Pharmacokinetics and Pharmacodynamics
Pharmacokinetics is currently defined as the study of the time course of drug absorption, distribution, metabolism, and excretion. Clinical pharmacokinetics is the application of pharmacokinetic principles to the safe and effective therapeutic management of drugs in an individual patient. Primary goals of clinical pharmacokinetics include enhancing efficacy and decreasing toxicity of a patient’s drug therapy. The development of strong correlations between drug concentrations and their pharmacologic responses has enabled clinicians to apply pharmacokinetic principles to actual patient situations.
Pharmacodynamics refers to the relationship between drug concentration at the site of action and the resulting effect, including the time course and intensity of therapeutic and adverse effects. The effect of a drug present at the site of achievement is determined by that drug’s binding with a receptor. Receptors may be present on neurons in the central nervous system (i.e., opiate receptors) to depress pain sensation, on cardiac muscle to affect the intensity of contraction, or even within bacteria to disrupt maintenance of the bacterial cell wall
- Pharmacokinetic and Pharmacodynamic Parameters
- Drug biotransformation reactions
- Drug interactions and pharmacological compatibilities
- Absorption and Distribution of Drugs
- Biotransformation/Metabolism
- Excretion of Drugs
- Pharmacodynamics
- Novel options for the pharmacological treatment of chronic diseases
- PK and PD in New Drug Development
- Routes of Drug Administration
- Pharmacokinetics Associations
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Pharmacokinetics and Pharmacodynamics Conference Speakers
Recommended Sessions
- Chemical and Pharmaceutical Engineering
- Drug Design And Development
- Drug Formulation Procedures
- Drug Product Manufacturing
- Biomarkers in Drug Design
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