基本药理学概念

Bryan M. Cook, Lindsay Urben
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引用次数: 0

摘要

药代动力学和药效学原理具体描述了药物和人体相互作用的不同方式。药代动力学主要关注药物在体内的吸收、在各组织中的分布、人体如何代谢和分解药物,以及任何剩余药物或代谢物的消除。此外,必须考虑患者的特定特征,如合并症和器官功能障碍,因为它们也可能影响药物的吸收、分布、代谢和消除。药效学涉及药物影响身体的不同方式,特别是当与不同受体相互作用时以及随后引发生理反应的生化反应。不同的药物特异性,如亲和力、疗效和激动作用,也在患者对药物的反应中起作用。当药代动力学和药效学的概念结合在一起时,可以利用计算机模型和模拟来帮助预测基于不同剂量参数的药物的预期生理效应,同时考虑到组织分布和代谢。本综述包含6幅图,5张表,21篇参考文献。关键词:生物相,隔室分布,环境敏感半衰期,剂量-反应关系,药效学,药代动力学,药物基因组学,受体致敏
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Basic Pharmacologic Concepts
Pharmacokinetic and pharmacodynamic principles specifically describe the different ways a drug and the body interact with each other. Pharmacokinetics focuses mainly on the absorption of medications into the body, the distribution into various tissues, how the body metabolizes and breaks down medications, and the elimination of any remaining medication or metabolites. Moreover, patient-specific characteristics, such as comorbidities and organ dysfunction, must be considered as they may also influence a drug’s absorption, distribution, metabolism, and elimination. Pharmacodynamics involves the different ways a medication affects the body, particularly when interacting with different receptors and the subsequent biochemical actions that elicit physiologic responses. Different drug-specific properties, such as affinity, efficacy, and agonism, also play a role in a patient’s response to the medication. When the concepts of pharmacokinetics and pharmacodynamics are joined together, computer models and simulations can be utilized to help predict the expected physiologic effects of a drug based on varying dosing parameters while taking tissue distribution and metabolism into consideration. This review contains 6 figures, 5 tables and 21 references. Keywords: biophase, compartment distribution, context-sensitive half-time, dose-response relationship, pharmacodynamics, pharmacokinetics, pharmacogenomics, receptor sensitization
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