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Physical-chemical properties of furosemide nanocrystals developed using rotation revolution mixer.
Barbosa, Sávio Fujita; Takatsuka, Takayuki; Tavares, Guilherme Diniz; Araújo, Gabriel Lima Barros; Wang, Hui; Vehring, Reinhard; Löbenberg, Raimar; Bou-Chacra, Nádia Araci.
Afiliação
  • Barbosa SF; a Faculty of Pharmaceutical Sciences , University of São Paulo , São Paulo , São Paulo , Brazil.
  • Takatsuka T; b Thinky Corporation , Tokyo , Japan.
  • Tavares GD; c Course of Pharmacy, Department of Biochemistry , Institute of Biology, State University of Campinas , Campinas , São Paulo , Brazil , and.
  • Araújo GL; a Faculty of Pharmaceutical Sciences , University of São Paulo , São Paulo , São Paulo , Brazil.
  • Wang H; d Faculty of Pharmacy and Pharmaceutical Sciences , Katz Group-Rexall Centre for Pharmacy & Health Research, University of Alberta , Edmonton , Alberta , Canada.
  • Vehring R; d Faculty of Pharmacy and Pharmaceutical Sciences , Katz Group-Rexall Centre for Pharmacy & Health Research, University of Alberta , Edmonton , Alberta , Canada.
  • Löbenberg R; d Faculty of Pharmacy and Pharmaceutical Sciences , Katz Group-Rexall Centre for Pharmacy & Health Research, University of Alberta , Edmonton , Alberta , Canada.
  • Bou-Chacra NA; a Faculty of Pharmaceutical Sciences , University of São Paulo , São Paulo , São Paulo , Brazil.
Pharm Dev Technol ; 21(7): 812-822, 2016 Nov.
Article em En | MEDLINE | ID: mdl-27825283
ABSTRACT
Recently, several approaches have been reported to improve the dissolution rate and bioavailability of furosemide, a class IV drug. However, to the best of our knowledge, none of them proposed nanocrystals. In the last decade, nanocrystals successfully addressed solubility issues by increasing surface area and saturation solubility, both leading to an increase in the dissolution rate of poor water soluble drugs. The preparation of furosemide nanocrystals was by a rotation revolution mixer method. Size distribution and morphology were performed using laser diffraction and scanning electron microscopy, respectively. In addition, differential scanning calorimetry, thermogravimetry, X-ray powder diffraction (XRD) and low frequency shift-Raman spectroscopy allowed investigating the thermal properties and crystalline state. Solubility saturation and intrinsic dissolution rate (IDR) studies were conducted. The thermal analysis revealed lower melting range for the nanocrystals comparing to furosemide. Moreover, a slight crystalline structure change to the amorphous state was observed by XRD and confirmed by low frequency shift Raman. The particle size was reduced to 231 nm with a polydispersity index of 0.232, a 30-fold reduction from the original powder. Finally, the saturation solubility and IDR showed a significant increase. Furosemide nanocrystals showed potential for development of innovative formulations as an alternative to the commercial products.
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nanopartículas / Furosemida Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nanopartículas / Furosemida Idioma: En Ano de publicação: 2016 Tipo de documento: Article