Impact of Venlafaxine on Platelet Count and Activity-Case Report and Narrative Review.

Venlafaxine (VEN) is considered to be one of the most effective antidepressants. It belongs to the group of serotonin (5-HT) and noradrenaline (NA) reuptake inhibitors (SNRIs). NA and 5-HT have receptors on the surface of platelets and are involved in platelet aggregation. In this case study, we present the case of a patient treated for one of the types of myeloproliferative neoplasm (MPN), essential thrombocythemia (ET), in whom VEN was added to pharmacotherapy during the treatment of a severe episode of depression with psychotic symptoms. We observed a gradual reduction in platelet count when increasing the dose of VEN. We also present a narrative review of literature about the effect of VEN on platelet counts and activity. We conclude that, in the group of patients taking VEN, attention should be paid to the rare adverse effect of a decrease in the number of platelets.

Sense of taste in patients after cochlear implantation-preliminary study.

Background: Taste is the leading sense in how we determine the quality of consumed food. Proper gustatory sensation largely determines the well-being and health of an organism, and this affects their quality of life. Objectives: The aim of the present study was to estimate the risk of early taste disorders following implantation surgery. Methods: Twenty patients underwent a taste test before, 1 day after, and 1 month after cochlear implantation. The taste sensations of sweet, sour, salty, and bitter were determined. Results: Statistical analysis showed no significant differences (p > 0.05) between individual tests among the entire study group. After dividing the respondents into smoking (n=6) and non-smoking (n=14) groups, only a weak correlation (p = 0.043) was found between the results of the first and second examination in the smoker group. However, a statistically significant decrease in the number of saline-sensitive (p<0.001) and acid-sensitive (p = 0.042) subjects was observed. Conclusion: These findings suggest that people after a cochlear implant may have transient taste disorders. Taste disorder called dysgeusia may be an early complication after the implantation procedure contributing to deterioration of patients quality of life.

Insights into Primary Ion Exchange between Ion-Selective Membranes and Solution. From Altering Natural Isotope Ratios to Isotope Dilution Inductively Coupled Plasma Mass Spectrometry Studies.

Although ion-selective electrodes have been routinely used for decades now, there are still gaps in experimental evidence regarding how these sensors operate. This especially applies to the exchange of primary ions occurring for systems already containing analyte ions from the pretreatment step. Herein, for the first time, we present an insight into this process looking at the effect of altered ratios of naturally occurring analyte isotopes and achieving isotopic equilibrium. Benefiting from the same chemical properties of all isotopes of analyte ions and spatial resolution offered by laser ablation and inductively coupled plasma mass spectrometry, obtaining insights into primary ion diffusion in the preconditioned membrane is possible. For systems that have reached isotopic equilibrium in the membrane through ion exchange and between the membrane phase and the sample, quantification of primary ions in the membrane is possible using an isotope dilution approach for a heterogeneous system (membrane-liquid sample). Experimental results obtained for silver-selective membrane show that the primary ion diffusion coefficient in the preconditioned membrane is close to (6 ± 1) × 10-9 cm2/s, being somewhat lower compared to the previously reported values for other cations. Diffusion of ions in the membrane is the rate limiting step in achieving isotopic exchange equilibrium between the ion-selective membrane phase and sample solution. On the contrary to previous reports, quantification of silver present in the membrane clearly shows that contact of the membrane with silver nitrate solution of concentration 10-3 M leads to pronounced accumulation of silver ions in the membrane, reaching almost 150% of ion exchanger amount. The magnitude of this effect increases for higher concentration of the electrolyte in the solution.

Effect of exogenous butyrate on the gastrointestinal tract of sheep. I. Structure and function of the rumen, omasum, and abomasum.

