<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-27T15:56:46Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/12751" metadataPrefix="marc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/12751</identifier><datestamp>2024-09-04T14:52:20Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Bezerra Souza, Adriana</subfield>
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      <subfield code="a">Fernández García, Raquel</subfield>
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      <subfield code="a">Rodrigues, Gabriela F.</subfield>
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      <subfield code="a">Bolas Fernández, Francisco</subfield>
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      <subfield code="a">Dalastra Laurenti, Marcia</subfield>
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      <subfield code="a">Passero, Luiz Felipe</subfield>
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      <subfield code="a">Lalatsa, Aikaterini</subfield>
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      <subfield code="a">Serrano López, Dolores Remedios</subfield>
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      <subfield code="c">2019-07-20</subfield>
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      <subfield code="a">Leishmaniasis is a neglected tropical disease a_ecting more than 12 million people worldwide, which in its visceral clinical form (VL) is characterised by the accumulation of parasites in the liver and spleen, and can lead to death if not treated. Available treatments are not well tolerated due to severe adverse e_ects, need for parenteral administration and patient hospitalisation, and long duration of expensive treatments. These treatment realities justify the search for new e_ective drugs, repurposing existing licensed drugs towards safer and non-invasive cost-e_ective medicines for VL.
In this work, we provide proof of concept studies of butenafine and butenafine self-nanoemulsifying drug delivery systems (B-SNEDDS) against Leishmania infantum. Liquid B-SNEDDS were optimised using design of experiments, and then were spray-dried onto porous colloidal silica carriers to produce solid-B-SNEDDS with enhanced flow properties and drug stability. Optimal liquid B-SNEDDS consisted of Butenafine:Capryol 90:Peceol:Labrasol (3:49.5:24.2:23.3 w/w), which were then sprayed-dried with Aerosil 200 with a final 1:2 (Aerosil:liquid B-SNEDDS w/w) ratio. Spray-dried particles exhibited near-maximal drug loading, while maintaining excellent powder flow properties (angle of repose &lt;10_) and sustained release in acidic gastrointestinal media. Solid-B-SNEDDS demonstrated greater selectivity index against promastigotes and L. infantum-infected amastigotes than butenafine alone. Developed oral solid nanomedicines enable the non-invasive and safe administration of butenafine as a cost-e_ective and readily scalable repurposed medicine for VL.</subfield>
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      <subfield code="a">Bezerra Souza, A., Fernández García, R., Rodrigues, G. F. et al. «Repurposing Butenafine as An Oral Nanomedicine for Visceral Leishmaniasis». Pharmaceutics, vol. 11, n.o 7, julio de 2019, p. 353. DOI.org (Crossref), https://doi.org/10.3390/pharmaceutics11070353.</subfield>
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      <subfield code="a">10.3390/pharmaceutics11070353</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.14352/12751</subfield>
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      <subfield code="a">https://doi.org/10.3390/pharmaceutics11070353</subfield>
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      <subfield code="a">Repurposing Butenafine as An Oral Nanomedicine for Visceral Leishmaniasis</subfield>
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