84 research outputs found

    Synthesis, structure and properties of V(III,IV and V) complexes with ONO Schiff bases

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    The synthesis and physicochemical properties of vanadium(III,IV,V) complexes with Schiff base ligands based on 3,5-dibromo-4-methoxy-salicylaldehyde and phenylacetic hydrazide (H2L1), 5-chlorosalicylaldehyde and 4-hydroxybenzhydrazide (H2L2) and 5- chlorosalicylaldehyde and 2-hydroxybenzhydrazide (H2L3) were presented. The formulas of the complexes {[V(L1)(HL2)]·EtOH (1), [VO(L2)(phen)]·2H2O (2) and [VO(L3)(EtO)] (3)} were proposed based on the elemental analysis, IR and UV-Vis spectra. Additionally, the IR and UV-Vis spectra (in solvents as well as in a solid state) have been discussed from the vanadium oxidation state point of view. The single crystal structure of 3 shows triclinic, P-1 space group, structure is stabilized by hydrogen bonds and strong π-π stacking interactions. The oxidation state of the metal centre was also confirmed by the magnetic susceptibility measurements. The stability of the complexes was measured in pH = 7.00 and in pH = 2.00 which allows to evaluate the use of these compounds as insulin mimetic compounds

    Reducing Conditions Favor Magnetosome Production in Magnetospirillum magneticum AMB-1

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    Magnetotactic bacteria (MTB) are a heterogeneous group of Gram-negative prokaryotes, which all produce special magnetic organelles called magnetosomes. The magnetosome consists of a magnetic nanoparticle, either magnetite (Fe3O4) or greigite (Fe3S4), embedded in a membrane, which renders the systems colloidaly stable, a desirable property for biotechnological applications. Although these bacteria are able to regulate the formation of magnetosomes through a biologically-controlled mechanism, the environment in general and the physico–chemical conditions surrounding the cells in particular also influence biomineralization. This work thus aims at understanding how such external conditions, in particular the extracellular oxidation reduction potential, influence magnetite formation in the strain Magnetospirillum magneticum AMB-1. Controlled cultivation of the microorganisms was performed at different redox potential in a bioreactor and the formation of magnetosomes was assessed by microscopic and spectroscopic techniques. Our results show that the formation of magnetosomes is inhibited at the highest potential tested (0 mV), whereas biomineralization is facilitated under reduced conditions (-500 mV). This result improves the understanding of the biomineralization process in MTB and provides useful information in sight of a large scale production of magnetosomes for different applications

    The care of advanced COPD patients

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    Przewlekła obturacyjna choroba płuc (POChP) jest czwartą przyczyną zgonów na świecie. Około 20% chorych na POChP w Polsce cierpi na jej zaawansowaną postać, w której rokowanie jest poważne. Leczenie chorych na zaawansowaną POChP to postępowanie mające na celu opanowanie uporczywych objawów takich jak: duszność, kaszel, zmęczenie, wyczerpanie, a także często współwystępujących dolegliwości — depresji i lęku. Leczenie ma na celu zapobieganie zaostrzeniom choroby, które pogarszają jakość życia i stanowią ryzyko zgonu. Światowa Organizacja Zdrowia zaleca, aby w przewlekłych chorobach integrować działanie personelu medycznego ze wsparciem pozamedycznym (np. pomocą społeczną, wolontariatem). Z uwagi na niezadawalającą jakość życia, brak umiejętności radzenia sobie z chorobą i częste zaostrzenia u chorych na zaawansowaną POChP w Gdańskim Uniwersytecie Medycznym zaproponowano zintegrowany model opieki, zakładający połączenie kompleksowej medycznej opieki ze wsparciem domowym i społecznym. Jego celem było zmniejszenie liczby zaostrzeń w przebiegu POChP (zwłaszcza wymagających leczenia szpitalnego), a także zmniejszenie kosztów opieki nad chorymi na zaawansowaną POChP, oraz poprawa jakości życia i radzenia sobie pacjentów z chorobą.Chronic obstructive pulmonary disease (COPD) is a fourth cause of mortality worldwide. The 20% of COPD patients in Poland suffer from advanced disease. COPD usually gets gradually worse over time. In advanced COPD prognosis is bad. The main goal of management patients with advanced COPD is reducing symptoms: shortness of breath, cough, fatigue and often occurring depression and anxiety. The treatment prevents acute exacerbations of the disease. Exacerbations are the cause of the decrease of the quality of life and the risk factor of death. World Health Organization recommends in chronic diseases to integrate the action of the medical and the non-medical stuff (welfare and volunteers). Medical University of Gdansk developed ‘Pomeranian Model of Integrated Care for Patients with advanced COPD’. The main goal of it was to decrease the number of exacerbations (especially requiring the hospitalization) and in result, limit the cost of care, improve the quality of life of patients with advanced COPD and to help them to cope with disease

    No advantage of antimicrobial prophylaxis in AML/MDS/CMML patients treated with azacitidine—a prospective multicenter study by the Polish Adult Leukemia Group

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    IntroductionInfections represent one of the most frequent causes of death of higher-risk MDS patients, as reported previously also by our group. Azacitidine Infection Risk Model (AIR), based on red blood cell (RBC) transfusion dependency, neutropenia <0.8 × 109/L, platelet count <50 × 109/L, albumin <35g/L, and ECOG performance status ≥2 has been proposed based on the retrospective data to estimate the risk of infection in azacitidine treated patients.MethodsThe prospective non-intervention study aimed to identify factors predisposing to infection, validate the AIR score, and assess the impact of antimicrobial prophylaxis on the outcome of azacitidine-treated MDS/AML and CMML patients.ResultsWe collected data on 307 patients, 57.6 % males, treated with azacitidine: AML (37.8%), MDS (55.0%), and CMML (7.1%). The median age at azacitidine treatment commencement was 71 (range, 18-95) years. 200 (65%) patients were assigned to higher risk AIR group. Antibacterial, antifungal, and antiviral prophylaxis was used in 66.0%, 29.3%, and 25.7% of patients, respectively. In total, 169 infectious episodes (IE) were recorded in 118 (38.4%) patients within the first three azacitidine cycles. In a multivariate analysis ECOG status, RBC transfusion dependency, IPSS-R score, and CRP concentration were statistically significant for infection development (p < 0.05). The occurrence of infection within the first three azacitidine cycles was significantly higher in the higher risk AIR group – 47.0% than in lower risk 22.4% (odds ratio (OR) 3.06; 95% CI 1.82-5.30, p < 0.05). Administration of antimicrobial prophylaxis did not have a significant impact on all-infection occurrence in multivariate analysis: antibacterial prophylaxis (OR 0.93; 0.41-2.05, p = 0.87), antifungal OR 1.24 (0.54-2.85) (p = 0.59), antiviral OR 1.24 (0.53-2.82) (p = 0.60).DiscussionThe AIR Model effectively discriminates infection-risk patients during azacitidine treatment. Antimicrobial prophylaxis does not decrease the infection rate
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