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Detailed chemical characterization and molecular modeling of serotonin inclusion complex with unmodified β-cyclodextrin

In this study, we analyzed the capability of unmodified β-cyclodextrin (β-CD) to form the stable complex with serotonin hydrochloride (SER), as an important neurotransmitter in the brain. The stable β-CD: SER formulation was prepared and characterized using spectroscopic, thermal, molecular docking,...

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Detalles Bibliográficos
Autores principales: Fateminasab, F., Bordbar, A.K., Shityakov, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458498/
https://www.ncbi.nlm.nih.gov/pubmed/31008382
http://dx.doi.org/10.1016/j.heliyon.2019.e01405
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author Fateminasab, F.
Bordbar, A.K.
Shityakov, S.
author_facet Fateminasab, F.
Bordbar, A.K.
Shityakov, S.
author_sort Fateminasab, F.
collection PubMed
description In this study, we analyzed the capability of unmodified β-cyclodextrin (β-CD) to form the stable complex with serotonin hydrochloride (SER), as an important neurotransmitter in the brain. The stable β-CD: SER formulation was prepared and characterized using spectroscopic, thermal, molecular docking, and molecular dynamics techniques, revealing the phenomenon of H-bond formations and the domination of hydrophobic forces between the host molecule and its guest via the amine group of SER and the narrow side of β-CD. The complexation mechanism was mainly enthalpy-driven, representing the improvement in SER photo-stability. Overall, the results highlighted the possibility to use this formulation with improved stability in clinical practice for treatment and prevention of various depressive conditions, such as anxiety disorders.
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spelling pubmed-64584982019-04-19 Detailed chemical characterization and molecular modeling of serotonin inclusion complex with unmodified β-cyclodextrin Fateminasab, F. Bordbar, A.K. Shityakov, S. Heliyon Article In this study, we analyzed the capability of unmodified β-cyclodextrin (β-CD) to form the stable complex with serotonin hydrochloride (SER), as an important neurotransmitter in the brain. The stable β-CD: SER formulation was prepared and characterized using spectroscopic, thermal, molecular docking, and molecular dynamics techniques, revealing the phenomenon of H-bond formations and the domination of hydrophobic forces between the host molecule and its guest via the amine group of SER and the narrow side of β-CD. The complexation mechanism was mainly enthalpy-driven, representing the improvement in SER photo-stability. Overall, the results highlighted the possibility to use this formulation with improved stability in clinical practice for treatment and prevention of various depressive conditions, such as anxiety disorders. Elsevier 2019-04-09 /pmc/articles/PMC6458498/ /pubmed/31008382 http://dx.doi.org/10.1016/j.heliyon.2019.e01405 Text en © 2019 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Fateminasab, F.
Bordbar, A.K.
Shityakov, S.
Detailed chemical characterization and molecular modeling of serotonin inclusion complex with unmodified β-cyclodextrin
title Detailed chemical characterization and molecular modeling of serotonin inclusion complex with unmodified β-cyclodextrin
title_full Detailed chemical characterization and molecular modeling of serotonin inclusion complex with unmodified β-cyclodextrin
title_fullStr Detailed chemical characterization and molecular modeling of serotonin inclusion complex with unmodified β-cyclodextrin
title_full_unstemmed Detailed chemical characterization and molecular modeling of serotonin inclusion complex with unmodified β-cyclodextrin
title_short Detailed chemical characterization and molecular modeling of serotonin inclusion complex with unmodified β-cyclodextrin
title_sort detailed chemical characterization and molecular modeling of serotonin inclusion complex with unmodified β-cyclodextrin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458498/
https://www.ncbi.nlm.nih.gov/pubmed/31008382
http://dx.doi.org/10.1016/j.heliyon.2019.e01405
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