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Active Targeted Nanoemulsions for Repurposing of Tegaserod in Alzheimer’s Disease Treatment

Background and Purpose: The activation of 5-HT(4) receptors with agonists has emerged as a valuable therapeutic strategy to treat Alzheimer’s disease (AD) by enhancing the nonamyloidogenic pathway. Here, the potential therapeutic effects of tegaserod, an effective agent for irritable bowel syndrome,...

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Autores principales: Séguy, Line, Guyon, Léna, Maurel, Manon, Verdié, Pascal, Davis, Audrey, Corvaisier, Sophie, Lisowski, Vincent, Dallemagne, Patrick, Groo, Anne-Claire, Malzert-Fréon, Aurélie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540544/
https://www.ncbi.nlm.nih.gov/pubmed/34683919
http://dx.doi.org/10.3390/pharmaceutics13101626
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author Séguy, Line
Guyon, Léna
Maurel, Manon
Verdié, Pascal
Davis, Audrey
Corvaisier, Sophie
Lisowski, Vincent
Dallemagne, Patrick
Groo, Anne-Claire
Malzert-Fréon, Aurélie
author_facet Séguy, Line
Guyon, Léna
Maurel, Manon
Verdié, Pascal
Davis, Audrey
Corvaisier, Sophie
Lisowski, Vincent
Dallemagne, Patrick
Groo, Anne-Claire
Malzert-Fréon, Aurélie
author_sort Séguy, Line
collection PubMed
description Background and Purpose: The activation of 5-HT(4) receptors with agonists has emerged as a valuable therapeutic strategy to treat Alzheimer’s disease (AD) by enhancing the nonamyloidogenic pathway. Here, the potential therapeutic effects of tegaserod, an effective agent for irritable bowel syndrome, were assessed for AD treatment. To envisage its efficient repurposing, tegaserod-loaded nanoemulsions were developed and functionalized by a blood–brain barrier shuttle peptide. Results: The butyrylcholinesterase inhibitory activity of tegaserod and its neuroprotective cellular effects were highlighted, confirming the interest of this pleiotropic drug for AD treatment. In regard to its drugability profile, and in order to limit its peripheral distribution after IV administration, its encapsulation into monodisperse lipid nanoemulsions (Tg-NEs) of about 50 nm, and with neutral zeta potential characteristics, was performed. The stability of the formulation in stock conditions at 4 °C and in blood biomimetic medium was established. The adsorption on Tg-NEs of peptide-22 was realized. The functionalized NEs were characterized by chromatographic methods (SEC and C(18)/HPLC) and isothermal titration calorimetry, attesting the efficiency of the adsorption. From in vitro assays, these nanocarriers appeared suitable for enabling tegaserod controlled release without hemolytic properties. Conclusion: The developed peptide-22 functionalized Tg-NEs appear as a valuable tool to allow exploration of the repurposed tegaserod in AD treatment in further preclinical studies.
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spelling pubmed-85405442021-10-24 Active Targeted Nanoemulsions for Repurposing of Tegaserod in Alzheimer’s Disease Treatment Séguy, Line Guyon, Léna Maurel, Manon Verdié, Pascal Davis, Audrey Corvaisier, Sophie Lisowski, Vincent Dallemagne, Patrick Groo, Anne-Claire Malzert-Fréon, Aurélie Pharmaceutics Article Background and Purpose: The activation of 5-HT(4) receptors with agonists has emerged as a valuable therapeutic strategy to treat Alzheimer’s disease (AD) by enhancing the nonamyloidogenic pathway. Here, the potential therapeutic effects of tegaserod, an effective agent for irritable bowel syndrome, were assessed for AD treatment. To envisage its efficient repurposing, tegaserod-loaded nanoemulsions were developed and functionalized by a blood–brain barrier shuttle peptide. Results: The butyrylcholinesterase inhibitory activity of tegaserod and its neuroprotective cellular effects were highlighted, confirming the interest of this pleiotropic drug for AD treatment. In regard to its drugability profile, and in order to limit its peripheral distribution after IV administration, its encapsulation into monodisperse lipid nanoemulsions (Tg-NEs) of about 50 nm, and with neutral zeta potential characteristics, was performed. The stability of the formulation in stock conditions at 4 °C and in blood biomimetic medium was established. The adsorption on Tg-NEs of peptide-22 was realized. The functionalized NEs were characterized by chromatographic methods (SEC and C(18)/HPLC) and isothermal titration calorimetry, attesting the efficiency of the adsorption. From in vitro assays, these nanocarriers appeared suitable for enabling tegaserod controlled release without hemolytic properties. Conclusion: The developed peptide-22 functionalized Tg-NEs appear as a valuable tool to allow exploration of the repurposed tegaserod in AD treatment in further preclinical studies. MDPI 2021-10-06 /pmc/articles/PMC8540544/ /pubmed/34683919 http://dx.doi.org/10.3390/pharmaceutics13101626 Text en © 2021 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 Article
Séguy, Line
Guyon, Léna
Maurel, Manon
Verdié, Pascal
Davis, Audrey
Corvaisier, Sophie
Lisowski, Vincent
Dallemagne, Patrick
Groo, Anne-Claire
Malzert-Fréon, Aurélie
Active Targeted Nanoemulsions for Repurposing of Tegaserod in Alzheimer’s Disease Treatment
title Active Targeted Nanoemulsions for Repurposing of Tegaserod in Alzheimer’s Disease Treatment
title_full Active Targeted Nanoemulsions for Repurposing of Tegaserod in Alzheimer’s Disease Treatment
title_fullStr Active Targeted Nanoemulsions for Repurposing of Tegaserod in Alzheimer’s Disease Treatment
title_full_unstemmed Active Targeted Nanoemulsions for Repurposing of Tegaserod in Alzheimer’s Disease Treatment
title_short Active Targeted Nanoemulsions for Repurposing of Tegaserod in Alzheimer’s Disease Treatment
title_sort active targeted nanoemulsions for repurposing of tegaserod in alzheimer’s disease treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540544/
https://www.ncbi.nlm.nih.gov/pubmed/34683919
http://dx.doi.org/10.3390/pharmaceutics13101626
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