JoVE Logo

Sign In

3.25 : Steady State Concentration

A steady state refers to the level of a drug in the body once it has reached an equilibrium between administration and elimination. It represents the point at which the drug administration rate equals the drug elimination rate, resulting in a relatively constant concentration in the body over time. The dynamic equilibrium is crucial to ensure the drug's effectiveness with minimal risk of toxicity.

Most drugs are administered in repeated doses at fixed intervals or through continuous intravenous infusions to achieve a steady state. After each dose, the drug is absorbed, distributed, metabolized, and eliminated from the body. As subsequent doses are administered, the drug accumulates until the amount eliminated from the body in each dosing interval matches the amount administered. This leads to a stable concentration being maintained within a predictable range.

The rate at which a drug reaches a steady state depends on its half-life, which is the time it takes for the body to eliminate half of the drug. A drug typically takes around four to five half-lives to reach a steady state. During this time, the drug concentration gradually increases until it reaches a plateau where the administration and elimination rates become equal.

Once a steady state is achieved, the drug's concentration fluctuates within a narrow therapeutic range, ensuring a consistent pharmacological effect. Deviations from the steady-state concentration may lead to suboptimal treatment or increased risk of adverse effects. Factors such as patient characteristics, drug interactions, and changes in drug clearance should be considered when determining the optimal dosing strategy to achieve and maintain a steady state.

Tags

Steady State ConcentrationDrug AdministrationDrug EliminationDynamic EquilibriumDrug Half lifePharmacological EffectTherapeutic RangeDosing StrategyDrug InteractionsDrug Clearance

From Chapter 3:

article

Now Playing

3.25 : Steady State Concentration

Pharmacokinetics

4.2K Views

article

3.1 : פרמקוקינטיקה (Pharmacokinetics): סקירה כללית

Pharmacokinetics

5.5K Views

article

3.2 : מנגנון ספיגת תרופות: הובלת קרום פסיבית

Pharmacokinetics

3.6K Views

article

3.3 : מנגנון ספיגת תרופות: הובלת קרום בתיווך נשא

Pharmacokinetics

3.5K Views

article

3.4 : ספיגת תרופות: גורמים המשפיעים על ספיגת מערכת העיכול

Pharmacokinetics

3.8K Views

article

3.5 : זמינות ביולוגית: סקירה כללית

Pharmacokinetics

2.7K Views

article

3.6 : גורמים המשפיעים על זמינות ביולוגית: ביטול מעבר ראשון

Pharmacokinetics

6.1K Views

article

3.7 : שקילות ביולוגית: סקירה כללית

Pharmacokinetics

916 Views

article

3.8 : אפקט מעבר ראשון

Pharmacokinetics

5.1K Views

article

3.9 : מהלך הזמן של השפעת התרופה

Pharmacokinetics

1.9K Views

article

3.10 : הפצת תרופות: קשירת רקמות

Pharmacokinetics

2.5K Views

article

3.11 : מחסומים פיזיולוגיים

Pharmacokinetics

3.4K Views

article

3.12 : הפצת תרופות: קשירת חלבון פלזמה

Pharmacokinetics

4.8K Views

article

3.13 : דגמי תא: דגם תא יחיד

Pharmacokinetics

2.1K Views

article

3.14 : דגמי תאים: דגם שני תאים

Pharmacokinetics

5.2K Views

See More

JoVE Logo

Privacy

Terms of Use

Policies

Research

Education

ABOUT JoVE

Copyright © 2025 MyJoVE Corporation. All rights reserved