Alcorn Jane, McNamara Patrick J
College of Pharmacy and Nutrition, University of Saskatchewan, 110 Science Place, SK, S7N 5C9, Saskatoon, Canada.
Adv Drug Deliv Rev. 2003 Apr 29;55(5):667-86. doi: 10.1016/s0169-409x(03)00030-9.
In addition to differences in the pharmacodynamic response in the infant, the dose and the pharmacokinetic processes acting upon that dose principally determine the efficacy and/or safety of a therapeutic or inadvertent exposure. At a given dose, significant differences in therapeutic efficacy and toxicant susceptibility exist between the newborn and adult. Immature pharmacokinetic processes in the newborn predominantly explain such differences. With infant development, the physiological and biochemical processes that govern absorption, distribution, metabolism, and excretion undergo significant growth and maturational changes. Therefore, any assessment of the safety associated with an exposure must consider the impact of these maturational changes on drug pharmacokinetics and response in the developing infant. This paper reviews the current data concerning the growth and maturation of the physiological and biochemical factors governing absorption, distribution, metabolism, and excretion. The review also provides some insight into how these developmental changes alter the efficiency of pharmacokinetics in the infant. Such information may help clarify why dynamic changes in therapeutic efficacy and toxicant susceptibility occur through infancy.
除了婴儿药效学反应的差异外,剂量以及作用于该剂量的药代动力学过程主要决定了治疗性或意外接触的疗效和/或安全性。在给定剂量下,新生儿和成年人在治疗效果和毒物易感性方面存在显著差异。新生儿不成熟的药代动力学过程主要解释了这些差异。随着婴儿的发育,支配吸收、分布、代谢和排泄的生理和生化过程会发生显著的生长和成熟变化。因此,任何关于接触安全性的评估都必须考虑这些成熟变化对发育中婴儿药物药代动力学和反应的影响。本文综述了有关支配吸收、分布、代谢和排泄的生理和生化因素的生长和成熟的现有数据。该综述还深入探讨了这些发育变化如何改变婴儿药代动力学的效率。这些信息可能有助于阐明为什么在婴儿期治疗效果和毒物易感性会发生动态变化。