Vocabulary Flashcards
Absorption
Process by which a drug enters the circulatory system.
The Pharmacokinetic Processes
Absorption, Distribution, Metabolism, and Elimination (ADME)
Addiction
Dependence characterized by a received need to take a drug to attain the psychological and physical effects of mood altering substances.
Affinity
Natural attraction; the strength by which a particular chemical messenger binds to its receptor site on a cell.
Agonist
Drug that mimics the action of a neurotransmitter when it binds to a particular receptor site - i.e. & triggers the cell’s response in a manner similar to the action of the body’s own chemical messenger.
Anaphylactic Reaction
Severe allergic response resulting in immediate life-threatening respiratory distress, usually followed by vascular collapse & shock accompanied w/ hives.
Angiodema
Abnormal accumulation of fluid in tissue.
Antagonist
Drug that neutralizes or counteracts the effects of a neurotransmitter or another drug when it binds to a particular receptor site.
Antigen
Foreign substance that is recognized by the immune system & induces the immune system to produce antibodies to defend against the foreign substance.
Bioavalibility
Degree to which a drug or other substance becomes available to the target tissue after administration.
Blood-Brain Barrier
Fortified area that prevents many substances from entering the cerebro-spinal fluid from the blood. This area is formed by glial cells that envelope capillaries in the fcentral nervous system. This creates a shield that blocks many water-soluble compounds, but is permeable to lipid-soluble substances.
Ceiling Effect
Point @ which no clinical response occurs w/ increased dosage of a drug.
Clearance
Rate @ which a drug is eliminated from a specific volume of blood per unit of time.
Contraindication
Any disease, condition, or symptom for which a drug will not be beneficial & may be harmful.
Body Molecules drugs ca combine with:
Enzymes, Nucleic Acids, Receptors, Transport Proteins
Duration of Action
Length of time a drug gives the desired response/remains at the therapeutic level.
Elimination
Removal of a drug or the drugs metabolites from the body by excretion.
First-Order
Drugs for which the rate of elimination is concentration dependent
First Pass Effect
Extent to which a drug is metabolized by the liver before reaching full body circulation. This can substantially decrease bioavailability of certain drugs when administered orally, in which case administration by injection is required.
Half-Life
Time necessary for the body to eliminate half of the drug in the body @ any 1 time (written as T 1/2).
Induction
Process by which a drug increases the concentration of certain enzymes that affect the pharmacologic response to other drugs.
Inhibition
Process by which a drug blocks enzyme activity & impairs the metabolism of another drug.
Loading Dose
Amt of a drug that will bring the blood concentration rapidly to a therapeutic level.
Maintinance Dose
Amt of a drug administered at regular intervals to keep the blood concentration @ a therapeutic level. An important factor in determining this, is a drug’s clearance rate.