FoM:L3 - Pharmacokinetics 1, administration and absorption Flashcards

1
Q

What are the 4 main factors in pharmacokinetics? Briefly outline each one

A

Absorption - outside the body into the blood
Distribution - blood into extravascular tissue
Metabolism - back into blood/metabolites
Excretion - from the blood to outside the body

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2
Q

What are the main routes of drug administration?

A
  • local: topical
  • systemic: enteral or parenteral
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3
Q

What is the function of an enteric coating?

A

prevents disintegration in the stomach

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4
Q

What are extended release drugs?

A
  • tablets have been modified so drug is slowly released through permeable membrane
  • reduce frequency of dosing
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5
Q

What are parenteral formulations?

A
  • injectables
  • liquid or lyophilised
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6
Q

What are the types of topical formations?

A
  • cutaneous
  • inhaled
  • eye/nasal drops
  • implants
  • suppositories
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7
Q

Where do most oral drugs get absorbed?

A
  • small intestine
  • except alcohol and aspirin
  • rate impacted by whether food has been eaten as well as if liquid/solid meals
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8
Q

What is the pathway of an oral drug?

A
  • absorbed in stomach/small intestine
  • travel to the liver
  • reaches general circulation
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9
Q

What is first-pass metabolism?

A
  • first time a drug passes through the liver before entering systemic circulation
  • affects bioavailability
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10
Q

What enteral routes avoid first-pass metabolism?

A
  • buccal
  • sublingual
  • rectal
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11
Q

What are the types of parenteral administration?

A
  • IV - instantaneous
  • IM - intermediate
  • SC - slow
    all avoid 1st-pass metabolism and GI tract
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12
Q

What are the topical routes of action?

A
  • transdermal - slow, lipophilic drug
  • inhaled - rapid, low dose, targeted
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13
Q

How might penetration of membranes or barriers occur?

A
  • simple diffusion
  • facilitated diffusion
  • active transport
  • aqueous pores
  • intercellular junctions
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14
Q

How do lipid soluble drugs pass through membranes?

A

simple diffusion

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15
Q

How do low MW, water soluble drugs pass through membranes?

A
  • diffusion through aqueous channel
  • carrier mediated transport (including passive and active)
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16
Q

How do drugs with MW > 200 move through membranes?

A

diffuse through intercellular junctions

17
Q

What impacts simple diffusion?

A
  • concentration gradient
  • temperature
  • area
  • permeability
  • thickness
  • ionic charge and pH
18
Q

How does ionisation impact drug absorption?

A
  • some are weak acids and weak bases
  • acidic drug in acidic envt or basic drug in basic envt : drug will cross (non-ionised)
  • acidic drug in basic envt or basic drug in acidic envt : drug will not cross (ionised)
19
Q

What is bioavailability?

A
  • fraction of the administered dose reaching general circulation unchanged
  • constant for a drug given by a specific route: independent of drug dose
20
Q

How do you calculate bioavailable dose?

A

Administered dose x bioavailability