Lecture 4 Flashcards

1
Q

pharmacodynamics

A

what the drug does to the body

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

pharmacokinetics

A

what the body does to the drug

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

how does pharmacokinetics work

A

The branch of pharmacology that studies the behaviour of drugs as they move into, around and out of the body.

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

ADME process

A
  • absorption
  • distrabution
  • metabolsim
  • excretion
  • urine
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

plasma concentration time profile or curve

A
  • blood concentration in blood against time
  • helps define the therapeutic window
  • most drugs produce dose dependent plasma concentration time profiles
  • width of the window shows how safe a drug is for patients
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

ADME 1- Absorption

A
  • Drug Absorption is process
    whereby ingested drug molecules relocate from interior of GI-tract into the portal blood (drains from gut into the liver)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

reasons for poor absorption

A
1- drug is too big (>600g/mol)
2- drug is not greasy enough 
3- drug carries a charge 
4- drug is metabolised in gut wall
5- drug is pumped back into gut
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

ADME 2- Distrabution

A
  • where drugs go in the blood stream depends on their physicochemical properties
  • drugs remain in the blood mainly
  • other drugs pentrate tissues
  • getting drugs into the brain is harder because of the blood brain barrier
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Hydrophilic drugs

A
  • not vulnerable to protein binding

- most drug ciculates in blood as unbound or free drug

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

Lipophilic Drugs

A
  • vulnerable ot protein binding
  • most drugs cicruclates in blood while bound to plasma proteins
  • 10% bound drug
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Lipophilic drugs

A
  • vulnerable to protein binding
  • most drugs circulates in blood while bound to plasma protein
  • 90% bound drug
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

ADME 3- Metbabolism

A

the chemical alteration of drugs by drugs metabolising enzymes in the body.

  • drugs eneter the body if they are lipphilic bu they might accumulate in body tissues
  • the body converts them into water soluble metabolites
  • the body expresses the hundred of drug metabolsiing enzymes
  • protect us against driugs, pollutants ect
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what happens to drugs when they are metabolised

A
  • reduces activity of drugs
  • some drugs are inactive until metabolised (pro drugs)
  • some drugs metabolites are toxic
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

ADME - excrection

A

“The permanent removal of
unchanged drugs from the
body via body fluids and secretions, expired air or tissue shedding.
- 25-30% of current medicine is not metabolsied
- these drugs are excreted unchanged by the kidneys to the urine
- other drugs are excreted unchnaged into the bile
- other minor routes of include breast milk,expired air, sweat
- membrane transporters act as excretory drug pumps into urine, bile, milk ect

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

Examples of hydrophilic drugs

A
  • penicillins
  • cephalosporins
  • gentamycin
  • metformin
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Examples of lipohilic drugs

A
  • morphine
  • diazepam
  • chlorpromazine