Table. I.
Permeability values of Vandetanib across MDCK cell monolayers
Permeability (×106)cm/sec |
||||
---|---|---|---|---|
Cell line | Drug ± Inhibitor | A-B | B-A | Efflux Ratio |
MDCK-WT | Vandetanib | 7.57±0.52 | 8.08±0.17 | 1.06 |
MDCK-MDR1 | Vandetanib | 5.73±0.29 | 4.66±0.26 | 0.81 |
MDCK-Bcrp1 | Vandetanib | 5.66±1.26 | 42.32±2.64 | 7.5 |
Vandetanib+Ko143 | 8.58±0.63 | 8.58±0.69 | 1 | |
Vandetanib+Everolimus | 7.29±1.24 | 10.03±0.79 | 1.4 | |
Vandetanib+Temsirolimus | 10.80±1.22 | 11.81±0.30 | 1.1 |