Otsuka M, Matsuda Y
Department of Pharmaceutical Technology, Kobe Pharmaceutical University, Japan.
J Pharm Sci. 1994 Jul;83(7):956-61. doi: 10.1002/jps.2600830708.
The release of pentoxifylline from matrix tablets containing palmitic or behenic acids, as waxes, and prepared via cogrinding was investigated. X-ray powder diffraction analysis of the ground drug-wax indicated that particle size could be reduced by grinding without polymorphic transformation. After the coground mixed powder was compressed at 1000 kg/cm2, the drug-release rate from the tablet was evaluated in pH 6.8 buffer at 37 degrees C. The drug-release profiles could be fitted to the Cobby model. The release rate decreased with an increased grinding time and increased significantly with an increased proportion of the drug. The drug-release rate constant from the matrix was calculated using the Cobby equation and the drug-release profiles. Scanning electron microphotographs of the coground product after dissolution tests suggested that mechanochemical energy had been used to cover the drug particles.