Thermodynamical properties of the relativistic quantum scalar plasma

The thermodynamical properties of the relativistic quantum scalar plasma (i.e. a system of spin one-half baryons interacting through a scalar field) are studied in the Hartree approximation.     

Effects of an admixture and fast neutron irradiation on thermal properties of sodium potassium sulphate crystals

The differential thermal analysis curves and the specific heat at constant pressure,C _p, of pure and Cu²⁺-doped sodium potassium sulphate crystals were studied. Different neutron fluences were used up to 2.6×10¹⁰ n/cm², in the temperature range 300–500 K. Impurity incorporation generally increased the specific heat up to a maximum at 5% Cu²⁺ content. The peaks for the doped crystals were shifted to lower temperature as a result of neutron irradiation. This behaviour is discussed on the basis of defects induced by irradiation.

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Zusammenfassung Es wurden die DTA-Kurven und die spezifische Wärme bei konstantem DruckC _p von reinen, mit Cu²⁺ versetzten Natriumkaliumsulfatkristallen untersucht. Im Temperaturbereich 300–500 K wurden verschiedene Neutronenströme bis zu 2,6×10¹⁰ n/cm² verwendet. Der Einbau von Verunreinigungen erhöht im allgemeinen die spezifische Wärme bis zu einem Maximum bei einem Cu²⁺ Gehalt von 5%. Im Ergebnis der Neutronenbestrahlung verschieben sich die Peaks für die versetzten Kristalle in Richtung niedrigerer Temperaturen. Dieses Verhalten wird auf der Basis strahlungsinduzierter Defekte besprochen.

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_p . 300–500 2,6 · 10¹⁰ n/². 5%. , . , .

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It is a great pleasure for us to express our deepest gratitude to Prof. Dr. Younis S. Selim for his guidance throughout this work and for providing the irradiation facilities.     

Fonctions holomorphes bornees sur la boule unite deC n

Sans résumé     

Biaryl scaffold-focused virtual screening for anti-aggregatory and neuroprotective effects in Alzheimer’s disease

Background

Alzheimer’s disease (AD) is a primary cause of dementia in ageing population affecting more than 35 million people around the globe. It is a chronic neurodegenerative disease caused by defected folding and aggregation of amyloid beta (Aβ) protein. Aβ is formed by the cleavage of membrane embedded amyloid precursor protein (APP) by using enzyme ‘transmembrane aspartyl protease, β-secretase’. Inhibition of β-secretase is a viable strategy to prevent neurotoxicity in AD. Another strategy in the treatment of AD is inhibition of acetylcholinesterase. This inhibition reduces the degradation of acetylcholine and temporarily restores the cholinergic function of neurons and improves cognitive function. Monoamine oxidase and higher glutamate levels are also found to be linked with Aβ peptide related oxidative stress. Oxidative stress leads to reduced activity of glutamate synthase resulting in significantly higher level of glutamate in brain. The aim of this study is to perform in silico screening of a virtual library of biaryl scaffold containing compounds potentially used for the treatment of AD. Screening was done against the primary targets of AD therapeutics, acetylcholinesterase, β-secretase (BACE1), Monoamine oxidases (MAO) and N-Methyl-D-aspartate (NMDA) receptor. Compounds were screened for their inhibitory potential by employing molecular docking approach using AutoDock vina. Binding energy scores were embodied in the heatmap to display varies strengths of interactions of the ligands targeting AD.

Results

Several ligands showed notable interaction with at least two targets, but the strong interaction with all the targets is shown by very few ligands. The pharmacokinetics of the interacting ligands was also predicted. The interacting ligands have good drug-likeness and brain availability essential for drugs with intracranial targets.

Conclusion

These results suggest that biaryl scaffold may be pliable to drug development for neuroprotection in AD and that the synthesis of further analogues to optimize these properties should be considered.

