Chitosan and its derivatives as nanocarriers for siRNA delivery
| Main Author: | |
|---|---|
| Publication Date: | 2012 |
| Other Authors: | , |
| Format: | Article |
| Language: | eng |
| Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
| Download full: | http://hdl.handle.net/10400.1/2099 |
Summary: | The ability to specifically silence genes using siRNA has enormous potential for treating genetic diseases. However, siRNA instability and biodistribution issues still need to be overcome, and adequate delivery vehicles have proven indispensable in conveying siRNA to its target. Chitosan is a promising biopolymer for siRNA delivery, its interest stemming from its safety, biodegradability, mucoadhesivity, permeation enhancing effect and cationic charge, as well as amenability to undergo chemical modifications. Chitosan and its derivatives can be readily arranged into complexes or nanoparticles able to entrap and carry siRNA. Specific strategies have been adopted to improve chitosan-based vectors with regard to transfectability. However, further efforts are required to verify their value and adapt them to enhance therapeutic output prior to clinical application. This review emphasizes the potential of chitosan and its derivatives to develop nanocarriers for siRNA delivery. The properties of chitosan that are significant for transfectability and the most relevant findings are assessed. |
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Chitosan and its derivatives as nanocarriers for siRNA deliveryChitosanChitosan derivativesFormulation parametersGene silencingNanocarrierssiRNA deliveryThe ability to specifically silence genes using siRNA has enormous potential for treating genetic diseases. However, siRNA instability and biodistribution issues still need to be overcome, and adequate delivery vehicles have proven indispensable in conveying siRNA to its target. Chitosan is a promising biopolymer for siRNA delivery, its interest stemming from its safety, biodegradability, mucoadhesivity, permeation enhancing effect and cationic charge, as well as amenability to undergo chemical modifications. Chitosan and its derivatives can be readily arranged into complexes or nanoparticles able to entrap and carry siRNA. Specific strategies have been adopted to improve chitosan-based vectors with regard to transfectability. However, further efforts are required to verify their value and adapt them to enhance therapeutic output prior to clinical application. This review emphasizes the potential of chitosan and its derivatives to develop nanocarriers for siRNA delivery. The properties of chitosan that are significant for transfectability and the most relevant findings are assessed.SapientiaAl-Qadi, SoniaGrenha, AnaRemuñán-López, Carmen2013-01-16T13:38:34Z20122012-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.1/2099engAUT: AMG02212;info: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:RCAAP2025-02-18T17:35:35Zoai:sapientia.ualg.pt:10400.1/2099Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T20:28:02.885953Repositórios 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 |
Chitosan and its derivatives as nanocarriers for siRNA delivery |
| title |
Chitosan and its derivatives as nanocarriers for siRNA delivery |
| spellingShingle |
Chitosan and its derivatives as nanocarriers for siRNA delivery Al-Qadi, Sonia Chitosan Chitosan derivatives Formulation parameters Gene silencing Nanocarriers siRNA delivery |
| title_short |
Chitosan and its derivatives as nanocarriers for siRNA delivery |
| title_full |
Chitosan and its derivatives as nanocarriers for siRNA delivery |
| title_fullStr |
Chitosan and its derivatives as nanocarriers for siRNA delivery |
| title_full_unstemmed |
Chitosan and its derivatives as nanocarriers for siRNA delivery |
| title_sort |
Chitosan and its derivatives as nanocarriers for siRNA delivery |
| author |
Al-Qadi, Sonia |
| author_facet |
Al-Qadi, Sonia Grenha, Ana Remuñán-López, Carmen |
| author_role |
author |
| author2 |
Grenha, Ana Remuñán-López, Carmen |
| author2_role |
author author |
| dc.contributor.none.fl_str_mv |
Sapientia |
| dc.contributor.author.fl_str_mv |
Al-Qadi, Sonia Grenha, Ana Remuñán-López, Carmen |
| dc.subject.por.fl_str_mv |
Chitosan Chitosan derivatives Formulation parameters Gene silencing Nanocarriers siRNA delivery |
| topic |
Chitosan Chitosan derivatives Formulation parameters Gene silencing Nanocarriers siRNA delivery |
| description |
The ability to specifically silence genes using siRNA has enormous potential for treating genetic diseases. However, siRNA instability and biodistribution issues still need to be overcome, and adequate delivery vehicles have proven indispensable in conveying siRNA to its target. Chitosan is a promising biopolymer for siRNA delivery, its interest stemming from its safety, biodegradability, mucoadhesivity, permeation enhancing effect and cationic charge, as well as amenability to undergo chemical modifications. Chitosan and its derivatives can be readily arranged into complexes or nanoparticles able to entrap and carry siRNA. Specific strategies have been adopted to improve chitosan-based vectors with regard to transfectability. However, further efforts are required to verify their value and adapt them to enhance therapeutic output prior to clinical application. This review emphasizes the potential of chitosan and its derivatives to develop nanocarriers for siRNA delivery. The properties of chitosan that are significant for transfectability and the most relevant findings are assessed. |
| publishDate |
2012 |
| dc.date.none.fl_str_mv |
2012 2012-01-01T00:00:00Z 2013-01-16T13:38:34Z |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
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http://hdl.handle.net/10400.1/2099 |
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eng |
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eng |
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AUT: AMG02212; |
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openAccess |
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application/pdf |
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