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Solid-state characterization of Felodipine-Soluplus amorphous solid dispersions.
Lu, Jiannan; Cuellar, Kristina; Hammer, Nathan I; Jo, Seongbong; Gryczke, Andreas; Kolter, Karl; Langley, Nigel; Repka, Michael A.
Afiliação
  • Lu J; a Department of Pharmaceutics and Drug Delivery , School of Pharmacy, the University of Mississippi, University , MS , USA .
  • Cuellar K; b Department of Chemistry and Biochemistry , The University of Mississippi, University , MS , USA .
  • Hammer NI; b Department of Chemistry and Biochemistry , The University of Mississippi, University , MS , USA .
  • Jo S; a Department of Pharmaceutics and Drug Delivery , School of Pharmacy, the University of Mississippi, University , MS , USA .
  • Gryczke A; c BASF SE, Global Development and Technical Marketing , Ludwigshafen , Germany .
  • Kolter K; d BASF SE, R&D Product Management Excipients , Ludwigshafen , Germany .
  • Langley N; e BASF Corporation , Tarrytown , NY , USA , and.
  • Repka MA; a Department of Pharmaceutics and Drug Delivery , School of Pharmacy, the University of Mississippi, University , MS , USA .
Drug Dev Ind Pharm ; 42(3): 485-96, 2016.
Article em En | MEDLINE | ID: mdl-26530290
ABSTRACT
The aim of the current study is to develop amorphous solid dispersion (SD) via hot melt extrusion technology to improve the solubility of a water-insoluble compound, felodipine (FEL). The solubility was dramatically increased by preparation of amorphous SDs via hot-melt extrusion with an amphiphilic polymer, Soluplus® (SOL). FEL was found to be miscible with SOL by calculating the solubility parameters. The solubility of FEL within SOL was determined to be in the range of 6.2-9.9% (w/w). Various techniques were applied to characterize the solid-state properties of the amorphous SDs. These included Fourier Transform Infrared Spectrometry spectroscopy and Raman spectroscopy to detect the formation of hydrogen bonding between the drug and the polymer. Scanning electron microscopy was performed to study the morphology of the SDs. Among all the hot-melt extrudates, FEL was found to be molecularly dispersed within the polymer matrix for the extrudates containing 10% drug, while few small crystals were detected in the 30 and 50% extrudates. In conclusion, solubility of FEL was enhanced while a homogeneous SD was achieved for 10% drug loading.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polietilenoglicóis / Polivinil / Felodipino / Química Farmacêutica Idioma: En Revista: Drug Dev Ind Pharm Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polietilenoglicóis / Polivinil / Felodipino / Química Farmacêutica Idioma: En Revista: Drug Dev Ind Pharm Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos