Publicação
Understanding the Solubility behaviour of Ibuprofen and Xylitol in Natural Deep Eutectic Systems through Hansen Solubility Parameters and Physicochemical Properties
| Resumo: | Most of the recent studies have been praising the peculiar ability of deep eutectic systems (DES), especially the natural-based ones (designated by NADES), in dissolving a wide variety of compounds. Despite their remarkable physicochemical properties, it is still true that little is known about the factors that would help to comprehend their interesting behaviour when they are used as solvents. Hence, it is important to gather as many tools as possible that can be useful for understanding it. First, the affinity degrees between the two selected compounds (Ibuprofen and Xylitol) and the various NADES, were analysed using Hansen Solubility Parameters (HSPs), which confirmed to be a good tool for screening good and bad NADES for solubilising Ibuprofen and Xylitol. Although, in general, the empirical models (EM) such as the one proposed by Hoftyzer-Van Krevelen and Fedors (HKF) and Yamamoto (Ymt) performed better than the semi-empirical models (SEM), when it came to assessing affinity, it was found that this actually depends on the type of assessment carried out, i.e., if it is in 1- or 2-dimension. Furthermore, it was also found that, except for the dispersive parameter (δd), all the others play a significant role in the interaction between the two compounds and NADES, especially the total solubility parameter (δt). Finally, the correlations between a set of physiochemical properties of NADES and the solubility data were evaluated in this work where it was possible to conclude that surface tension, density and molar volume are those that present the highest contribution for the variations in the solubility. |
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| Autores principais: | Fernandes, Cláudio C. |
| Outros Autores: | Paiva, Alexandre; Haghbakhsh, Reza; Duarte, Ana Rita C. |
| Assunto: | Correlation Hansen solubility parameters Ibuprofen Natural deep eutectic systems Physicochemical properties Xylitol Electronic, Optical and Magnetic Materials Atomic and Molecular Physics, and Optics Condensed Matter Physics Spectroscopy Physical and Theoretical Chemistry Materials Chemistry |
| Ano: | 2025 |
| País: | Portugal |
| Tipo de documento: | artigo |
| Tipo de acesso: | acesso aberto |
| Instituição associada: | Universidade Nova de Lisboa |
| Idioma: | inglês |
| Origem: | Repositório Institucional da UNL |
| Resumo: | Most of the recent studies have been praising the peculiar ability of deep eutectic systems (DES), especially the natural-based ones (designated by NADES), in dissolving a wide variety of compounds. Despite their remarkable physicochemical properties, it is still true that little is known about the factors that would help to comprehend their interesting behaviour when they are used as solvents. Hence, it is important to gather as many tools as possible that can be useful for understanding it. First, the affinity degrees between the two selected compounds (Ibuprofen and Xylitol) and the various NADES, were analysed using Hansen Solubility Parameters (HSPs), which confirmed to be a good tool for screening good and bad NADES for solubilising Ibuprofen and Xylitol. Although, in general, the empirical models (EM) such as the one proposed by Hoftyzer-Van Krevelen and Fedors (HKF) and Yamamoto (Ymt) performed better than the semi-empirical models (SEM), when it came to assessing affinity, it was found that this actually depends on the type of assessment carried out, i.e., if it is in 1- or 2-dimension. Furthermore, it was also found that, except for the dispersive parameter (δd), all the others play a significant role in the interaction between the two compounds and NADES, especially the total solubility parameter (δt). Finally, the correlations between a set of physiochemical properties of NADES and the solubility data were evaluated in this work where it was possible to conclude that surface tension, density and molar volume are those that present the highest contribution for the variations in the solubility. |
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