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Life Science Dictionary

Bioavailability

Pharmacology

Say it: by-oh-uh-vay-luh-BIL-ih-tee

Bioavailability is the fraction of a drug dose that reaches the general circulation unchanged, along with how quickly it gets there.

Definition

What is bioavailability?

Bioavailability is the share of a dose of a drug that actually reaches the general bloodstream in active form, from where it can be carried to its site of action. It is expressed as a fraction or percentage, given the symbol F, and also covers the rate at which the drug arrives. A drug injected into a vein counts as 100 percent bioavailable, because none is lost on the way in.

Other routes lose some of the dose. A swallowed tablet has to dissolve, cross the gut lining and pass through the liver before reaching the rest of the body, and enzymes in the gut wall and liver may break part of it down first, the first-pass effect. Poor solubility, stomach acid, binding to food or other drugs, and quick passage through the gut can lower bioavailability further. The antibiotic gentamicin is barely absorbed by mouth and must be injected.

Bioavailability is measured by plotting blood concentration against time after a dose and comparing the area under the curve with that after an intravenous dose. Two products of the same drug, such as a brand and a generic, are bioequivalent when their curves closely match, which matters most for drugs with a narrow therapeutic index.

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Where does the word “bioavailability” come from?

bio-
lifeGreek bios

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