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dc.contributor.authorSánchez, María Teresa
dc.contributor.authorRuiz, María Adolfina
dc.contributor.authorCastán, Herminia
dc.contributor.authorMorales Hernández, María Encarnación 
dc.date.accessioned2024-02-08T09:59:24Z
dc.date.available2024-02-08T09:59:24Z
dc.date.issued2018-01
dc.identifier.citationEuropean Journal of Pharmaceutical Sciences Volume 112, 15 January 2018, Pages 63-70es_ES
dc.identifier.urihttps://hdl.handle.net/10481/88699
dc.description.abstractAbstract Vulvovaginal candidosis caused by Candida spp. is the most prevalent vaginal infection in Europe and the second one in EE.UU, so it has become a major female concern. Probiotics bacteria have been proposed as an alternative treatment with the aim of avoiding the adverse effects associated with conventional therapies including antibiotics and other aggressive drugs for the vaginal mucosa and microbiota. The purpose of this work was to design and develop a novel vaginal tablet that contained Lactobacillus spp. bacteria as a treatment against vulvovaginal infections. A total of 21 two-layers vaginal tablets, which contained different polymeric ratios, were proposed. However, formulation F4 (20 mg Na-CMC; 50 mg Carbopol® 934; 20 mg chitosan) was selected as optimal according to its swelling index and dissolution/erosion capability. F4 tablets showed suitable technological properties for vaginal administration as well as mucoadhesion time (24.36 ± 0.88 h) and force (0.0941 N). Disintegration assay in simulated vaginal fluid (SVF, pH 5.5) showed that effervescent layer disappeared in 27.48 ± 0.05 s whilst matrix layer was totally gelled in 1 h. Two different release profiles were achieved; on the one hand, a promptly release due to the dissolution of both effervescent layer and matrix layer's surface (1.10 × 108 CFU/g), on the second hand, a prolonged released of the remaining bacteria until 24 h (5.48 × 107 CFU/g). For stability and storage study, it was found that bacteria viability was constant until 90 days in both ways of storage, in a desiccator and at room temperature, with a final dosage of 108 CFU/g which was considered appropriate for vaginal therapy (108–1010 CFU/g).es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.titleA novel double-layer mucoadhesive Tablet containing probiotic strain for vaginal administration: Design, development and technological evaluationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.1016/j.ejps.2017.11.006
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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