Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/58060

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dc.contributor.authorMiranda, Margarida Silvapor
dc.contributor.authorRodrigues, Márcia T.por
dc.contributor.authorDomingues, Rui Miguel Andradepor
dc.contributor.authorCosta, Rui R.por
dc.contributor.authorPaz, Elvirapor
dc.contributor.authorRodríguez-Abreu, Carlospor
dc.contributor.authorFreitas, Paulopor
dc.contributor.authorAlmeida, B. G.por
dc.contributor.authorCarvalho, M. Alicepor
dc.contributor.authorGonçalves, Carine Machadopor
dc.contributor.authorFerreira, Catarina Machadopor
dc.contributor.authorTorrado, Egídiopor
dc.contributor.authorReis, R. L.por
dc.contributor.authorPedrosa, Jorgepor
dc.contributor.authorGomes, Manuela E.por
dc.date.accessioned2019-01-11T12:24:29Z-
dc.date.available2019-09-01T06:00:53Z-
dc.date.issued2018-08-
dc.identifier.issn2192-2640-
dc.identifier.urihttps://hdl.handle.net/1822/58060-
dc.description.abstractTuberculosis (TB) is an infectious disease which affects millions of people worldwide. Inhalable polymeric dry powders are promising alternatives as anti-TB drug carriers to the alveoli milieu and infected macrophages, with potential to significantly improve the therapeutics efficiency. Here, the development of a magnetically responsive microparticulate system for pulmonary delivery of an anti-TB drug candidate (P3) is reported. Microparticles (MPs) are developed based on a cast method using calcium carbonate sacrificial templates and incorporate superparamagnetic iron oxide nanoparticles to concentrate MPs in alveoli and enable drug on demand release upon actuation of an external alternate magnetic field (AMF). The MPs are shown to be suitable for P3 delivery to the lower airways and for alveolar macrophage phagocytosis. The developed MPs reveal unique and promising features to be used as an inhalable dry powder allowing the AMF control over dosage and frequency of drug delivery anticipating improved TB treatments.por
dc.description.sponsorshipThe authors wish to acknowledge the financial support from the Portuguese Foundation for Science and Technology (FCT) for the postdoctoral grant of M.S.M. (SFRH/BPD/110868/2015) and R.M.A.D (SFRH/BPD/112459/2015), FCT grant of E.T. (IF/01390/2014) and Recognize project (UTAP-ICDT/CTM-BIO/0023/2014). This article is also a result of the project “Accelerating tissue engineering and personalized medicine discoveries by the integration of key enabling nanotechnologies, marine-derived biomaterials and stem cells,” supported by Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF). The authors acknowledge the financial support from the European Union Framework Programme for Research and Innovation HORIZON 2020, under the TEAMING Grant Agreement No. 739572 – The Discoveries CTR.por
dc.language.isoengpor
dc.publisherWileypor
dc.relationinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/137422/PTpor
dc.rightsopenAccesspor
dc.subjectBiomaterialspor
dc.subjectInhalable dry powderspor
dc.subjectMagnetic drug targetingpor
dc.subjectMicroparticulate systemspor
dc.subjectRemotely controlled drug releasepor
dc.titleDevelopment of Inhalable Superparamagnetic Iron Oxide Nanoparticles (SPIONs) in microparticulate system for antituberculosis drug deliverypor
dc.typearticlepor
dc.peerreviewedyespor
oaire.citationStartPagee1800124-1por
oaire.citationEndPagee1800124-12por
oaire.citationIssue15por
oaire.citationVolume7por
dc.identifier.eissn2192-2659-
dc.identifier.doi10.1002/adhm.201800124por
dc.identifier.pmid29797461por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersionpor
dc.subject.wosScience & Technologypor
sdum.journalAdvanced Healthcare Materialspor
Aparece nas coleções:ICVS - Artigos em revistas internacionais / Papers in international journals

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