Yayın: 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 | 2026-01-04T12:47:57Z | |
| dc.date.issued | 2019-04-01 | |
| dc.description.abstract | AbstractThe 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. | |
| dc.description.uri | https://doi.org/10.1111/jvp.12763 | |
| dc.description.uri | https://pubmed.ncbi.nlm.nih.gov/30933367 | |
| dc.description.uri | https://dx.doi.org/10.1111/jvp.12763 | |
| dc.description.uri | https://avesis.deu.edu.tr/publication/details/260bbee3-4847-42cd-bdb7-b0a25a2e0329/oai | |
| dc.description.uri | https://hdl.handle.net/11468/17717 | |
| dc.description.uri | https://hdl.handle.net/20.500.12395/38084 | |
| dc.identifier.doi | 10.1111/jvp.12763 | |
| dc.identifier.eissn | 1365-2885 | |
| dc.identifier.endpage | 659 | |
| dc.identifier.issn | 0140-7783 | |
| dc.identifier.openaire | doi_dedup___::8befd057315a543dc5d5eb923f88b39e | |
| dc.identifier.orcid | 0000-0003-3168-2510 | |
| dc.identifier.orcid | 0000-0003-1567-991x | |
| dc.identifier.orcid | 0000-0003-2411-7492 | |
| dc.identifier.orcid | 0000-0002-9017-763x | |
| dc.identifier.orcid | 0000-0002-8674-4873 | |
| dc.identifier.pubmed | 30933367 | |
| dc.identifier.scopus | 2-s2.0-85063720229 | |
| dc.identifier.startpage | 654 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12597/37295 | |
| dc.identifier.volume | 42 | |
| dc.identifier.wos | 000501034000011 | |
| dc.language.iso | eng | |
| dc.publisher | Wiley | |
| dc.relation.ispartof | Journal of Veterinary Pharmacology and Therapeutics | |
| dc.rights | OPEN | |
| dc.subject | levamisole | |
| dc.subject | Cross-Over Studies | |
| dc.subject | Bioavailability | |
| dc.subject | Antinematodal Agents | |
| dc.subject | Injections, Subcutaneous | |
| dc.subject | Biological Availability | |
| dc.subject | Injections, Intramuscular | |
| dc.subject | Turtles | |
| dc.subject | Levamisole | |
| dc.subject | red-eared slider turtles | |
| dc.subject | Area Under Curve | |
| dc.subject | Injections, Intravenous | |
| dc.subject | Red-Eared Slider Turtles | |
| dc.subject | Animals | |
| dc.subject | Pharmacokinetics | |
| dc.subject | bioavailability | |
| dc.subject | pharmacokinetics | |
| dc.subject | Half-Life | |
| dc.subject.sdg | 3. Good health | |
| dc.title | Pharmacokinetics of levamisole in the red‐eared slider turtles (Trachemys scripta elegans) | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
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Good health"},"provenance":null},{"subject":{"scheme":"FOS","value":"0403 veterinary science"},"provenance":null},{"subject":{"scheme":"FOS","value":"03 medical and health sciences"},"provenance":null},{"subject":{"scheme":"FOS","value":"0302 clinical medicine"},"provenance":null},{"subject":{"scheme":"keyword","value":"Levamisole"},"provenance":null},{"subject":{"scheme":"keyword","value":"red-eared slider turtles"},"provenance":null},{"subject":{"scheme":"keyword","value":"Area Under Curve"},"provenance":null},{"subject":{"scheme":"keyword","value":"Injections, Intravenous"},"provenance":null},{"subject":{"scheme":"keyword","value":"Red-Eared Slider Turtles"},"provenance":null},{"subject":{"scheme":"keyword","value":"Animals"},"provenance":null},{"subject":{"scheme":"keyword","value":"Pharmacokinetics"},"provenance":null},{"subject":{"scheme":"keyword","value":"bioavailability"},"provenance":null},{"subject":{"scheme":"keyword","value":"pharmacokinetics"},"provenance":null},{"subject":{"scheme":"keyword","value":"Half-Life"},"provenance":null}],"mainTitle":"Pharmacokinetics of levamisole in the red‐eared slider turtles (<i>Trachemys scripta elegans</i>)","subTitle":null,"descriptions":["<jats:title>Abstract</jats:title><jats:p>The pharmacokinetics and bioavailability of levamisole were determined in red‐eared slider turtles after single intravenous (<jats:styled-content style=\"fixed-case\">IV</jats:styled-content>), intramuscular (<jats:styled-content style=\"fixed-case\">IM</jats:styled-content>), and subcutaneous (<jats:styled-content style=\"fixed-case\">SC</jats:styled-content>) 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 <jats:styled-content style=\"fixed-case\">IV</jats:styled-content>,<jats:styled-content style=\"fixed-case\"> IM</jats:styled-content>, and <jats:styled-content style=\"fixed-case\">SC</jats:styled-content> routes, respectively. The total clearance and volume of distribution at steady state for the <jats:styled-content style=\"fixed-case\">IV</jats:styled-content> route were 0.14 L hr<jats:sup>−1</jats:sup> kg<jats:sup>−1</jats:sup> and 0.81 L/kg, respectively. 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| local.import.source | OpenAire | |
| local.indexed.at | WOS | |
| local.indexed.at | Scopus | |
| local.indexed.at | PubMed |
