Pharmacokinetics 1 Flashcards

1
Q

pharmacokinetics studies what 3 things?

A

how drugs enter and leave the body. plasma drug concentrations vs. time. what the body does to a drug.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

ADME

A

absorption from site of administration. distribution within body. metabolism. excretion.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

pharmacokinetic properties of drugs are ___ and ____? provides what clinically relevant information (4)?

A

distinct + drug specific. optimal route of drug admin, required drug dose + dosing interval, variations in drug levels in disease, how to optimize drug therapies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

movement of drug molecules in body: 3?

A

bulk flow, passive diffusion, transport/carrier systems.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

movement of drug molecules in body: bulk flow?

A

drug moves in bloodstream around body, lymphatic system, cerebrospinal fluid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

movement of drug molecules in body: passive diffusion depends on?

A

drug concentration gradient. rate is very drug specific, depends on ionization/lipid solubility, molecular size.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

2 types of drug administration

A

systemic: use blood as delivery system. local: drug given directly to site of action.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

oral administration: aka? absorption %?

A

enteral administration. less than 100%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

why is GI tract absorption less than 100%? (6)

A

disintegration/solubility. drug ionization. stability (stomach acid). gastric emptying, GI motility. GI blood flow. first pass effect

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

gastric emptying/GI motility: most of drug absorbed where? slowed by?

A

upper GI. gastric emptying slowed by food.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

bio-availability def? aka? partial loss due to?

A

“F”: perception of dose entering circulation. partial loss due to metabolism or excretion.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

first pass effect: aka? what?

A

pre-systemic elimination. GI blood first enters hepatic portal circulation so partial loss due to metabolism or ecretion.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

first pass effect: direct effect on? likely to vary with? examples?

A

therapeutic outcome, varies with liver function. ASA 30% lost. morphine 70% lost. nitroglycerin 99% lost.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

advantages of oral route (3)

A

no need for drug to be pure/sterile. common, easy for patient, no pain. cheap formulations, multi dose bottles.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

disadvantages of oral route (5)

A

requires conscious cooperative patient. slow so not good for emergencies. variable absorption/bioavailibility. loss of drug if patient vomits. potential for upper GI tract irritation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

rectal administration: speed? first pass effect?

A

rapid absorption possible; less first pass effect.

17
Q

rectal administration: good for patients who?

A

cannot swallow, unconscious. won’t swallow - children or psychotics. may be vomiting

18
Q

parental means? does not mean?

A

NOT by enteral route, doesn’t mean only by injection

19
Q

sublingual route: what? ___ entry to? first pass?

A

drug place under tongue = direct entry to systemic circulation, no first pass

20
Q

sublingual route: speed? pH? so? pros?

A

rapid absorption despite low area. pH about 7 so avid labile drugs are stable. fast, easy, comfortable.