Wilkinson G R 377-90, 1975

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چکیده

This paper described a pharmacokinetic model for the hepatic elimination of drugs based on the relationship between the involved physiological factors including the new concept of "intrinsic clearance." It was shown that such a unifying model could describe the known effects of perturbations in the determinants on a drug's blood concentration-time profile caused by disease-states, drug interactions, interindividual variability in drug metabolizing ability, and route of administration. A generalizable classification was developed that allowed prediction of in vivo disposition characteristics according to the particular drug's intrinsic clearance. [The SCI indicates that this paper has been cited in more than 1,335 publications, making it the most-cited paper published in this journal]

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تاریخ انتشار 2004