguish between pre-existing volatiles and those formed during oxidation, nor can they assess the formation rates of oxidation products. We subjected PUR soft foam to oxidative treatment in a continuous air flow at 120 ◦C. Emissions were convectively transferred from the foam to an exhaust port and analyzed using a thermodesorption–gas chromatography–mass spectrometry (TD-GC-MS) system, with external calibration employed for the quantification of selected analytes. The study identified hydroperoxide formation and degradation as key mechanisms in the breakdown of the polyether soft segments. This process predominantly produces volatiles, such as carboxylic acids, formates, acetates, alpha-hydroxy-ketones, (unsaturated) aldehydes, substituted dioxolanes and dioxanes, glycols, and allyl ethers. Volatiles associated with the degradation of the hard segments include aniline, benzoxazole, 2-methylbenzoxazole, and benzaldehyde. This experimental setup enables reproducible qualitative and quantitative analysis of volatiles formed during the oxidative degradation of PUR soft foams, providing new insights into the segment-dependent chemical pathways of the polymer’s molecular breakdown

The role of fire and mechanical clearing in the management of Chromolaena odorata.

Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg, 2006.The effects of fire and mechanical clearing were investigated for their potential in assisting with the eradication of Chromolaena odorata (previously Eupatorium odoratum). The study was divided into two focus areas, the first focused on mechanical clearing of dense stands of C. odorata on three sites and the second focused on the long term influences of a single burn on C. odorata plants in the different size categories. For mechanical clearing, two key issues were investigated; namely whether this type of clearing procedure was effective in dense C. odorata stands and whether rehabilitation was necessary in these cleared areas. The study was conducted from July 2002 to June 2004. The area was subject to a severe drought throughout the duration of the study. The severe drought had a large influence on the result in both focus areas. A bulldozer was found to be a very effective at clearing dense C. odorata stands. Results from the mechanical clearing study showed that there was still a large viable grass seed population in the areas that had been covered by a dense stand of C. odorata plants for over three years. Thus, indigenous plants were able to re-colonize the area after removal of C. odorata without human intervention, even thought the area was experiencing a severe drought. The density of C. odorata seedlings emerging in the cleared areas was far lower than expected. The C. odorata density in the permanent plots, for seedlings that germinated in the first season after clearing (SeptemberOctober 2002), was only 0.25,0.03 and 0.72 per 5 m2 in the three sites respectively by the end of the study in June 2004. For the C. odorata seedlings that germinated in the second season (September-October 2003) the density was, 0.5, 0.56 and 1.06 per 5 m2 in the three sites respectively by the end of the study in June 2004. It was suspected that the drought influenced seed germination. Unfortunately the number of C. odorata seedlings was so low, that no significant relationship could be found between grass and C. odorata seedling density. By the end of the study the grass fuel mass in all the rehabilitated sites was already over 3000 kg ha-1, even though the area was experiencing a severe drought. This grass fuel load, when burnt, will assist land managers in controlling C. odorata plants, especially seedlings. Very few other alien invasive plant species emerged in the cleared areas. At the Mhlosinga site, Senna pendula made up less than one percent of the herbaceous species composition and only a single Ricinus communis plant was recorded. No alien plant species were recorded on the other two sites. Results from the burning trials revealed that plants in all the size categories were affected by fire. Greater fuel masses and fire intensities were required to kill larger C. odorata plants relative to smaller ones. Fire was found to be very effective at eliminating small and medium size C. odorata plants. Fire applied as a once off treatment had a significant long-term effect on the C. odorata population. The following fuel loads were required to achieve 80% mortality in this 11 study: for small plants a fuel load of over 4000 kg ha-I, for medium plants a fuel load over 4200 kg ha-I and for large plants a fuel load over 4600 kg ha-I. Little difference could be detected between a head or a back burn, as both fire types had their own advantages and disadvantages. Although some of the C. odorata plants in the burnt plots had not perished by the time of the first investigation, following the burn (February 2003), by the time of the second investigation (June 2004), many of these plants had eventually succumbed. These results highlighted the fact that plants which are damaged by fire were more likely to persish during an extended droughts period, than plants which were not subjected to fire. Results from the control plots, in the burning trials, for medium and large plants showed dramatic increases in density over time. Tagged individuals from the control plots did reveal that some of the medium and large plants did die during the drought, although the amount was negligible when compared to the number of new plants growing into the new size categories. A large proportion of the small plants in the control plots also survived the drought with many of them even growing into the medium category. The difference between the control plots and the burnt plots was obvious and significant, especially once the fuel mass exceeded 3783 kg ha-I. Results from this study show that fire can be used as a very effective tool in assisting land managers to control C. odorata in open savanna bushveld

