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Polysaccharide-Based Carriers for Pulmonary Insulin Delivery: The Potential of Coffee as an Unconventional Source

Non-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 g...

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Autores principales: Valente, Sara A., Lopes, Guido R., Ferreira, Isabel, Galrinho, Miguel F., Almeida, Margarida, Ferreira, Paula, Cruz, Maria T., Coimbra, Manuel A., Passos, Cláudia P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10144660/
https://www.ncbi.nlm.nih.gov/pubmed/37111698
http://dx.doi.org/10.3390/pharmaceutics15041213
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author Valente, Sara A.
Lopes, Guido R.
Ferreira, Isabel
Galrinho, Miguel F.
Almeida, Margarida
Ferreira, Paula
Cruz, Maria T.
Coimbra, Manuel A.
Passos, Cláudia P.
author_facet Valente, Sara A.
Lopes, Guido R.
Ferreira, Isabel
Galrinho, Miguel F.
Almeida, Margarida
Ferreira, Paula
Cruz, Maria T.
Coimbra, Manuel A.
Passos, Cláudia P.
author_sort Valente, Sara A.
collection PubMed
description Non-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.
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spelling pubmed-101446602023-04-29 Polysaccharide-Based Carriers for Pulmonary Insulin Delivery: The Potential of Coffee as an Unconventional Source Valente, Sara A. Lopes, Guido R. Ferreira, Isabel Galrinho, Miguel F. Almeida, Margarida Ferreira, Paula Cruz, Maria T. Coimbra, Manuel A. Passos, Cláudia P. Pharmaceutics Article Non-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. MDPI 2023-04-11 /pmc/articles/PMC10144660/ /pubmed/37111698 http://dx.doi.org/10.3390/pharmaceutics15041213 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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/).
spellingShingle Article
Valente, Sara A.
Lopes, Guido R.
Ferreira, Isabel
Galrinho, Miguel F.
Almeida, Margarida
Ferreira, Paula
Cruz, Maria T.
Coimbra, Manuel A.
Passos, Cláudia P.
Polysaccharide-Based Carriers for Pulmonary Insulin Delivery: The Potential of Coffee as an Unconventional Source
title Polysaccharide-Based Carriers for Pulmonary Insulin Delivery: The Potential of Coffee as an Unconventional Source
title_full Polysaccharide-Based Carriers for Pulmonary Insulin Delivery: The Potential of Coffee as an Unconventional Source
title_fullStr Polysaccharide-Based Carriers for Pulmonary Insulin Delivery: The Potential of Coffee as an Unconventional Source
title_full_unstemmed Polysaccharide-Based Carriers for Pulmonary Insulin Delivery: The Potential of Coffee as an Unconventional Source
title_short Polysaccharide-Based Carriers for Pulmonary Insulin Delivery: The Potential of Coffee as an Unconventional Source
title_sort polysaccharide-based carriers for pulmonary insulin delivery: the potential of coffee as an unconventional source
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10144660/
https://www.ncbi.nlm.nih.gov/pubmed/37111698
http://dx.doi.org/10.3390/pharmaceutics15041213
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