Development and validation of a simple and sensitive high performance liquid chromatographic method for the simultaneous determination of anastrozole, bicalutamide, tamoxifen, and their synthetic impurities


Autoria(s): Gomes, Fabio Pereira; Garcia, Pedro Lopez
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

14/10/2013

14/10/2013

2012

Resumo

A simple and sensitive analytical method for simultaneous determination of anastrozole, bicalutamide, and tamoxifen as well as their synthetic impurities, anastrozole pentamethyl, bicalutamide 3-fluoro-isomer, and tamoxifen e-isomer, was developed and validated by using high performance liquid chromatography (HPLC). The separation was achieved on a Symmetry (R) C-8 column (100 x 4.6 mm i.d., 3.5 mu m) at room temperature (+/- 24 degrees C), with a mobile phase consisting of acetonitrile/water containing 0.18% N,N dimethyloctylamine and pH adjusted to 3.0 with orthophosphoric acid (46.5/53.5, v/v) at a flow rate of 1.0 mL min(-1) within 20 min. The detection was made at a wavelength of 270 nm by using ultraviolet (UV) detector. No interference peaks from excipients and relative retention time indicated the specificity of the method. The calibration curve showed correlation coefficients (r) > 0.99 calculated by linear regression and analysis of variance (ANOVA). The limit of detection (LOD) and limit of quantitation (LOQ), respectively, were 2.2 and 6.7 mu g mL(-1) for anastrozole, 2.61 and 8.72 mu g mL(-1) for bicalutamide, 2.0 and 6.7 mu g mL(-1) for tamoxifen, 0.06 and 0.22 mu g mL(-1) for anastrozole pentamethyl, 0.02 and 0.07 mu g mL(-1) for bicalutamide 3-fluoro-isomer, and 0.002 and 0.007 mu g mL(-1) for tamoxifen e-isomer. Intraday and interday relative standard deviations (RSDs) were <2.0% (drugs) and <10% (degradation products) as well as the comparison between two different analysts, which were calculated by f test. (C) 2012 Elsevier B.V. All rights reserved.

International Postgraduate Research Scholarship (IPRS)

International Postgraduate Research Scholarship (IPRS)

University of Queensland Centennial Scholarship (UQCent)

University of Queensland Centennial Scholarship (UQCent)

Council for Scientific and Technological Development (CNPq)

Council for Scientific and Technological Development (CNPq)

Identificador

TALANTA, AMSTERDAM, v. 101, n. 41334, supl. 1, Part 1, pp. 495-503, 42309, 2012

0039-9140

http://www.producao.usp.br/handle/BDPI/34476

10.1016/j.talanta.2012.10.004

http://dx.doi.org/10.1016/j.talanta.2012.10.004

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

AMSTERDAM

Relação

TALANTA

Direitos

closedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #HPLC METHOD VALIDATION #SYNTHETIC IMPURITIES #ONCOLOGIC DRUGS #TANDEM MASS-SPECTROMETRY #LC ASSAY-METHOD #HUMAN PLASMA #ELECTROPHORESIS METHOD #DEGRADATION-PRODUCTS #MAIN METABOLITES #HPLC METHOD #QUANTIFICATION #ROBUSTNESS #CITRATE #CHEMISTRY, ANALYTICAL
Tipo

article

original article

publishedVersion