Week 2 - Pharmacokinetics - Review Questions Flashcards

1
Q

Compare different routes of administration and their reason for use.

A
  • PO is easiest and most common
  • IV is quickest and can deliver large amounts over time (infusion)
  • IM or Subcut is used for slower rate
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2
Q

What routes are required for specific sites?

A
  • Inhalation for respiratory
  • Epithetlial for skin, cornea, nasal mucosa
  • Subling for rapid absorption into systemic circulation, bypass liver
  • Rectal for GI or when PO/IV not possible
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3
Q

How will drug lipid-solubility affect absorption and distribution?

A
  • Higher lipid-solubility = faster absorption across membranes
  • High lipid-soluble distribute throughout body
  • Low lipid-soluble/insoluble distribute in plasma and interstitial fluid
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4
Q

Contrast effects of pH on absorption of drug from different area of GI tract.

A
  • Acidic drug (Aspirin pH3.5) absorbed in the stomach

- Basic drug (Atropine pH9.8) absorbed in the small intestine

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5
Q

A drug has a Vd of 10, what is its distribution and what are the consequences?

A
  • Accumulate in the fat

- Stay in te system for longer

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6
Q

Define “first pass metabolism”

A

Drug may be substantially metabolised during first passage through the liver before entering systemic circulation.

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7
Q

Define the Single Compartment Model

A

The body is a single well-stirred compartment

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8
Q

Define First Order Kinetics

A

Rate of excretion is dependent on drug [plasma]

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9
Q

What are two types of reactions that occur between drugs as a result of their pharmacokinetic properties?

A
  • Elimination rate and half-life can determine rate of repeated dose
  • If drug [plasma] not decreased or not cleared, the amount absorbed will add on to the current amount. Until rate of elimination = rate of absorption; and plateau achieved.
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10
Q

Why is Aspirin absorbed in the stomach?

A

Aspirin takes uncharged form to get through charge selective membrane, and changes to charged form to stay in blood.

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11
Q

What is ADME of Pharmacokinetics?

A

Administration/Absorption
Dsitribution
Metabolism
Excretion

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12
Q

Define the Two Compartment Model

A

Central compartment = Plasma

Peripheral compartment = Bodily tissues

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13
Q

Ethanol Absorption

A

Rapidly absorbed from the stomach and intestines

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14
Q

Ethanol Distribution

A
  • Lipid-soluble; quick distribution
  • Rapid absorption and high portal vein [ ]
    = large amount of systemic circulation
  • Slow absorption
    = high 1st pass metabolism in liver
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15
Q

Ethanol Metabolism

A
  • Dehyrdogenase cycle
  • Larger % cleared by1st pass metabolism
  • 90% metabolised
  • Metabolism reduced due to limited cofactor (NAD+) {10drinks need 1.5kg NAD+}
  • 0.5kg ethanol removed at 8g/hr (long)
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16
Q

What is the metabolic process of ethanol during Dehydrogenase?

A

Ethanol -> Acetaldehyde by Alcohol dehydrogenase

Acetaldehyde -> Acetic Acide by Aldehyde dehydrogenase

17
Q

Ethanol Excretion

A

Follows zero order kinetics where excretion from plasma is linear
Therefore removed at a constant rate independant of plasm [ ]

18
Q

Define zero order kinetics

A

Rate of excretion independant of drug plasm []