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
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
14/10/2013
14/10/2013
2012
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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 |
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 |