Zein-based nanoparticles as oral carriers for insulin delivery

Zein, the major storage protein from corn, has a GRAS (Generally Regarded as Safe) status and may be easily transformed into nanoparticles, offering significant payloads for protein materials without affecting their stability. In this work, the capability of bare zein nanoparticles (mucoadhesive) an...

Descripción completa

Detalles Bibliográficos
Autores: Reboredo-Fuentes, C. (Cristian)|||/items/33a5afad-e78b-4aac-9847-14421580f6de, Gonzalez-Navarro, C.J. (Carlos Javier)|||/items/480527b9-23db-4625-b9e0-a91f385e9a1a, Martínez-López, A.L. (Ana Luisa)|||/items/c09a6a4f-fa01-4f50-b224-ad0ce9731cea, Martinez-Oharriz, C. (Cristina)|||/items/e9c18b09-044e-4df2-9269-5875b2c8e1ef, Sarmento, B. (Bruno)|||/items/01a87ac2-1a6b-47e8-a5f1-b4c01de792f2, Irache, J.M. (Juan Manuel)|||/items/c7cbbe9e-faeb-47e1-b7e8-2d956ca50173
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:inglés
OAI Identifier:oai:dadun.unav.edu:10171/113129
Acceso en línea:https://hdl.handle.net/10171/113129
Access Level:acceso abierto
Palabra clave:Zein
insulin
nanoparticles
mucus-permeating
poly(ethylene glicol)
oral delivery
Descripción
Sumario:Zein, the major storage protein from corn, has a GRAS (Generally Regarded as Safe) status and may be easily transformed into nanoparticles, offering significant payloads for protein materials without affecting their stability. In this work, the capability of bare zein nanoparticles (mucoadhesive) and nanoparticles coated with poly(ethylene glycol) (mucus-permeating) was evaluated as oral carriers of insulin (I-NP and I-NP-PEG, respectively). Both nanocarriers displayed sizes of around 270 nm, insulin payloads close to 80 µg/mg and did not induce cytotoxic effects in Caco-2 and HT29-MTX cell lines. In Caenorhabditis elegans, where insulin decreases fat storage, I-NP-PEG induced a higher reduction in the fat content than I-NP and slightly lower than the control (Orlistat). In diabetic rats, nanoparticles induced a potent hypoglycemic effect and achieved an oral bioavailability of 4.2% for I-NP and 10.2% for I-NP-PEG. This superior effect observed for I-NP-PEG would be related to their capability to diffuse through the mucus layer and reach the surface of enterocytes (where insulin would be released), whereas the mucoadhesive I-NP would remain trapped in the mucus, far away from the absorptive epithelium. In summary, PEG-coated zein nanoparticles may be an interesting device for the effective delivery of proteins through the oral route.