Role of P-Glycoprotein Inhibitors in the Bioavailability Enhancement of Solid Dispersion of Darunavir

Table 4

Apparent permeability coefficients (cm/s). Data presented as mean ± SD, for each formulation.

Formulation code	Equation of graph between drug conc. inside sac (µg/ml) and time (sec)		Apparent permeability coefficient; (×10^−6 cm/sec); mean ± SD
Drug
Drug + Ritonavir
SD7

SD7 = (DRV : Kolliphor TPGS = 1 : 2 w/w, spray drying).