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http://hdl.handle.net/2445/130535
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DC Field | Value | Language |
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dc.contributor.author | Vila Estapé, Jordi | - |
dc.contributor.author | Hebert, Adelaide A. | - |
dc.contributor.author | Torrelo, Antonio | - |
dc.contributor.author | López, Yuly | - |
dc.contributor.author | Tato, Marta | - |
dc.contributor.author | García Castillo, María | - |
dc.contributor.author | Cantón, Rafael | - |
dc.date.accessioned | 2019-03-19T16:55:21Z | - |
dc.date.available | 2019-03-19T16:55:21Z | - |
dc.date.issued | 2019 | - |
dc.identifier.issn | 1478-7210 | - |
dc.identifier.uri | http://hdl.handle.net/2445/130535 | - |
dc.description.abstract | Introduction: Impetigo is the most common bacterial skin infection in children. Treatment is becoming complicated due to the development of antimicrobial resistance, especially in the main pathogen, Staphylococcus aureus. Ozenoxacin, a novel non-fluorinated topical quinolone antimicrobial, has demonstrated efficacy in impetigo. Areas covered: This article reviews the microbiology, pharmacodynamic and pharmacokinetic properties of ozenoxacin, and its clinical and microbiological efficacy in impetigo. Expert opinion: In an environment of increasing antimicrobial resistance and concurrent slowdown in antimicrobial development, the introduction of a new agent is a major event. Ozenoxacin is characterized by simultaneous affinity for DNA gyrase and topoisomerase IV, appears to be impervious to certain efflux pumps that confer bacterial resistance to other quinolones, shows low selection of resistant mutants, and has a mutant prevention concentration below its concentration in skin. These mechanisms protect ozenoxacin against development of resistance, while the absence of a fluorine atom in its structure confers a better safety profile versus fluoroquinolones. In vitro studies have demonstrated high potency of ozenoxacin against staphylococci and streptococci including resistant strains of S. aureus. Clinical trials of ozenoxacin in patients with impetigo reported high clinical and microbiological success rates. Preserving the activity and availability of ozenoxacin through antimicrobial stewardship is paramount. | - |
dc.format.extent | 10 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | Taylor&Francis | - |
dc.relation.isformatof | Reproducció del document publicat a: http://dx.doi.org/10.1080/14787210.2019.1573671 | - |
dc.relation.ispartof | Expert Review of Anti-infective Therapy, 2019, vol. 17, num. 3, p. 159-168 | - |
dc.relation.uri | http://dx.doi.org/10.1080/14787210.2019.1573671 | - |
dc.rights | cc-by-nc-nd (c) Vila et al., 2019 | - |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/es/ | * |
dc.source | Articles publicats en revistes (ISGlobal) | - |
dc.subject.classification | Malalties de la pell | - |
dc.subject.classification | Malalties bacterianes | - |
dc.subject.other | Skin diseases | - |
dc.subject.other | Bacterial diseases | - |
dc.title | Ozenoxacin: a review of preclinical and clinical efficacy | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.date.updated | 2019-02-14T15:29:15Z | - |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
Appears in Collections: | Articles publicats en revistes (ISGlobal) |
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File | Description | Size | Format | |
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VilaJ_Expert_Rev_Anti_Infect_Ther_2019.pdf | 673.47 kB | Adobe PDF | View/Open |
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