Pharmacokinetic predictions in children by using the physiologically based pharmacokinetic modelling

被引:37
作者
Bouzom, F. [1 ]
Walther, B. [1 ]
机构
[1] Technol Servier, F-45007 Orleans 1, France
关键词
ADME; children; PBPK;
D O I
10.1111/j.1472-8206.2008.00648.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nowadays, 50-90% of drugs used in children have never been actually studied in this population. Consequently, either our children are often exposed to the risk of adverse drug events or to lack of efficacy, or they are unable to benefit from a number of therapeutic advances offered to adults, as no clinical study has been properly performed in children. Actually the main methods used to calculate the dose for a child are based on allometric methods taking into account different categories of age, the body weight and/or the body surface area. Unfortunately, these calculation methods consider the children as small adults, which is not the case. Physiologically based pharmacokinetics is one way to integrate the physiological changes occurring in the childhood and to anticipate their impact on the pharmacokinetic processes: absorption, distribution, metabolism and excretion/elimination. From different examples, the application of this modelling approach is discussed as a possible and valuable method to minimize the ethical and technical difficulties of conducting research in children.
引用
收藏
页码:579 / 587
页数:9
相关论文
共 58 条
[1]   Potassium homeostasis: ontogenic aspects [J].
Aizman, R ;
Grahnquist, L ;
Celsi, G .
ACTA PAEDIATRICA, 1998, 87 (06) :609-617
[2]   Pharmacokinetics in the newborn [J].
Alcorn, J ;
McNamara, PJ .
ADVANCED DRUG DELIVERY REVIEWS, 2003, 55 (05) :667-686
[3]  
Alcorn J, 2002, CLIN PHARMACOKINET, V41, P1077, DOI 10.2165/00003088-200241130-00005
[4]   Acetaminophen developmental pharmacokinetics in premature neonates and infants - A pooled population analysis [J].
Anderson, BJ ;
van Lingen, RA ;
Hansen, TG ;
Lin, YC ;
Holford, NHG .
ANESTHESIOLOGY, 2002, 96 (06) :1336-1345
[5]   DEVELOPMENTAL PATTERNS OF RENAL FUNCTIONAL MATURATION COMPARED IN HUMAN NEONATE [J].
ARANT, BS .
JOURNAL OF PEDIATRICS, 1978, 92 (05) :705-712
[6]   Guidelines on paediatric dosing on the basis of developmental physiology and pharmacokinetic considerations [J].
Bartelink, Imke H. ;
Rademaker, Carin M. A. ;
Schobben, Alfred F. A. M. ;
van den Anker, John N. .
CLINICAL PHARMACOKINETICS, 2006, 45 (11) :1077-1097
[7]   Characterizing uncertainty and variability in physiologically based pharmacokinetic models: State of the science and needs for research and implementation [J].
Barton, Hugh A. ;
Chiu, Weihsueh A. ;
Setzer, R. Woodrow ;
Andersen, Melvin E. ;
Bailer, A. John ;
Bois, Frederic Y. ;
DeWoskin, Robert S. ;
Hays, Sean ;
Johanson, Gunnar ;
Jones, Nancy ;
Loizou, George ;
MacPhail, Robert C. ;
Portier, Christopher J. ;
Spendiff, Martin ;
Tan, Yu-Mei .
TOXICOLOGICAL SCIENCES, 2007, 99 (02) :395-402
[9]   Developmental pharmacokinetics of morphine and its metabolites in neonates, infants and young children [J].
Bouwmeester, NJ ;
Anderson, BJ ;
Tibboel, D ;
Holford, NHG .
BRITISH JOURNAL OF ANAESTHESIA, 2004, 92 (02) :208-217
[10]  
Brightman FA, 2006, DRUG METAB DISPOS, V34, P94, DOI 10.1124/dmd.105.004838