Drug Administration Flashcards

1
Q

Drug Concentration

A

Plasma concentration over time results from the ratio between absorption and degradation

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2
Q

Intracranial (i.c.) and Intracerebroventricular (i.c.v) Administration:

A

• Administered directly into brain region (i.c) or into ventricles containing cerebral spinal fluid to carry drug throughout brain (i.c.v)
• Not systemic, not concerned with blood concentration
• Often used in experimental settings
Very high peak

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3
Q

Oral Administration (p.o)

A

• Drug administered through tablets, pills, liquid
• Must dissolve in stomach fluid and pass through stomach wall, or be absorbed through the small intestine
• Must be resistant to stomach acid and digestion
• Peak is much small because some of the drug has already been metabolized by the time it reaches the blood stream
• Food in stomach causes delayed absorption
Relatively cheap, easy, and safe (less chance of an overdose)

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4
Q

First Pass Effect:

A
  • All drugs taken orally first pass through the liver, which contains lots of enzymes
    • Causes degradation of drugs, many drugs will not get the chance to reach the blood stream before it is metabolized by the liver
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5
Q

Intravenous (i.v) Administration:

A

• Goes directly into the blood, very quick onset
• Most rapid effect
High risk of abuse and overdose

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6
Q

Intramuscular (i.m) Administration:

A
  • Slower, but absorbs more than IV administration
    • Needs to move through muscle cells, blood flow in area increases absorption
    • Drugs suspended in oil results in slower, sustained absorption (cannabis oil can result in the drug staying in your system for a very long time)
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7
Q

Subcutaneous (s.c) Administration:

A
  • Administered just below the skin
    • Absorption depends on blood flow to site
    • Slow and steady
    • Has to absorb through several layers of skin
    • No sharp peak, overall blood concentration lower because of metabolism
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8
Q

Inhalation:

A

• Very rapid absorption
• Very rapid effect, blood from capillaries of lungs goes straight to the brain without returning to the heart first
Similar function to IV and IM

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9
Q

Intraperitoneal (i.p.) Administration:

A

• Common in lab animals, rare for human
• Injection into peritoneal cavity (space surrounding abdominal organs)
• Convenient, relatively quick absorption
Function of peak concentration varies depending on injection location

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