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Suada Cipurković

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Nowadays, bottled water has become part of the lifestyle, replacing tap water, and water from freestanding dispensers is increasingly being used. The main goal of this research was to determine the health suitability of bottled water in freestanding dispensers. The research included the microbiological analysis of a total of 100 samples of bottled water from freestanding dispensers. The samples were mostly taken in the wider area of the city of Doboj (doctor's offices, shops, public buildings), and one dispenser in the city of Tuzla. Water samples were taken twice, in the period from April to June 2022. Water samples from 6 different manufacturers (Vivia, Kristal, Nevra, Gora, Aqua doria, Aqua team) were analyzed. 9% of water samples (9/100) were microbiologically correct. Microbiologically defective samples contained a higher total number of bacteria at 22°C and 37°C, as well as a higher number of coliform bacteria than the maximum allowed values. No significant differences in microbiological quality were found between older and/or recently installed water dispensers, as well as in terms of environmental conditions, while visible differences were observed between dispensers that were regularly hygienically maintained.KEYWORDS:dispensers; bottled water; coliform bacteria; biofilms; total bacteria count

A. Cipurković, S. Marić, E. Horozić, D. Husejnagić, Suada Cipurković

Copper (II) complexes with commercial antibiotics, amoxicillin (AMX), azithromycin (AZT) and ciprofloxacin (CFL) were synthesized and isolated as solids. Structures of the isolated products were determined by FTIR spectroscopy. Antibacterial activities were determined on reference bacterial strains from the ATCC collection by diffusion technique. The results show that AMX and CFL coordinate Cu (II) ion as bidentate O-donor ligand. AZT coordinates metal center as bidentate NO-donor ligand. A difference in the morphology of antibiotic crystals and the synthesized complexes was found. Complex of Cu (AMX)2 show complete absence of antibacterial activity, while the other com-plexes show the same or even lower activity than the parent ligands.  

A. Avdić, A. Kurtcehajic, Vesna Hadžiavdić, Amela Hercegovac, Aldijana Dautbašić, Senad Brzović, Suad Širanović, Maja Podjanin, Jasmina Dedić et al.

Molecular-genetic diagnostics of polygenic diseases is a new and interesting area in laboratory diagnostics, especially in the area of cardiovascular diseases, as one of the leading causes of mortality in the world population. Aims: The aim of the paper was to analyse variants of the endothelial nitric oxide synthase gene (NOS3) (Glu298Asp/G894T) in the human population of Tuzla Canton in relation to cardiovascular diseases. Study Design: The study included 112 respondents of both sexes over 18 years old. The experimental group for the analysis of the polymorphism (Glu298Asp) of the endothelial nitric oxide synthase gene included 56 respondents of both sexes with cardiovascular disease (hypertension), while the control group comprised 56 healthy respondents of both sexes without a prior history of cardiovascular disease (sample/control). Place and Duration of Study: Blood sampling was performed at Medical Center "Plava Poliklinika", “Plava Medical Group”, Department of Biochemistry, Microbiology and Genetics, Tuzla. DNA isolation and molecular-genetic analysis of the samples were performed in Laboratory for scientific research at the Department of Biology, Faculty of Natural Sciences and Mathematics in Tuzla. Methodology: The genotyping of eNOS Glu298Asp polymorphism for all respondents was determined by an optimized method based on PCR-RFLP reaction. Results: In the total sample of respondents, the highest genotype frequencies of the eNOS gene were recorded for the GG genotype (53.5%) and the GT genotype (35.7%). The lowest frequency was recorded for the TT genotype, which was 10.8%. Conclusion: The results obtained in the study provide good guidelines for further study of a molecular-genetic association between a high number of gene candidates and cardiovascular diseases, which will contribute to the incorporation of these results into the existing regional and European genetic database.

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