Canonical Question
PK – Absorption
Master answer
DEFINITION
The fraction of drug that reaches the circulation compared with the same dose given intravenously. (%)
(or)
The ratio of the area under the stated concentration–time curve (AUC) divided by the area under the i.v. concentration–time curve. (%)

FACTORS AFFECTING BIOAVAILABILITY
- Pharmaceutical factors
- Preparation: Decreasing order: Solutions > Suspensions > Capsule > Tablet > Coated tablet
- Particle Size
- Salt form
- Crystal forms have better availability compared to amorphous forms
- Degree of ionization: – Non-ionised, lipid soluble drugs – higher bioavailability
- Pharmacological factors
- Gastric Emptying and GI Motility
- GI Diseases: Coeliac, Crohn’s
- Timing in relation to food intake
- First pass metabolism: The degree of metabolic breakdown of an orally administered drug that occurs in the intestine or liver before it reaches the systemic circulation.
- Drug-Drug interactions
- Pharmacogenetic factors
- Other factors:
- Area of absorptive surface
- State of circulation (shock, tissue perfusion)
- Hepatic Insufficiency, Poor renal function
- Route of administration
Sources: Cross and Plunkett. Physics, Pharmacology, Physiology for Anaesthetists. Goodman & Gilman’s Pharmacological Basis of Therapeutics. Katzung Clinical Pharmacology
JC 2020
Exam appearances
| Exam | Exact wording | Relationship | Success |
|---|---|---|---|
| 2017B Q22 | Define bioavailability. Outline the factors which affect it. | historical_member | — |
| 2020A Q15 | Define bioavailability (10% of marks). Outline the factors which affect it (90% of marks). | historical_member | — |