Population pharmacokinetics of pyrazinamide in elephants

This study was undertaken to characterize the population pharmacokinetics (PK), therapeutic dose, and preferred route of administration for pyrazinamide (PZA) in elephants. Twenty‐three African ( Loxodonta africana ) and Asian ( Elephas maximus ) elephants infected with or in contact with others culture positive for Mycobacterium tuberculosis were dosed under treatment conditions. PZA was dosed daily at 20–30 mg/kg via oral (fasting or nonfasting state) or rectal (enema or suppository) administration. Blood samples were collected 0–24 h postdose. Population PK was estimated using nonlinear mixed effect modeling. Drug absorption was rapid with T max at or before 2 h regardless of the method of drug administration. C max at a mean dose of 25.6 (±4.6) mg/kg was 19.6 (±9.5  μ g/mL) for PZA given orally under fasting conditions. Under nonfasting conditions at a mean dose of 26.1 ± 4.2 mg/kg, C max was 25% (4.87 ± 4.89  μ g/mL) and area under concentration curve ( AUC ) was 30% of the values observed under fasting conditions. Mean rectal dose of 32.6 ± 15.2 mg/kg yielded C max of 12.3 ± 6.3  μ g/mL, but comparable AUC to PZA administered orally while fasting. Both oral and rectal administration of PZA appeared to be acceptable and oral dosing is preferred because of the higher C max and lower inter‐subject variability. A starting dose of 30 mg/kg is recommended with drug monitoring between 1 and 2 h postdose. Higher doses may be required if the achieved C max values are below the recommended 20–50  μ g/mL range.