Pharmacokinetics of enrofloxacin and danofloxacin in premature calves
dc.contributor.author | Corum, Orhan | |
dc.contributor.author | Altan, Feray | |
dc.contributor.author | Yildiz, Ramazan | |
dc.contributor.author | Ider, Merve | |
dc.contributor.author | Ok, Mahmut | |
dc.contributor.author | Uney, Kamil | |
dc.date.accessioned | 2024-04-24T17:11:47Z | |
dc.date.available | 2024-04-24T17:11:47Z | |
dc.date.issued | 2019 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | The aim of this study was to determine the pharmacokinetics/pharmacodynamics of enrofloxacin (ENR) and danofloxacin (DNX) following intravenous (IV) and intramuscular (IM) administrations in premature calves. The study was performed on twenty-four calves that were determined to be premature by anamnesis and general clinical examination. Premature calves were randomly divided into four groups (six premature calves/group) according to a parallel pharmacokinetic (PK) design as follows: ENR-IV (10 mg/kg, IV), ENR-IM (10 mg/kg, IM), DNX-IV (8 mg/kg, IV), and DNX-IM (8 mg/kg, IM). Plasma samples were collected for the determination of tested drugs by high-pressure liquid chromatography with UV detector and analyzed by noncompartmental methods. Mean PK parameters of ENR and DNX following IV administration were as follows: elimination half-life (t(1/2 lambda z)) 11.16 and 17.47 hr, area under the plasma concentration-time curve (AUC(0-48)) 139.75 and 38.90 hr*mu g/ml, and volume of distribution at steady-state 1.06 and 4.45 L/kg, respectively. Total body clearance of ENR and DNX was 0.07 and 0.18 L hr(-1) kg(-1), respectively. The PK parameters of ENR and DNX following IM injection were t(1/2 lambda z) 21.10 and 28.41 hr, AUC(0-48) 164.34 and 48.32 hr*mu g/ml, respectively. The bioavailability (F) of ENR and DNX was determined to be 118% and 124%, respectively. The mean AUC(0-48CPR)/AUC(0-48ENR) ratio was 0.20 and 0.16 after IV and IM administration, respectively, in premature calves. The results showed that ENR (10 mg/kg) and DNX (8 mg/kg) following IV and IM administration produced sufficient plasma concentration for AUC(0-24)/minimum inhibitory concentration (MIC) and maximum concentration (C-max)/MIC ratios for susceptible bacteria, with the MIC90 of 0.5 and 0.03 mu g/ml, respectively. These findings may be helpful in planning the dosage regimen for ENR and DNX, but there is a need for further study in naturally infected premature calves. | en_US |
dc.identifier.doi | 10.1111/jvp.12787 | |
dc.identifier.endpage | 631 | en_US |
dc.identifier.issn | 0140-7783 | |
dc.identifier.issn | 1365-2885 | |
dc.identifier.issue | 6 | en_US |
dc.identifier.pmid | 31190327 | |
dc.identifier.scopus | 2-s2.0-85067616256 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | 624 | en_US |
dc.identifier.uri | https://doi.org/10.1111/jvp.12787 | |
dc.identifier.uri | https://hdl.handle.net/11468/17718 | |
dc.identifier.volume | 42 | en_US |
dc.identifier.wos | WOS:000501034000007 | |
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 | Danofloxacin | en_US |
dc.subject | Enrofloxacin | en_US |
dc.subject | Pharmacokinetics | en_US |
dc.subject | Premature Calves | en_US |
dc.title | Pharmacokinetics of enrofloxacin and danofloxacin in premature calves | en_US |
dc.title | Pharmacokinetics of enrofloxacin and danofloxacin in premature calves | |
dc.type | Article | en_US |