The Bioequivalence Determination of Two Different Formulations of Enrofloxacin in Heifers Following Intramuscular Administration
dc.authorid | Yilmaz, Ismet/0000-0001-8680-3098 | |
dc.authorid | Elmas, Muammer/0000-0001-9059-7151 | |
dc.authorwosid | Yilmaz, Ismet/H-4144-2019 | |
dc.authorwosid | Yılmaz, ismet/AAG-8946-2019 | |
dc.authorwosid | Elmas, Muammer/B-1013-2008 | |
dc.contributor.author | Yilmaz, Ismet | |
dc.contributor.author | Elmas, Muammer | |
dc.date.accessioned | 2024-08-04T21:01:19Z | |
dc.date.available | 2024-08-04T21:01:19Z | |
dc.date.issued | 2010 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | The aim of this study was to evaluate the bioequivalence (BE) of two medicinal products of enrofloxacin, which have been also marketed as 10% injectable solution in Turkey, after the intramuscular injection (IM) at a single dose of 2.5 mg/kg of BW in the heifers. The present study was performed on healthy 6 Swiss-Brown (12-18 months and 340-400 kg BW) heifers. This study was carried out on the based a single dose cross-over design. Blood samples were taken into sterilized tubes just before, and 10(th), 20(th), 30(th), 45(th), 60(th) and 90(th) min. and 2(th), 3(th), 4(th), 6(th), 8(th), 12(th) and 24(th) h following injections. The plasma concentrations of enrofloxacin (ENR) were measured by high performance liquid chromatography (HPLC) following the extraction process. The plasma concentration-time curves for each animals showed that both products distributed according two-compartment open model. The basic pharmacokinetic parameters at this study were only the AUC(0-24) and AUC(total) were statistically significant (P<0.05) before logarithmic (log) transformation. Log transformed the AUC(0-24), AUC(total) and C(max) parameters and observed t(max) were used in BE evaluation. Minimum, maximum and mean AUC(0-24) AUC(total) and C(max) for A and B products were found in the acceptable ranges (70-143%). For the t(max) value log transformation has not been done and that were determined within the limits 80-125%. As a result; it is concluded that both products could be used instead of each other as an inter-changeable drugs. | en_US |
dc.identifier.endpage | 382 | en_US |
dc.identifier.issn | 1300-6045 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.startpage | 377 | en_US |
dc.identifier.uri | https://hdl.handle.net/11616/104290 | |
dc.identifier.volume | 16 | en_US |
dc.identifier.wos | WOS:000278340800004 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.language.iso | en | en_US |
dc.publisher | Kafkas Univ, Veteriner Fakultesi Dergisi | en_US |
dc.relation.ispartof | Kafkas Universitesi Veteriner Fakultesi Dergisi | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Bioequivalence | en_US |
dc.subject | Enrofloxacin | en_US |
dc.subject | Heifer | en_US |
dc.title | The Bioequivalence Determination of Two Different Formulations of Enrofloxacin in Heifers Following Intramuscular Administration | en_US |
dc.type | Article | en_US |