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A New Ferulic Acid-Nicotinamide Cocrystal With Improved Solubility and Dissolution Performance.
Chaves Júnior, José Venâncio; Dos Santos, Jonh Anderson Borges; Lins, Taynara Batista; de Araújo Batista, Rayanne Sales; de Lima Neto, Severino Antônio; de Santana Oliveira, Artur; Nogueira, Fernando Henrique Andrade; Gomes, Ana Paula Barreto; de Sousa, Damião Pergentino; de Souza, Fábio Santos; Aragão, Cícero Flávio Soares.
Afiliación
  • Chaves Júnior JV; Department of Pharmacy, Postgraduate Program in Pharmaceutical Sciences, Federal University of Rio Grande do Norte, Natal 59010-115, Brazil.
  • Dos Santos JAB; Department of Pharmacy, Postgraduate Program in Pharmaceutical Sciences, Federal University of Rio Grande do Norte, Natal 59010-115, Brazil.
  • Lins TB; Department of Pharmaceutical Sciences, Federal University of Paraíba, João Pessoa 58051-970, Brazil.
  • de Araújo Batista RS; Department of Pharmaceutical Sciences, Federal University of Paraíba, João Pessoa 58051-970, Brazil.
  • de Lima Neto SA; Department of Pharmaceutical Sciences, Federal University of Paraíba, João Pessoa 58051-970, Brazil.
  • de Santana Oliveira A; Department of Pharmacy, Postgraduate Program in Pharmaceutical Sciences, Federal University of Rio Grande do Norte, Natal 59010-115, Brazil.
  • Nogueira FHA; Department of Pharmacy, Postgraduate Program in Pharmaceutical Sciences, Federal University of Rio Grande do Norte, Natal 59010-115, Brazil.
  • Gomes APB; Department of Pharmacy, Postgraduate Program in Pharmaceutical Sciences, Federal University of Rio Grande do Norte, Natal 59010-115, Brazil.
  • de Sousa DP; Department of Pharmaceutical Sciences, Federal University of Paraíba, João Pessoa 58051-970, Brazil.
  • de Souza FS; Department of Pharmaceutical Sciences, Federal University of Paraíba, João Pessoa 58051-970, Brazil.
  • Aragão CFS; Department of Pharmacy, Postgraduate Program in Pharmaceutical Sciences, Federal University of Rio Grande do Norte, Natal 59010-115, Brazil. Electronic address: cicero.aragao@yahoo.com.br.
J Pharm Sci ; 109(3): 1330-1337, 2020 03.
Article en En | MEDLINE | ID: mdl-31821823
ABSTRACT
Among the various strategies for increasing aqueous solubility of pharmaceutical substances, cocrystals have been emerging as a promising alternative. The ferulic acid (FEA) is a molecule with limited aqueous solubility, but with an interesting pharmacological activity, highlighting its antitumor potential. This study presents the characterization and physicochemical properties of a new cocrystal based on FEA and nicotinamide (NIC). The FEA-NIC cocrystal was obtained by solvent evaporation technique and physicochemically characterized by differential scanning calorimetry, powder X-ray diffraction, Fourier transform infrared spectroscopy, solid-state nuclear magnetic resonance and scanning electron microscopy. The content determination and dissolution profile in different media were analyzed by high-performance liquid chromatography. The results obtained with the characterization techniques indicated the obtainment of an anhydrous cocrystal of FEA and NIC at a 11 molar ratio. The method was reproducible and obtained a high yield, of approximately 99%. In addition, a 70% increase in the FEA solubility in the cocrystal and a better dissolution performance than the physical mixture in pH 6.8 were achieved.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Niacinamida Idioma: En Revista: J Pharm Sci Año: 2020 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Niacinamida Idioma: En Revista: J Pharm Sci Año: 2020 Tipo del documento: Article País de afiliación: Brasil