The solubility of Ca(OH)<Subscript>2</Subscript> in extremely concentrated NaOH solutions at 25°C

The solubility of Ca(OH)₂ in aqueous NaOH solutions up to 12.50 M at 25°C has been determined. The solubility data obtained for NaOH concentrations lower than 3 M was compared with those published in the literature. The solubility of Ca(OH)₂ steadily decreases with the increasing NaOH concentration. The solubility data obtained at a constant ionic strength (I = 1 M Na(Cl,OH)) enabled the determination of the conditional solubility product of Ca(OH)₂(s) (lgL_Ca(OH)2 = − 4.10 ± 0.02). Formation of the hydroxo complex CaOH⁺(aq) was invoked to describe the variation of [Ca²⁺]_T with [OH⁻]_T. Its conditional stability constant was found to be lgK_CaOH+ = 0.97 ± 0.02. The experimental protocol employed was proven to be suitable for accurate solubility determinations in rapidly equilibrating systems comprising of highly concentrated, alkaline solutions and containing analytes in the ppm range.      

Structure-based design of supercharged, highly thermoresistant antibodies

Mutation of surface residues to charged amino acids increases resistance to aggregation and can enable reversible unfolding. We have developed a protocol using the Rosetta computational design package that "supercharges" proteins while considering the energetic implications of each mutation. Using?a homology model, a single-chain variable fragment antibody was designed that has a markedly enhanced resistance to thermal inactivation and displays an unanticipated ≈30-fold improvement in affinity. Such supercharged antibodies should prove useful for assays in resource-limited settings and for developing reagents with improved shelf lives.     

Universal flow-driven conical emission in ultrarelativistic heavy-ion collisions

The double-peak structure observed in soft-hard hadron correlations is commonly interpreted as a signature for a Mach cone generated by a supersonic jet interacting with the hot and dense medium created in ultrarelativistic heavy-ion collisions. We show that it can also arise due to averaging over many jet events in a transversally expanding background. We find that the jet-induced away-side yield does not depend on the details of the energy-momentum deposition in the plasma, the jet velocity, or the system size. Our claim can be experimentally tested by comparing soft-hard correlations induced by heavy-flavor jets with those generated by light-flavor jets.     

Properties of Sizeable [n]Cycloparaphenylenes as Molecular Models of Single‐Wall Carbon Nanotubes Elucidated by Raman Spectroscopy: Structural and Electron‐Transfer Responses under Mechanical Stress

[n]Cycloparaphenylenes behave as molecular templates of “perfectly chemically defined” single‐wall carbon nanotubes. These [n]CPP molecules have electronic, mechanical, and chemical properties in size correspondence with their giant congeners. Under mechanical stress, they form charge‐transfer salts, or complexes with fullerene, by one‐electron concave–convex electron transfer.     

Charge shift bonding concept in radical π-dimers

We show that pancake bonding in radical π-dimers display features of charge shift (CS) bonding. While the CS bonding concept has been developed to interpret the unusual aspects of σ-bonds around centers with a large number of lone pairs, such as F(2) and HOOH, we find a similar role played by the nonbonding or slightly bonding π-electron pairs in π-stacking radical dimers. Arguments and computational evidence indicate that the CS bonding concept developed by Shaik and Hiberty et al. captures essential features of the intermolecular bonding in radical π-dimers in which the overlap of the two radical centered singly occupied molecular orbitals (SOMOs) play a crucial role. By using the tetracyanoethylene anion dimer, [TCNE](2)(2-), as a model, we show that compared to CAS(2,2) calculations, significant binding contributions are recovered in the calculations simply by including selected intrapair excitations of the SOMO-SOMO bonding orbitals and the nonbonding π-orbitals. This observation is the basis for the analogy of chemical bonding between pancake bonded radical π-dimers and other charge shift bonded molecules, such as F(2). By extending the CS bonding concept to a new class of molecules, we find a novel application of the lone pair bond weakening effect (LPBWE) in which the doubly occupied π-orbitals play the role of lone pairs.     

Exvivo ultrasound attenuation coefficient for human cervical and uterine tissue from 5 to 10 MHz

Attenuation estimation and imaging in the cervix has been utilized to evaluate the onset of cervical ripening during pregnancy. This feature has also been utilized for the acoustic characterization of leiomyomas and myometrial tissue. In this paper, we present direct narrowband substitution measurement values of the variation in the ultrasonic attenuation coefficient in ex vivo human uterine and cervical tissue, in the 5-10 MHz frequency range. At 5 MHz, the attenuation coefficient values are similar for the different orientations of uterine tissue with values of 4.1-4.2 dB/cm, 5.1 dB/cm for the leiomyoma, and 6.3 dB/cm for the cervix. As the frequency increases, the attenuation coefficient values increase and are also spread out, with a value of approximately 12.6 dB/cm for the uterus (both parallel and perpendicular), 16.0 for the leiomyoma, and 26.8 dB/cm for the cervix at 10 MHz. The attenuation coefficient measured increases monotonically over the frequency range measured following a power law.     

How to remove barriers to medicines trade in emerging economies: the role of medicines regulatory authority in Serbia

The primary role of European pharmaceutical legislation is to safeguard public health while encouraging the development of the pharmaceutical industry, creation of single market for pharmaceuticals with removed barriers to medicines trade. This article presents some important characteristics of pharmaceutical legislation in Serbia, the potential EU candidate country, and the latest improvements of existing national pharmaceutical legislation. Additional explanation is given for the Serbian negotiations with World Trade Organization and measures taken for the harmonisation with Agreements on Technical barriers to Trade (TBT), especially with Agreement on Trade-Related Intellectual Property Rights. Current status of Serbian pharmaceutical market is described, with the highlight of domestic manufacturers??capacity to comply with European Union requirements. National medicines agency is described in the framework of European medicines quality infrastructure. The role and responsibility of national medicines authority to assure access to quality, safe and efficacious medicines on Serbian market is described. The special emphasis is given to agency’s role in harmonisation process, in terms of removing unnecessary barriers to medicines trade in Serbia.     

Dextran‐Based Self‐Healing Hydrogels Formed by Reversible Diels–Alder Reaction under Physiological Conditions

A dextran‐based self‐healing hydrogel is prepared by reversible Diels–Alder reaction under physiological conditions. Cytocompatible fulvene‐modified dextran as main polymer chains and dichloromaleic‐acid‐modified poly(ethylene glycol) as cross‐linkers are used. Both macro‐ and microscopic observation as well as the rheological recovery test confirm the self‐healing property of the dextran‐l‐poly(ethylene glycol) hydrogels (“l” means “linked‐by”). In addition, scanning electrochemical microscopy is used to qualitatively and quantitatively in situ track the self‐healing process of the hydrogel for the first time. It is found that the longitudinal depth of scratch on hydrogel surface almost completely healed at 37 °C after 7 h. This work represents a facile approach for fabrication of polysaccharide self‐healing hydrogel, which can be potentially used in several biomedical fields.