Drug absorption & distribution (L5) Flashcards

1
Q

what is pharmacokinetics (PK)?

A

what the body does to the drug

ADME 
• absorption 
• distribution 
• metabolism 
• excretion
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2
Q

what is pharmacodynamics (PD)?

A

what the drug does to the body

time course and mechanism of therapeutic effects

how the drug works

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3
Q

what happens in absorption?

A

transfer of an exogenous compound from site of administration into the systemic circulation

  • usually needs to pass cell membranes
  • passive diffusion doen conc gradient
  • active transport
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4
Q

what are the 3 types of administration routes for a drug?

A

IV
oral
dermal

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5
Q

how do you decide which route is best?

A
  • physiochemical properties
  • therapeutic aims
  • patient preferences
  • pharmacokinetic properties
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6
Q

when is parental delivery needed?

A
  • when drug is poorly absorbed
  • drug is unstable or metabolised in GI tract
  • rapid onset of action is needed
  • high dose control is needed
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7
Q

parental delivery includes…

A

intravenous - bolus or infusion

intramuscular - injected dose is stored in the muscle and diffuses over time

subcutaneous - bolus or infusion

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8
Q

how is the small intestine involved in absorption?

A

site of absorption of most orally administered exogenous compounds

large, highly permeable SA
excellent blood supply

enterocytes of epithelium contain metabolic enzymes and transporters

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9
Q

what is first pass metabolism?

A

a phenomenon of drug metabolism whereby the concentration of a drug is greatly reduced before it reaches the systemic circulation

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10
Q

what are other absorption routes?

A
  • sublingual
  • inhalation
  • rectal
  • vaginal
  • transdermal
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11
Q

absorption in the sublingual route

A

under the tongue

films and sprays

excellent network of capillaries under the tongue - drug delivered directly into the blood stream

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12
Q

absorption by inhalation

A

inhalation of powders, gases and suspensions

excellent network of capillaries under the tongue - drug delivered directly into the blood stream

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13
Q

absorption in the rectal route

A

suppositories and enemas

useful for treating illnesses where vomiting is a symptom

good blood supply

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14
Q

absorption in the vaginal route

A

gels, pessaries and rings

can ensure local drug efficacy with reduced systemic side effects

good blood supply

pH variances through the menstruation cycle may affect absorption

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15
Q

absorption in the transdermal route

A

even highly lipid soluble chemicals are slow to enter the bloodstream through the skin

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16
Q

what factors affect absorption via the skin?

A
  • size of drug molecule
  • membrane permeability of drug delivery system
  • skin hydration
  • pKa of drug
  • drug metabolism by skin flora
  • lipid solubility
17
Q

what are class I drugs?

A

high permeability and high solubility

often these drugs are absorbed faster than excreted due to their high solubility

e.g. propranolol

18
Q

what are class II drugs?

A

high permeability and low solubility

bioavailability and distribution is limited by the time taken for the drug to dissolve

e.g. naproxen

19
Q

what are class III drugs?

A

low permeability and high solubility

a very solvent drug that is limited by its ability to pass through membranes

e.g. ranitidine

20
Q

what are class IV drugs?

A

low permeability and low solubility

drugs with very low bioavailability - not good at crossing membranes or being dissolved

e.g. paclitaxel

21
Q

what factors affect absorption?

A
  • blood flow
  • absorptive SA
  • contact time at absorptive surface
  • gastric emptying
22
Q

what is Cmax?

A

maximum concentration of compound after dosing

23
Q

what is Tmax?

A

time taken to reach maximum drug conc

24
Q

what is the area under the curve (AUC)?

A

considered a measure of systemic exposure

25
Q

what is bioavailability (F)?

A

the extent of absorption - how much is available to have an effect on the body

comparison using IV dosing

26
Q

what do you need to know to work out bioavailability?

A
  • how much exposure using IV route
  • how much exposure using oral route
  • IV dose administered
  • oral dose administered
27
Q

equation for bioavailability

A

F = (AUCoral/AUCiv) x (DOSEiv/DOSEoral)

lower bioavailability means more of the oral dose is lost

28
Q

how is IV and oral bioavailability different?

A

IV administration - whole dose goes straight into the bloodstream

oral administration - some drug lost to first pass metabolism, lower overall exposure (lower AUC)