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dc.contributor.authorAbidin, Ismin Zainol
dc.contributor.authorFehrenbach, Gustavo Waltzer
dc.contributor.authorGately, Noel
dc.date.accessioned2024-04-11T14:01:34Z
dc.date.available2024-04-11T14:01:34Z
dc.date.copyright2024
dc.date.issued2024-03-08
dc.identifier.citationAbidin, I.Z., Murphy, E.J., Fehrenbach, G., Gately, N. (2024). Chitosan-(poly)acrylic acid polyelectrolyte complexes: enhanced mucoadhesion and sustained drug release in vaginal tabletsCarbohydrate Polymer Technologies and Applications. 7, 100480. https://doi.org/10.1016/j.carpta.2024.100480en_US
dc.identifier.issn2666-8939
dc.identifier.urihttps://research.thea.ie/handle/20.500.12065/4790
dc.description.abstractPolyelectrolyte complexes (PECs) have emerged as promising vehicles for medical applications, attributable to their non-toxicity, non-immunogenicity, and ability for controlled drug release. Notably, their inherent mucoadhesive properties are being leveraged for sustained drug delivery across mucosal barriers, including vaginal, ocular, nasal, and buccal membranes. This study delves into the formulation and effects of chitosan-(poly)acrylic acid-based PEC for vaginal tablet applications. A comparative analysis of various polymer combinations was conducted, emphasizing the differential impacts of low versus high-molecular weight chitosan. Results highlighted that PECs augmented the flowability of powder mixtures and bolstered the tablets' physical properties. Moreover, PEC-enhanced formulations exhibited a pronounced increase in swelling efficiency, with swelling index values reaching up to 92.67 % ± 1.90, ensuring structural integrity during dissolution. In ex vivo mucoadhesion tests, tablets from PEC mixes demonstrated extended adhesion, surpassing 48 h for certain formulations. The optimized PEC formulation successfully achieved sustained drug release while retaining tablet adhesion for the duration of the release period.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.ispartofCarbohydrate Polymer Technologies and Applicationsen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectPolyelectrolyte complexen_US
dc.subjectChitosanen_US
dc.subject(Poly)acrylic aciden_US
dc.subjectMucoadhesive vaginal tableten_US
dc.subjectSustained releaseen_US
dc.subjectSwellingen_US
dc.titleChitosan-(poly)acrylic acid polyelectrolyte complexes: enhanced mucoadhesion and sustained drug release in vaginal tabletsen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.contributor.affiliationTechnological University of the Shannon: Midlands Midwesten_US
dc.contributor.sponsorAIT President's Seed Fund PSF2017-IMen_US
dc.identifier.doi10.1016/j.carpta.2024.100480en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2912-4210en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-5620-0058en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-9389-3391en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-2610-2975en_US
dc.rights.accessrightsinfo:eu-repo/semantics/openAccessen_US
dc.subject.departmentPRISM: Polymer, Recycling, Industrial, Sustainability and Manufacturing Institute: TUS Midlandsen_US
dc.type.versioninfo:eu-repo/semantics/publishedVersionen_US
dc.relation.projectidPSF2017-IMen_US


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States