Activity of zinc oxide and zinc borate nanoparticles against resistant bacteria in an experimental lung cancer model

dc.authorid0000-0002-3506-0324
dc.authorid0000-0003-3824-2462
dc.authorid0000-0003-0877-453X
dc.authorid0000-0002-1523-9116
dc.authorid0000-0003-2391-8191
dc.authorid0000-0003-4578-9474
dc.contributor.authorCelebi, Demet
dc.contributor.authorCelebi, Ozgur
dc.contributor.authorTaghizadehghalehjoughi, Ali
dc.contributor.authorBaser, Sumeyye
dc.contributor.authorAydin, Elif
dc.contributor.authorCalina, Daniela
dc.contributor.authorCharvalos, Ekaterina
dc.date.accessioned2025-05-20T18:59:29Z
dc.date.issued2024
dc.departmentBilecik Şeyh Edebali Üniversitesi
dc.description.abstractBackground Recent research indicates a prevalence of typical lung infections, such as pneumonia, in lung cancer patients. Klebsiella pneumoniae, Pseudomonas aeruginosa, and Acinetobacter baumannii stand out as antibiotic-resistant pathogens. Given this, there is a growing interest in alternative therapeutic avenues. Boron and zinc derivatives exhibit antimicrobial, antiviral, and antifungal properties. Objectives This research aimed to establish the effectiveness of ZnO and ZB NPs in combating bacterial infections in lung cancer cell lines. Methods Initially, this study determined the minimal inhibitory concentration (MIC) and fractional inhibitory concentration (FIC) of zinc oxide nanoparticles (ZnO NPs) and zinc borate (ZB) on chosen benchmark strains. Subsequent steps involved gauging treatment success through a lung cancer-bacteria combined culture and immunohistochemical analysis. Results The inhibitory impact of ZnO NPs on bacteria was charted as follows: 0.97 mu g/mL for K. pneumoniae 700603, 1.95 mu g/mL for P. aeruginosa 27853, and 7.81 mu g/mL for Acinetobacter baumannii 19,606. In comparison, the antibacterial influence of zinc borate was measured as 7.81 mu g/mL for Klebsiella pneumoniae 700603 and 500 mu g/mL for both P. aeruginosa 27853 and A.baumannii 19606. After 24 h, the cytotoxicity of ZnO NPs and ZB was analyzed using the MTT technique. The lowest cell viability was marked in the 500 mu g/mL ZB NPs group, with a viability rate of 48.83% (P < 0.001). However, marked deviations appeared at ZB concentrations of 61.5 mu g/mL (P < 0.05) and ZnO NPs at 125 mu g/mL. Conclusion A synergistic microbial inhibitory effect was observed when ZnO NP and ZB were combined against the bacteria under investigation.
dc.identifier.doi10.1007/s40199-024-00505-2
dc.identifier.endpage206
dc.identifier.issn2008-2231
dc.identifier.issue1
dc.identifier.pmid38366078
dc.identifier.scopusqualityQ1
dc.identifier.startpage197
dc.identifier.urihttps://doi.org/10.1007/s40199-024-00505-2
dc.identifier.urihttps://hdl.handle.net/11552/8452
dc.identifier.volume32
dc.identifier.wosWOS:001163214700001
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWoS
dc.indekslendigikaynakPubMed
dc.indekslendigikaynakWoS - Science Citation Index Expanded
dc.language.isoen
dc.publisherSpringer Int Publ Ag
dc.relation.ispartofDaru-Journal of Pharmaceutical Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250518
dc.subjectAcinetobacter Baumannii
dc.subjectZnO NP
dc.subjectZinc borate
dc.subjectKlebsiella pneumoniae
dc.subjectPseudomonas aeruginosa
dc.subjectLung cancer
dc.titleActivity of zinc oxide and zinc borate nanoparticles against resistant bacteria in an experimental lung cancer model
dc.typeArticle

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