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Chitosan Glutamate-Coated Niosomes: A Proposal for Nose-to-Brain Delivery
The aim of this in vitro study is to prepare and characterize drug free and pentamidine loaded chitosan glutamate coated niosomes for intranasal drug delivery to reach the brain through intranasal delivery. Mucoadhesive properties and stability testing in various environments were evaluated to exami...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027090/ https://www.ncbi.nlm.nih.gov/pubmed/29565809 http://dx.doi.org/10.3390/pharmaceutics10020038 |
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author | Rinaldi, Federica Hanieh, Patrizia N. Chan, Lik King Nicholas Angeloni, Livia Passeri, Daniele Rossi, Marco Wang, Julie Tzu-Wen Imbriano, Anna Carafa, Maria Marianecci, Carlotta |
author_facet | Rinaldi, Federica Hanieh, Patrizia N. Chan, Lik King Nicholas Angeloni, Livia Passeri, Daniele Rossi, Marco Wang, Julie Tzu-Wen Imbriano, Anna Carafa, Maria Marianecci, Carlotta |
author_sort | Rinaldi, Federica |
collection | PubMed |
description | The aim of this in vitro study is to prepare and characterize drug free and pentamidine loaded chitosan glutamate coated niosomes for intranasal drug delivery to reach the brain through intranasal delivery. Mucoadhesive properties and stability testing in various environments were evaluated to examine the potential of these formulations to be effective drug delivery vehicles for intranasal delivery to the brain. Samples were prepared using thin film hydration method. Changes in size and ζ-potential of coated and uncoated niosomes with and without loading of pentamidine in various conditions were assessed by dynamic light scattering (DLS), while size and morphology were also studied by atomic force microscopy (AFM). Bilayer properties and mucoadhesive behavior were investigated by fluorescence studies and DLS analyses, respectively. Changes in vesicle size and ζ-potential values were shown after addition of chitosan glutamate to niosomes, and when in contact with mucin solution. In particular, interactions with mucin were observed in both drug free and pentamidine loaded niosomes regardless of the presence of the coating. The characteristics of the proposed systems, such as pentamidine entrapment and mucin interaction, show promising results to deliver pentamidine or other possible drugs to the brain via nasal administration. |
format | Online Article Text |
id | pubmed-6027090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60270902018-07-13 Chitosan Glutamate-Coated Niosomes: A Proposal for Nose-to-Brain Delivery Rinaldi, Federica Hanieh, Patrizia N. Chan, Lik King Nicholas Angeloni, Livia Passeri, Daniele Rossi, Marco Wang, Julie Tzu-Wen Imbriano, Anna Carafa, Maria Marianecci, Carlotta Pharmaceutics Article The aim of this in vitro study is to prepare and characterize drug free and pentamidine loaded chitosan glutamate coated niosomes for intranasal drug delivery to reach the brain through intranasal delivery. Mucoadhesive properties and stability testing in various environments were evaluated to examine the potential of these formulations to be effective drug delivery vehicles for intranasal delivery to the brain. Samples were prepared using thin film hydration method. Changes in size and ζ-potential of coated and uncoated niosomes with and without loading of pentamidine in various conditions were assessed by dynamic light scattering (DLS), while size and morphology were also studied by atomic force microscopy (AFM). Bilayer properties and mucoadhesive behavior were investigated by fluorescence studies and DLS analyses, respectively. Changes in vesicle size and ζ-potential values were shown after addition of chitosan glutamate to niosomes, and when in contact with mucin solution. In particular, interactions with mucin were observed in both drug free and pentamidine loaded niosomes regardless of the presence of the coating. The characteristics of the proposed systems, such as pentamidine entrapment and mucin interaction, show promising results to deliver pentamidine or other possible drugs to the brain via nasal administration. MDPI 2018-03-22 /pmc/articles/PMC6027090/ /pubmed/29565809 http://dx.doi.org/10.3390/pharmaceutics10020038 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rinaldi, Federica Hanieh, Patrizia N. Chan, Lik King Nicholas Angeloni, Livia Passeri, Daniele Rossi, Marco Wang, Julie Tzu-Wen Imbriano, Anna Carafa, Maria Marianecci, Carlotta Chitosan Glutamate-Coated Niosomes: A Proposal for Nose-to-Brain Delivery |
title | Chitosan Glutamate-Coated Niosomes: A Proposal for Nose-to-Brain Delivery |
title_full | Chitosan Glutamate-Coated Niosomes: A Proposal for Nose-to-Brain Delivery |
title_fullStr | Chitosan Glutamate-Coated Niosomes: A Proposal for Nose-to-Brain Delivery |
title_full_unstemmed | Chitosan Glutamate-Coated Niosomes: A Proposal for Nose-to-Brain Delivery |
title_short | Chitosan Glutamate-Coated Niosomes: A Proposal for Nose-to-Brain Delivery |
title_sort | chitosan glutamate-coated niosomes: a proposal for nose-to-brain delivery |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027090/ https://www.ncbi.nlm.nih.gov/pubmed/29565809 http://dx.doi.org/10.3390/pharmaceutics10020038 |
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