SOAP: solutions to often asked problems. Choice of antihistamines for urticaria.
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Carboxylate-bridged chain complexes of Co(II) (the diaquacobalt(II) mono- and ,-dialkanoates) form two homologous series of layered compounds which have been fully characterised both structurally and magnetically. The crystal structures of two selected members, [Co[CH3(CH2)10COO]2(H2O)2] and [Co[CH3(CH2)18COO]2(H2O)2], have been solved by X-ray powder diffraction and selected-area electron diffraction methods, and refined by the Rietveld technique. Crystal data: monoclinic, P 2(1)/a; a=9.688(1), b=7.5495(9), c=37.281(5) A, =96.70(3) primary, Z=4; and monoclinic, P 2(1)/a; a=9.7260(7), b=7.5477(7), c=57.53(1) A, =94.66(4) primary, Z=4, respectively. Their isomorphous structures contain layers of octahedral diaquacobalt(II) ions bonded to two chemically inequivalent alkanoates, one chelating and one bridging two Co atoms about 6.3 A apart, thus confirming the rare anti-anti conformation mode of the -RCOO groups recently proposed for diaquacobalt(II) ,-dodecanedioate. Extensive magnetic characterisation allowed estimation of the feeble antiferromagnetic coupling, which is weaker in the mono- than in the dialkanoate series.
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The electrophoretic mobilities of copper phthalocyanine particles, dispersed in isoparaffin solutions containing zirconium octanoate, have been determined using phase-analysis light scattering. All the samples studied contained trace concentrations of water. The mobility values were converted to zeta potentials using the Hückel equation. All the systems studied exhibited a pronounced maximum in zeta potential as the zirconium octanoate concentration increased. The maximum occurred at a bulk zirconium octanoate concentration equivalent to that required for complete coverage of the particles. The zeta potential data were converted to surface charge density values through the use of the Poisson-Boltzmann equation. The latter were in the range 0.4 to 2.5 µC m-2. A simple two equation site binding theory, which considered the dissociation of zirconium octanoate and the subsequent adsorption of ions at a generic surface site, was successfully applied to the surface charge data. It is proposed that the maximum in the zeta potential and surface charge as a function of zirconium octanoate concentration was observed due to the preferential location of ZrO2+ ions at the particle surface, followed by charge neutralization with octanoate anions. It is suggested that water facilitates the dissociation process of the zirconium octanoate, although it does not directly contribute to the surface charge itself. Two plausible qualitative mechanisms are described. The first involves the presence of water at the particle-solution interface, whilst the second considers the formation of micelles in the bulk isoparaffin phase. Copyright 1999 Academic Press.
The interfacial tensions of lauric and myristic acid sodium salt water solutions were measured at the air/water interface at 20 degrees C and at the air/0.01 M NaOH water solution interface at 20 degrees and 40 degrees C. On the basis of these results the dependence of standard free energy of adsorption (DeltaG(0)) on the interface coverage (Theta) was determined from the Blomgren-Bockris isotherm. According to these dependencies the interactions of adsorbed molecules were discussed and dielectric constants of the adsorbed monolayer were estimated. Copyright 1999 Academic Press.
The contact angle, θ, of a small bubble on a flat solid substrate was measured as a function of bubble radius, R. The observed deviation of the contact angle from 90 degrees can be accounted for in terms of a negative line tension, tau. The measured values of |tau|/gamma(f), where gamma(f) is the film tension, ranged between 0.15 and 0.6 mm and are proportional to the height, h, of the Plateau border, with |tau| congruent with1.7gamma(f)h. Copyright 2001 Academic Press.
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OBJECTIVE: To define the frequency and prognostic implications of SIRS criteria in critically ill patients hospitalized in European ICUs. DESIGN AND SETTING: Cohort, multicentre, observational study of 198 ICUs in 24 European countries. PATIENTS AND INTERVENTIONS: All 3,147 new adult admissions to participating ICUs between 1 and 15 May 2002 were included. Data were collected prospectively, with common SIRS criteria. RESULTS: During the ICU stay 93% of patients had at least two SIRS criteria [respiratory rate (82%), heart rate (80%)]. The frequency of having three or four SIRS criteria vs. two was higher in infected than non-infected patients (p < 0.01). In non-infected patients having more than two SIRS criteria was associated with a higher risk of subsequent development of severe sepsis (odds ratio 2.6, p < 0.01) and septic shock (odds ratio 3.7, p < 0.01). Organ system failure and mortality increased as the number of SIRS criteria increased. CONCLUSIONS: Although common in the ICU, SIRS has prognostic importance in predicting infections, severity of disease, organ failure and outcome.
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Studying membrane proteins represents a major challenge in protein biochemistry, with one of the major difficulties being the problems encountered when working outside the natural lipid environment. In vitro studies such as crystallization are reliant on the successful solubilization or reconstitution of membrane proteins, which generally involves the careful selection of solubilizing detergents and mixed lipid/detergent systems. This review will concentrate on the methods currently available for efficient reconstitution and solubilization of membrane proteins through the use of detergent micelles, mixed lipid/detergent micelles and bicelles or liposomes. We focus on the relevant molecular properties of the detergents and lipids that aid understanding of these processes. A significant barrier to membrane protein research is retaining the stability and function of the protein during solubilization, reconstitution and crystallization. We highlight some of the lessons learnt from studies of membrane protein folding in vitro and give an overview of the role that lipids can play in stabilizing the proteins.
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Eighteen water-soluble food dyes have been studied by chromatography on thin layers of anion-exchange (AG 1-X4, DEAE-cellulose, PAB-cellulose and chitosan) and cation-exchange (Dowex 50-X4, Rexyn 102 and humic acid) materials; layers of silanised silica gel impregnated with cationic or anionic detergent were also used. Fourteen of the dyes were separated, but the two orange and the two black dyes were not. Some applications of the techniques to commercial products are reported.