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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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Detalles Bibliográficos
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
Descripción
Sumario: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.