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Targeting lung macrophages for fungal and parasitic pulmonary infections with innovative amphotericin B dry powder inhalers

dc.contributor.authorde Pablo, E
dc.contributor.authorO'Connell, Peter
dc.contributor.authorFernández García, Raquel
dc.contributor.authorMarchand, Sandrine
dc.contributor.authorChauzy, A.
dc.contributor.authorTewes, F
dc.contributor.authorDea Ayuela, María Auxiliadora
dc.contributor.authorKumar, D.
dc.contributor.authorBolas Fernández, Francisco
dc.contributor.authorBallesteros Papantonakis, María De La Paloma
dc.contributor.authorTorrado Durán, Juan José
dc.contributor.authorHealy, Anne Marie
dc.contributor.authorSerrano López, Dolores Remedios
dc.date.accessioned2023-06-22T12:41:12Z
dc.date.available2023-06-22T12:41:12Z
dc.date.issued2023-03-25
dc.description.abstractThe incidence of fungal pulmonary infections is known to be on the increase, and yet there is an alarming gap in terms of marketed antifungal therapies that are available for pulmonary administration. Amphotericin B (AmB) is a highly efficient broad-spectrum antifungal only marketed as an intravenous formulation. Based on the lack of effective antifungal and antiparasitic pulmonary treatments, the aim of this study was to develop a carbohydrate-based AmB dry powder inhaler (DPI) formulation, prepared by spray drying. Amorphous AmB microparticles were developed by combining 39.7% AmB with 39.7% γ-cyclodextrin, 8.1% mannose and 12.5% leucine. An increase in the mannose concentration from 8.1 to 29.8%, led to partial drug crystallisation. Both formulations showed good in vitro lung deposition characteristics (80% FPF< 5 µm and MMAD < 3 µm) at different air flow rates (60 and 30 L/min) when used with a DPI, but also during nebulisation upon reconstitution in water.en
dc.description.departmentDepto. de Farmacia Galénica y Tecnología Alimentaria
dc.description.facultyFac. de Farmacia
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia e Innovacion de España
dc.description.sponsorshipScience Foundation Ireland
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/76894
dc.identifier.doi10.1016/j.ijpharm.2023.122788
dc.identifier.issn0378-5173
dc.identifier.officialurlhttps://www.sciencedirect.com/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/73046
dc.journal.titleInternational journal of pharmaceutics
dc.language.isoeng
dc.page.initial122788
dc.publisherElsevier
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subject.cdu615.4
dc.subject.keywordAmphotericin B
dc.subject.keywordPulmonary administration
dc.subject.keywordSpray drying
dc.subject.keywordDry powder inhaler
dc.subject.keywordASAP
dc.subject.keywordAmorphous
dc.subject.keywordCrystalline
dc.subject.ucmTecnología farmaceútica
dc.titleTargeting lung macrophages for fungal and parasitic pulmonary infections with innovative amphotericin B dry powder inhalersen
dc.typejournal article
dc.volume.number635
dspace.entity.typePublication
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relation.isAuthorOfPublication85c3c6ba-b0e6-4fcd-af4f-51fb29942894
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relation.isAuthorOfPublication.latestForDiscoverya577e97d-a6c8-4552-8c78-f35c42216b92

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