Pharmacology: Pharmacokinetic Principles and Drug Absorption, Distribution, and Elimination Flashcards
Cp
Plasma concentration of drug
Pharmacokinetics
The study of the liberation, absorption, distribution, metabolism, and excretion of drugs in the body
Css
Plasma concentration of an infused drug at steady state
Co
Plasma concentration of a drug extrapolated to time of administration, assuming completed absorption and distribution
AUC
Area under the curve of plasma concentration of a drug vs. time
F
- Bioavailability
- The fraction of the dose of a drug that reaches the systemic circulation in an active form
S
Fraction of a drug composition that is the active form
Bioavailability
area under the curve of drug/area under the curve of drug if infused in vitro
Bioequivalent drug preparations
Preparations for which equal doses by same route of administration produce identical AUCs
Vd
- Volume of distribution
- The hypothetical volume needed to contain the drug in the body at the concenttration found in plasma after the drug has been distributed throughout the body
- = drug in body/plasma concentration of drug
ke
Elimination rate constant
Ke for first order kinetics
- Dependent on plasma concentration of drug at concentrations that do not saturate the elimination mechanism
- Has units of time-1
Ke for zero order elimination kinetics
- A rate not dependent on plasma concentration of drug
- Requires plasma concentration of drug sufficient to saturate the elimination mechanism
- Units of amount/time
Clearance rate for first order elimination kinetics
- The hypothetical volume of fluid cleared of a drug per unit of time
- Clearance rate is independent of plasma drug concentration
- Constant with time
Clearance rate for zero order elimination kinetics
- The amount of drug cleared per unit of time
- Clearance rate is independent of plasma drug concentration