Quality by Design Approach for the Development of Liposome Carrying Ghrelin for Intranasal Administration
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10316/105332 https://doi.org/10.3390/pharmaceutics13050686 |
Resumo: | The therapeutic use of peptides has increasingly recognized in the development of new therapies. However, the susceptible enzymatic cleavage is a barrier that needs to overcome. Nose-to-brain delivery associated with liposomes can protect peptides against biodegradation and improve the accessibility to brain targets. The aim was to develop a liposomal formulation as ghrelin carrier. The quality by design (QbD) approach was used as a strategy for method development. The initial risk assessments were carried out using a fishbone diagram. A screening design study was performed for the critical material attributes/critical process parameters (CMAs/CPPs) on critical quality attributes (CQAs). Liposomes were obtained by hydrating phospholipid films, followed by extrusion or homogenization, and coated with chitosan. The optimized liposome formulation was produced by high-pressure homogenization coated with chitosan, and the resulted were liposomes size 72.25 ± 1.46 nm, PDI of 0.300 ± 0.027, the zeta potential of 50.3 ± 1.46 mV, and encapsulation efficiency of 53.2%. Moreover, chitosan coating improved performance in ex vivo permeation and mucoadhesion analyzes when compared to the uncoated liposome. In this context, chitosan coating is essential for the performance of the formulations in the ex vivo permeation and mucoadhesion analyzes. The intranasal administration of ghrelin liposomes coated with chitosan offers an innovative opportunity to treat cachexia. |
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Quality by Design Approach for the Development of Liposome Carrying Ghrelin for Intranasal Administrationghrelinintranasal routliposomesquality by design (QbD)cachexiaundernourishmentstarvationThe therapeutic use of peptides has increasingly recognized in the development of new therapies. However, the susceptible enzymatic cleavage is a barrier that needs to overcome. Nose-to-brain delivery associated with liposomes can protect peptides against biodegradation and improve the accessibility to brain targets. The aim was to develop a liposomal formulation as ghrelin carrier. The quality by design (QbD) approach was used as a strategy for method development. The initial risk assessments were carried out using a fishbone diagram. A screening design study was performed for the critical material attributes/critical process parameters (CMAs/CPPs) on critical quality attributes (CQAs). Liposomes were obtained by hydrating phospholipid films, followed by extrusion or homogenization, and coated with chitosan. The optimized liposome formulation was produced by high-pressure homogenization coated with chitosan, and the resulted were liposomes size 72.25 ± 1.46 nm, PDI of 0.300 ± 0.027, the zeta potential of 50.3 ± 1.46 mV, and encapsulation efficiency of 53.2%. Moreover, chitosan coating improved performance in ex vivo permeation and mucoadhesion analyzes when compared to the uncoated liposome. In this context, chitosan coating is essential for the performance of the formulations in the ex vivo permeation and mucoadhesion analyzes. The intranasal administration of ghrelin liposomes coated with chitosan offers an innovative opportunity to treat cachexia.MDPI2021-05-10info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/105332http://hdl.handle.net/10316/105332https://doi.org/10.3390/pharmaceutics13050686eng1999-4923Barros, Cecília deAranha, NorbertoSeverino, PatríciaSouto, Eliana B.Zielińska, AleksandraLopes, AndréRios, AlessandraBatain, FernandoCrescencio, KessiChaud, MarcoAlves, Thaisinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-02-17T10:24:46Zoai:estudogeral.uc.pt:10316/105332Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:21:55.557763Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Quality by Design Approach for the Development of Liposome Carrying Ghrelin for Intranasal Administration |
title |
Quality by Design Approach for the Development of Liposome Carrying Ghrelin for Intranasal Administration |
spellingShingle |
Quality by Design Approach for the Development of Liposome Carrying Ghrelin for Intranasal Administration Barros, Cecília de ghrelin intranasal rout liposomes quality by design (QbD) cachexia undernourishment starvation |
title_short |
Quality by Design Approach for the Development of Liposome Carrying Ghrelin for Intranasal Administration |
title_full |
Quality by Design Approach for the Development of Liposome Carrying Ghrelin for Intranasal Administration |
title_fullStr |
Quality by Design Approach for the Development of Liposome Carrying Ghrelin for Intranasal Administration |
title_full_unstemmed |
Quality by Design Approach for the Development of Liposome Carrying Ghrelin for Intranasal Administration |
title_sort |
Quality by Design Approach for the Development of Liposome Carrying Ghrelin for Intranasal Administration |
author |
Barros, Cecília de |
author_facet |
Barros, Cecília de Aranha, Norberto Severino, Patrícia Souto, Eliana B. Zielińska, Aleksandra Lopes, André Rios, Alessandra Batain, Fernando Crescencio, Kessi Chaud, Marco Alves, Thais |
author_role |
author |
author2 |
Aranha, Norberto Severino, Patrícia Souto, Eliana B. Zielińska, Aleksandra Lopes, André Rios, Alessandra Batain, Fernando Crescencio, Kessi Chaud, Marco Alves, Thais |
author2_role |
author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Barros, Cecília de Aranha, Norberto Severino, Patrícia Souto, Eliana B. Zielińska, Aleksandra Lopes, André Rios, Alessandra Batain, Fernando Crescencio, Kessi Chaud, Marco Alves, Thais |
dc.subject.por.fl_str_mv |
ghrelin intranasal rout liposomes quality by design (QbD) cachexia undernourishment starvation |
topic |
ghrelin intranasal rout liposomes quality by design (QbD) cachexia undernourishment starvation |
description |
The therapeutic use of peptides has increasingly recognized in the development of new therapies. However, the susceptible enzymatic cleavage is a barrier that needs to overcome. Nose-to-brain delivery associated with liposomes can protect peptides against biodegradation and improve the accessibility to brain targets. The aim was to develop a liposomal formulation as ghrelin carrier. The quality by design (QbD) approach was used as a strategy for method development. The initial risk assessments were carried out using a fishbone diagram. A screening design study was performed for the critical material attributes/critical process parameters (CMAs/CPPs) on critical quality attributes (CQAs). Liposomes were obtained by hydrating phospholipid films, followed by extrusion or homogenization, and coated with chitosan. The optimized liposome formulation was produced by high-pressure homogenization coated with chitosan, and the resulted were liposomes size 72.25 ± 1.46 nm, PDI of 0.300 ± 0.027, the zeta potential of 50.3 ± 1.46 mV, and encapsulation efficiency of 53.2%. Moreover, chitosan coating improved performance in ex vivo permeation and mucoadhesion analyzes when compared to the uncoated liposome. In this context, chitosan coating is essential for the performance of the formulations in the ex vivo permeation and mucoadhesion analyzes. The intranasal administration of ghrelin liposomes coated with chitosan offers an innovative opportunity to treat cachexia. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-05-10 |
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 |
http://hdl.handle.net/10316/105332 http://hdl.handle.net/10316/105332 https://doi.org/10.3390/pharmaceutics13050686 |
url |
http://hdl.handle.net/10316/105332 https://doi.org/10.3390/pharmaceutics13050686 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
1999-4923 |
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:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799134109529800704 |