Validation of a high performance liquid chromatographic method for quantitative determination of boldine in fluid extract of boldo

A simple and specific method was validated for quantification of boldine in fluid extract of boldo (Peumus boldus Mol.) using high-performance liquid chromatography. A reversed-phase C<sub>18</sub> , Phenomenex® (150 x 4.6 mm, 4 µm) column was employed. The mobile phase consisted of 0....

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Autores principales: Casal, Francieli, Mallmann, Michele, Pedroni, Helen C., Grazziotin, Manoela M., Tasso, Leandro
Formato: Articulo Comunicacion
Lenguaje:Inglés
Publicado: 2011
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/8224
http://www.latamjpharm.org/resumenes/30/4/LAJOP_30_4_2_11.pdf
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id I19-R120-10915-8224
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
Extractos Vegetales
boldine; high-performance liquid chromatography; Peumus boldus Mol.; quality control; validation
Cromatografía
Control de Calidad
spellingShingle Farmacia
Extractos Vegetales
boldine; high-performance liquid chromatography; Peumus boldus Mol.; quality control; validation
Cromatografía
Control de Calidad
Casal, Francieli
Mallmann, Michele
Pedroni, Helen C.
Grazziotin, Manoela M.
Tasso, Leandro
Validation of a high performance liquid chromatographic method for quantitative determination of boldine in fluid extract of boldo
topic_facet Farmacia
Extractos Vegetales
boldine; high-performance liquid chromatography; Peumus boldus Mol.; quality control; validation
Cromatografía
Control de Calidad
description A simple and specific method was validated for quantification of boldine in fluid extract of boldo (Peumus boldus Mol.) using high-performance liquid chromatography. A reversed-phase C<sub>18</sub> , Phenomenex® (150 x 4.6 mm, 4 µm) column was employed. The mobile phase consisted of 0.1 % trifluoroacetic acid and acetonitrile (78:22, v/v) at a flow rate of 0.8 mL/min. The column was maintained at 30 °C and the boldine peak detection was performed at a wavelength of 281 nm. The parameters used in the validation process were: linearity, specificity, precision, accuracy, limit of detection, limit of quantification and robustness. The validated method was selective and linear (r≥0.9991) for boldine concentration considering 5.0, 10.0, 15.0, 20.0 and 25.0 micro;g/mL. The recovery ranged from 90.93 % to 96.24 % and the limit of quantification was 2.41 micro;g/mL. The precision determined was reported as RSD (1.73 %). The method can be successfully applied to measure boldine concentrations in Boldo extract and be included in routine analysis of quality control.
format Articulo
Comunicacion
author Casal, Francieli
Mallmann, Michele
Pedroni, Helen C.
Grazziotin, Manoela M.
Tasso, Leandro
author_facet Casal, Francieli
Mallmann, Michele
Pedroni, Helen C.
Grazziotin, Manoela M.
Tasso, Leandro
author_sort Casal, Francieli
title Validation of a high performance liquid chromatographic method for quantitative determination of boldine in fluid extract of boldo
title_short Validation of a high performance liquid chromatographic method for quantitative determination of boldine in fluid extract of boldo
title_full Validation of a high performance liquid chromatographic method for quantitative determination of boldine in fluid extract of boldo
title_fullStr Validation of a high performance liquid chromatographic method for quantitative determination of boldine in fluid extract of boldo
title_full_unstemmed Validation of a high performance liquid chromatographic method for quantitative determination of boldine in fluid extract of boldo
title_sort validation of a high performance liquid chromatographic method for quantitative determination of boldine in fluid extract of boldo
publishDate 2011
url http://sedici.unlp.edu.ar/handle/10915/8224
http://www.latamjpharm.org/resumenes/30/4/LAJOP_30_4_2_11.pdf
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