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Hi all,
How one interpret the data from P-gp chemical knockout model? To be precise
based on the fold change in brain to plasma ratio, how do you classify the
compounds as poor, moderate or good Pgp substrate in this model? Any
literature reference in this regard would be highly appreciated and finally
how reliable chemical knockout data in comparison to genetic models?
Regards
Young
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At the recent ASCPT meeting, J Polli gave a talk entitled Efflux Transporters in the Blood
Brain Barrier: Why Clinically Relevent Drug Interactions are Unlikely
You might try looking for some of his publications.
Susan
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