     

Complexation of Pu(IV) with the natural siderophore desferrioxamine B and the redox properties of Pu(IV)(siderophore) complexes

The bioavailability and mobility of Pu species can be profoundly affected by siderophores and other oxygen-rich organic ligands. Pu(IV)(siderophore) complexes are generally soluble and may constitute with other soluble organo-Pu(IV) complexes the main fraction of soluble Pu(IV) in the environment. In order to understand the impact of siderophores on the behavior of Pu species, it is important to characterize the formation and redox behavior of Pu(siderophore) complexes. In this work, desferrioxamine B (DFO-B) was investigated for its capacity to bind Pu(IV) as a model siderophore and the properties of the complexes formed were characterized by optical spectroscopy measurements. In a 1:1 Pu(IV)/DFO-B ratio, the complexes Pu(IV)(H2DFO-B)4+, Pu(IV)(H1DFO-B)3+, Pu(IV)(DFO-B)2+, and Pu(IV)(DFO-B)(OH)+ form with corresponding thermodynamic stability constants log beta1,1,2 = 35.48, log beta1,1,1 = 34.87, log beta1,1,0 = 33.98, and log beta1,1,-1 = 27.33, respectively. In the presence of excess DFO-B, the complex Pu(IV)H2(DFO-B)22+ forms with the formation constant log beta2,1,2 = 62.30. The redox potential of the complex Pu(IV)H2(DFO-B)22+ was determined by cyclic voltammetry to be E1/2 = -0.509 V, and the redox potential of the complex Pu(IV)(DFO-B)2+ was estimated to be E1/2 = -0.269 V. The redox properties of Pu(IV)(DFO-B)2+ complexes indicate that Pu(III)(siderophore) complexes are more than 20 orders of magnitude less stable than their Pu(IV) analogues. This indicates that under reducing conditions, stable Pu(siderophore) complexes are unlikely to persist.     

A new micropatterning method of soft substrates reveals that different tumorigenic signals can promote or reduce cell contraction levels

In tissues, cell microenvironment geometry and mechanics strongly impact on cell physiology. Surface micropatterning allows the control of geometry while deformable substrates of tunable stiffness are well suited for the control of the mechanics. We developed a new method to micropattern extracellular matrix proteins on poly-acrylamide gels in order to simultaneously control cell geometry and mechanics. Microenvironment geometry and mechanics impinge on cell functions by regulating the development of intra-cellular forces. We measured these forces in micropatterned cells. Micropattern geometry was streamlined to orient forces and place cells in comparable conditions. Thereby force measurement method could be simplified and applied to large-scale experiment on chip. We applied this method to mammary epithelial cells with traction force measurements in various conditions to mimic tumoral transformation. We found that, contrary to the current view, all transformation phenotypes were not always associated to an increased level of cell contractility.     

Modelling carbon dioxide molecule interacting with aquaglyceroporin and aquaporin-1 channels

Aquaporin (AQP) is a family of membrane proteins that enable water and small individual molecules to permeate cell membranes. Examples of these protein channels are aquaglyceroporin and aquaporin-1 (AQP1). Here, we investigate the permeability of carbon dioxide $(\hbox {CO}_2)$ ( CO 2 ) through both aquglyceroporin and AQP1 channels and explain their selectivity mechanisms. We provide a mathematical model which determines the molecular interaction potential between carbon dioxide molecule and an AQP channel. We evaluate this interaction using two approaches, namely discrete-continuum and completed discrete approaches. Both calculations agree well and our results indicate the acceptance of $(\hbox {CO}_2)$ ( CO 2 ) molecule into these channels which is in good agreement with other recent studies.     

Reliability of a consecutive (r, s)-out-of-(m, n):F lattice system with conditions on the number of failed components in the system

A consecutive(r, s)-out-of-(m, n):F lattice system which is defined as a two-dimensional version of a consecutive k-out-of-n:F system is used as a reliability evaluation model for a sensor system, an X-ray diagnostic system, a pattern search system, etc. This system consists of m × n components arranged like an (m, n) matrix and fails iff the system has an (r, s) submatrix that contains all failed components. In this paper we deal a combined model of a k-out-of-mn:F and a consecutive (r, s)-out-of-(m, n):F lattice system. Namely, the system has one more condition of system down, that is the total number of failed components, in addition to that of a consecutive (r, s)-out-of-(m, n):F lattice system. We present a method to obtain reliability of the system. The proposed method obtains the reliability by using a combinatorial equation that does not depend on the system size. Some numerical examples are presented to show the relationship between component reliability and system reliability.