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Phase diagrams of PEG(1000,1500,2000,4000,6000) + lithium citrate + water ATPSs, and the partitioning of salbutamol at T = 298.15 K

Salbutamol is a drug used to treat the pulmonary diseases by ameliorate the medium and large airways in the lungs. Partitioning of salbutamol drug on the aqueous two-phase systems (ATPSs) of PEG(1000,1500,2000,4000,6000) + trilithium citrate + water was determined at T = 298.15 K. The effect of mole...

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Autores principales: Nemati-Kande, Ebrahim, Azizi, Zolfa, Mokarizadeh, Marziyeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852274/
https://www.ncbi.nlm.nih.gov/pubmed/36658224
http://dx.doi.org/10.1038/s41598-023-28046-9
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author Nemati-Kande, Ebrahim
Azizi, Zolfa
Mokarizadeh, Marziyeh
author_facet Nemati-Kande, Ebrahim
Azizi, Zolfa
Mokarizadeh, Marziyeh
author_sort Nemati-Kande, Ebrahim
collection PubMed
description Salbutamol is a drug used to treat the pulmonary diseases by ameliorate the medium and large airways in the lungs. Partitioning of salbutamol drug on the aqueous two-phase systems (ATPSs) of PEG(1000,1500,2000,4000,6000) + trilithium citrate + water was determined at T = 298.15 K. The effect of molecular mass of polymer (MMP) on the binodal and tie-line compositions were studied. Results showed that the biphasic area was extended as the MMP was increased. The salting-out ability were quantified using the Setschenow model, and the binodal curves were modeled by a nonlinear 3-parameter equation. Furthermore, electrolyte Wilson along with the osmotic virial models have adequately been implemented to fit the tie-line compositions. Also, the studied ATPSs were implemented to study the partitioning of salbutamol drug on the salt-affluent and polymer-affluent phases. It is observed that, ATPSs of PEG(1000) is premium to extract the salbutamol to the polymer-affluent phase, where, the ATPSs of PEG(6000) is more favorable to extract the drug to the salt-affluent phase.
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spelling pubmed-98522742023-01-21 Phase diagrams of PEG(1000,1500,2000,4000,6000) + lithium citrate + water ATPSs, and the partitioning of salbutamol at T = 298.15 K Nemati-Kande, Ebrahim Azizi, Zolfa Mokarizadeh, Marziyeh Sci Rep Article Salbutamol is a drug used to treat the pulmonary diseases by ameliorate the medium and large airways in the lungs. Partitioning of salbutamol drug on the aqueous two-phase systems (ATPSs) of PEG(1000,1500,2000,4000,6000) + trilithium citrate + water was determined at T = 298.15 K. The effect of molecular mass of polymer (MMP) on the binodal and tie-line compositions were studied. Results showed that the biphasic area was extended as the MMP was increased. The salting-out ability were quantified using the Setschenow model, and the binodal curves were modeled by a nonlinear 3-parameter equation. Furthermore, electrolyte Wilson along with the osmotic virial models have adequately been implemented to fit the tie-line compositions. Also, the studied ATPSs were implemented to study the partitioning of salbutamol drug on the salt-affluent and polymer-affluent phases. It is observed that, ATPSs of PEG(1000) is premium to extract the salbutamol to the polymer-affluent phase, where, the ATPSs of PEG(6000) is more favorable to extract the drug to the salt-affluent phase. Nature Publishing Group UK 2023-01-19 /pmc/articles/PMC9852274/ /pubmed/36658224 http://dx.doi.org/10.1038/s41598-023-28046-9 Text en © The Author(s) 2023 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
Nemati-Kande, Ebrahim
Azizi, Zolfa
Mokarizadeh, Marziyeh
Phase diagrams of PEG(1000,1500,2000,4000,6000) + lithium citrate + water ATPSs, and the partitioning of salbutamol at T = 298.15 K
title Phase diagrams of PEG(1000,1500,2000,4000,6000) + lithium citrate + water ATPSs, and the partitioning of salbutamol at T = 298.15 K
title_full Phase diagrams of PEG(1000,1500,2000,4000,6000) + lithium citrate + water ATPSs, and the partitioning of salbutamol at T = 298.15 K
title_fullStr Phase diagrams of PEG(1000,1500,2000,4000,6000) + lithium citrate + water ATPSs, and the partitioning of salbutamol at T = 298.15 K
title_full_unstemmed Phase diagrams of PEG(1000,1500,2000,4000,6000) + lithium citrate + water ATPSs, and the partitioning of salbutamol at T = 298.15 K
title_short Phase diagrams of PEG(1000,1500,2000,4000,6000) + lithium citrate + water ATPSs, and the partitioning of salbutamol at T = 298.15 K
title_sort phase diagrams of peg(1000,1500,2000,4000,6000) + lithium citrate + water atpss, and the partitioning of salbutamol at t = 298.15 k
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852274/
https://www.ncbi.nlm.nih.gov/pubmed/36658224
http://dx.doi.org/10.1038/s41598-023-28046-9
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