Development of Novel In Silico Model to Predict Corneal Permeability for Congeneric Drugs: A QSPR Approach
Figure 2
(a) Mean concentration (μg/mL) versus time (min) plot for all the fluoroquinolones in group A (ofloxacin, pefloxacin, gatifloxacin, and sparfloxacin). (b) Mean concentration (μg/mL) versus time (min) plot for all the fluoroquinolones in group B (levofloxacin, norfloxacin, ciprofloxacin, lomefloxacin, and moxifloxacin).
