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Deep eutectic solvents for antiepileptic drug phenytoin solubilization: thermodynamic study

Thermodynamic investigations provide information about the solute-solvent interactions in the selection of the proper solvent for different fields of pharmaceutical sciences. Especially, the study of antiepileptic drugs in solutions (ethanol/co-solvent) has been a subject of interest owing to their...

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Autores principales: Shekaari, Hemayat, Zafarani-Moattar, Mohammed Taghi, Mokhtarpour, Masumeh, Faraji, Saeid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8677722/
https://www.ncbi.nlm.nih.gov/pubmed/34916530
http://dx.doi.org/10.1038/s41598-021-03212-z
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author Shekaari, Hemayat
Zafarani-Moattar, Mohammed Taghi
Mokhtarpour, Masumeh
Faraji, Saeid
author_facet Shekaari, Hemayat
Zafarani-Moattar, Mohammed Taghi
Mokhtarpour, Masumeh
Faraji, Saeid
author_sort Shekaari, Hemayat
collection PubMed
description Thermodynamic investigations provide information about the solute-solvent interactions in the selection of the proper solvent for different fields of pharmaceutical sciences. Especially, the study of antiepileptic drugs in solutions (ethanol/co-solvent) has been a subject of interest owing to their effect in the systems using interaction with a number of important biological membranes. This work focuses on the measurement of density and speed of sound of the phenytoin (PTH) in ethanol/deep eutectic solvents (choline chloride:ethylene glycol, and choline chloride:glycerol) solutions as the innovative class of green solvents at temperature range (288.15 to 318.15) K. It was determined Hansen solubility parameters for assessment of PTH interactions in the solvent media. Some thermophysical parameters including apparent molar volumes Vϕ, apparent molar isobaric expansion [Formula: see text] , and Hepler’s constant, apparent molar isentropic compressibility κ(φ) were obtained and calculated using these data. To correlate  the Vϕ and κ(φ) values, the Redlich-Meyer equation was used to calculate the number of quantities containing standard partial molar volume and partial molar isentropic compressibility. Finally, [Formula: see text] values showed a strong interaction between PTH and solvent (ethanol/DES (ChCl:EG)). The thermodynamic analysis of the studied system also plays a crucial role in the pharmaceutical industry.
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spelling pubmed-86777222021-12-20 Deep eutectic solvents for antiepileptic drug phenytoin solubilization: thermodynamic study Shekaari, Hemayat Zafarani-Moattar, Mohammed Taghi Mokhtarpour, Masumeh Faraji, Saeid Sci Rep Article Thermodynamic investigations provide information about the solute-solvent interactions in the selection of the proper solvent for different fields of pharmaceutical sciences. Especially, the study of antiepileptic drugs in solutions (ethanol/co-solvent) has been a subject of interest owing to their effect in the systems using interaction with a number of important biological membranes. This work focuses on the measurement of density and speed of sound of the phenytoin (PTH) in ethanol/deep eutectic solvents (choline chloride:ethylene glycol, and choline chloride:glycerol) solutions as the innovative class of green solvents at temperature range (288.15 to 318.15) K. It was determined Hansen solubility parameters for assessment of PTH interactions in the solvent media. Some thermophysical parameters including apparent molar volumes Vϕ, apparent molar isobaric expansion [Formula: see text] , and Hepler’s constant, apparent molar isentropic compressibility κ(φ) were obtained and calculated using these data. To correlate  the Vϕ and κ(φ) values, the Redlich-Meyer equation was used to calculate the number of quantities containing standard partial molar volume and partial molar isentropic compressibility. Finally, [Formula: see text] values showed a strong interaction between PTH and solvent (ethanol/DES (ChCl:EG)). The thermodynamic analysis of the studied system also plays a crucial role in the pharmaceutical industry. Nature Publishing Group UK 2021-12-16 /pmc/articles/PMC8677722/ /pubmed/34916530 http://dx.doi.org/10.1038/s41598-021-03212-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shekaari, Hemayat
Zafarani-Moattar, Mohammed Taghi
Mokhtarpour, Masumeh
Faraji, Saeid
Deep eutectic solvents for antiepileptic drug phenytoin solubilization: thermodynamic study
title Deep eutectic solvents for antiepileptic drug phenytoin solubilization: thermodynamic study
title_full Deep eutectic solvents for antiepileptic drug phenytoin solubilization: thermodynamic study
title_fullStr Deep eutectic solvents for antiepileptic drug phenytoin solubilization: thermodynamic study
title_full_unstemmed Deep eutectic solvents for antiepileptic drug phenytoin solubilization: thermodynamic study
title_short Deep eutectic solvents for antiepileptic drug phenytoin solubilization: thermodynamic study
title_sort deep eutectic solvents for antiepileptic drug phenytoin solubilization: thermodynamic study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8677722/
https://www.ncbi.nlm.nih.gov/pubmed/34916530
http://dx.doi.org/10.1038/s41598-021-03212-z
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