While several authors demonstrated a clear trend towards underprediction with highly bound drugs [ 30 , 31 , 32 ], others reported a lack of correlation between free fraction and prediction bias [ 29 , 33 ] or mixed effects depending on the physicochemical characteristics of the drug (acidic, basic or neutral) [ 28 ].
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Relevance of In Vitro Metabolism Models to PET Radiotracer Development: Prediction of In Vivo Clearance in Rats from Microsomal Stability Data.
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