Antivirals/Antifungals Flashcards

1
Q

Name a M2 ion channel inhibitor and explain how they work.

A
  • amantadine
  • prevents uncoating of virus (an early step in replication)
  • virustatic
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2
Q

Are M2 ion channel blockers prone to resistance?

A

Yes, resistance develops in 30% in a few days (due to resistance in M2 gene)

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3
Q

What is the spectrum of amantadine?

A

prevents and treats influenza A

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4
Q

Describe M2 ion channel inhibitor pharmacokinetics

A
  • completely absorbed

- eliminated unchanged in urine

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5
Q

what are the side effects of M2 ion channel blockers

A
  • amphetamine like effects

- mild GI upset

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6
Q

Name 2 neuraminidase inhibitor and how the work.

A
  • zanamivir
  • oseltamivir
  • inhibits viral neuraminidase –> impairs release and spread of influenza virions by causing them to stick together
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7
Q

What is the spectrum of neuraminidase inhibitor?

A

prevents and treats influenza A and B infections

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8
Q

Describe the neuraminidase inhibitor pharmacokinetics.

A
  • zanamivir (powder) is only 3% absorbed, then eliminated unchanged via urine. 1D dose causes active drug in the lungs for 24 hours
  • oseltamivir ~80% absorbed, eliminated unchanged in urine. Elimination t1/2 = 3 hours
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9
Q

What are the side effects of zanamivir and oseltamivir?

A

Z - rare bronchospasm

O - nausea and vomiting

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10
Q

Give an example of a DNA polymerase inhibitor and explain how they work.

A
  • acyclovir
  • acyclovir becomes acyclovir-triphosphate and takes the place of guanosine in the DNA. This competitively inhibits viral DNA polymerase and causes DNA chain termination.
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11
Q

What is the difference between zanamivir and oseltamivir?

A

Z - inhaled powder

O - oral tablet prodrug

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12
Q

Describe the resistance that occurs in DNA polymerase inhibitors

A

resistance only develops in immunocompromised pts during prolonged therapy.

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13
Q

What is the spectrum of DNA polymerase inhibitors?

A
  • treatment, prevention and suppression of HSV and VZV infection
  • only ganciclovir is used for CMV infection
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14
Q

Describe the pharmacokinetics of DNA polymerase inhibitors.

A
  • 15% of oral absorbed

- eliminated unchanged in urine

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