Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/113662
DC FieldValueLanguage
dc.contributor.authorValente, Sara A.-
dc.contributor.authorLopes, Guido R.-
dc.contributor.authorFerreira, Isabel-
dc.contributor.authorGalrinho, Miguel F.-
dc.contributor.authorAlmeida, Margarida-
dc.contributor.authorFerreira, Paula-
dc.contributor.authorCruz, Maria T.-
dc.contributor.authorCoimbra, Manuel A.-
dc.contributor.authorPassos, Cláudia P.-
dc.date.accessioned2024-02-26T09:21:17Z-
dc.date.available2024-02-26T09:21:17Z-
dc.date.issued2023-04-11-
dc.identifier.issn1999-4923pt
dc.identifier.urihttps://hdl.handle.net/10316/113662-
dc.description.abstractNon-invasive routes for insulin delivery are emerging as alternatives to currently painful subcutaneous injections. For pulmonary delivery, formulations may be in powdered particle form, using carriers such as polysaccharides to stabilise the active principle. Roasted coffee beans and spent coffee grounds (SCG) are rich in polysaccharides, namely galactomannans and arabinogalactans. In this work, the polysaccharides were obtained from roasted coffee and SCG for the preparation of insulin-loaded microparticles. The galactomannan and arabinogalactan-rich fractions of coffee beverages were purified by ultrafiltration and separated by graded ethanol precipitations at 50% and 75%, respectively. For SCG, galactomannan-rich and arabinogalactan-rich fractions were recovered by microwave-assisted extraction at 150 °C and at 180 °C, followed by ultrafiltration. Each extract was spray-dried with insulin 10% (w/w). All microparticles had a raisin-like morphology and average diameters of 1-5 µm, which are appropriate for pulmonary delivery. Galactomannan-based microparticles, independently of their source, released insulin in a gradual manner, while arabinogalactan-based ones presented a burst release. The microparticles were seen to be non-cytotoxic for cells representative of the lung, specifically lung epithelial cells (A549) and macrophages (Raw 264.7) up to 1 mg/mL. This work shows how coffee can be a sustainable source of polysaccharide carriers for insulin delivery via the pulmonary route.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationThe authors thank Fundação para a Ciência e Tecnologia (FCT) co-financed by Programa Operacional Competitividade e Internacionalização, Portugal 2020 and União Europeia by the FEDER (FCT—Compete2020—Portugal 2020—FEDER/EU) N POCI-01-0145-FEDER-029560, project “PulManCar”. This research was also funded by University of Aveiro and FCT/MCTES, supporting LAQV-REQUIMTE (FCT UIDB/50006/2020) research unit, and CICECO-Aveiro Institute of Materials (UIDB/50011/2020, UIDP/50011/2020 & LA/P/0006/2020). Thanks are also due to CIBB (projects UIDB/04539/2020, UIDP/04539/2020 and LA/P/0058/2020)pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectdrug deliverypt
dc.subjectprotein deliverypt
dc.subjectmicroparticlespt
dc.subjectarabinogalactanspt
dc.subjectgalactomannanspt
dc.subjectinhalationpt
dc.titlePolysaccharide-Based Carriers for Pulmonary Insulin Delivery: The Potential of Coffee as an Unconventional Sourcept
dc.typearticle-
degois.publication.firstPage1213pt
degois.publication.issue4pt
degois.publication.titlePharmaceuticspt
dc.peerreviewedyespt
dc.identifier.doi10.3390/pharmaceutics15041213pt
degois.publication.volume15pt
dc.date.embargo2023-04-11*
uc.date.periodoEmbargo0pt
item.cerifentitytypePublications-
item.languageiso639-1en-
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0003-1084-1041-
Appears in Collections:FFUC- Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais
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