Your browser doesn't support javascript.
loading
Unexpected solvent impact in the crystallinity of praziquantel/poly(vinylpyrrolidone) formulations. A solubility, DSC and solid-state NMR study.
Costa, Emanuel D; Priotti, Josefina; Orlandi, Silvina; Leonardi, Darío; Lamas, María C; Nunes, Teresa G; Diogo, Hermínio P; Salomon, Claudio J; Ferreira, M João.
Afiliación
  • Costa ED; CQE, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisbon, Portugal.
  • Priotti J; IQUIR-CONICET, Suipacha 531, 2000 Rosario, Argentina; Área Técnica Farmacéutica, Facultad de Cs. Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, 2000 Rosario, Argentina.
  • Orlandi S; Área Técnica Farmacéutica, Facultad de Cs. Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, 2000 Rosario, Argentina.
  • Leonardi D; IQUIR-CONICET, Suipacha 531, 2000 Rosario, Argentina; Área Técnica Farmacéutica, Facultad de Cs. Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, 2000 Rosario, Argentina.
  • Lamas MC; IQUIR-CONICET, Suipacha 531, 2000 Rosario, Argentina; Área Técnica Farmacéutica, Facultad de Cs. Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, 2000 Rosario, Argentina.
  • Nunes TG; CQE, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisbon, Portugal.
  • Diogo HP; CQE, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisbon, Portugal.
  • Salomon CJ; IQUIR-CONICET, Suipacha 531, 2000 Rosario, Argentina; Área Técnica Farmacéutica, Facultad de Cs. Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, 2000 Rosario, Argentina. Electronic address: csalomon@fbioyf.unr.edu.ar.
  • Ferreira MJ; CQE, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisbon, Portugal. Electronic address: m.joao.ferreira@tecnico.ulisboa.pt.
Int J Pharm ; 511(2): 983-93, 2016 Sep 25.
Article en En | MEDLINE | ID: mdl-27506511
The saturation solubility of PVP:PZQ physical mixtures (PMs) and solid dispersions (SDs) prepared from ethanol (E/E) or ethanol/water (E/W) by the solvent evaporation method at 1:1, 2:1 and 3:1 ratio (w/w) was determined. The presence of PVP improves the solubility of PZQ (0.31±0.01mg/mL). A maximum of 1.29±0.03mg/mL of PZQ in solution was achieved for the 3:1 SD (E/E). The amount of PZQ in solution depends on the amount of polymer and on the preparation method. Solid-state NMR (ssNMR) and DSC were used to understand this behavior. Results show that PMs are a mixture of crystalline PZQ with the polymer, while SDs show different degrees of drug amorphization depending on the solvent used. For E/W SDs, PZQ exists in amorphous and crystalline states, with no clear correlation between the amount of crystalline PZQ and the amount of PVP. For E/E SDs, formulations with a higher percentage of PZQ are amorphous with the components miscible in domains larger than 3nm ((1)H ssNMR relaxation measurements). Albeit its higher saturation solubility, the 3:1 E/E PVP:PZQ sample has a significant crystalline content, probably due to the water introduced by the polymer. High PVP content and small crystal size account for this result.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Praziquantel / Solventes / Povidona / Antihelmínticos Idioma: En Revista: Int J Pharm Año: 2016 Tipo del documento: Article País de afiliación: Portugal Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Praziquantel / Solventes / Povidona / Antihelmínticos Idioma: En Revista: Int J Pharm Año: 2016 Tipo del documento: Article País de afiliación: Portugal Pais de publicación: Países Bajos