| dc.contributor.author | Guerrero, Laura | |
| dc.contributor.author | Martínez - Olondris, Pilar | |
| dc.contributor.author | Rigol, Montserrat | |
| dc.contributor.author | Esperatti, Mariano | |
| dc.contributor.author | Esquinas, Cristina | |
| dc.contributor.author | Luque, Néstor | |
| dc.contributor.author | Piñer, Raquel | |
| dc.contributor.author | Torres, Antoni | |
| dc.contributor.author | Soy, Dolors | |
| dc.date.accessioned | 2026-01-08T08:53:18Z | |
| dc.date.available | 2026-01-08T08:53:18Z | |
| dc.date.issued | 2010-01-01 | |
| dc.identifier.citation | Guerrero 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):391-8 | es |
| dc.identifier.issn | 1437-4331 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12412/6974 | |
| dc.description.abstract | Background: 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.iso | eng | es |
| dc.title | Development and validation of high performance liquid chromatography method to determine linezolid concentration in pig pulmonary tissue. | es |
| dc.title.alternative | Development and validation of high performance liquid chromatography method to determine linezolid concentration in pig pulmonary tissue. | es |
| dc.type | article | es |
| dc.identifier.doi | 10.1515/CCLM.2010.078 | |
| dc.issue.number | 3 | es |
| dc.journal.title | Clinical Chemistry & Laboratory Medicine | es |
| dc.page.initial | 391 | es |
| dc.page.final | 398 | es |
| dc.relation.projectID | PI07/0419 | es |
| dc.relation.references | 10.1515/cclm.2010.078 | es |
| dc.rights.accessRights | openAccess | es |
| dc.subject.keyword | HPLC | es |
| dc.subject.keyword | Linezolid | es |
| dc.subject.keyword | Validation | es |
| dc.volume.number | 48 | es |