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Antipsychotics-Loaded Nanometric Emulsions for Brain Delivery
Antipsychotic drugs have numerous disabling side effects, and many are lipophilic, making them hard to formulate at high strength. Incorporating them into nanometric emulsions can increase their solubility, protect them from degradation, and increase their brain delivery, being a promising strategy...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9611456/ https://www.ncbi.nlm.nih.gov/pubmed/36297609 http://dx.doi.org/10.3390/pharmaceutics14102174 |
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author | Pires, Patrícia C. Paiva-Santos, Ana Cláudia Veiga, Francisco |
author_facet | Pires, Patrícia C. Paiva-Santos, Ana Cláudia Veiga, Francisco |
author_sort | Pires, Patrícia C. |
collection | PubMed |
description | Antipsychotic drugs have numerous disabling side effects, and many are lipophilic, making them hard to formulate at high strength. Incorporating them into nanometric emulsions can increase their solubility, protect them from degradation, and increase their brain delivery, being a promising strategy to overcome the current treatment gap. A thorough review was performed to assess the true potential of these formulations for antipsychotic drugs brain delivery. Intranasal administration was preferred when compared to oral or intravenous administration, since it allowed for direct brain drug transport and reduced systemic drug distribution, having increased efficacy and safety. Moreover, the developed systems increased antipsychotic drug solubility up to 4796 times (when compared to water), which is quite substantial. In the in vivo experiments, nanometric emulsions performed better than drug solutions or suspensions, leading to improved brain drug targeting, mainly due to these formulation’s excipients (surfactants and cosolvents) permeation enhancing capability, added to a small droplet size, which leaves a large surface area available for drug absorption to occur. Thus, even if it is difficult to conclude on which formulation composition leads to a best performance (high number of variables), overall nanometric emulsions have proven to be promising strategies to improve brain bioavailability of antipsychotic drugs. |
format | Online Article Text |
id | pubmed-9611456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96114562022-10-28 Antipsychotics-Loaded Nanometric Emulsions for Brain Delivery Pires, Patrícia C. Paiva-Santos, Ana Cláudia Veiga, Francisco Pharmaceutics Review Antipsychotic drugs have numerous disabling side effects, and many are lipophilic, making them hard to formulate at high strength. Incorporating them into nanometric emulsions can increase their solubility, protect them from degradation, and increase their brain delivery, being a promising strategy to overcome the current treatment gap. A thorough review was performed to assess the true potential of these formulations for antipsychotic drugs brain delivery. Intranasal administration was preferred when compared to oral or intravenous administration, since it allowed for direct brain drug transport and reduced systemic drug distribution, having increased efficacy and safety. Moreover, the developed systems increased antipsychotic drug solubility up to 4796 times (when compared to water), which is quite substantial. In the in vivo experiments, nanometric emulsions performed better than drug solutions or suspensions, leading to improved brain drug targeting, mainly due to these formulation’s excipients (surfactants and cosolvents) permeation enhancing capability, added to a small droplet size, which leaves a large surface area available for drug absorption to occur. Thus, even if it is difficult to conclude on which formulation composition leads to a best performance (high number of variables), overall nanometric emulsions have proven to be promising strategies to improve brain bioavailability of antipsychotic drugs. MDPI 2022-10-12 /pmc/articles/PMC9611456/ /pubmed/36297609 http://dx.doi.org/10.3390/pharmaceutics14102174 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Pires, Patrícia C. Paiva-Santos, Ana Cláudia Veiga, Francisco Antipsychotics-Loaded Nanometric Emulsions for Brain Delivery |
title | Antipsychotics-Loaded Nanometric Emulsions for Brain Delivery |
title_full | Antipsychotics-Loaded Nanometric Emulsions for Brain Delivery |
title_fullStr | Antipsychotics-Loaded Nanometric Emulsions for Brain Delivery |
title_full_unstemmed | Antipsychotics-Loaded Nanometric Emulsions for Brain Delivery |
title_short | Antipsychotics-Loaded Nanometric Emulsions for Brain Delivery |
title_sort | antipsychotics-loaded nanometric emulsions for brain delivery |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9611456/ https://www.ncbi.nlm.nih.gov/pubmed/36297609 http://dx.doi.org/10.3390/pharmaceutics14102174 |
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