EO 004 Flashcards
(119 cards)
[EO 004.01] What is pharmacology?
The study of how the body and drugs interact.
[EO 004.01] What are the 2 sub-categories of pharmacology?
- Pharmacokinetics
- Pharmacodynamics
[EO 004.01] What are the 4 processes of pharmacokinetics?
- Absorption
- Distribution
- Metabolism
- Elimination
[EO 004.01] What are the 2 properties that affect pharmacokinetics?
- Properties of drug
- Properties of patient
[EO 004.01] List 3 properties of drugs or patients that pharmacokinetics helps determine.
- Onset of drug
- Concentration of drug in the body
- Potency of drug
- Half-life/metabolism
- Bioavailability
- Drug-Drug influence (inhibit vs induce)
[EO 004.01] Define absorption.
How the drug gets into systemic circulation or other site of action.
[EO 004.01] List the 4 general methods of absorption.
- Passive diffusion
- Facilitated diffusion
- Active transport
- Endo/exocytsosis
[EO 004.01] List a 3 routes of administration.
- IV/IO
- IM
- SQ
- Oral
- Sublingual
- Transdermal/topical
- Inhalation
- Rectal
[EO 004.01] List a few factors that affect absorption.
- Formulation of med
- Route
- Surface Area
- pH of GI tract
- Perfusion at absorption site
- Contact time
- Solubility of med
- Molecular size of med
[EO 004.01] Define bioavailability.
The percentage of a dose that reaches systemic circulation.
[EO 004.01] Define distribution.
Movement of a drug throughout the body.
[EO 004.01] What is Volume of Distribution?
The amount of fluid a drug needs to be dissolved in to produce the same concentration in plasma.
This is important since the concentration of a drug in plasma shows the dose available to enter tissues from the blood stream.
[EO 004.01] What is the formula for Volume of Distribution?
Vd = amount/concentration
ex. Vd = 50mg/1mg per L = 0.05/0.001 = 50 L
[EO 004.01] List a few factors affecting distribution.
- Blood flow
- Capillary permeability
- Drug structure
- Binding to compounds in body
[EO 004.01] What’s the difference between bound and unbound drugs?
Bound drugs cannot leave systemic circulation, not active.
Unbound drugs are able to leave systemic circulation into tissues.
[EO 004.01] What is a drug reservoire?
A place where drugs are bound and dissolved for long periods of time.
[EO 004.01] What is the blood-brain barrier?
Tight capillaries that heavily restrict movement of substances from blood into the brain.
[EO 004.01] Define metabolism as it relates to pharmacokinetics.
The process of chemically modifying drugs within the body to create new compounds called metabolites.
[EO 004.01] What is a pro-drug?
A drug intended to be metabolized to reach its active form.
[EO 004.01] Where are most drugs metabolized?
The liver.
[EO 004.01] List a couple factors affecting metabolism
- Individual variations
- 1st pass metabolism
- Capacity limitations
- Drug interactions
[EO 004.01] What is 1st pass metabolism?
The amount of drug metabolized before reaching systemic circulation.
[EO 004.01] What are a few factors that stem from individual variation?
- Blood flow to liver
- Liver enzyme activity
- Disease/illness of liver
- Drug distribution
- Genetics (general metabolism)
[EO 004.01] What is capacity limitation?
The maximum rate of enzymes to metabolize a substance.