Your browser doesn't support javascript.
loading
Pharmacokinetics of levamisole in the red-eared slider turtles (Trachemys scripta elegans).
Corum, Orhan; Durna Corum, Duygu; Atik, Orkun; Altan, Feray; Er, Ayse; Uney, Kamil.
Affiliation
  • Corum O; Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Kastamonu, Kastamonu, Turkey.
  • Durna Corum D; Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Kastamonu, Kastamonu, Turkey.
  • Atik O; Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Afyon Kocatepe, Afyonkarahisar, Turkey.
  • Altan F; Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Dicle, Diyarbakir, Turkey.
  • Er A; Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Selcuk, Konya, Turkey.
  • Uney K; Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Selcuk, Konya, Turkey.
J Vet Pharmacol Ther ; 42(6): 654-659, 2019 Nov.
Article in En | MEDLINE | ID: mdl-30933367
The pharmacokinetics and bioavailability of levamisole were determined in red-eared slider turtles after single intravenous (IV), intramuscular (IM), and subcutaneous (SC) administration. Nine turtles received levamisole (10 mg/kg) by each route in a three-way crossover design with a washout period of 30 days. Blood samples were collected at time 0 (pretreatment), and at 0.25, 0.5, 1, 1.5, 3, 6, 9, 12, 18, 24, 36, and 48 hr after drug administration. Plasma levamisole concentrations were determined by a high-performance liquid chromatography assay. Data were analyzed by noncompartmental methods. The mean elimination half-life was 5.00, 7.88, and 9.43 hr for IV, IM, and SC routes, respectively. The total clearance and volume of distribution at steady state for the IV route were 0.14 L hr-1  kg-1 and 0.81 L/kg, respectively. For the IM and SC routes, the peak plasma concentration was 9.63 and 10.51 µg/ml, respectively, with 0.5 hr of Tmax . The bioavailability was 93.03 and 115.25% for the IM and SC routes, respectively. The IM and SC route of levamisole, which showed the high bioavailability and long t1/2ʎz , can be recommended as an effective way for treating nematodes in turtles.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Turtles / Levamisole / Antinematodal Agents Type of study: Prognostic_studies Limits: Animals Language: En Journal: J Vet Pharmacol Ther Year: 2019 Document type: Article Affiliation country: Turkey Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Turtles / Levamisole / Antinematodal Agents Type of study: Prognostic_studies Limits: Animals Language: En Journal: J Vet Pharmacol Ther Year: 2019 Document type: Article Affiliation country: Turkey Country of publication: United kingdom