Lipophilicity was evaluated as a possible mechanism for drug retardation fr
om a glyceryl monostearate matrix system. Lipophilicity of the glyceryl mon
ostearate matrix system was studied using contact angle measurement of wate
r droplets on the surface of compressed disks, extrudate ascension of water
, and movement of water through a powder mixture packed in a high-performan
ce liquid chromatographic (HPLC) column. Increase in glyceryl monostearate
content resulted in an increase in water droplet contact angle, decrease in
the rate of water ascending the extrudate, and increase in the pressure va
lues as a function of flow rare of water moving through the powder mixture.
These could be clue to the increase in lipophilicity of the matrix, render
ing the matrix less wettable. As a result, the rate of water penetration in
to the matrix decreased, and the drug release could be sustained.