Clearance and bioavailability study through arterio-venous drug concentrations relationship.
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[1] P. Fagiolino,et al. Is saliva suitable as a biological fluid in relative bioavailability studies? Analysis of its performance in a 4 × 2 replicate crossover design , 2011, European Journal of Drug Metabolism and Pharmacokinetics.
[2] A. Scaramelli,et al. Influence of Efflux Transporters on Drug Metabolism , 2011, Clinical pharmacokinetics.
[3] S. Kaasa,et al. Early pharmacokinetics of nasal fentanyl: is there a significant arterio-venous difference? , 2008, European Journal of Clinical Pharmacology.
[4] M. Vázquez,et al. The Influence of Cardiovascular Physiology on Dose/Pharmacokinetic and Pharmacokinetic/Pharmacodynamic Relationships , 2006, Clinical pharmacokinetics.
[5] G. Hoizey,et al. Arterio-venous ethanol levels in blood and plasma after intravenous injection in rabbits. , 1998, Alcohol.
[6] N. Benowitz,et al. Arteriovenous differences in plasma concentration of nicotine and catecholamines and related cardiovascular effects after smoking, nicotine nasal spray, and intravenous nicotine , 1997, Clinical pharmacology and therapeutics.
[7] M. Vázquez,et al. Post-prandial reabsorption of paracetamol , 1994 .
[8] W. L. Chiou,et al. Determination of the steady‐state volume of distribution using arterial and venous plasma data from constant infusion studies with procainamide , 1982, The Journal of pharmacy and pharmacology.
[9] J. Posti. Saliva-plasma drug concentration ratios during absorption: theoretical considerations and pharmacokinetic implications. , 1982, Pharmaceutica acta Helvetiae.