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Transdermal therapeutic systems for memantine delivery. Comparison of passive and iontophoretic transport

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Transdermal therapeutic systems for memantine delivery. Comparison of passive and iontophoretic transport

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dc.contributor.author Del Rio-Sancho, S. es_ES
dc.contributor.author Serna-Jiménez, C.E. es_ES
dc.contributor.author Sebastián-Morelló, M. es_ES
dc.contributor.author Calatayud-Pascual, M.A. es_ES
dc.contributor.author Balaguer-Fernández, C. es_ES
dc.contributor.author Femenia-Font, A. es_ES
dc.contributor.author Kalia, Y.N. es_ES
dc.contributor.author MERINO SANJUÁN, VIRGINIA es_ES
dc.contributor.author Lopez-Castellano, A. es_ES
dc.date.accessioned 2020-11-05T04:32:59Z
dc.date.available 2020-11-05T04:32:59Z
dc.date.issued 2017-01-30 es_ES
dc.identifier.issn 0378-5173 es_ES
dc.identifier.uri http://hdl.handle.net/10251/154101
dc.description.abstract [EN] Memantine is a non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist used in the treatment of moderate to severe dementia including the symptoms of Alzheimer's disease (AD). It is administered orally but compliance, swallowing problems and the routine use of multiple medications in elderly AD patients means that an alternative route of administration would be of interest. The aim of the present. study was to develop memantine hydrochloride occlusive transdermal therapeutic systems (TI'S) for passive and iontophoretic delivery across the skin. Polyvinyl pyrrolidone (PVP) and a mixture with polyvinyl alcohol (PVA) were employed as polymeric matrices. The study involved the TTS characterization in addition to quantification of the memantine transport across porcine skin in vitro. The evaluation of the ITS physical properties suggested that systems were made more mechanically resistant by including PVA (6%) or high concentrations of PVP (24%). Moreover, a linear correlation was observed between the concentration of PVP and the bioadhesion of the systems. Drug delivery expefiments showed that the highest transdermal flux provided by a passive TTS (PVP 24% w/w limonene) was 8.89 +/- 0.81 mu g cm(-2) h(-1) whereas the highest iontophoretic transport was 46.4 +/- 3.6 mu g cm(-2) h(-1). These innovative TTS would enable two dosage regimens that could lead to therapeutic plasma concentrations. es_ES
dc.description.sponsorship The authors wish to thank the "Generalitat Valenciana" (AP-114/09; AP-155/10; AP-175/11) and the "Universidad CEU Cardenal Herrera" for their financial support. The authors also thank Pharsight corp. for the academic license of WinNonlin 5.0.1. es_ES
dc.language Inglés es_ES
dc.publisher Elsevier es_ES
dc.relation.ispartof International Journal of Pharmaceutics es_ES
dc.rights Reserva de todos los derechos es_ES
dc.subject Memantine es_ES
dc.subject Transdermal delivery es_ES
dc.subject Occlusive-systems es_ES
dc.subject Chemical penetration enhancers es_ES
dc.subject Iontophoresis es_ES
dc.title Transdermal therapeutic systems for memantine delivery. Comparison of passive and iontophoretic transport es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.1016/j.ijpharm.2016.11.038 es_ES
dc.relation.projectID info:eu-repo/grantAgreement/Generalitat Valenciana//AP-114%2F09/ES/Estudio de la administración transdérmica de memantina para el tratamiento de la enfermedad de Alzheimer/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/Generalitat Valenciana//AP-155%2F10/ES/Estudio de la administración transdérmica de memantina para el tratamiento de la enfermedad de Alzheimer./ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/Generalitat Valenciana//AP-175%2F11/ES/Desarrollo de un parche transdérmico de memantina para el tratamiento de la enfermedad de Alzheimer en fases avanzadas/ es_ES
dc.rights.accessRights Cerrado es_ES
dc.description.bibliographicCitation Del Rio-Sancho, S.; Serna-Jiménez, C.; Sebastián-Morelló, M.; Calatayud-Pascual, M.; Balaguer-Fernández, C.; Femenia-Font, A.; Kalia, Y.... (2017). Transdermal therapeutic systems for memantine delivery. Comparison of passive and iontophoretic transport. International Journal of Pharmaceutics. 517(1-2):104-111. https://doi.org/10.1016/j.ijpharm.2016.11.038 es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion https://doi.org/10.1016/j.ijpharm.2016.11.038 es_ES
dc.description.upvformatpinicio 104 es_ES
dc.description.upvformatpfin 111 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 517 es_ES
dc.description.issue 1-2 es_ES
dc.identifier.pmid 27865983 es_ES
dc.relation.pasarela S\365980 es_ES
dc.contributor.funder Generalitat Valenciana es_ES
dc.contributor.funder Universidad CEU Cardenal Herrera es_ES


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