Pharmacokinetics of levamisole in the red-eared slider turtles (Trachemys scripta elegans)
dc.contributor.author | Corum, Orhan | |
dc.contributor.author | Durna Corum, Duygu | |
dc.contributor.author | Atik, Orkun | |
dc.contributor.author | Altan, Feray | |
dc.contributor.author | Er, Ayse | |
dc.contributor.author | Uney, Kamil | |
dc.date.accessioned | 2024-04-24T17:11:46Z | |
dc.date.available | 2024-04-24T17:11:46Z | |
dc.date.issued | 2019 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | 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 mu g/ml, respectively, with 0.5 hr of T-max. 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 t(1/2z), can be recommended as an effective way for treating nematodes in turtles. | en_US |
dc.identifier.doi | 10.1111/jvp.12763 | |
dc.identifier.endpage | 659 | en_US |
dc.identifier.issn | 0140-7783 | |
dc.identifier.issn | 1365-2885 | |
dc.identifier.issue | 6 | en_US |
dc.identifier.pmid | 30933367 | |
dc.identifier.scopus | 2-s2.0-85063720229 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | 654 | en_US |
dc.identifier.uri | https://doi.org/10.1111/jvp.12763 | |
dc.identifier.uri | https://hdl.handle.net/11468/17717 | |
dc.identifier.volume | 42 | en_US |
dc.identifier.wos | WOS:000501034000011 | |
dc.identifier.wosquality | Q2 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.relation.ispartof | Journal of Veterinary Pharmacology and Therapeutics | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Bioavailability | en_US |
dc.subject | Levamisole | en_US |
dc.subject | Pharmacokinetics | en_US |
dc.subject | Red-Eared Slider Turtles | en_US |
dc.title | Pharmacokinetics of levamisole in the red-eared slider turtles (Trachemys scripta elegans) | en_US |
dc.title | Pharmacokinetics of levamisole in the red-eared slider turtles (Trachemys scripta elegans) | |
dc.type | Article | en_US |