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dc.contributor.authorRolón, Miriam Soledad 
dc.contributor.authorHanna, Eustine
dc.contributor.authorVega Gómez, María Celeste 
dc.contributor.authorCoronel, Cathia Cecilia 
dc.contributor.authorDea-Ayuela, María Auxiliadora
dc.contributor.authorSerrano, Dolores Remedios
dc.contributor.authorLalatsa, Aikaterini
dc.contributor.otherFundación Moisés Bertonies
dc.date.accessioned2026-01-28T20:13:51Z
dc.date.available2026-01-28T20:13:51Z
dc.date.issued2022-08-29
dc.identifier.citationRolon, M., Hanna, E., Vega, C., Coronel, C., Dea-Ayuela, M. A., Serrano, D. R., & Lalatsa, A. (2022). Solid Nanomedicines of Nifurtimox and Benznidazole for the Oral Treatment of Chagas Disease. Pharmaceutics, 14(9), Artículo 1822. https://doi.org/10.3390/pharmaceutics14091822en
dc.identifier.issn1999-4923es
dc.identifier.otherhttps://doi.org/10.3390/pharmaceutics14091822es
dc.identifier.urihttp://hdl.handle.net/20.500.14066/4744
dc.descriptionCorrespondence: drserran@ucm.es (D.R.S.); aikaterini.lalatsa@strath.ac.uk (A.L.); Tel.: +44-141-548-2675 (A.L.).en
dc.descriptionThis article belongs to the Section Nanomedicine and Nanotechnology.en
dc.description.abstractChagas disease (CD) is a parasitic zoonosis endemic in Central and South America affecting nearly 10 million people, with 100 million people at high risk of contracting the disease. Treatment is only effective when received at the early stages of the disease and it involved two drugs (nifurtimox (NFX) and benznidazole (BNZ)). Both treatments require multiple daily administrations of high doses, suffer from variable efficacy and insufficient efficacy in chronic CD, many side effects, and a very long duration of treatment that results in poor compliance, while combined available therapies that lead to reduced duration of treatment are not available and polypharmacy reduces compliance and increases the cost further. Here we present self-nanoemulsified drug delivery systems (SNEDDS) able to produce easily scalable combined formulations of NFX and BNZ that can allow for tailoring of the dose and can be easily converted to oral solid dosage form by impregnation on mesoporous silica particles. SNEDDS demonstrated an enhanced solubilisation capacity for both drugs as demonstrated by flow-through studies and in vitro lipolysis studies. High loading of SNEDDS to Syloid 244 and 3050 silicas (2:1 w/w) allowed clinically translatable amounts of both NFX and BNZ to be loaded. Tablets prepared from NFX-BNZ combined SNEDDS loaded on Syloid 3050 silicas demonstration near complete dissolution in the flow through cell apparatus compared to NFX and BNZ commercial tablets respectively (Lampit® and Rochagan®). NFX-BNZ-SNEDDS demonstrated nanomolar efficacy in epimastigotes and amastigotes of T. cruzi with acceptable selectivity indexes and demonstrated enhanced survival and reduced parasitaemia in acute murine experimental models of CD. Thus, the results presented here illustrate the ability for an easily scalable and personalised combination oral therapy prepared from GRAS excipients, enabling treatment access worldwide for the treatment of CD.es
dc.description.sponsorshipConsejo Nacional de Ciencia y Tecnologíaes
dc.format.extent25 páginases
dc.language.isoenges
dc.publisherMultidisciplinary Digital Publishing Institutees
dc.rightsAtribución/Reconocimiento 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.classification6. Producción y tecnología industriales
dc.subject.classification6.16. Manufacture of basic pharmaceutical products and pharmaceutical preparationsen
dc.subject.otherBenznidazolees
dc.subject.otherChagas diseasees
dc.subject.otherNifurtimoxes
dc.subject.otherSelf-nanoemulsifying drug delivery systems (SNEDDS)es
dc.subject.otherSilicon dioxide (silica)es
dc.subject.otherSolid self-nanoemulsifying drug delivery systems (solid-SNEDDS)es
dc.subject.otherTrypanosomiasises
dc.titleSolid nanomedicines of nifurtimox and benznidazole for the oral treatment of Chagas diseasees
dc.typeinfo:eu-repo/semantics/articlees
dc.typeinfo:eu-repo/semantics/publishedVersiones
dc.identifier.doi10.3390/pharmaceutics14091822es
dc.description.fundingtextPrograma Paraguayo para el Desarrollo de la Ciencia y Tecnología. Programa Nacional de Incentivo a los Investigadoreses
dc.description.fundingtextPrograma Paraguayo para el Desarrollo de la Ciencia y Tecnología. Proyectos de investigación y desarrolloes
dc.issue.number9es
dc.journal.titlePharmaceuticses
dc.relation.projectCONACYT14-INV-022es
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.copyright© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).es
dc.volume.number14es


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Atribución/Reconocimiento 4.0 Internacional
Except where otherwise noted, this item's license is described as Atribución/Reconocimiento 4.0 Internacional