Unit 1 Flashcards
Pharmacokinetics
describes the four stages a drug goes through in the body: absorption, distribution, metabolism, and excretion
the process a drug goes through in our body is?
ADME: absorption, distribution, metabolism, and excretion
Pharmacodynamics
refers to the effects of drugs in the body and the mechanism of their action
Drug bioavailability
the ability of a drug or other chemical to be taken up by the body and made available in the tissue where it is needed
Pharmacogenetics
the study of how people’s genes affect their response to medicines
Pharmacognosy
the study of natural products and their potential for medicinal use
Toxicology
the study of how chemicals, substances, and situations can harm living organisms and the environment
Pharmacoeconomics
measuring costs and outcomes associated with the use of pharmaceuticals in health-care delivery
Where does a medication get distributed after consumed orally?
It goes through stomach -> liver -> portal circulation
The first pass effect
the inactivation of orally or enterally administered drugs in the liver and intestines by enzymes
What is the transdermal route of medication delivery beneficial for?
medication that must be administered over a longer period of time to control symptoms
Side effect
anticipated, well-known consequence of the drug targeting other cells rather than just its target cell
Adverse effect
unanticipated effect of a drug that may be harmful to the patient
Free/unbound drug
the portion of the drug that is dissolved in plasma water
T/F: only free and unbound drugs will pass from the bloodstream to tissues where drug-receptor interactions will occur.
True. The protein-bound portion of the drug is inactive.
Blood-brain barrier
tightly woven mesh of capillaries that protect the brain from potentially dangerous substances, such as poisons or viruses
What can get through the blood-brain barrier?
Only certain medications made of lipids (fats) or those with a “carrier” can get through the blood-brain barrier
Everything that enters the bloodstream is metabolized by ______
the liver
Biotransformations
chemical metabolizing done by the liver
Phase I-III biotransformations
Phase I - change an inactive drug -> active called a prodrug. Prodrugs improve a medication’s effectiveness.
Phase II - couple the drug molecule with another molecule in conjugation to change it from active -> inactive again to be excreted.
Phase III - may also occur after Phase II, but not always. This is where conjugates & metabolites are excreted from cells.
Disruptions of drug metabolism:
depot binding and enzyme induction
Depot binding
the coupling of drug molecules with inactive sites in the body, resulting in the drug not being accessible for metabolism
Enzyme Induction
Enzymes are induced by repeated use of the same drug, so the body becomes accustomed to the constant presence of the drug and compensates by increasing the production of the enzyme necessary for the drug’s metabolism. This contributes to a condition referred to as tolerance and causes clients to require ever-increasing doses of certain drugs to produce the same effect
What is the most common route of drug excretion?
The kidneys