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Preparation and characterization of new salts of tioconazole. Comparison of their dissolution performance.
Moroni, Aldana B; Mayoral, Elena Pérez; Lionello, Diego F; Vega, Daniel R; Kaufman, Teodoro S; Calvo, Natalia L.
Afiliação
  • Moroni AB; Área de Análisis de Medicamentos, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario e Instituto de Química Rosario (IQUIR. CONICET-UNR), Suipacha 531, S2002LRK, Rosario, Argentina.
  • Mayoral EP; Departamento de Química Inorgánica y Química Técnica, Universidad Nacional de Educación a Distancia, UNED, Urbanización Monte Rozas, Avenida Esparta s/n, Ctra. de Las Rozas al Escorial Km 5, 28232 Las Rozas-Madrid, Spain.
  • Lionello DF; Departamento Física de la Materia Condensada, Gerencia de Investigación y Aplicaciones, Centro Atómico Constituyentes, Comisión Nacional de Energía Atómica e Instituto Jorge A. Sabato, Universidad Nacional General San Martín, Av. Gral. Paz 1499, B1650KNA San Martín, Buenos Aires, Argentina.
  • Vega DR; Departamento Física de la Materia Condensada, Gerencia de Investigación y Aplicaciones, Centro Atómico Constituyentes, Comisión Nacional de Energía Atómica y Escuela de Ciencia y Tecnología, Universidad Nacional General San Martín, Av. Gral. Paz 1499, B1650KNA San Martín, Buenos Aires, Argentina.
  • Kaufman TS; Área de Análisis de Medicamentos, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario e Instituto de Química Rosario (IQUIR. CONICET-UNR), Suipacha 531, S2002LRK, Rosario, Argentina. Electronic address: kaufman@iquir-conicet.gov.ar.
  • Calvo NL; Área de Análisis de Medicamentos, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario e Instituto de Química Rosario (IQUIR. CONICET-UNR), Suipacha 531, S2002LRK, Rosario, Argentina. Electronic address: calvo@iquir-conicet.gov.ar.
Int J Pharm ; 652: 123855, 2024 Mar 05.
Article em En | MEDLINE | ID: mdl-38280497
ABSTRACT
Tioconazole is an effective antifungal agent with very low solubility in aqueous media, which limits its bioavailability and efficacy. Aiming to overcome the drug limitations by improving the solubility of this active pharmaceutical ingredient, solution precipitation techniques were employed to prepare four new crystalline salts, namely the mesylate, tosylate, maleate (11), and fumarate (11) hemihydrate. The thermal stabilities, dissolution properties, and structural characteristics of the solids were determined, and the study was extended to compare their properties with the already-known oxalate salt. The structural characterization of the new phases was carried out using a multi-method approach, which included thermal (differential scanning calorimetry and thermogravimetry), diffractometric (powder X-ray diffraction), and spectroscopic (near-infrared and mid-infrared) methodologies. The determination of the melting point of the salts confirmed the findings made by thermal methods. Functional characteristics of the salts, involving their intrinsic dissolution rates were also determined. It was found that the salts exhibited improved thermal stability and that the nature of the counterion modulated their dissolution characteristics. The salts displayed better intrinsic dissolution rates than the free base, to the point of being "highly soluble" according to the Biopharmaceutical Classification System. At pH 4.3, the sulfonic acid derivatives exhibited better dissolution rates than their carboxylic acid-derived counterparts, greatly improved regarding bare tioconazole. The results suggest that the salts have great potential to be used as replacements for the free base; in principle, careful salt selection may help to fulfill each solubility need for the different scenarios where the drug may be used.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sais / Imidazóis Idioma: En Revista: Int J Pharm Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Argentina País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sais / Imidazóis Idioma: En Revista: Int J Pharm Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Argentina País de publicação: Holanda