Plasma clearance

Journal of Veterinary Pharmacology and Therapeutics - Tập 27 Số 6 - Trang 415-425 - 2004
Pierre‐Louis Toutain1, Alain Bousquet‐mélou1
1Physiologie et Toxicologie Expérimentales

Tóm tắt

Plasma (total, systemic…) clearance is determined by all the individual metabolizing/eliminating organ clearances and involves mainly liver and kidney clearances. Plasma clearance (a volume per time, i.e. a flow) expresses the overall ability of the body to eliminate a drug by scaling the drug elimination rate (amount per time) by the corresponding plasma concentration level. The interpretation of plasma clearance and inter‐species comparisons are made easier by computing the overall body extraction ratio (from 0 to 1), which is the ratio of the body clearance divided by cardiac output. Plasma clearance is the most important pharmacokinetic parameter because it is the only one which controls the overall drug exposure (for a given bioavailability) and it is the parameter which allows computation of the dosage required to maintain an average steady‐state plasma concentration.

Từ khóa


Tài liệu tham khảo

Baggot J.D., 1977, Principles of Drug Disposition in Domestic Animals: the Basis of Veterinary Clinical Pharmacology

Baggot J.D., 1973, Species differences in plasma protein binding of morphine and codeine, American Journal of Veterinary Research, 34, 571

10.1007/BF01065654

10.2460/ajvr.2000.61.24

10.1530/jrf.0.1160199

10.2746/042516402776249191

Chiou W.L., 1982, The physiological significance of total body clearance in pharmacokinetic studies, Journal of Clinical and Hospital Pharmacy, 7, 25

Combie J.D., 1983, Pharmacokinetics and protein binding of morphine in horses, American Journal of Veterinary Research, 44, 870

10.1111/j.1365-2885.1993.tb00285.x

Hinderling P.H., 1997, Red blood cells: a neglected compartment in pharmacokinetics and pharmacodynamics, Pharmacological Reviews, 49, 279

10.2165/00003088-199528020-00005

10.1016/S0924-8579(02)00025-0

10.1080/10826079308019595

Marroum P.J., 1994, Pharmacokinetics and pharmacodynamics of acepromazine in horses, American Journal of Veterinary Research, 55, 1428, 10.2460/ajvr.1994.55.10.1428

Riviere J.E., 1999, Comparative Pharmacokinetics. Principles, Techniques and Applications

10.1016/S0272-0590(83)80020-7

Rowland M., 1995, Clinical Pharmacokinetics. Concepts and Applications

Schulz M., 1997, Therapeutic and toxic blood concentrations of more than 500 drugs, Pharmazie, 52, 895

10.1002/cpt197824152

10.1208/ps040438

10.1016/S1090-0233(02)00271-X

10.1046/j.1365-2885.2002.00442.x

10.2746/042516402776185985

Toutain P.L., 2002, 14th International Conference of Racing Analysts and Veterinarians, 19

10.1002/jps.2600750309

10.1111/j.1365-2885.1994.tb00278.x

Toutain P.L., 2000, Benazeprilat disposition and effect in dogs revisited with a pharmacokinetic/pharmacodynamic modeling approach, Journal of Pharmacology and Experimental Therapeutics, 292, 1087

10.1016/S0034-5288(02)00039-5

Wilkinson G.R., 1987, Clearance approaches in pharmacology, Pharmacological Reviews, 39, 1