HPLC method for assessment of in vitro and in vivo recovery of gatifloxacin using microdialysis

A simple and sensitive HPLC method was validated for assessment of in vitro and in vivo recovery of gatifloxacin using microdialysis. The validation parameters of linearity, precision, accuracy and limit of detection were studied as well as stability. Correlation coefficient (r<sup>2</sup&g...

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Autores principales: Tasso, Leandro, Bettoni, Clarissa C., Dalla Costa, Teresa
Formato: Articulo
Lenguaje:Inglés
Publicado: 2011
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/8164
http://www.latamjpharm.org/resumenes/30/3/LAJOP_30_3_1_8.pdf
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id I19-R120-10915-8164
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
gatifloxacin; high performance liquid chromatography; microdialysis; no net flux; probe recovery
Técnicas de Química Analítica
spellingShingle Farmacia
gatifloxacin; high performance liquid chromatography; microdialysis; no net flux; probe recovery
Técnicas de Química Analítica
Tasso, Leandro
Bettoni, Clarissa C.
Dalla Costa, Teresa
HPLC method for assessment of in vitro and in vivo recovery of gatifloxacin using microdialysis
topic_facet Farmacia
gatifloxacin; high performance liquid chromatography; microdialysis; no net flux; probe recovery
Técnicas de Química Analítica
description A simple and sensitive HPLC method was validated for assessment of in vitro and in vivo recovery of gatifloxacin using microdialysis. The validation parameters of linearity, precision, accuracy and limit of detection were studied as well as stability. Correlation coefficient (r<sup>2</sup>) obtained was > 0.999 for all calibration curves (20-600 ng.mL<sup>-1</sup>). Intra- and inter-day precision, expressed as the relative standard deviation (RSD) were less than 1.59 % and 1.33 %, respectively. Acceptable accuracy was achieved for all concentrations (99.17-101.35 %). The limit of quantification of the method was 20 ng.mL<sup>-1</sup>. The method showed the stability of gatifloxacin when submitted to different conditions. The validated method was applied to study calibration of microdialysis probes. The probe recovery was determined by no net flux experiment in vitro and in vivo. The in vitro and in vivo recovery for gatifloxacin was 30.9 ± 2.9 % and 28.9 ± 0.8 %, respectively. No differences were found between the two approaches. The HPLC method offers advantages because it has no extra sample handling steps; it is sensitive and can be used to determine free concentrations of gatifloxacin in tissues.
format Articulo
Articulo
author Tasso, Leandro
Bettoni, Clarissa C.
Dalla Costa, Teresa
author_facet Tasso, Leandro
Bettoni, Clarissa C.
Dalla Costa, Teresa
author_sort Tasso, Leandro
title HPLC method for assessment of in vitro and in vivo recovery of gatifloxacin using microdialysis
title_short HPLC method for assessment of in vitro and in vivo recovery of gatifloxacin using microdialysis
title_full HPLC method for assessment of in vitro and in vivo recovery of gatifloxacin using microdialysis
title_fullStr HPLC method for assessment of in vitro and in vivo recovery of gatifloxacin using microdialysis
title_full_unstemmed HPLC method for assessment of in vitro and in vivo recovery of gatifloxacin using microdialysis
title_sort hplc method for assessment of in vitro and in vivo recovery of gatifloxacin using microdialysis
publishDate 2011
url http://sedici.unlp.edu.ar/handle/10915/8164
http://www.latamjpharm.org/resumenes/30/3/LAJOP_30_3_1_8.pdf
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AT dallacostateresa hplcmethodforassessmentofinvitroandinvivorecoveryofgatifloxacinusingmicrodialysis
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