Quiz Eight #2 Flashcards
Disintegration
Breakdown into smaller particles
Absorption
Movement of drug particles from GI tract to body fluids through:
- passive absorption
- active absorption
- pinocytosis
Lipid soluble
Pass rapidly through GI membrane and blood brain barrier
Water soluble
Require enzyme or protein to pass through membrane
Bioavailability
% of drug that the body can now use
Distribution
Drug becomes available to body fluid and tissues
Protein binding
Drug must go where protein is going
-portion of drug that is bound is inactive other portion is free
-drugs bound by protein are going to remain in system a little bit longer
Free drugs
What is available to go to site of action and do what it needs to do
-when free level drug decreases, protein bound drugs release some of drug into free until the drug is out of the system.
Volume of drug distribution (Vd)
Amount of the drug in the body/plasma concentration
Liver
The main organ for metabolism
1/2 life
The time it takes one one half of drug concentration to be eliminated.
- and then half of that and half of that until drug is gone
Excretion(elimination)
Kidneys-Urine Liver-bile Intestines-feces Lungs-Co2,H2O Skin-sweat Milk ducts-breast milk
Creatinine clearance
Difference between your urine and your blood creatinine levels
Pharmacodynamics
The study of drug concentrations and its effects of the body
Primary effect
The desired/wanted effect
Secondary effect
Side effect
Dose response
Amount of drug needed for desired effect, one patient may need more of a drug than somebody else
Maximal efficacy
Medication is no longer more effective even if given more
Peak
Point where drug reaches maximal effect but is not toxic
Duration
The time period in which the drug is effective while in the therapeutic range