Analytical Procedure for the Determination of Tulathromycin in Swine Plasma

For the measurement of tulathromycin distribution in swine plasma an accurate and reliable analytical method was developed. The extraction was performed with oxalic acid buffer (pH=4.0). Plasma samples were cleaned up by solid phase extraction procedure using polymeric cartriges. Chromatographic sep...

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Main Authors: Gajda Anna, Posyniak Andrzej, Błądek Tomasz
Format: Article
Language:English
Published: Sciendo 2013-06-01
Series:Bulletin of the Veterinary Institute in Pulawy
Subjects:
Online Access:https://doi.org/10.2478/bvip-2013-0035
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spelling doaj-b9e4fc05a0504ce5aee264b98831a7b02021-09-22T06:13:23ZengSciendoBulletin of the Veterinary Institute in Pulawy2300-32352013-06-0157219119510.2478/bvip-2013-0035Analytical Procedure for the Determination of Tulathromycin in Swine PlasmaGajda Anna0Posyniak Andrzej1Błądek Tomasz2Department of Pharmacology and Toxicology, National Veterinary Research Institute, 24-100Pulawy, PolandDepartment of Pharmacology and Toxicology, National Veterinary Research Institute, 24-100Pulawy, PolandDepartment of Pharmacology and Toxicology, National Veterinary Research Institute, 24-100Pulawy, PolandFor the measurement of tulathromycin distribution in swine plasma an accurate and reliable analytical method was developed. The extraction was performed with oxalic acid buffer (pH=4.0). Plasma samples were cleaned up by solid phase extraction procedure using polymeric cartriges. Chromatographic separation was achieved on a C 18 analytical column using mobile phase consisting of acetonitrile, 0.1% formic acid in gradient mode. Detection was carried out by liquid chromatography tandem mass spectrometry. Azithromycin was used as internal standard. The method has been successfully validated. The recovery from spiked samples ranged from 94% to 110%. The limit of detection was 2 ng/mL and the limit of quantification was 5 ng/mL. The method was developed to investigate the pharmacokinetics of tulathromycin in swine plasma. Applicability of the method was tested with plasma from swine administered with a single dose of tulathromycin.https://doi.org/10.2478/bvip-2013-0035swinetulathromycinplasmavalidation
collection DOAJ
language English
format Article
sources DOAJ
author Gajda Anna
Posyniak Andrzej
Błądek Tomasz
spellingShingle Gajda Anna
Posyniak Andrzej
Błądek Tomasz
Analytical Procedure for the Determination of Tulathromycin in Swine Plasma
Bulletin of the Veterinary Institute in Pulawy
swine
tulathromycin
plasma
validation
author_facet Gajda Anna
Posyniak Andrzej
Błądek Tomasz
author_sort Gajda Anna
title Analytical Procedure for the Determination of Tulathromycin in Swine Plasma
title_short Analytical Procedure for the Determination of Tulathromycin in Swine Plasma
title_full Analytical Procedure for the Determination of Tulathromycin in Swine Plasma
title_fullStr Analytical Procedure for the Determination of Tulathromycin in Swine Plasma
title_full_unstemmed Analytical Procedure for the Determination of Tulathromycin in Swine Plasma
title_sort analytical procedure for the determination of tulathromycin in swine plasma
publisher Sciendo
series Bulletin of the Veterinary Institute in Pulawy
issn 2300-3235
publishDate 2013-06-01
description For the measurement of tulathromycin distribution in swine plasma an accurate and reliable analytical method was developed. The extraction was performed with oxalic acid buffer (pH=4.0). Plasma samples were cleaned up by solid phase extraction procedure using polymeric cartriges. Chromatographic separation was achieved on a C 18 analytical column using mobile phase consisting of acetonitrile, 0.1% formic acid in gradient mode. Detection was carried out by liquid chromatography tandem mass spectrometry. Azithromycin was used as internal standard. The method has been successfully validated. The recovery from spiked samples ranged from 94% to 110%. The limit of detection was 2 ng/mL and the limit of quantification was 5 ng/mL. The method was developed to investigate the pharmacokinetics of tulathromycin in swine plasma. Applicability of the method was tested with plasma from swine administered with a single dose of tulathromycin.
topic swine
tulathromycin
plasma
validation
url https://doi.org/10.2478/bvip-2013-0035
work_keys_str_mv AT gajdaanna analyticalprocedureforthedeterminationoftulathromycininswineplasma
AT posyniakandrzej analyticalprocedureforthedeterminationoftulathromycininswineplasma
AT bładektomasz analyticalprocedureforthedeterminationoftulathromycininswineplasma
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