How Can Biomolecules Improve Mucoadhesion of Oral Insulin? A Comprehensive Insight using Ex-Vivo, In Silico, and In Vivo Models

Bibliographic Details
Main Author: Amaral, Mariana
Publication Date: 2020
Other Authors: Martins, Ana Sofia, Catarino, José, Faísca, Pedro, Kumar, Pradeep, Pinto, João F., Pinto, Rui, Correia, Isabel, Ascensão, Lia, Afonso, Ricardo A., Gaspar, M. Manuela, Charmier, Adília J., Figueiredo, Isabel Vitória, Reis, Catarina Pinto
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://hdl.handle.net/10316/105819
https://doi.org/10.3390/biom10050675
Summary: Currently, insulin can only be administered through the subcutaneous route. Due to the flaws associated with this route, it is of interest to orally deliver this drug. However, insulin delivered orally has several barriers to overcome as it is degraded by the stomach's low pH, enzymatic content, and poor absorption in the gastrointestinal tract. Polymers with marine source like chitosan are commonly used in nanotechnology and drug delivery due to their biocompatibility and special features. This work focuses on the preparation and characterization of mucoadhesive insulin-loaded polymeric nanoparticles. Results showed a suitable mean size for oral administration (<600 nm by dynamic laser scattering), spherical shape, encapsulation efficiency (59.8%), and high recovery yield (80.6%). Circular dichroism spectroscopy demonstrated that protein retained its secondary structure after encapsulation. Moreover, the mucoadhesive potential of the nanoparticles was assessed in silico and the results, corroborated with ex-vivo experiments, showed that using chitosan strongly increases mucoadhesion. Besides, in vitro and in vivo safety assessment of the final formulation were performed, showing no toxicity. Lastly, the insulin-loaded nanoparticles were effective in reducing diabetic rats' glycemia. Overall, the coating of insulin-loaded nanoparticles with chitosan represents a potentially safe and promising approach to protect insulin and enhance peroral delivery.
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spelling How Can Biomolecules Improve Mucoadhesion of Oral Insulin? A Comprehensive Insight using Ex-Vivo, In Silico, and In Vivo Modelsmarine-derived biomoleculesdiabetes mellitusinsulinmucoadhesionnanoparticleoral deliveryAdhesivesAdministration, OralAnimalsCaco-2 CellsChitosanHumansInsulinMaleMouth MucosaNanoparticlesOral Mucosal AbsorptionRatsRats, WistarCell AdhesionCurrently, insulin can only be administered through the subcutaneous route. Due to the flaws associated with this route, it is of interest to orally deliver this drug. However, insulin delivered orally has several barriers to overcome as it is degraded by the stomach's low pH, enzymatic content, and poor absorption in the gastrointestinal tract. Polymers with marine source like chitosan are commonly used in nanotechnology and drug delivery due to their biocompatibility and special features. This work focuses on the preparation and characterization of mucoadhesive insulin-loaded polymeric nanoparticles. Results showed a suitable mean size for oral administration (<600 nm by dynamic laser scattering), spherical shape, encapsulation efficiency (59.8%), and high recovery yield (80.6%). Circular dichroism spectroscopy demonstrated that protein retained its secondary structure after encapsulation. Moreover, the mucoadhesive potential of the nanoparticles was assessed in silico and the results, corroborated with ex-vivo experiments, showed that using chitosan strongly increases mucoadhesion. Besides, in vitro and in vivo safety assessment of the final formulation were performed, showing no toxicity. Lastly, the insulin-loaded nanoparticles were effective in reducing diabetic rats' glycemia. Overall, the coating of insulin-loaded nanoparticles with chitosan represents a potentially safe and promising approach to protect insulin and enhance peroral delivery.MDPI2020-04-27info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://hdl.handle.net/10316/105819https://hdl.handle.net/10316/105819https://doi.org/10.3390/biom10050675eng2218-273XAmaral, MarianaMartins, Ana SofiaCatarino, JoséFaísca, PedroKumar, PradeepPinto, João F.Pinto, RuiCorreia, IsabelAscensão, LiaAfonso, Ricardo A.Gaspar, M. ManuelaCharmier, Adília J.Figueiredo, Isabel VitóriaReis, Catarina Pintoinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2023-03-09T21:31:12Zoai:estudogeral.uc.pt:10316/105819Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T05:56:14.807033Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv How Can Biomolecules Improve Mucoadhesion of Oral Insulin? A Comprehensive Insight using Ex-Vivo, In Silico, and In Vivo Models
title How Can Biomolecules Improve Mucoadhesion of Oral Insulin? A Comprehensive Insight using Ex-Vivo, In Silico, and In Vivo Models
spellingShingle How Can Biomolecules Improve Mucoadhesion of Oral Insulin? A Comprehensive Insight using Ex-Vivo, In Silico, and In Vivo Models
Amaral, Mariana
marine-derived biomolecules
diabetes mellitus
insulin
mucoadhesion
nanoparticle
oral delivery
Adhesives
Administration, Oral
Animals
Caco-2 Cells
Chitosan
Humans
Insulin
Male
Mouth Mucosa
Nanoparticles
Oral Mucosal Absorption
Rats
Rats, Wistar
Cell Adhesion
title_short How Can Biomolecules Improve Mucoadhesion of Oral Insulin? A Comprehensive Insight using Ex-Vivo, In Silico, and In Vivo Models
title_full How Can Biomolecules Improve Mucoadhesion of Oral Insulin? A Comprehensive Insight using Ex-Vivo, In Silico, and In Vivo Models
title_fullStr How Can Biomolecules Improve Mucoadhesion of Oral Insulin? A Comprehensive Insight using Ex-Vivo, In Silico, and In Vivo Models
title_full_unstemmed How Can Biomolecules Improve Mucoadhesion of Oral Insulin? A Comprehensive Insight using Ex-Vivo, In Silico, and In Vivo Models
title_sort How Can Biomolecules Improve Mucoadhesion of Oral Insulin? A Comprehensive Insight using Ex-Vivo, In Silico, and In Vivo Models
author Amaral, Mariana
author_facet Amaral, Mariana
Martins, Ana Sofia
Catarino, José
Faísca, Pedro
Kumar, Pradeep
Pinto, João F.
