T2 - One-Comp Open Model Flashcards
What factors do rate and extent of tissue distribution depend on?
- Blood flow to organs
- Physiological properties of drug
- Affinity of tissues for drug (binding)
- Size of organ (Large = greater distribution)
What are the basic assumption of a 1-COM model?
- The body is single uniform compartment
- Instantaneous administration of entire does
- Rapid distribution throughout the body
- Drug elimination starts immediately upon administration
- The simplest representation of drug disposition
What should we do if drug distribution is rapid enough?
Treat that body as a simple compartment
What is considered in a well-stirred model?
There is uniform and instantaneous distribution
What is Db?
Administration of a dose into a single compartment
What is Vd?
-The apparent volume of distribution found in the single compartment
-Not the actual volume, theoretically to which the drug distributes
- Porportional to dose and concentration in plasma
What is C0p?
Plasma concnetraion at time 0
How do we calculate C0p?
What is k?
- Elimination rate constant
- Proportion of the rate of drug elimination and the amount of drug in the body at any given time
- The rate of drug elimination changes as the amount of drug in the body changes
- The summation of all elimination processes
How do we calculate k?
What is the importance of calculating k?
-Gives us a constant fractional amount of drug that is eliminated
-Allows us to summarize drug elimination independent of amount of drug in body and independent of time (straight line relationship)
What is the 1-COM model used for?
- Predict concentrations in plasma not tissue
- Assume that tissue concentrations decline proportionally with plasma concentrations
What concentrations in the tissue be the same as plasma?
Tissues have different concentration than other tissues, but changes in tissue concentrations are proportional to plasma concentrations
Identify the dependent and independent variable of first order processes?
Rate elimination is dependent on amount of drug at a given time
Elimination rate constant is independent on amount of drug at a given time
Clearance is independent of change in concentration of drug
What is half-life?
The time it takes for drug concentration to drop by 50%