3&4 - Drug absorption Flashcards
Are strong or weak acids & bases better at being absorbed in the intestine
Weak - strong acids & bases are ionised at the pH of the intestine
Factors affection GI absorption of drugs (4)
GI motility
Splanchic blood flow
Particle size & formulation
Physiochemical factors
What causes gastric stasis and what does it do to absorption
Migraine, diabetic neuropathy
- decreased drug absorption
GI motility - Coeliac disease
Increased and decreased absorption of what drugs
Increased - thyroxine & digoxin
Decreased - propranolol, cotrimoxazol, cephalexin
GI motility - food _ drug absorption
Decreases
Metaclopramide affects _ receptors
Muscarinic
Example of a physiochemical factor - drug / drug interaction
Bile & warfarin
Compete for uptake transporters
Example of drug not absorbed
Mesalazine - for Crohn’s disease
1st pass metabolism - drugs excreted in faeces
Benzyl penicillin & insulin
Inactivated by gastric acid
1st pass metabolism - drugs metabolised a gut wall
Monoamines by MAO
Eg of 2 drugs with low hepatic extraction ratio
Paracetamol
Warfarin
Eg of 2 drugs with intermediate hepatic extraction ratio
Aspirin
Codeine
Eg of 2 drugs with high hepatic extraction ratio
Morphine
Propranolol
Route of cutaneous administration
Epidermis —> dermis —> hypodermis
Adv & disadv of cutaneous administration
Adv - skips 1st pass metabolism
Dis - variability in application of topically applied drugs