The authors studied several important factors which influence in vitro drug
release from suppositories. The biopharmaceutical aspect makes it essentia
l to know these factors. The suppositories contained antirheumatic piroxica
m, which was used as the model substance. Fourteen lipophilic and hydrophil
ic suppository bases with various hydroxyl numbers were tested experimental
ly. beta-cyclodextrin was used to increase solubility, while tensides with
different hydrophilic/lipophilic balance values sewed to increase moistenin
g and pharmacon liberation. The best results were obtained with suppositori
es prepared with the Witepsol H 15 vehicle, when this base was used no prob
lems of production technology were encountered, the physical parameters of
the suppositories (solidity, disintegration time) were adequate and the in
vitro pharmacon liberation was also optimal. Acceptor phases with different
pH values were used during the membrane diffusion studies, and the best re
sult was obtained with a pH of 7.5.