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The contribution of dispersion and digestion in the stomach to the bioavailability of poorly water‐soluble drugs administered in lipid‐based formulations was assessed by comparison of intraduodenal (ID) and peroral (p.o.) administration using cinnarizine (CZ) as a model drug. Differences in the dispersion and digestion in the gastric and intestinal compartments for medium‐chain triacylglycerides (MCT)...
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