The aim of this study was to determine the effect of exogenous butyrate on the structure and selected functions of the stomach in sheep. Eighteen rams (30.8 ± 2.1 kg; 12 to 15 mo of age) were allocated to the study and fed a diet for 14 d without (CTRL) or with sodium butyrate (BUT; 36 g/kg of offered DM). Neither DMI nor initial BW differed between treatments (P ≥ 0.61), but final BW was greater for BUT compared with CTRL (P = 0.03). Butyrate concentration in the reticuloruminal fluid and abomasal digesta was greater for BUT compared with CTRL (P ≤ 0.01), but total short-chain fatty acids (SCFA) concentration, as well as concentration of other SCFA, did not differ between treatments (P ≥ 0.07). Relative to BW, reticuloruminal tissue mass tended (P = 0.09) to be greater and omasal digesta was less (P = 0.02) for BUT compared with CTRL. Dietary butyrate did not affect ruminal papillae length, width, and density nor did it affect ruminal epithelium thickness (P ≥ 0.12) in the ventral sac of the rumen. However, the DM of ruminal epithelium (mg/cm2) tended (P = 0.06) to be greater for BUT compared with CTRL. Omasal and abomasal epithelium thicknesses were greater (P ≤ 0.05) for BUT compared with CTRL. Mitosis-to-apoptosis ratio in the abomasal epithelium was less for BUT compared with CTRL (P = 0.04). Finally, the mRNA expression of peptide transporter 1 in the omasal epithelium was less (P = 0.02) and mRNA expression of monocarboxylate transporter 1 in the abomasal epithelium tended (P = 0.07) to be greater for BUT compared with CTRL. It can be concluded that exogenous butyrate supplementation affected not only the rumen but also omasum and abomasum in sheep.

Direct determination of δ44/42 Ca isotope ratio by ion chromatography/low-resolution multicollector ICPMS.

High-precision on-line procedure for measurement of calcium isotopic ratio by coupling ion chromatography to multicollector inductively coupled plasma mass spectrometry was developed. Calcium separation from the sample matrix was achieved on an ion chromatography column-IonPac CS16-ID 3 mm connected with CERS 500 2 mm suppressor and followed by multicollector inductively coupled plasma mass spectrometry calcium isotopic ratio determination. Dry plasma mode was used with Aridus II desolvation system. To sustained samples with high level of total dissolved salts as well as account capacity of applied analytical column, the method has been optimized regarding calcium isotope ratio measurements with low-resolution mass spectrometry. Mass discrimination and instrument drift were corrected by sample-standard bracketing method using the 44 Ca/42 Ca isotope ratio of SRM 915a as a standard. Good accuracy and reasonable precision of calcium isotope ratio (generally 0.20‰ [2SD]) were achieved, which are comparable to off-line Ca separation and continuous measurement. The reproducibility of the proposed analytical procedure was verified by measuring the SRM 915a standard as a sample randomly over 3 months (n = 56). Applicability of the protocol was demonstrated for matrix-rich natural water samples, coral samples, and bone standard reference materials.

Introducing Cobalt(II) Porphyrin/Cobalt(III) Corrole Containing Transducers for Improved Potential Reproducibility and Performance of All-Solid-State Ion-Selective Electrodes.

A novel solid contact type for all-solid-state ion-selective electrodes is introduced, yielding high stability and reproducibility of potential readings between sensors as well as improved analytical performance. The transducer phase herein proposed takes advantage of the presence of porphyrinoids containing the same metal ion at different oxidation states. In contrast to the traditional approach, the compounds of choice are not a redox pair; although they have different oxidation states, they cannot be electrochemically driven one to another. The compounds of choice were cobalt(II) porphyrin and cobalt(III) corrole-both characterized by a high stability of the coordinated metal ions in their respective redox states and electrical neutrality, as well as relatively high lipophilicity. The porphyrinoids were used together with carbon nanotubes to yield transducer layers for ion-selective electrodes. As a result, we obtained a high stability of potential readings of the resulting ion-selective electrodes together with good reproducibility between different sensor batches. Moreover, advantageously the presence of porphyrinoids in the transducer phase results in improvement of the analytical performance of the sensors: linear response range and selectivity due to interactions with membrane components, resulting in tailoring of ion fluxes through the membrane phase. Thus, carbon nanotubes with the cobalt(II) porphyrin/cobalt(III) corrole system are promising alternatives for existing transducer systems for potentiometric sensors.

