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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...

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Detalles Bibliográficos
Autores principales: Pires, Patrícia C., Paiva-Santos, Ana Cláudia, Veiga, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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.
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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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