bioavailabilty

in pharmacokinetics
https://doi.org/10.1351/goldbook.BT06813
Ratio of the systemic exposure from extravascular (ev) exposure to that following intravenous (iv) exposure as described by the equation: \[F=\frac{A_{\text{ev}}\ D_{\text{iv}}}{B_{\text{iv}}\ D_{\text{ev}}}\] where F is the bioavailabilty, A and B are areas under the (plasma) concentration-time curve following extravascular and intravenous administration, respectively, and Dev and Div are the administered extravascular and intravenous doses.
Source:
PAC, 2004, 76, 1033. 'Glossary of terms used in toxicokinetics (IUPAC Recommendations 2003)' on page 1041 (https://doi.org/10.1351/pac200476051033)