High precision direct analysis of magnesium isotope ratio by ion chromatography/multicollector-ICPMS using wet and dry plasma conditions.

In this work the applicability of Ion Chromatography (IC) coupled to Multicollector Inductively Coupled Plasma Mass Spectrometry (MC-ICPMS) for on-line magnesium isotope ratio analysis was explored. Various instrumental setups were employed to enable continuous magnesium separation from the sample matrix by IC followed by MC-ICPMS. The performance of two separation columns IonPac CS16 (ID 5mm or ID 3mm) connected with appropriate CERS 500 suppressors (4mm or 2mm) using dry and wet plasma conditions was compared. With the use of ID 3mm column and 2mm suppressor it was possible to apply dry plasma mode with Aridus II desolvation system. Mass discrimination and instrument drift were corrected by sample-standard bracketing method using the 26Mg/24Mg isotope ratio of DSM-3 as standard. Good accuracy and high precision of the magnesium isotope ratio (generally 0.15‰ (2SD)) were achieved for wet and dry plasma modes; both were comparable to off-line Mg separation and continuous measurement. The sensitivity of MC-ICPMS measurements with dry plasma was 25 times higher in comparison to wet plasma conditions. Robustness and applicability of the method was demonstrated for matrix-rich natural water and rock samples magnesium isotope analysis.

On the use of certified reference materials for assuring the quality of results for the determination of mercury in environmental samples.

This work focused on the development and validation of methodologies for the accurate determination of mercury in environmental samples and its further application for the preparation and certification of new reference materials (RMs). Two certified RMs ERM-CC580 (inorganic matrix) and ERM-CE464 (organic matrix) were used for the evaluation of digestion conditions assuring the quantitative recovery of mercury. These conditions were then used for the digestion of new candidates for the environmental RMs: bottom sediment (M_2 BotSed), herring tissue (M_3 HerTis), cormorant tissue (M_4 CormTis), and codfish muscle (M_5 CodTis). Cold vapor atomic absorption spectrometry (CV AAS) and inductively coupled plasma mass spectrometry (ICP MS) were used for the measurement of mercury concentration in all RMs. In order to validate and assure the accuracy of results, isotope dilution mass spectrometry (IDMS) was applied as a primary method of measurement, assuring the traceability of obtained values to the SI units: the mole, the kilogram, and the second. Results obtained by IDMS using n(200Hg)/n(202Hg) ratio, with estimated combined uncertainty, were as follows: (916 ± 41)/[4.5 %] ng g-1 (M_2 BotSed), (236 ± 14)/[5.9 %] ng g-1 (M_3 HerTis), (2252 ± 54)/[2.4 %] ng g-1 (M_4 CormTis), and (303 ± 15)/[4.9 %] ng g-1 (M_CodTis), respectively. Different types of detection techniques and quantification (external calibration, standard addition, isotope dilution) were applied in order to improve the quality of the analytical results. The good agreement (within less than 2.5 %) between obtained results and those derived from the Inter-laboratory Comparison, executed by the Institute of Nuclear Chemistry and Technology (Warsaw, Poland) on the same sample matrices, further validated the analytical procedures developed in this study, as well as the concentration of mercury in all four new RMs. Although the developed protocol enabling the metrological certification of the reference value was exemplified by the determination of mercury in environmental samples, it could be considered as valid for any certification procedure required whenever new certified RMs are introduced.

Bio-transformation of selenium in Se-enriched bacterial strains of Lactobacillus casei.

