Clinical Pharmacokinetics 🏥 Flashcards
Clearance
Clearance is defined as the volume of blood cleared of drug per unit time and predicts the rate of elimination in relation to drug concentration.
Half-life
Half-life is the time taken for the plasma concentration of a drug to reduce by half and is related to volume of distribution and clearance in determining dosing regimens.
Volume of Distribution
Volume of distribution is a measure of the apparent space in the body available to contain the drug, allowing for the conversion of concentrations to amounts.
Drug Infusion
During constant IV infusion, every half-life the drug concentration changes by 50% of the difference between the steady-state concentration and the current concentration.
Factors Affecting Half-life
Obesity, pathologic fluid accumulation, CYP induction, CYP inhibition, aging, cardiac failure, liver failure, and renal failure can impact the half-life of drugs.
Zero Order Elimination
Observed in drugs like aspirin at high doses, ethanol, and phenytoin, where a constant amount of drug is eliminated per unit of time regardless of drug concentration.
Clinical Pharmacokinetics
Clinical pharmacokinetics aims to design dosage regimens to optimize therapeutic response of a drug and minimize the chance of adverse reactions.
First-order kinetics
First-order kinetics of drug elimination describes drugs where the rate of drug elimination is directly proportional to the drug concentration, often observed due to unsaturated physiological elimination mechanisms.
First Order Kinetics
A constant fraction of the drug is eliminated per unit of time, and plotting the log of concentration against time yields a straight line.
Half-life
The time required to reduce the amount of drug in the body by 50% during elimination, and determines the rate at which blood concentration rises and falls.
Half-life Graphical Determination
Half-life can also be determined graphically by plotting the percentage of steady-state plasma concentration against time.
Saturation Kinetics
Some drugs exhibit saturation kinetics of elimination where the elimination rate is maximal and independent of drug concentration, resembling zero-order kinetics.