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

Author:

Valente Sara A.1ORCID,Lopes Guido R.1ORCID,Ferreira Isabel23ORCID,Galrinho Miguel F.1ORCID,Almeida Margarida4,Ferreira Paula4ORCID,Cruz Maria T.23ORCID,Coimbra Manuel A.1ORCID,Passos Cláudia P.1ORCID

Affiliation:

1. LAQV-REQUIMTE, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal

2. Center for Neuroscience and Cell Biology, University of Coimbra, 3004-517 Coimbra, Portugal

3. Faculty of Pharmacy, University of Coimbra, 3000-548 Coimbra, Portugal

4. CICECO, Department of Materials and Ceramic Engineering, University of Aveiro, 3810-193 Aveiro, Portugal

Abstract

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.

Funder

Fundação para a Ciência e Tecnologia

University of Aveiro

CICECO-Aveiro Institute of Materials

CIBB

Publisher

MDPI AG

Subject

Pharmaceutical Science

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