Effects of food on drug therapy Flashcards
(13 cards)
drug absorption
- The presence of food & nutrients in the stomach/intestine can alter absorption of a drug
– Often ↓/interferes with absorption
for some medications, bioavailability is _ when taken with food
greater
bioavailability
fraction of an administered drug that reaches systemic circulation
– If administered by IV, bioavailability is 100%
– Oral administration is associated with lower bioavailability
delayed gastric emptying:
Rate of gastric emptying is influenced by the presence of food in the stomach & the type of meal or food ingested
– High-fibre or high-fat meals can delay gastric emptying
chelation
- Occurs between certain medications & divalent or trivalent cations
– e.g., Fe, Ca, Mg, Zn, Al - Can lead to reduced drug absorption
– Most commonly seen with tetracycline and fluoroquinolone antibiotics (e.g., ciprofloxacin, cephalosporin) - Optimally, will stop non-critical supplements for the duration of the antibiotic prescription
pH of the GI tract:
- Situations resulting in changes to the gastric (stomach) pH can reduce drug absorption
many meds treating _ aim to reduce the pH of the stomach
GERD
– e.g., antacids, H2-receptor antagonists (e.g., Pepcid) or proton-pump inhibitors
Physical incompatibilities between enteral feed and medications include
leads to…
– Granulation
– gel formation
– Separation of the enteral product
this leads to:
- clogged feeding tubes
- interrruption of delivery of nutrition to the patient
*Drug formulations that CAN cause granulation and gel formation include:
– Ciprofloxacin suspension (Cipro),
– Chlorpromazine (thorazine) concentrate,
– ferrous sulfate elixir,
– Guaifenesin (Robitussin), and
– Metoclopramide (Reglan) syrup
albumin
- Albumin is the most important drug -binding protein in the blood
- Patients with albumin levels <30 g/L have ↑ risk of adverse drug effects
– A lower dose of highly protein-bound drugs (e.g., warfarin; phenytoin) is recommended for patients with low albumin levels
enzyme systems in the _ and _ are responsible for much of the drug metabolizing activity in the body
liver & intestinal tract
food can inhibit or increase metabolism of medication by
enhancing the activity of these enzyme systems
– e.g., consumption of grapefruit & related citrus fruits inhibits the cytochrome P-450 3A4 enzyme system responsible for oxidative metabolism of many oral medications
Occasionally there is competition between food & drugs for metabolizing enzymes in the
liver
– When this is the case, more of the drug is likely to be circulated, which can lead to a toxic effect