Photolysis of CH3CHO at 248 nm: Evidence of triple fragmentation from primary quantum yield of CH3 and HCO radicals and H atoms

Radical quantum yields have been measured following the 248 nm photolysis of acetaldehyde, CH3CHO. HCO radical and H atom yields have been quantified by time resolved continuous wave Cavity Ring Down Spectroscopy in the near infrared following their conversion to HO2 radicals by reaction with O2. The CH3 radical yield has been determined using the same technique following their conversion into CH3O2. Absolute yields have been deduced for HCO radicals and H atoms through fitting of time resolved HO2 profiles, obtained under various O2 concentrations, to a complex model, while the CH3 yield has been determined relative to the CH3 yield from 248 nm photolysis of CH3I. Time resolved HO2 profiles under very low O 2 concentrations suggest that another unknown HO2 forming reaction path exists in this reaction system besides the conversion of HCO radicals and H atoms by reaction with O2. HO2 profiles can be well reproduced under a large range of experimental conditions with the following quantum yields: CH3CHO+hν248nm → CH 3CHO*, CH3CHO* → CH3+HCO φ1a = 0.125±0.03, CH3CHO* → CH 3+H+CO φ1e = 0.205±0.04, CH 3CHO* o2→ CH3CO+HO2 φ1f = 0.07±0.01. The CH3O2 quantum yield has been determined in separate experiments as φCH3 = 0.33 ± 0.03 and is in excellent agreement with the CH3 yields derived from the HO2 measurements considering that the triple fragmentation (R1e) is an important reaction path in the 248 nm photolysis of CH3CHO. From arithmetic considerations taking into account the HO2 and CH3 measurements we deduce a remaining quantum yield for the molecular pathway: CH3CHO* → CH 4+CO φ1b = 0.6. All experiments can be consistently explained with absence of the formerly considered pathway: CH 3CHO* → CH3CO+H φ1c = 0. © 2014 AIP Publishing LLC.Fil: Pranay Morajkar. University Of Lille.; FranciaFil: Bossolasco, Adriana Gabriela. University Of Lille.; Francia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Schoemaecker, Coralie. University Of Lille.; FranciaFil: Fittschen, Christa. University Of Lille.; Franci

Speciation of manganese in a synthetic recycling slag relevant for lithium recycling from lithium-ion batteries

Lithium aluminum oxide has previously been identified to be a suitable compound to recover lithium (Li) from Li-ion battery recycling slags. Its formation is hampered in the presence of high concentrations of manganese (9 wt.% MnO2). In this study, mock-up slags of the system Li2O-CaO-SiO2-Al2O3-MgO-MnOx with up to 17 mol% MnO2-content were prepared. The manganese (Mn)-bearing phases were characterized with inductively coupled plasma optical emission spectrometry (ICP-OES), X-ray diffraction (XRD), electron probe microanalysis (EPMA), and X-ray absorption near edge structure analysis (XANES). The XRD results confirm the decrease of LiAlO2 phases from Mn-poor slags (7 mol% MnO2) to Mn-rich slags (17 mol% MnO2). The Mn-rich grains are predominantly present as idiomorphic and relatively large (>50μm) crystals. XRD, EPMA and XANES suggest that manganese is present in the form of a spinel solid solution. The absence of light elements besides Li and O allowed to estimate the Li content in the Mn-rich grain, and to determine a generic stoichiometry of the spinel solid solution, i.e., (Li(2x)Mn2+(1−x))1+x(Al(2−z),Mn3+z)O4. The coefficients x and z were determined at several locations of the grain. It is shown that the aluminum concentration decreases, while the manganese concentration increases from the start (x: 0.27;z: 0.54) to the end (x: 0.34;z: 1.55) of the crystallization