BACKGROUND: Selenium is an element of very great importance for the proper functioning of the human body, mainly due to its antioxidant properties. Selenium exhibits a preventive effect in the case of cardiovascular disease, the immune system, male infertility and inhibits the toxic action of other agents. Selenium is important for Hashimoto's disease. Intake of selenium in the diet slows the aging process. The biological and toxicological effects of selenium strongly depend on its chemical form. Some organisms for example: plant, yeast, are capable of metabolizing low bioavailable selenium compounds (inorganic selenium) into its high bioavailable forms (organic selenium). OBJECTIVE: The aim of this study was to investigate the bio-transformation of selenium by Lactobacillus bacteria towards the characterisation of selenium metabolites. MATERIAL AND METHODS: The speciation of selenium was evaluated by high performance liquid chromatography with inductively coupled plasma mass spectrometry detector. The extraction of selenium species from lyophilized bacteria was executed with water, the mixture of lipase and protease, as well as lisozyme and sodium dodecyl sulphate. RESULTS: All investigated bacteria strains cultivated in the presence of Na2SeO3 effectively uptake selenium. Surprisingly, none of the applied extraction media exhibited a strong power to release the majority of the uptaken selenium compounds. Thus a maximum of 10% of the selenium was extracted from bacteria exposed to the enzymes. However, it was found that Lactobacillus bacteria are able to metabolize inorganic ions of selenium (IV) into Se-methionine, Se-methyloselenocysteine and other unidentified forms. CONCLUSIONS: The study confirmed the ability of probiotic bacteria to biotransform inorganic selenium into its organic derivatives. Therefore, Se-enriched bacteria can be considered as an addition to the functional food. KEY WORDS: selenium speciation, extraction procedure, Lactobacillus casei bacteria, Lactic acid bacteria (LAB), HPLC ICP-MS, functional food.

Inductively coupled plasma mass spectrometry in comparison with neutron activation and ion chromatography with UV/VIS detection for the determination of lanthanides in plant materials.

Analytical performance of inductively coupled plasma mass spectrometry (ICP-MS) for determination of lanthanides in plant materials was investigated and compared with neutron activation analysis (NAA) as well as ion chromatography (IC) with UV-VIS detection. Two sample preparation protocols were tested: (i) microwave assisted digestion by concentrated nitric acid; (ii) microwave digestion involving silica and fluoride removal, followed by the selective and quantitative lanthanides group separation from the plant matrix. Several Certified Reference Materials (CRM) of plant origin were used for the evaluation of the accuracy of the applied analytical procedures. The consistency of results, obtained by various methods, enabled to establish the tentative recommended values (TRV) for several missing elements in one of CRMs. The ICP-MS, due to its very high sensitivity, has the potential to contribute to this aim. The discrepancy of the results obtained by various methods was discussed in a view of possible matrix effects related to the composition of investigated materials.

Dithizone modified gold nanoparticles films for potentiometric sensing.

For the first time, application of a membrane composed of gold nanoparticles decorated with complexing ligand for potentiometric sensing is shown. Gold nanoparticles drop cast from a solution form a porous structure on a substrate electrode surface. Sample cations can penetrate the gold nanoparticles layer and interact with ligand acting as a charged ionophore, resulting in Nernstian potentiometric responses. Anchoring of complexing ligand on the gold surface abolishes the necessity of ionophore application. Moreover, it opens the possibility of preparation of potentiometric sensors using chelators of significantly different selectivity patterns further enhanced by the absence of polymeric membrane matrix. This was clearly seen, for example, for gold nanoparticles stabilizing the applied ligand-dithizone-thiol conformation leading to a high potentiometric selectivity toward copper ions, much higher than that of ionophores typically used to induce selectivity for polymeric ion-selective membranes.

Microspheres aided introduction of ionophore and ion-exchanger to the ion-selective membrane.

In this work a novel method for introduction of ionophore and ion-exchanger to the ion-selective polyacrylate based membrane is proposed. These compounds (and optionally primary ions) are introduced to polyacrylate microspheres, used to prepare ion-selective membrane. The approach proposed here can be used to prepare membranes containing primary ions equally distributed through the receptor phase, i.e. membranes that do not require conditioning in primary ions solution and are free from problems related to slow diffusion of primary ions. Thus obtained sensors were characterized with linear responses (also at relatively high activities) and high selectivities, despite considerable reduction of ionophore and ion-exchanger amount introduced to the membrane. To be able to prepare ion-selective membranes using this approach, a method for quantification of ionophore and ion-exchanger introduced into microspheres is required. In this work a novel method utilizing high performance liquid chromatography (HPLC) with DAD or FLD detection is proposed. Incorporation of ionophore and ion-exchanger into the microspheres was achieved either by absorption into ready spheres or in course of photopolymerization of polymeric beads. The obtained results have proven that both procedures led to incorporation of ionophore/ion-exchanger into polymeric spheres, however, the content of the compounds in the spheres post process is different from their ratio in solution from which they had been introduced. These effects need to be considered/compensated while preparing microspheres containing ion-selective membranes. As a model system poly(n-butyl acrylate) spheres, silver selective ionophore and sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate were chosen, resulting ultimately in silver-selective electrodes.

