Simultaneous determination of cyclophosphamide and Ifosfamide in plasma using SPE-HPLC-UV method

A reproducible and selective method for the simultaneous determination of cyclophosphamide (CP) and ifosfamide (IF) in plasma has been developed and validated using isocratic elution. The assay is performed by HPLC-UV, with a C18 column (5μm, 150 x 4 mm) and detection in 195 nm. The mobile phase was...

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Detalles Bibliográficos
Autores principales: Martins, Isarita, Souza, Jeferson O., Sanson, Ananda L., Vieira, Elisabeth, Guisti-Paiva, Alexandre
Formato: Articulo
Lenguaje:Inglés
Publicado: 2009
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/7723
http://www.latamjpharm.org/trabajos/28/1/LAJOP_28_1_1_6_O9LZ159788.pdf
Aporte de:
id I19-R120-10915-7723
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
antineoplastic drugs; HPLC; cyclophosphamide; Ifosfamide; simultaneous determination
Productos químicos y drogas
Evaluación de drogas
Toxicología
Preparaciones farmacéuticas
spellingShingle Farmacia
antineoplastic drugs; HPLC; cyclophosphamide; Ifosfamide; simultaneous determination
Productos químicos y drogas
Evaluación de drogas
Toxicología
Preparaciones farmacéuticas
Martins, Isarita
Souza, Jeferson O.
Sanson, Ananda L.
Vieira, Elisabeth
Guisti-Paiva, Alexandre
Simultaneous determination of cyclophosphamide and Ifosfamide in plasma using SPE-HPLC-UV method
topic_facet Farmacia
antineoplastic drugs; HPLC; cyclophosphamide; Ifosfamide; simultaneous determination
Productos químicos y drogas
Evaluación de drogas
Toxicología
Preparaciones farmacéuticas
description A reproducible and selective method for the simultaneous determination of cyclophosphamide (CP) and ifosfamide (IF) in plasma has been developed and validated using isocratic elution. The assay is performed by HPLC-UV, with a C18 column (5μm, 150 x 4 mm) and detection in 195 nm. The mobile phase was constituted by phosphate buffer 10 mM pH 6.0: acetonitrile (77.25:22.75), with a flow of 1 mL/min. SPE was used for sample clean-up in a range from 3 (LOQ) to 540 μM. The repeatability coefficients of variation (CV) ranged from 0.5 to 7.8% and the intermediate precision CVs varied from 0.9 to 5.7%. Extraction efficacy and accuracy varied from 94 to 115%. The simple method may permit the determination of cyclophosphamide and ifosfamide in plasma, simultaneously, to pharmacokinetics and bioequivalence studies.
format Articulo
Articulo
author Martins, Isarita
Souza, Jeferson O.
Sanson, Ananda L.
Vieira, Elisabeth
Guisti-Paiva, Alexandre
author_facet Martins, Isarita
Souza, Jeferson O.
Sanson, Ananda L.
Vieira, Elisabeth
Guisti-Paiva, Alexandre
author_sort Martins, Isarita
title Simultaneous determination of cyclophosphamide and Ifosfamide in plasma using SPE-HPLC-UV method
title_short Simultaneous determination of cyclophosphamide and Ifosfamide in plasma using SPE-HPLC-UV method
title_full Simultaneous determination of cyclophosphamide and Ifosfamide in plasma using SPE-HPLC-UV method
title_fullStr Simultaneous determination of cyclophosphamide and Ifosfamide in plasma using SPE-HPLC-UV method
title_full_unstemmed Simultaneous determination of cyclophosphamide and Ifosfamide in plasma using SPE-HPLC-UV method
title_sort simultaneous determination of cyclophosphamide and ifosfamide in plasma using spe-hplc-uv method
publishDate 2009
url http://sedici.unlp.edu.ar/handle/10915/7723
http://www.latamjpharm.org/trabajos/28/1/LAJOP_28_1_1_6_O9LZ159788.pdf
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AT vieiraelisabeth simultaneousdeterminationofcyclophosphamideandifosfamideinplasmausingspehplcuvmethod
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