Related Experiment Video
Updated: Jan 13, 2026

A Novel Method of Drug Administration to Multiple Zebrafish Danio rerio and the Quantification of Withdrawal
Published on: November 12, 2014
Pharmacokinetics and Withdrawal Time of Doxycycline in Snakehead (Channa striata) Following Oral Medication
Nguyen Quoc Thinh1, Han Chi Thien1, Mathias Devreese2
1College of Aquaculture and Fisheries, Can Tho University, Can Tho, Vietnam.
Abstract:
The study consisted of two experiments. First, a PK experiment was set up with a single oral dose at 20 mg/kg body weight, and second, a withdrawal time determination study, where the fish were fed once a day for 5 consecutive days at the same dosage. The DOX concentration in medicated feed, fish muscle, plasma, liver, and kidney was analysed by LC-MS/MS. Phoenix 8.1 and WT 1.4 software were used in the calculation for PK parameters and withdrawal time, respectively. DOX was absorbed quickly into plasma after oral medication with an absorption half-life T1/2abs of 0.12 h, reaching the Cmax (116 μg/L) at 1 h (Tmax). DOX distribution was highest in the kidney, followed by the liver and plasma. The high DOX concentration in the kidney and liver supports the possibility of using DOX to treat relevant bacterial infections in snakehead. In conclusion, DOX is rapidly absorbed in snakehead after oral medication, has a significant tissue distribution, followed by slow elimination. Finally, after feeding medicated feed for 5 consecutive days, the withdrawal times of DOX in composite muscle and skin samples of snakehead were 4 days and 6 days (at 28.5°C) according to the maximum residue limits set by the European Commission (100 μg/kg for bovine, porcine and poultry) and Japanese authority (50 μg/kg), respectively.
Related Concept Videos
Indirect-Acting Cholinergic Agonists: Pharmacokinetics
Reversible agents containing quaternary amines, such as neostigmine and edrophonium, are not easily absorbed orally because they...
Chronopharmacokinetics: Time-Dependent Pharmacokinetics
Time-dependent pharmacokinetics refers to non-cyclical changes in drug rate processes over a period of time. It can lead to nonlinear pharmacokinetics, where the relationship between drug concentration and time is not proportional. Non-cyclical...
Dosage Regimen: Multiple Oral Dosage
Kinetics of Drug Elimination
Drug clearance depends on the rate of drug elimination and its plasma concentration. Another important parameter is the half-life of a drug, which is the time required for its concentration to decrease by half. In most cases, drug clearance follows first-order...
Cholinergic Antagonists: Pharmacokinetics
Hepatic Drug Excretion: Enterohepatic Cycling
Post-release drugs and metabolites can be reabsorbed into the body from the intestine. For conjugated metabolites like glucuronides, reabsorption requires enzymatic hydrolysis by intestinal microflora. This...

