Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/66811
Title: Determination of stress-induced degradation products of cetirizine dihydrochloride by a stability-indicating RP-HPLC method
Author: Flórez, P.
Pérez Lozano, Pilar
García Montoya, Encarna
Ticó Grau, Josep R.
Miñarro Carmona, Montserrat
Jo, E.
Suñé i Negre, Josep M. (Josep Maria)
Keywords: Cromatografia de líquids
Desenvolupament de medicaments
Antihistamínics
Liquid chromatography
Drug development
Antihistamines
Issue Date: 9-Dec-2014
Publisher: BioMed Central
Abstract: A new, simple and accurate stability-indicating reverse phase high performance liquid chromatography method was developed and validated during the early stage of drug development of an oral lyophilizate dosage form of cetirizine dihydrochloride. For RP-HPLC analysis it was used an Eclipse XDB C8 column 150 mm × 4.6 mm, 5 μm (Agilent columns, Barcelona, Spain) as the stationary phase with a mobile phase consisted of a mixture of 0.2 M K2HPO4 pH 7.00 and acetonitrile (65:35, v/v) at a flow rate of 1 mL min −1. Detection was performed at 230 nm using diode array detector. The method was validated in accordance with ICH guidelines with respect to linearity, accuracy, precision, specificity, limit of detection and quantification. The method results in excellent separation between the drug substance and its stress-induced degradation products. The peak purity factor is >950 for the drug substance after all types of stress, which confirms the complete separation of the drug substance peak from its stress induced degradation products. Regression analysis showed r2 > 0.999 for cetirizine dihydrochloride in the concentration range of 650 μg mL −1 to 350 μg mL−1 for drug substance assay and a r2 > 0.999 in the concentration range of 0.25 μg mL−1 to 5 μg mL−1 for degradation products. The method presents a limit of detection of 0.056 μg mL −1 and a limit of quantification of 0.25 μg mL−1. The obtained results for precision and accuracy for drug substance and degradation products are within the specifications established for the validation of the method. The proposed stability-indicating method developed in the early phase of drug development proved to be a simple, sensitive, accurate, precise, reproducible and therefore useful for the following stages of the cetirizine dihydrochloride oral lyophilizate dosage form development.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1186/s40199-014-0082-5
It is part of: DARU Journal of Pharmaceutical Sciences, 2014, vol. 22, num. 82
Related resource: http://dx.doi.org/10.1186/s40199-014-0082-5
URI: http://hdl.handle.net/2445/66811
ISSN: 1560-8115
Appears in Collections:Articles publicats en revistes (Farmàcia, Tecnologia Farmacèutica i Fisicoquímica)

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