pharm chapter 2 part 1 Flashcards
drug
affects the physiological processes of a living organism
pharmacology
study of drugs
chemical name
describes drugs composition and molecular structure
generic name
official name approved by health canada
trade name
proprietary name. has TM.
drugs are classified by
properties, structure and therapeutic use
pharmaceutics
study of how different drug forms influence effects on body.
enteric coating
prevents pill form breaking down in acidic environments like the stomach. instead goes to intestine
thin film drugs
dissolve in buccal tissue
combination dosage forms
multiple drugs in one dose
time release technology
drugs are slowly released in GI tract for prolonged absorption
pharmacokinetics
what the body does to the drug. from when its put in body to when it metabolizes and leaves. ADME
ADME
absorption, distribution, metabolism, excretion.
pharmacokinetics- absorption
movement of drug from site into bloodstream
bioavailability
extent of drug absorption
first pass effect
drugs pass through liver first and then reduces bioavailability
enteral route
drug absorbed through the mucosa of stomach or large intestine. oral, sublingual, buccal, rectal. GI tract
sublingual and buccal route
Sublingual- absorption site under the tongue
buccal- between cheek and gums.
both have rapid absorption; area is highly vascular.
parenteral route definition
anything other than GI tract. Usually injection.
parenteral route examples
intraderm, subcutanenous, intravenous, intramuscular, intrathecally, intra articularly, intra arterially
topical route
application to various body surfaces. ex- skin, eyes, ears, vag, nose, rectum, lungs.
transdermal route
administration through adhesive drug patches
inhalation route
type of topical, inhaled into lungs as small particles
pharmacokinetics- distribution
transportation of drug by bloodstream to site of action.
areas of first distribution
places of extensive blood supply.
heart, liver, kidney, brain
albumin
most common blood protein, carries most protein-bound drug molecules
active and inactive drugs
active- free/ not bound to albumin
inactive- bound to albumin
low albumin levels can contribute to
drug toxicity and less inactive drug
pharmacokinetics- metabolism
aka biotransformation
liver does it
alters drug to make it more or less usable by the body.
which organ is most responsible for metabolizing
the liver
cytochrome P450 enzymes
microsomal enzymes. targeted to metabolize lipophilic drugs
lipophilic enzymes
fat loving, difficult to eliminate
hydrophilic enzymes
water loving, easier to metabolize
substrates
target drugs of specific enzymes
enzyme inhibitors
decrease metabolism
enzyme inducers
stimulate metabolism
excretion
elimination of drugs from body, kidney is most responsible, liver and bowel,
renal excretion
affected by kidney disease
biliary excretion
affected by liver disease