Please use this identifier to cite or link to this item: http://repositorio.ufla.br/jspui/handle/1/50850
Title: Theoretical construction of thermodynamic relations for a solvent-controlled phase transition to improve the bioavailability of drugs: a case study of indomethacin
Keywords: Bioavailability
Indomethacin
DFT methods
Polymorphic phase transition
Thermodynamic functions
Biodisponibilidade
Indometacina
Métodos DFT
Transição de fase polimórfica
Funções termodinâmicas
Issue Date: 2022
Publisher: Egyptian Chemical Society
Citation: BRITO, K. P. S. de et al. Theoretical construction of thermodynamic relations for a solvent-controlled phase transition to improve the bioavailability of drugs: a case study of indomethacin. Egyptian Journal of Chemistry, Cairo, v. 65, n. 7, p. 465-472, 2022. DOI: 10.21608/EJCHEM.2021.104860.4841.
Abstract: The thermodynamic aspects of the polymorphic phase transition from α-indomethacin to γ-indomethacin are the fundamental key to find the most bioavailable phase of indomethacin. In the present work, varying the solvent permittivity changes the polymorphic transitions. Hence, the thermodynamic properties such as enthalpy, Gibbs free energy, and entropy of both indomethacin polymorphs are determined in terms of the solvent permittivity at T0=298.15 K and P0=1 atm., which are crucially related to the stability, spontaneity, and reversibility of the polymorphic transformation.
URI: 10.21608/EJCHEM.2021.104860.4841
http://repositorio.ufla.br/jspui/handle/1/50850
Appears in Collections:DQI - Artigos publicados em periódicos

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