Experimental study on stability of different solid contact arrangements of ion-selective electrodes.

Comparison of potentials stability of different types of solid contact lead selective electrodes is presented. Conducting polymer based sensors (hydrophilic and conducting - poly(3,4-ethylenedioxythiophene) or hydrophobic and semiconducting-polyoctylthiophene) were studied in parallel with coated wire and hydrogel (poly(hydroxyethylmethacrylate)) contact electrodes. The within day and between days potential stability was compared, highlighting the effect of sensor storing conditions. The obtained results clearly demonstrate that different conclusions on stability of sensors' potential can be drawn depending on experimental protocol applied. Polyoctylthiophene based contacts show superior within day stability with no influence of dry storage. On the other hand, a chronopotentiometric method of stability evaluation clearly prefers poly(3,4-ethylenedioxythiophene) based sensors, pointing to smallest resistance and polarizability. It is clearly shown that the choice of experimental conditions applied to test stability can favor particular type of contact used. The inductively coupled plasma mass spectrometry with laser ablation (LA-ICP-MS) experiments conducted for different arrangements tested has shown that for poly(3,4-ethylenedioxythiophene) and poly(hydroxyethylmethacrylate) type contacts longer contact time with lead(II) solution results in changes in the elemental composition of the transducer layer. On the other hand, in line with high stability observed under potentiometric conditions, no changes were seen for polyoctylthiophene based transducer.

Poly(n-butyl acrylate) based lead (II) selective electrodes.

Poly(n-butyl acrylate) membranes for potentiometric ion-selective electrodes were developed and studied on example of lead-selective sensors. A novel approach resulting in Nernstian responses of tested sensor was proposed. Introduction of 5% (w/w) hydroxyethyl methacrylate into n-butyl acrylate moiety resulted in significant improvement of sensor analytical parameters. For the latter membrane material linear responses were obtained within lead activities range from 10(-2) to 10(-9) mol/dm(3), while for poly(n-butyl acrylate) based membranes pretreated in the same manner super-Nernstian behavior was obtained in a parallel experiment. Electrochemical impedance spectroscopy studies did not reveal significant differences between these two membranes, also similar lead ions diffusion coefficients were determined using inductively coupled plasma mass spectrometry with laser ablation.The difference between two kinds of membranes was found to concern higher Pb(II) ions contents in the surface part of the membrane with hydroxyethyl methacrylate, resulting in balanced Pb ions fluxes from/to the membrane.

Composite polyacrylate-poly(3,4- ethylenedioxythiophene) membranes for improved all-solid-state ion-selective sensors.

A novel type of self-plasticizing polyacrylate-based membrane was developed for all-solid-state ion-selective potentiometric electrodes. The membrane composition contains a conducting polymer (CP): poly(3,4-ethylenedioxythiophene) end capped with methacrylate groups, chemically grafted with the membrane during the photopolymerization step. This composition results in ion-selective membranes with the following advantages: lower electrical resistance compared to the CP-free membrane, facile ion-to-electron transduction between the membrane and the electrode support, controlled low activity of analyte ions, and high concentration of interferent ions (incorporated with the CP) within the membrane, potentially resulting in improved analytical parameters. Ca2+- and K+-selective membranes were chosen as model systems to study the effect of pretreatment and CP content on the potentiometric sensor's characteristics. For Ca2+ sensors, reproducible and stable Nernstian characteristics were obtained within the range from 0.1 to 10(-9) M CaCl2, without a time-consuming preconditioning step. For K+-selective sensors, the influence on Nernstian response range was observed for varying KCl concentrations in the conditioning solution, with the lowest detection limit found close to 10(-8) M KCl. Mass spectrometry coupled with laser ablation studies of the membranes revealed that in this case the detection limit is not related to primary ion content in the membrane contacting a sample solution, but is affected by interfering ion concentration close to the membrane surface.

