Drug Administration Flashcards
Drug Concentration
Plasma concentration over time results from the ratio between absorption and degradation
Intracranial (i.c.) and Intracerebroventricular (i.c.v) Administration:
• 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
Oral Administration (p.o)
• 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)
First Pass Effect:
- 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
Intravenous (i.v) Administration:
• Goes directly into the blood, very quick onset
• Most rapid effect
High risk of abuse and overdose
Intramuscular (i.m) Administration:
- 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)
Subcutaneous (s.c) Administration:
- 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
Inhalation:
• 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
Intraperitoneal (i.p.) Administration:
• 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