Pharma Week 2 Flashcards
is the study of the effect of drugs on the body.
Pharmacodynamics
Drugs act within the body to mimic the actions of the body’s own chemical messengers.
Pharmacodynamics
is the body’s physiological response to changes in drug concentration at the site of action
Dose-Response Relationship
refers to the amount of drug needed to elicit a specific physiologic response to a drug
Potency
magnitude of effect a drug can cause when exerting its maximal effect.
Efficacy
the point at which increasing a drug dosage no longer increases the desired therapeutic response.
Maximal efficacy
describes the relationship between the therapeutic dose of a drug (ED50) and the toxic dose of a drug (TD50)
Therapeutic Index – (TI)
is the dose of a drug that produces a therapeutic response in 50% of the population.
Therapeutic dose of a drug
is the dose that produces a toxic response in 50% of the population.
Toxic dose of a drug
is the time it takes for a drug to reach the minimum effective concentration (MEC) after administration.
Time from drug administration to first observable effect (T0-T1)
Onset
occurs when it reaches its highest concentration in the blood/plasma concentration. T0-T2
Peak
is the length of time the drug exerts a therapeutic effect. period from onset until the drug effect is no longer seen. T1-T3
Duration of action
can be determined by measuring peak and trough drug levels.
Drug concentration
highest plasma concentration. 30 minutes after infusion.
Peak
lowest plasma concentration. 30 minutes prior to the next infusion.
Trough
Certain portion of drug molecule (active site) selectively combines with some molecular structure (reactive site) on the cell to produce a biologic effect
Drug-Receptor Interaction
drugs act at specific areas on cell membranes; react with certain chemicals to cause an effect within the cell
Receptor site
specific chemical (key) approaches a cell membrane and finds fit (the lock) at receptor site- affects enzyme system within cell- produce certain effects. Drug+Receptor=Effect
“Lock and Key Theory”
Interferes with enzyme systems that act as catalyst from various chemical reactions
If single step in one of enzyme system is blocked- normal function is disrupted
Drug-Enzyme Interaction
Act by biophysical means that do not affect cellular/enzymatic reactions.
drugs do not bind to receptors but instead saturate the water or lipid part of a cell- drug actions occur based on the degree of saturation. Neutralization of stomach acid by antacids.
Nonspecific Drug Interaction
Specific action on cellular structures that are unique to the microbe. All chemotherapeutic agents would act only in one enzyme system needed for life of a pathogen or neoplastic cell.
It is essential to the pathogen but not to the host.
Selective toxicity
always desirable/physiologic effects
Primary
desirable or undesirable
Example: Diphenhydramine (Benadryl)
Primary effect: antihistamine; treat symptoms of allergy Secondary: Drowsiness
Secondary
few seconds to minutes
- IV, SL, Inhalations
Rapid