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Charge effect of a liposomal delivery system encapsulating simvastatin to treat experimental ischemic stroke in rats

BACKGROUND AND AIMS: Although the beneficial effects of statins on stroke have been widely demonstrated both in experimental studies and in clinical trials, the aim of this study is to prepare and characterize a new liposomal delivery system that encapsulates simvastatin to improve its delivery into...

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Autores principales: Campos-Martorell, Mireia, Cano-Sarabia, Mary, Simats, Alba, Hernández-Guillamon, Mar, Rosell, Anna, Maspoch, Daniel, Montaner, Joan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935044/
https://www.ncbi.nlm.nih.gov/pubmed/27418824
http://dx.doi.org/10.2147/IJN.S107292
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author Campos-Martorell, Mireia
Cano-Sarabia, Mary
Simats, Alba
Hernández-Guillamon, Mar
Rosell, Anna
Maspoch, Daniel
Montaner, Joan
author_facet Campos-Martorell, Mireia
Cano-Sarabia, Mary
Simats, Alba
Hernández-Guillamon, Mar
Rosell, Anna
Maspoch, Daniel
Montaner, Joan
author_sort Campos-Martorell, Mireia
collection PubMed
description BACKGROUND AND AIMS: Although the beneficial effects of statins on stroke have been widely demonstrated both in experimental studies and in clinical trials, the aim of this study is to prepare and characterize a new liposomal delivery system that encapsulates simvastatin to improve its delivery into the brain. MATERIALS AND METHODS: In order to select the optimal liposome lipid composition with the highest capacity to reach the brain, male Wistar rats were submitted to sham or transitory middle cerebral arterial occlusion (MCAOt) surgery and treated (intravenous [IV]) with fluorescent-labeled liposomes with different net surface charges. Ninety minutes after the administration of liposomes, the brain, blood, liver, lungs, spleen, and kidneys were evaluated ex vivo using the Xenogen IVIS(®) Spectrum imaging system to detect the load of fluorescent liposomes. In a second substudy, simvastatin was assessed upon reaching the brain, comparing free and encapsulated simvastatin (IV) administration. For this purpose, simvastatin levels in brain homogenates from sham or MCAOt rats at 2 hours or 4 hours after receiving the treatment were detected through ultra-high-protein liquid chromatography. RESULTS: Whereas positively charged liposomes were not detected in brain or plasma 90 minutes after their administration, neutral and negatively charged liposomes were able to reach the brain and accumulate specifically in the infarcted area. Moreover, neutral liposomes exhibited higher bioavailability in plasma 4 hours after being administered. The detection of simvastatin by ultra-high-protein liquid chromatography confirmed its ability to cross the blood–brain barrier, when administered either as a free drug or encapsulated into liposomes. CONCLUSION: This study confirms that liposome charge is critical to promote its accumulation in the brain infarct after MCAOt. Furthermore, simvastatin can be delivered after being encapsulated. Thus, simvastatin encapsulation might be a promising strategy to ensure that the drug reaches the brain, while increasing its bioavailability and reducing possible side effects.
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spelling pubmed-49350442016-07-14 Charge effect of a liposomal delivery system encapsulating simvastatin to treat experimental ischemic stroke in rats Campos-Martorell, Mireia Cano-Sarabia, Mary Simats, Alba Hernández-Guillamon, Mar Rosell, Anna Maspoch, Daniel Montaner, Joan Int J Nanomedicine Original Research BACKGROUND AND AIMS: Although the beneficial effects of statins on stroke have been widely demonstrated both in experimental studies and in clinical trials, the aim of this study is to prepare and characterize a new liposomal delivery system that encapsulates simvastatin to improve its delivery into the brain. MATERIALS AND METHODS: In order to select the optimal liposome lipid composition with the highest capacity to reach the brain, male Wistar rats were submitted to sham or transitory middle cerebral arterial occlusion (MCAOt) surgery and treated (intravenous [IV]) with fluorescent-labeled liposomes with different net surface charges. Ninety minutes after the administration of liposomes, the brain, blood, liver, lungs, spleen, and kidneys were evaluated ex vivo using the Xenogen IVIS(®) Spectrum imaging system to detect the load of fluorescent liposomes. In a second substudy, simvastatin was assessed upon reaching the brain, comparing free and encapsulated simvastatin (IV) administration. For this purpose, simvastatin levels in brain homogenates from sham or MCAOt rats at 2 hours or 4 hours after receiving the treatment were detected through ultra-high-protein liquid chromatography. RESULTS: Whereas positively charged liposomes were not detected in brain or plasma 90 minutes after their administration, neutral and negatively charged liposomes were able to reach the brain and accumulate specifically in the infarcted area. Moreover, neutral liposomes exhibited higher bioavailability in plasma 4 hours after being administered. The detection of simvastatin by ultra-high-protein liquid chromatography confirmed its ability to cross the blood–brain barrier, when administered either as a free drug or encapsulated into liposomes. CONCLUSION: This study confirms that liposome charge is critical to promote its accumulation in the brain infarct after MCAOt. Furthermore, simvastatin can be delivered after being encapsulated. Thus, simvastatin encapsulation might be a promising strategy to ensure that the drug reaches the brain, while increasing its bioavailability and reducing possible side effects. Dove Medical Press 2016-06-29 /pmc/articles/PMC4935044/ /pubmed/27418824 http://dx.doi.org/10.2147/IJN.S107292 Text en © 2016 Campos-Martorell et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Campos-Martorell, Mireia
Cano-Sarabia, Mary
Simats, Alba
Hernández-Guillamon, Mar
Rosell, Anna
Maspoch, Daniel
Montaner, Joan
Charge effect of a liposomal delivery system encapsulating simvastatin to treat experimental ischemic stroke in rats
title Charge effect of a liposomal delivery system encapsulating simvastatin to treat experimental ischemic stroke in rats
title_full Charge effect of a liposomal delivery system encapsulating simvastatin to treat experimental ischemic stroke in rats
title_fullStr Charge effect of a liposomal delivery system encapsulating simvastatin to treat experimental ischemic stroke in rats
title_full_unstemmed Charge effect of a liposomal delivery system encapsulating simvastatin to treat experimental ischemic stroke in rats
title_short Charge effect of a liposomal delivery system encapsulating simvastatin to treat experimental ischemic stroke in rats
title_sort charge effect of a liposomal delivery system encapsulating simvastatin to treat experimental ischemic stroke in rats
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935044/
https://www.ncbi.nlm.nih.gov/pubmed/27418824
http://dx.doi.org/10.2147/IJN.S107292
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