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Electrospun poly(lactic acid) (PLA)/poly(butylene adipate-co-terephthalate) (PBAT) nanofibers for the controlled release of cilostazol.
Antunes, Lidiane Rodrigues; Breitenbach, Gabriela Lauer; Pellá, Michelly Cristina Galdioli; Caetano, Josiane; Dragunski, Douglas Cardoso.
Afiliação
  • Antunes LR; Master Program in Chemistry, State University of West Paraná, 645, Rua da Faculdade, Paraná, 85903-000 Toledo, Brazil.
  • Breitenbach GL; Center of Engineering and Exact Sciences, Centro de Engenharias e Ciências Exatas - State University of West Paraná, 645, Rua da Faculdade, Paraná, 85903-000 Toledo, Brazil.
  • Pellá MCG; Department of Chemistry, State University of Maringá, 5790, Av. Colombo, Paraná 87020-900, Maringá, Brazil. Electronic address: michellepella57@gmail.com.
  • Caetano J; Master Program in Chemistry, State University of West Paraná, 645, Rua da Faculdade, Paraná, 85903-000 Toledo, Brazil.
  • Dragunski DC; Master Program in Chemistry, State University of West Paraná, 645, Rua da Faculdade, Paraná, 85903-000 Toledo, Brazil. Electronic address: dcdragunski@gmail.com.
Int J Biol Macromol ; 182: 333-342, 2021 Jul 01.
Article em En | MEDLINE | ID: mdl-33798589
Drug delivery devices are attractive alternatives to drugs usually orally administrated. Therefore, this work aimed to produce PLA/PBAT-based nanofibers for the controlled release of cilostazol, evaluating the effect of different drug concentrations (20 and 30%) over the properties of the fibers. The fibers were characterized by scanning electron microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR), x-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric (TG/DTG), and mechanical analysis. SEM results indicated a high concentration of drug crystals on the surface of the fibers that contained 20% of cilostazol. These fibers were also thinner, more crystalline, less thermally stable, and less fragile in comparison to the fibers containing 30% of cilostazol, according to the XRD, DSC, TG/DTG, and mechanical results. The controlled release assays indicated that the fibers containing 20% of cilostazol would be attractive for short-term releases, reaching the equilibrium after approximately 6 h, while the ones containing 30% would ensure a slower release (~ 12 h). Despite the differences, both fibers would improve and enhance the efficiency of the treatment, and they would also prevent possible side effects caused by the drug to the gastric system.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poliésteres / Preparações de Ação Retardada / Nanofibras / Cilostazol Idioma: En Revista: Int J Biol Macromol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poliésteres / Preparações de Ação Retardada / Nanofibras / Cilostazol Idioma: En Revista: Int J Biol Macromol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil País de publicação: Holanda