In an in vitro study the release rates of zomepirac acid (I) and zomepirac sodium dihydrate (II) from suspensions in liquid paraffin towards an aqueous phase were determined. When calcium was added to the aqueous phase a cake of zomepiraccalcium was formed at the interface paraffin/buffer and the release rates of I and/or II decreased extensively. The influence of additives, i.e. Tween 80, PVP and lecithin, in the suspension on this caking process was determined. It was found that Tween 80 was the most effective additive. The results obtained were 'transformed' to the release of II from supp,>sitories (in vitro studies in a modified Paddle set-up). Again Tween 80 was the most effective additive; the influence of lecithin and PVP was negligible.The bionvailability of a drug after rectal administration in a suppository is sometimes incomplete and irregular. Causes of this irregular drug uptake are, among other things, variability in the spreading of the base, problems concerning the release of drug from the vehicle, dissolution of the drug and interactions between drug and vehicle compounds or physiological agents. Bioavailability studies with zomepirac showed a relatively low concentration in the blood after rectal application '. Further research pointed to an interaction of zomepirac with (physiologically) present
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