Basics Flashcards
1
Q
Absorption
A
Getting drug to blood
2
Q
Distribution
A
- Movement of drug to body’s tissue
- Results in therapeutic and adverse effects
3
Q
Metabolism
A
Breaking drug down
4
Q
Excretion
A
Getting drug out of body
5
Q
Factors Influencing Drug Absorption
A
- Route
- Drug properties
> molecular size, lipid solubility, pH - Pt properties
> surface area of absorptive site, blood flow to site of absorption
6
Q
Oral Route
A
- Most meds absorped in small intestine
- Due to first-pass metabolism, the oneset of action for most oral drugs is 30-60mins
7
Q
Sublingual
A
Absorbed into highly vascular tissue under tongue; rapid actions
8
Q
Topical
A
- Delivers drug directly to affected area
- Minimal systemic absorption
9
Q
Transdermal
A
- Provides constant rate of drug absorption
- Always apply to intact skin
> broken skin incrs absorption
10
Q
Intravenous (IV)
A
- Full strength: immediate onset & fully absorbed; more likely to cause toxic effects
- If admining more than 1 drug at same site, must be compatible
11
Q
Intramuscular (IM)
A
- Absorbed directly into capillaries in muscle & sent into circulation
- Men more vascular muscles than women; men reach a peak lvl faster than women
12
Q
Subcutaneous (SQ)
A
- Slowly absorbed; timing of absorption varies depending on fat content & state of local circulation
- Incrd adipose tissue = dcrd absorption (less capillaries)
13
Q
Bioavailability
A
- IV: 100% absorption, 100% biooavailable
- IM/SQ: 100% absorption, <100% bioavailable
- Oral: <100% absorption, 0-70% bioavailable
14
Q
Factors Affecting Distribution
A
-
Blood flow to organs/tissues
> areas of rapid perfusion/distribution: heart, liver, kidney, brain
> areas of slow distribution: muscle, skin, fat - Ability to cross blood-brain barrier or fetal/placental barrier
-
Drug properties
> Protein binding (albumin); highly protein bound = less available for distribution
> highly water soluble drugs stay in bloodstream; go more places
> highly lipid-soluble drugs more readily lipid cell membranes & deposit in adipose tissue
15
Q
Primary Site for Metabolism
A
- LIVER
- hepatic microsomal enzyme system (P-450 system)
- inactivates/breakdown drug for excretion; some to active form (prodrug)
- changes in hepatic microsomal enzyme can affect drug metabolism