Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/1591
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dc.contributor.authorDahdouh, Eliasen_US
dc.contributor.authorEL Khatib, Salahen_US
dc.contributor.authorBaydoun, Elias A-H.en_US
dc.contributor.authorAbdel-Massih, Roulaen_US
dc.date.accessioned2020-12-23T08:55:19Z-
dc.date.available2020-12-23T08:55:19Z-
dc.date.issued2017-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/1591-
dc.description.abstractBackground: Pectin is a heterogeneous polysaccharide present in plants and citrus fruits. It exhibits different beneficial biological activities. Conflicting reports exist about the antimicrobial effect of pectin and its derivatives. Objective: In this study, we investigate the antimicrobial effect of Modified Citrus Pectin (MCP) against Staphylococcus aureus, a pathogen showing increasing rates of antimicrobial resistance worldwide. Method: Forty-three clinical isolates of S. aureus were obtained from a hospital in North Lebanon. Minimum Inhibitory Concentrations (MICs) and Minimum Bactericidal Concentrations (MBCs) were determined using MCP after determining its optimum pH activity. The combination between MCP and cefotaxime was then investigated for S. aureus isolates using the checkerboard technique. Results and Discussion: The optimum pH for the activity of MCP was 6.0. MIC and MBC values against S. aureus ranged between 0.39-50 µg/µl and 3.13-50 µg/µl, respectively. These values are promising for using MCP in the inhibition of some S. aureus isolates at relatively low concentrations. Combination experiments showed an additive effect in most S. aureus strains between MCP and cefotaxime, and a synergistic effect in two strains. These preliminary findings open the way for further investigation into the therapeutic potential of MCP in the treatment of S. aureus infections. Conclusion: MCP demonstrates in vitro antimicrobial activity alone and in combination with cefotaxime against S. aureus. Keywords: Antibiotic resistance, checkerboard, combination therapy, modified citrus pectin, MRSA, Staphylococcus aureus.en_US
dc.language.isoengen_US
dc.subjectAntibiotic resistanceen_US
dc.subjectCheckerboarden_US
dc.subjectCombination therapyen_US
dc.subjectModified Citrus Pectinen_US
dc.subjectMRSAen_US
dc.subjectStaphylococcus aureusen_US
dc.titleAdditive effect of MCP in combination with cefotaxime against staphylococcus aureusen_US
dc.typeJournal Articleen_US
dc.contributor.affiliationDepartment of Biologyen_US
dc.description.volume13en_US
dc.description.issue7en_US
dc.description.startpage682en_US
dc.description.endpage688en_US
dc.date.catalogued2017-10-30-
dc.description.statusPublisheden_US
dc.identifier.OlibID174613-
dc.relation.ispartoftextMedicinal chemistryen_US
dc.provenance.recordsourceOliben_US
Appears in Collections:Department of Biology
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