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Journal of Pharmacokinetics and Biopharmaceutics|February 1, 1980
Mathematical basis and generalization of the Loo-Riegelman method for the determination of in vivo drug absorptionD P Vaughan, M DennisJournal of Pharmaceutical Sciences|May 1, 1978
Mathematical basis of point-area deconvolution method for determining in vivo input functionsD P Vaughan, M DennisThe Journal of Pharmacy and Pharmacology|June 1, 1976
A model independent method for estimating the in vivo release rate constant of a drug from its oral formulationsD P VaughanJournal of Pharmaceutical Sciences|February 1, 1984
Theorem on the apparent volume of distribution and the amount of drug in the body at steady stateD P VaughanJournal of Pharmaceutical Sciences|December 1, 1989
On the transformation of compartmental systems and the indeterminacy of the volume of distributionD P VaughanBritish Journal of Clinical Pharmacology|June 1, 1975
A general equation for the ratio of the areas below the blood or plasma concentration time-curves following intravenous and oral drug administration and its application to inter-subject variations in drug eliminationD P Vaughan, A TrainorJournal of Pharmacokinetics and Biopharmaceutics|March 12, 2010
Applications of a recirculatory stochastic pharmacokinetic model: limitations of compartmental modelsD P Vaughan, I HopeEuropean Journal of Clinical Pharmacology|December 19, 1975
General theory for rapidly establishing steady state drug concentrations using two consecutive constant rate intravenous infusionsD P Vaughan, G T TuckerJournal of Pharmaceutical Sciences|April 1, 1976
Simple transformation method for predicting plasma drug profiles from dissolution ratesD P Vaughan, R H LeachEuropean Journal of Clinical Pharmacology|January 1, 1976
General derivation of the ideal intravenous drug input required to achieve and maintain a constant plasma drug concentration. Theoretical application to lignocaine therapyD P Vaughan, G T TuckerPageof 107