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. 2014 Jun 27;16(5):1077–1084. doi: 10.1208/s12248-014-9639-y

Fig. 5.

Fig. 5

Simulated sensitivity of pharmacokinetic parameters to changing particle size after a single dose of 30 mg. Black line shows simulated exposures over a range of particle diameters assuming a monodisperse particle size distribution. Symbols show observed mean (±SD) exposures in study REL_BA1 for tablets containing coarsely and finely milled material with different polydisperse particle size distributions