Pharmacokinetics Flashcards
What are the factors affecting Drug absp/Bioavailability
- Drug factors (physiochemical properties, lipophilic, dosage form, solid, liquid)
- Gatric emptying rate, GI motility
- Disease state
- Other factors (Interaction with other drugs/food)
Where is the main site of Drug absp
Small intestines
Why small intestine is the main site of absp
Large SA, Good blood flow, Long residence time (~4h)
Definition of bioavailability (F)
A measure of the drug available to the systemic circulation over time after administration (usually oral).
How to calculate F
AUC (route of administration.) / AUC (IV)
Definition of PK
The action of the body to the drug which determines its concentration at the receptor site.
Why oral admin has low F
Incomplete absp
presystemic metabolism (First pass metab.)
What is the formula of Vd
Drug dose / [drug]plasma
What are the factors affecting Drug distribution
- body size
- Lipid solubility of drug
- protein-binding in tissues vs plasma
- Disease start that alter physiology
What are the factors affecting drug metabolism
- Delayed entry into the liver
- CYP enzyme inhibition by drugs (increase)
- CYP enzyme induction by drugs
- ethnicity/ genetics
- age , pathology
Major site of drug excretion
Kidney
Formula of Clearance
( [Drug]urine x Volurine/min ) / [drug]plama
Definition of renal clearance
Volume of blood cleared of drug appearing in urine per unit time
Effects of Drug metabolism
Metabolic inactivation, metabolic bioactivation, metabolic toxicity