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Utilizarea a di(m-s)-bis{cloro-[1-piridin-2-iletanon-4-metiltiosemicarbazono(1-)]cupru}, în calitate de substanţă cu activitate antimicrobiană faţă de Staphylococcus aureus

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dc.contributor.author Lozan-Tirsu, C.
dc.date.accessioned 2020-01-28T13:19:35Z
dc.date.available 2020-01-28T13:19:35Z
dc.date.issued 2014
dc.identifier.citation LOZAN-TIRSU, C. Utilizarea a di(m-s)-bis{cloro-[1-piridin-2-iletanon--metiltiosemicarbazono(1-)]cupru}, în calitate de substanţă cu activitate antimicrobiană faţă de Staphylococcus aureus. In: Curierul Medical. 2014, vol. 57, no 3, pp. 9-11. ISSN 1875-0666. en_US
dc.identifier.issn 1857-0666
dc.identifier.uri http://repository.usmf.md/handle/20.500.12710/7350
dc.identifier.uri http://moldmedjournal.md/wp-content/uploads/2016/09/Cm-3-57-Electornic-PDF-version.pdf
dc.description Department of Microbiology, Virusology and Immunology, Nicolae Testemitsanu State University of Medicine and Pharmacy, Chisinau, the Republic of Moldova en_US
dc.description.abstract Background: This work relates to chemistry and medicine, namely to a biologically active coordination compound of copper from the class of thiosemicarbazonates of transition metals, which can be used as substance with antimicrobial activity against Staphylococcus aureus. Material and methods: The antimicrobial activity has been studied in vitro in liquid nutritive media [peptone broth, 2%, pH 7.0] by means of using the method of successive dilutions. The substances were dissolved in DMSO at a concentration of 10 ml, the subsequent dilutions were prepared in peptone broth. The reference strains Staphylococcus aureus, Bacillus cereus, Escherichia coli, and Salmonella abony, Shigella sonnei were used as reference culture. Appreciation of the lowest inhibitory concentration and minimal bactericidal concentrations were performed by the standard method described in the literature. Results: The obtained experimental data show, that this di(m-S)-bis{chloro-[1-pyridine-2-ylethanone-4-methylthiosemicarbazonato(1-)]copper exhibits high antimicrobial activity against selective bacteria of the Staphylococcus aureus, that exceed 80-259 times the same characteristics of structural analogue. Conclusions: The new synthesized coordinative compounds of cooper demonstrate high bacteriostatic and bacteriocide activity against a wide spectrum of both gram-positive as well as gram-negative microorganisms. The experimentally obtained data demonstrate that (di(m-S)-bis{chloro-[1-pyridine2-ylethanone-4-methylthiosemicarbazonato(1-)]copper), show high selective antimicrobial activity against Staphylococcus aureus, which exceeds the analogous features of structural analogue by 80-259 times. Di(m-S)-bis{chloro-[1-pyridine-2-ylethanone-4-methylthiosemicarbazonato(1-)]copper) compounds have bacteriostatic and bacteriocide activity against gram-positive bacteria between the concentrations of 0.00056-0.14mg/ml and gramnegative bacteria between 0.58-75 mg/ml. The identified properties of nominated compounds present interest because of expanding arsenal of antimicrobial remedies and can be used for combating the strains of microorganisms which are resistant to traditional drugs en_US
dc.language.iso ro en_US
dc.publisher The Scientific Medical Association of the Republic of Moldova en_US
dc.relation.ispartof Curierul Medical
dc.subject gram-negative bacteria en_US
dc.subject gram-positive bacteria en_US
dc.subject antibacterial activity en_US
dc.subject.mesh Staphylococcus aureus--drug effects en_US
dc.subject.mesh Gram-Positive Bacteria en_US
dc.subject.mesh Gram-Positive Bacteria--pathogenicity en_US
dc.subject.mesh Semicarbazones--therapeutic use en_US
dc.subject.mesh Pyridines--therapeutic use en_US
dc.subject.mesh Anti-Bacterial Agents--therapeutic use en_US
dc.title Utilizarea a di(m-s)-bis{cloro-[1-piridin-2-iletanon-4-metiltiosemicarbazono(1-)]cupru}, în calitate de substanţă cu activitate antimicrobiană faţă de Staphylococcus aureus en_US
dc.title.alternative Usage of di(m-s)-bis{chloro-[1-pyridine-2-ylethanone4-methylthiosemicarbazonato(1-)]copper}, as substance with antimicrobial activity against Staphylococcus aureus en_US
dc.type Article en_US


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