Chapter 1 Flashcards
(190 cards)
What is pharmacokinetics?
Pharmacokinetics is the process of how medications travel through the body.
What are the 4 phases of pharmacokinetics?
- Absorption
- Distribution
- Metabolism
- Excretion
What is absorption in pharmacokinetics?
Absorption is the process of a medication moving from the site of administration into the bloodstream.
Where can absorption happen in the body?
Absorption can happen through the GI tract, muscle, skin, mucous membranes, or subcutaneous tissue.
What are the most common routes of medication administration?
Enteral (through the GI tract) and parenteral (by injection).
What does the rate of medication absorption affect?
It affects how soon the medication takes effect.
What does the route of administration affect?
It affects the rate and amount of absorption.
What does the amount of medication absorbed affect?
It affects the intensity of the medication’s effects.
What factors affect absorption of oral medications? (1 of 4)
Stability and solubility of the medication (how well it dissolves).
What factors affect absorption of oral medications? (2 of 4)
GI pH and gastric emptying time (how fast the stomach empties).
What factors affect absorption of oral medications? (3 of 4)
Whether food is in the stomach or intestines.
Whether food is in the stomach or intestines.
What factors affect absorption of oral medications? (4 of 4)
The form of the medication (like enteric-coated or extended-release).
What is a barrier to absorption for sublingual or buccal medications?
Swallowing the pill too soon — stomach acid breaks it down before it can work.
What is the absorption pattern for sublingual/buccal medications?
They absorb quickly into the bloodstream because of highly vascular mucous membranes.
What are barriers to absorption for vaginal or rectal medications?
Stool or infectious material can block contact with tissue, limiting absorption.
What is the barrier to absorption for intradermal and topical medications?
Because epidermal cells have close proximity and are tightly packed, absorption is slow and gradual.
How do intradermal and topical medications work?
They mainly have local effects, but can also work systemically—especially if the drug is lipid-soluble and passes into subcutaneous tissue.
Do intradermal/topical meds face a capillary barrier?
No. Capillary walls have large gaps between cells, so there’s no barrier to absorption into the bloodstream.
What is distribution in pharmacokinetics?
Distribution is the transportation of medications to sites of action by bodily fluids like blood.
How does circulation affect distribution?
Poor circulation (like in peripheral vascular disease or cardiac disease) can reduce blood flow, making it harder for medications to reach their target areas.
How does cell membrane permeability affect distribution?
Medications must pass through tissues and membranes to reach their target.
Lipid-soluble drugs (like nitroglycerin or levodopa) can cross the blood-brain barrier and placenta more easily.
How does protein binding affect distribution?
Medications bind to proteins in the blood (mostly albumin), which limits how much drug can leave the blood and reach body tissues.
What happens when two drugs compete for the same protein binding site?
They can displace each other, increasing the amount of free drug in the blood, which may cause toxicity