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Gibbs energy of transfer processes for the antimicrobial agent Triclosan from water to some organic solvents at 25.0 °C
Aragón, Diana M; Chiappetta, Diego A; Degrossi, José; Vargas, Edgar F; Bregni, Carlos; Sosnik, Alejandro; Martínez, Fleming.
Afiliação
  • Aragón, Diana M; National University of Colombia. Faculty of Sciences. Department of Pharmacy. Bogotá. CO
  • Chiappetta, Diego A; University of Buenos Aires. Faculty of Pharmacy and Biochemistry. Department of Pharmaceutical Technology. Buenos Aires. AR
  • Degrossi, José; University of Buenos Aires. Faculty of Pharmacy and Biochemistry. Department of Toxicology. Buenos Aires. AR
  • Vargas, Edgar F; Los Andes University. Faculty of Sciences. Department of Chemistry. Bogotá. CO
  • Bregni, Carlos; University of Buenos Aires. Faculty of Pharmacy and Biochemistry. Department of Pharmaceutical Technology. Buenos Aires. AR
  • Sosnik, Alejandro; University of Buenos Aires. Faculty of Pharmacy and Biochemistry. Department of Pharmaceutical Technology. Buenos Aires. AR
  • Martínez, Fleming; National University of Colombia. Faculty of Sciences. Department of Pharmacy. Bogotá. CO
Rev. colomb. ciencias quim. farm ; 37(2): 241-257, dic. 2008. tab, graf
Artigo em Inglês | LILACS | ID: lil-557448
Biblioteca responsável: CO136.3
ABSTRACT
The thermodynamic function Gibbs energy for the dissolution processes of triclosan (TS) was calculated from solubility values obtained at 25.0 °C in organic solvents with different hydrogen-bonding capability. TS solubility was determined in ethanol, octanol, water-saturated octanol, isopropyl myristate, chloroform, and heptane. The excess Gibbs energy and the activity coefficients of the solute were also calculated. In addition, the corresponding Gibbs energies of the drug transfer process from water to the organic solvents under investigation were also calculated by means of previous reports. In all cases, this thermodynamic property comprised a negative value, indicating the preference of TS for all the organic media evaluated.
RESUMEN
En este trabajo se presentan las energías de Gibbs para los procesos de disolución del triclosan (TS) en solventes orgánicos de diferente capacidad de formación de enlace de hidrógeno, las cuales fueron calculadas a partir de los valores de solubilidad a 25,0 °C. La solubilidad del TS se determinó en etanol, octanol, octanol saturado de agua, miristato de isopropilo, cloroformo, y heptano. Así mismo se calcularon las energías de Gibbs de exceso y los coeficientes de actividad del soluto en los mismos solventes. Adicionalmente, mediante el uso de valores previamente reportados en la literatura, se calcularon las energías de Gibbs de transferencia del TS desde el agua hasta los solventes orgánicos comprendidos en el estudio. En todos los casos, esta propiedad termodinámica fue negativa demostrando la preferencia del TS por los medios orgánicos evaluados.
Assuntos

Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: LILACS Assunto principal: Compostos Orgânicos / Solubilidade / Soluções / Solventes / Termodinâmica / Triclosan / Transferência de Energia Idioma: Inglês Revista: Rev. colomb. ciencias quim. farm Ano de publicação: 2008 Tipo de documento: Artigo

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Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: LILACS Assunto principal: Compostos Orgânicos / Solubilidade / Soluções / Solventes / Termodinâmica / Triclosan / Transferência de Energia Idioma: Inglês Revista: Rev. colomb. ciencias quim. farm Ano de publicação: 2008 Tipo de documento: Artigo