Abstract
Diclofenac sodium is a non-steroidal anti-inflammatory drug widely used in the treatment of ankylosing spondylitis, rheumatoid arthritis and osteoarthritis. In this context, a rapid onset of action is required. Thus, the aim of this study was to formulate diclofenac sodium-PVP K-30 fast release tablets from solid dispersions. The physical state and drug:carrier interactions were analyzed by X-ray diffraction and scanning electron microscopy and stability upon storage was also studied. Dissolution rate of diclofenac sodium from solid dispersions was markedly enhanced by increasing the polymer concentration.
Acknowledgments
The authors express their gratitude to the National University of Rosario (Argentina) and the National Council Research-CONICET (Argentina) for financial support and to L.M. Salvatierra, for his collaboration in obtaining some experimental data. D.L. gives thanks to National Council Research-CONICET (Argentina) for a fellowship.
Declaration of interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.