Pharmacology Chapter 1 Flashcards
Dissolution
dissolving of the smaller particles in the GI fluid before absorption
Breakdown of a tablet into smaller particles
disintegration
Pharmaceutic Phase
drug becomes a solution so it can cross the biologic membrane
process of drug movement to achieve drug action. (Absorption, Distribution, Protein Binding, Metabolism or Bio transformation, and Excretion or Elimination)
Pharmacokinetic Phase
passive absorption
drug does not require energy to move across the membrane. movement from higher concentration to lower concentration
type of movement that requires a carrier such as an enzyme or protein to move the drug against a concentration gradient
active absorption
pinocytosis
process by which cells carry a drug across membrane by engulfing the drug particles “blob”
REMEMBER
REMEMBER Drugs that are lipid soluble and non ionized are absorbed faster than water soluble and ionized drugs
first pass effect (hepatic first pass)
process in which drug passes to the liver first
bio-availability
% of administered drug does that reaches the systemic circulation– occurs after absorption and first pass metabolism
distribution
process by which the drug becomes available to the body fluids and body tissues
protein binding effect
Only drugs not bound to protein are active and can cause pharmacologic response
process by which the body inactivates or biotransforms the drugs (liver, renal excretion)
metabolism
half life
(t1/2) the time itakes for one half of the drug concentration to be eliminated
elimination
through the kidneys (urine) or bile, feces, lungs, saliva, sweat, and breast milk
creatinine clearance (CLcr)
used to determine renal function. compares creatinine levels in the urine and blood
Pharmacodynamics
study of the way drugs affect the body
“off label use”
not why the drug was preventedd/ prescribed but a desired side effect
agonist
drugs that produce s response like epinephrine
drugs hat block a response like atropine–a histamine
antagonists
Categories of Drug Action
1 stimulation or depression
2 replacement
3 inhibition or killing of organisms
4 irritation
therapeutic index
margin of safety of a drug through the use of a ratio that measures the effective (therapeutic) dose in 50% of people and lethal does in 50%of people. Closer to 1= greater risk of toxicity
peak drug level
highest plasma concentration of drug at specific time, measures the rate the drug is absorbed
trough drug level
lowest concentration of a drug, measures the rate the drug is eliminated
effects not related to desired drug effects
side effects
tachyphylaxis
rapid decrease in response to the drug, and “acute tolerance”
Nursing Process
Assessment Diagnosis Planning Interventions Evaluations
excipients
fillers and inert substances, used to allow drug to take particular shape and size and enhance drug dissolution
non specific drugs
can affect various sites
affect various receptors
non-selective sites