Pharmacokinetics simulation

From WikiMD.org
Jump to navigation Jump to search

Pharmacokinetics Simulation

Pharmacokinetics Simulation (pronunciation: far-ma-ko-ki-net-iks sim-yu-lay-shun) is a computational method used to predict the absorption, distribution, metabolism, and excretion (ADME) of drugs in the body. The term is derived from the Greek words pharmakon (drug) and kinetikos (moving, putting in motion).

Definition

Pharmacokinetics Simulation is a branch of pharmacokinetics that uses mathematical models to predict how the body will interact with a drug. It is a crucial tool in drug development and pharmacotherapy as it helps in understanding the behavior of a drug in the body over time.

Application

Pharmacokinetics Simulation is used in various stages of drug development. It helps in predicting the dosage, frequency, and duration of treatment. It is also used in clinical trials to predict the drug's behavior in the body, which aids in determining the safety and efficacy of the drug.

Related Terms

  • Pharmacodynamics: The study of the biochemical and physiological effects of drugs on the body.
  • Bioavailability: The extent and rate at which a drug is absorbed into a living system or is made available at the site of physiological activity.
  • Drug Metabolism: The process by which the body breaks down and converts medication into active chemical substances.
  • Drug Interaction: A situation in which a substance affects the activity of a drug when both are administered together.

See Also

External links

Esculaap.svg

This WikiMD dictionary article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski