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Development and validation of high performance liquid chromatography method to determine linezolid concentration in pig pulmonary tissue.

dc.contributor.authorGuerrero, Laura
dc.contributor.authorMartínez - Olondris, Pilar
dc.contributor.authorRigol, Montserrat
dc.contributor.authorEsperatti, Mariano
dc.contributor.authorEsquinas, Cristina
dc.contributor.authorLuque, Néstor
dc.contributor.authorPiñer, Raquel
dc.contributor.authorTorres, Antoni
dc.contributor.authorSoy, Dolors
dc.date.accessioned2026-01-08T08:53:18Z
dc.date.available2026-01-08T08:53:18Z
dc.date.issued2010-01-01
dc.identifier.citationGuerrero L, Martínez-Olondris P, Rigol M, Esperatti M, Esquinas C, Luque N, Piñer R, Torres A, Soy D. Development and validation of high performance liquid chromatography method to determine linezolid concentration in pig pulmonary tissue. Clin Chem Lab Med. 2010;48(3):391-8es
dc.identifier.issn1437-4331
dc.identifier.urihttps://hdl.handle.net/20.500.12412/6974
dc.description.abstractBackground: Linezolid is the first synthetic compound of a new group of antimicrobials, the oxazolidinones, which inhibit protein synthesis. It shows a broad spectrum of activity against Gram positive organisms. With respect to its pharmacokinetics, linezolid shows a relatively high volume of distribution and good penetration into inflammatory fluids, bone, fat and muscle. Methods: A reversed-phase isocratic high-performance liquid chromatographic method for linezolid analysis in piglet pulmonary tissue is described. Tissue samples and controls were prepared in 1=TBE (1 M Tris, 0.9 M boric acid, 0.01 M EDTA). The mobile phase consisted of 20% ultrafiltered water and 80% of (A) 15 mM potassium monohydrogen phosphate buffer (pHs5) with (B) acetonitrile (80%/20%; v/v). Samples were homogenized and precipitated with HClO4 3% (1/1, v/v). The injection volume was 100 mL. Ofloxacin was used as an internal standard. Results: The assay was linear over a linezolid concentration range: 1.6–100 mg/mL. The method provided good validation data (ns15): inaccuracy (3.6%), intra and inter-day variability (4.2% and 5.2%, respectively), recovery (91.8%), limit of detection (0.8 mg/mL) and quantitation (1.6 mg/mL) and acceptable stability within 24 h in the auto-sampler.es
dc.language.isoenges
dc.titleDevelopment and validation of high performance liquid chromatography method to determine linezolid concentration in pig pulmonary tissue.es
dc.title.alternativeDevelopment and validation of high performance liquid chromatography method to determine linezolid concentration in pig pulmonary tissue.es
dc.typearticlees
dc.identifier.doi10.1515/CCLM.2010.078
dc.issue.number3es
dc.journal.titleClinical Chemistry & Laboratory Medicinees
dc.page.initial391es
dc.page.final398es
dc.relation.projectIDPI07/0419es
dc.relation.references10.1515/cclm.2010.078es
dc.rights.accessRightsopenAccesses
dc.subject.keywordHPLCes
dc.subject.keywordLinezolides
dc.subject.keywordValidationes
dc.volume.number48es


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