Laser ablation inductively coupled plasma mass spectrometry assisted insight into ion-selective membranes.

Laser ablation inductively coupled plasma mass spectrometry was used to evaluate ion depth profiles across ion-selective membranes. Advantageously, this approach does not require incorporation of additional components (e.g., chromoionophore) in the membrane composition, as compared to that used in typical potentiometric applications. Moreover, comparison of the distribution of ions in differently pretreated membranes is possible. Concentration profiles of primary and interfering agent (Na+) ions were recorded, for example, of Pb2+-selective poly(vinyl chloride)-based membranes. It was found that the contents and the distribution of Pb(2+) and Na+ ions across the membrane is strongly dependent on the composition of the solutions to which both sides of the membrane are exposed during preconditioning and on the plasticizer included in the membrane formulation. Typical plasticizers, bis(2-ethylhexyl sebacate) (DOS) and the more polar 2-nitrophenyl octyl ether (o-NPOE), were used. It was found that faster ion transport occurs for o-NPOE, and the membrane saturation with Pb2+ ions was achieved within less than 20 h for a 400-microm-thick membrane. In the case of the less polar plasticizer DOS, due to slower rate of ion transport, even after 20 h, the Pb2+ concentration gradients were still visible within the membrane. On the basis of concentration profiles, primary ion diffusion coefficients in both membranes were calculated, and the value obtained for o-NPOE containing membrane was found to be approximately 2 times higher than for its DOS-plasticized counterpart.

Induction of unique structural changes in guanine-rich DNA regions by the triazoloacridone C-1305, a topoisomerase II inhibitor with antitumor activities.

We recently reported that the antitumor triazoloacridone, compound C-1305, is a topoisomerase II poison with unusual properties. In this study we characterize the DNA interactions of C-1305 in vitro, in comparison with other topoisomerase II inhibitors. Our results show that C-1305 binds to DNA by intercalation and possesses higher affinity for GC- than AT-DNA as revealed by surface plasmon resonance studies. Chemical probing with DEPC indicated that C-1305 induces structural perturbations in DNA regions with three adjacent guanine residues. Importantly, this effect was highly specific for C-1305 since none of the other 22 DNA interacting drugs tested was able to induce similar structural changes in DNA. Compound C-1305 induced stronger structural changes in guanine triplets at higher pH which suggested that protonation/deprotonation of the drug is important for this drug-specific effect. Molecular modeling analysis predicts that the zwitterionic form of C-1305 intercalates within the guanine triplet, resulting in widening of both DNA grooves and aligning of the triazole ring with the N7 atoms of guanines. Our results show that C-1305 binds to DNA and induces very specific and unusual structural changes in guanine triplets which likely plays an important role in the cytotoxic and antitumor activity of this unique compound.

MM/PBSA analysis of molecular dynamics simulations of bovine beta-lactoglobulin: free energy gradients in conformational transitions?

The pH-driven opening and closure of beta-lactoglobulin EF loop, acting as a lid and closing the internal cavity of the protein, has been studied by molecular dynamics (MD) simulations and free energy calculations based on molecular mechanics/Poisson-Boltzmann (PB) solvent-accessible surface area (MM/PBSA) methodology. The forms above and below the transition pH differ presumably only in the protonation state of residue Glu89. MM/PBSA calculations are able to reproduce qualitatively the thermodynamics of the transition. The analysis of MD simulations using a combination of MM/PBSA methodology and the colony energy approach is able to highlight the driving forces implied in the transition. The analysis suggests that global rearrangements take place before the equilibrium local conformation is reached. This conclusion may bear general relevance to conformational transitions in all lipocalins and proteins in general.