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The phenomenon of political evasiveness in the genre of a political interview has been the focus of several discourse studies employing conversation analysis, critical discourse analysis and the social psychology approach. Most of the above-mentioned studies focus on a detailed qualitative analysis of political discourse identifying a wide range of communication strategies that permit politicians to ambiguate their agency and at the same time boost their positive face. Since these strategies may change over time and also be subject to a culture specific environment, the aim of this paper is to discover a) which evasive communicative strategies were employed by Slovak politicians in 2012–2016, b) which lexical substitutions were most frequently used by them to avoid negative connotations of face-threatening questions, and finally, c) which cognitive frames formed a frequent conceptual background of their evasive political argumentation. The paper will draw on a combination of quantitative and qualitative approach to the analysis of non-replies devised by Bull and Mayer (1993) and critical discourse analysis in the sample of five Slovak radio interviews aired on the Rádio Express. The selection of interviews was not random- in each interview the politician was asked highly conflictual questions about bribery, embezzlement or disputes in the coalition. Based on qualitative research of Russian-Slovak political discourse (2009) by Dulebová it is hypothesized that a) the evasive strategy of 'attack' on the opposition and 'attack on the interviewer' would occur in our sample with the highest prominence in the speech of the former Prime Minister Fico, and b) the politicians accused of direct involvement in scandals would be the most evasive ones. [ABSTRACT FROM AUTHOR]

Highlights: [•] Analyte distribution constants between aqueous and phosphonium ionic liquid phases. [•] First time use of CMC determination of cationic micelle based on system peaks in CE. [•] CMC determination by system peaks provide good results but is time demanding. [•] Higher distribution constants were obtained using [P14444]OAc than [P14444]Cl. [•] The retention mechanism covers other than hydrophobic interaction. [Copyright &y& Elsevier]

CE has matured into a well-known and much used separation technique, with applications covering more or less all types of samples. EKC, which originally was developed for the separation of uncharged compounds, is still today under much development, with main focus on finding the perfect or ideal carriers (pseudo-stationary phase) for a broad range of analytes. In this review, the use of lipid dispersions as pseudostationary phases in EKC performed in capillaries and microchips, in addition to CE frontal analysis and partial filling EKC using lipid dispersions is discussed. Various types of lipid dispersions including liposomes, PEG-stabilized aggregates, proteoliposomes, lipid-based nanoparticles, and commercial lipid emulsions are described. The purpose of the review is to give the reader an overview of how EKC, CE frontal analysis, and partial filling EKC, have been applied to the study of interactions between analytes and lipid membranes. [ABSTRACT FROM AUTHOR]

Intravenous lipid emulsion is a recommended treatment for local anesthetic intoxication. The lipid sink theory hypothesizes that the mechanism behind the lipid treatment is the entrapment of toxic drugs in plasma, preventing them from reaching target receptors. Lipid sink treatment has also been used as a last refuge treatment for severe tricyclic antidepressant intoxication with seemingly beneficial results. We selected three drugs, i.e. amiodarone, ketamine, and amitriptyline, that can cause severe intoxication and compared their interactions with two commercial fat emulsions (Intralipid® and ClinOleic®) and one synthetic liposome (80:20 mol% phosphatidylcholine/phosphatidylglycerol) dispersion. The interaction studies were carried out by capillary electrokinetic chromatography and the retention factors and distributions constants of the drugs were calculated. The results demonstrate that there is stronger interaction between the drugs and the synthetic liposome dispersion than with the commercial emulsions. [ABSTRACT FROM AUTHOR]

fast and accurate micellar electrokinetic capillary chromatography (MEKC) method was developed for monitoring N-methyl-2-pyrrolidone (NMP) exposure. Baseline separation of NMP and its main metabolites: 5-hydroxy- N-methyl-2-pyrrolidone (5HNMP), N-methylsuccinimide (MSI), 2-hydroxy- N-methylsuccinimide (2HMSI), and 2-pyrrolidone (2P) was obtained within 6 min in an uncoated fused silica capillary using 5 mM phosphate buffer and 140 mM sodium dodecyl sulfate (pH 7.1) as background electrolyte (BGE). On-line UV-detection was performed at 200 nm and the applied electric field was 400 V cm. Possible interference of BGE-induced system peaks on separation was investigated by computer simulation and no such interference was observed. The developed MEKC method combined with solid phase extraction for sample preparation was successfully applied to the analysis of urine of rats exposed to NMP. The urinary excretion was determined in 0-6 h and 6-24 h specimens collected after an intragastic administration of 308 mg NMP / kg rat body weight. The results of NMP disposition kinetics in rat urine are reported for NMP and metabolites. [InlineMediaObject not available: see fulltext.] [ABSTRACT FROM AUTHOR]

The behavior of seven hydroxy anthraquinone derivatives was studied by capillary zone electrophoresis and micellar electrokinetic chromatography. The effects of buffer pH (6.5-10.8) and sodium dodecyl sulfate concentration (10-20 mmol L-1) on the effective mobilities of the analytes and their separation were tested. A comparison of the two optimized separation systems showed that micellar electrokinetic chromatography was superior as it permits separation of all the seven analytes within 15 min, using 15 mmol L-1 sodium dodecyl sulfate in 10 mmol L-1 tetraborate buffer, pH 8.5, at a voltage of 20 kV. The calibration curves were linear in the concentration range from 5.0 · 10-7 to 5.0 · 10-4 mol L-1 for most of the analytes, at a detection wavelength of 254 nm. LOD and LOQ values of the analytes were in the ranges of 2.10 · 10-7-1.28 · 10-6 mol L-1and 6.99 · 10-7-4.25 · 10-6 mol L-1, respectively. The proposed separation conditions were applied to determination of 1,2-dihydroxy anthraquinone (alizarin) and 1,2,4-trihydroxy anthraquinone (purpurin) in Rubia tinctorum aglycone and of the recently described 1-acetyl-2,4,5,7-tetrahydroxy-9,10-anthraquinone and 1-acetyl-2,4,5,7,8-pentahydroxy-9,10-anthraquinone in the mycelium of fungi Geosmithia lavendula. [ABSTRACT FROM AUTHOR]

Polymeric micelles of polystyrene-block-poly(methacrylic acid) with the shell containing various amounts of poly(2-vinylpyridine) chains were prepared by dialysis from 1,4-dioxane-rich mixtures into alkaline aqueous solutions. The structure of the polymeric nanoparticles was studied by light scattering, atomic force microscopy, fluorometry, and capillary zone electrophoresis. The presence of both weak polyacid and weak polybase in the corona allows the micelles to form fairly stable solutions in a broad pH range. Poly(methacrylic acid) blocks are dissociated in basic buffers, while poly(2-vinylpyridine) chains stabilize the micelles in acidic solutions. Besides the water-swollen shell, the inner parts of the micelles consist of the kinetically frozen polystyrene core and relatively rigid layer of poly(methacrylic acid) and poly(2-vinylpyridine) segments. An insufficient number of stabilizing polymer chain segments results in the aggregation of the micelles into clusters. [ABSTRACT FROM AUTHOR]