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dc.contributor.authorMcConville, Christopher
dc.contributor.authorMajor, Ian
dc.contributor.authorDevlin, Brid
dc.contributor.authorBrimer, Andrew
dc.date.accessioned2020-05-22T15:38:10Z
dc.date.available2020-05-22T15:38:10Z
dc.date.copyright2016
dc.date.issued2016-07
dc.identifier.citationMcConville, C., Major, I., Devlin, B., Brimer, A. (2016). Development of a multi-layered vaginal tablet containing Dapivirine, Levonorgestrel and Acyclovir for use as a multipurpose prevention technology. European Journal of Pharmaceutics and Biopharmaceutics. Jul;104:171-9. doi: 10.1016/j.ejpb.2016.05.003en_US
dc.identifier.issn0939-6411
dc.identifier.otherArticles - Materials Research Instituteen_US
dc.identifier.urihttp://research.thea.ie/handle/20.500.12065/3233
dc.description.abstractMultipurpose prevention technologies (MPTs) are preferably single dosage forms designed to simultaneously address multiple sexual and reproductive health needs, such as unintended pregnancy, HIV infection and other sexually transmitted infections (STIs). This manuscript describes the development of a range of multilayered vaginal tablets, with both immediate and sustained release layers capable of delivering the antiretroviral drug dapivirine, the contraceptive hormone levonorgestrel, and the anti-herpes simplex virus drug acyclovir at independent release rates from a single dosage form. Depending on the design of the tablet in relation to the type (immediate or sustained release) or number of layers, the dose of each drug could be individually controlled. For example one tablet design was able to provide immediate release of all three drugs, while another tablet design was able to provide immediate release of both acyclovir and levonorgestrel, while providing sustained release of Dapivirnie for up to 8 hours. A third tablet design was able to provide immediate release of both acyclovir and levonorgestrel, a large initial burst of Dapivirine, followed by sustained release of Dapivirine for up to 8 hours. All of the tablets passed the test for friability with a percent friability of less than 1%. The hardness of all tablet designs were between 115 and 153 Newtons, while their drug content met the European Pharmacopeia 2.9.40 Uniformity of Dosage units acceptance value at level 1 and 2. Finally, the accelerated stability of all three actives was significantly enhanced in comparison to a mixed drug control.en_US
dc.formatPDFen_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofEuropean Journal of Pharmaceutics and Biopharmaceuticsen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/ie/*
dc.subjectMultipurpose prevention technologyen_US
dc.subjectContraceptionen_US
dc.subjectSexually transmitted infectionsen_US
dc.subjectDapivirineen_US
dc.subjectLevonorgesterelen_US
dc.subjectAcycloviren_US
dc.titleDevelopment of a multi-layered vaginal tablet containing Dapivirine, Levonorgestrel and Acyclovir for use as a multipurpose prevention technology.en_US
dc.typeArticleen_US
dc.description.peerreviewyesen_US
dc.identifier.doidoi: 10.1016/j.ejpb.2016.05.003
dc.identifier.orcidhttps://orcid.org/0000-0002-1727-2454
dc.rights.accessOpen Accessen_US
dc.subject.departmentMaterials Research Instituteen_US


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Attribution-NonCommercial-NoDerivs 3.0 Ireland
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Ireland