Pinto, Rui
Correia, Isabel
Ascensão, Lia
Afonso, Ricardo A.
Gaspar, M. Manuela
Charmier, Adília J.
Figueiredo, Isabel Vitória
Reis, Catarina Pinto
author_role author
author2 Martins, Ana Sofia
Catarino, José
Faísca, Pedro
Kumar, Pradeep
Pinto, João F.
Pinto, Rui
Correia, Isabel
Ascensão, Lia
Afonso, Ricardo A.
Gaspar, M. Manuela
Charmier, Adília J.
Figueiredo, Isabel Vitória
Reis, Catarina Pinto
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Amaral, Mariana
Martins, Ana Sofia
Catarino, José
Faísca, Pedro
Kumar, Pradeep
Pinto, João F.
Pinto, Rui
Correia, Isabel
Ascensão, Lia
Afonso, Ricardo A.
Gaspar, M. Manuela
Charmier, Adília J.
Figueiredo, Isabel Vitória
Reis, Catarina Pinto
dc.subject.por.fl_str_mv marine-derived biomolecules
diabetes mellitus
insulin
mucoadhesion
nanoparticle
oral delivery
Adhesives
Administration, Oral
Animals
Caco-2 Cells
Chitosan
Humans
Insulin
Male
Mouth Mucosa
Nanoparticles
Oral Mucosal Absorption
Rats
Rats, Wistar
Cell Adhesion
topic marine-derived biomolecules
diabetes mellitus
insulin
mucoadhesion
nanoparticle
oral delivery
Adhesives
Administration, Oral
Animals
Caco-2 Cells
Chitosan
Humans
Insulin
Male
Mouth Mucosa
Nanoparticles
Oral Mucosal Absorption
Rats
Rats, Wistar
Cell Adhesion
description Currently, insulin can only be administered through the subcutaneous route. Due to the flaws associated with this route, it is of interest to orally deliver this drug. However, insulin delivered orally has several barriers to overcome as it is degraded by the stomach's low pH, enzymatic content, and poor absorption in the gastrointestinal tract. Polymers with marine source like chitosan are commonly used in nanotechnology and drug delivery due to their biocompatibility and special features. This work focuses on the preparation and characterization of mucoadhesive insulin-loaded polymeric nanoparticles. Results showed a suitable mean size for oral administration (<600 nm by dynamic laser scattering), spherical shape, encapsulation efficiency (59.8%), and high recovery yield (80.6%). Circular dichroism spectroscopy demonstrated that protein retained its secondary structure after encapsulation. Moreover, the mucoadhesive potential of the nanoparticles was assessed in silico and the results, corroborated with ex-vivo experiments, showed that using chitosan strongly increases mucoadhesion. Besides, in vitro and in vivo safety assessment of the final formulation were performed, showing no toxicity. Lastly, the insulin-loaded nanoparticles were effective in reducing diabetic rats' glycemia. Overall, the coating of insulin-loaded nanoparticles with chitosan represents a potentially safe and promising approach to protect insulin and enhance peroral delivery.
publishDate 2020
dc.date.none.fl_str_mv 2020-04-27
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://hdl.handle.net/10316/105819
https://hdl.handle.net/10316/105819
https://doi.org/10.3390/biom10050675
url https://hdl.handle.net/10316/105819
https://doi.org/10.3390/biom10050675
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2218-273X
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv MDPI
publisher.none.fl_str_mv MDPI
dc.source.none.fl_str_mv reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron:RCAAP
instname_str FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron_str RCAAP
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reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository.name.fl_str_mv Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
repository.mail.fl_str_mv info@rcaap.pt
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