WEEK 2 Flashcards
(68 cards)
WHAT ARE THE 3 PHARMACOLOGICAL PHASES?
- PHARMACEUTICAL PHASE (DISSOLUTION OF THE DRUG)
- PHARMACOKINETICS (BODY AFFECT TO THE DRUG)
- PHARMACODYNAMIC (DRUG AFFECT ON THE BODY)
WHAT IS PHARMOCOTHERAPEUTICS?
It’s the ability of a drug to treat or prevent illness. (drug action)
WHAT IS TOXICOLOGY?
its the study of adverse effects of drugs/chemicals on living organisms.
THE STUDY OF NATURAL VERSUS SYNTHETIC DRUG SOURCES IS CALLED?
Pharmacognosy
Liquids are the fastest to be absorbed while enteric-coated tablets are the slowest in oral drug absorption.
ENTERIC COATED DRUGS SHOULD NOT BE CRUSHED. This would cause disruption
of the tablet coating designed to protect the stomach lining
from the local effects of the drug and prevent the drug from
being prematurely disrupted by stomach acid.
true or false?
true.
what type of release allows
drugs to be released continuously and more slowly into the
bloodstream prolonging drug absorption
TIME RELEASED DOSAGE
opposite of time-released dosage?
IMMEDIATE RELEASE DOSAGE.
its the release all of the active
ingredients immediately upon dissolution in the gastrointestinal
tract.
Extended-release oral dosage forms must not be crushed, as
this could cause accelerated release of drug from the dosage
form and possible toxicity.
Drugs noted by SR (slow
release or sustained release), SA (sustained action), CR(controlled release), XL (extended length), and XT (extended
time). This includes granules capsule
TRUE OR FALSE?
TRUE
what drug delivery refers to drug products that dissolve in the mouth
and are absorbed through the oral mucosa.
THIN FILM DELIVERY
what pharmacokinetic process involves the movement of drugs from its site of administration into the bloodstream
ABSORPTION
fastest and slowest route for drug absorption
parenteral (fastest)
enteral
topical (slowest)
what route absorbs drugs through the mucosa of the stomach, large and small intestine
ENTERAL ROUTE
what route absorbs drugs directly into the circulation?
PARENTERAL ROUTE
FASTEST AND SLOWEST PARENTERAL ROUTES?
INTRAVENOUS AND INTRA-ARTERIAL (FASTEST)
INTRA MUSCULAR (due to the germ layers) AND SUBCUTANEOUS (due to the fatty tissues) (SLOWEST)
the four routes that uses the first pass effect
Hepatic arterial
Oral
Portal venous
Rectal
what pharmacokinetic process involves the transport of drugs by the bloodstream to the drug’s site of action
DISTRIBUTION
drugs are first distributed to areas with higher blood supply like the heart, brain, kidney before moving to areas with lower blood supply like the muscles, skin, fat.
true or false?
true
what is the most common blood protein that bounds to drug molecules
ALBUMIN
what is a drug-drug interaction?
is when one drug increases or decreases the action of the other drug that was administered concurrently
list and the transport mechanisms
- Passive diffusion: diffusion of drug from a higher concentration to a lower concentration. (for hypertension\drophobic and small drugs)
- Facilitated diffusion: diffusion of drug from a higher concentration to a lower concentration using a specialized protein. (for hydrophilic and large drugs )
- active transportation: diffusion of drug from a lower concentration to a higher concentration using ATP. (also for hydrophilic and large drugs)
-Endocytosis: is the movement of a substance into a cell (for extra large drugs).
What are the factors that affect bioavailability?
- first pass effect
(only 30% passes to the bloodstream) - solubility of drug
- instablity of environment
factors affecting distribution
- BLOOD FLOW
- areas with higher blood flow = higher distribution
- areas with lower blood flow = lower distribution - CAPILLARY PERMEABILITY (passage through capillary walls)
- increased C.P = increased distribution
- decreased C.P = decreased distribution - SOLUBILITY OF DRUG (how easily the drug moves around)
- Small, nonpolar, hydrophobic drugs will have higher solubility, therefore, higher distribution
- large, polar, hydrophilic drugs will have lower solubility and therefore lower distribution as well as albumin-binded drugs. - PROTEIN BINDING
the more protein binds to a drug, the less it would be distributed and vice versa - VOLUME OF DISTRIBUTION
- higher volume = higher penetration into tissues = higher distribution
- lower volume = lower penetration into tissues = lower distribution
what pharmacokinetic process involves the biochemical alteration of a drug
METABOLISM (biotransformation)
the organ most responsible for the biotransformation of drugs is the?
LIVER