Quality by Design Approach for the Development of Liposome Carrying Ghrelin for Intranasal Administration

Detalhes bibliográficos
Autor(a) principal: Barros, Cecília de
Data de Publicação: 2021
Outros Autores: Aranha, Norberto, Severino, Patrícia, Souto, Eliana B., Zielińska, Aleksandra, Lopes, André, Rios, Alessandra, Batain, Fernando, Crescencio, Kessi, Chaud, Marco, Alves, Thais
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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spelling 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
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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
instname_str 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
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