Pharmacokinetics Flashcards
Therapeutic Index
A measure of drug safety. it is a ratio between the dose that produces toxicity (in half the population) to the dose that provides clinical effects (in half the population)
Volume Distribution
The amount of drug which needs to be in the body to get a certain concentration in the plasma
Total Body Clearance
The sum of all clearances by the drug-metabolizing and drug eliminating organs
Factors that can affect elimination
Kidney function, blood flow, rate of drug metabolism
Dose vs Dosage
Dose is the amount of drug to be given at a specific time. Dosage is the full description of how the dose is administered (specific amount, number and frequency of doses and time frame)
Bioavailability
rate/extent to which a drug reaches systemic circulation
First order kinetics
amount of drug is less than available enzymes. metabolism depends on the amount of drug present
Zero order kinetics
amount of drug exceeds available enzymes and therefore metabolism is proportional to the rate of enzyme function
What needs to be done to metabolize (and then excrete) drugs (lipid-soluble)?
drugs need to be hydrophilic to be excreted by the kidneys. The drug is either oxidized, hydrolyzed or hydroxylated (H->OH) by cytochrome P450 in the liver. If the drug still cannot be excreted, it is attached to a larger, hydrophilic drug.
First Pass metabolism
concentration of a drug is greatly reduced before it reaches the systemic circulation (specifically when administered orally). drugs absorbed through the GI tract enter portal circulation and undergo metabolism in the liver prior to entering systemic circulation
Contraindications: relative vs absolute
contraindications are factors that if they are present, the drug shouldn’t be given. Relative: we don’t know much about the effects of the drug during pregnancy (but in an emergency we would give it). absolute: the patient is allergic and will die if it is given to them
Synergistic effects of two drugs
The sum of the effects of both drugs together is greater than each drug independently.
How does pregnancy affect plasma volume and cardiac output?
pregnant women have an increase in plasma and therefore there is a decrease in the concentration of certain drugs. Pregnant women have increased blood flow to organs - this means that they are absorbed more quickly and also excreted quickly (kidneys)
How does pregnancy affects GFR?
GFR is increased therefore the drug is eliminated more quickly
How does increased body fat during pregnancy affect drug distribution
gives lipophilic drugs a greater reservoir for distribution