TY - JOUR
T1 - The determination of miconazole and its related production impurities together with basic solution stability studies using a sub 2 μm chromatographic column
AU - O'Connor, N.
AU - Geary, M.
AU - Wharton, M.
AU - Sweetman, P.
PY - 2012/3
Y1 - 2012/3
N2 - A selective and sensitive method for the analysis of Miconazole and its associated impurities is developed. The separation is carried out using a Thermo Scientific Hypersil Gold C18 Column (50 mm × 4.6 mm i.d., 1.9 μm particle size) with a mobile phase of acetonitrilemethanolammonium acetate (1.5 w/v) (30:32:38 v/v) at a flow rate of 2.5 mL/min and UV detection at 235 nm. The method is validated according to ICH guidelines with respect to precision, accuracy, linearity, specificity, robustness, and limits of detection and quantification. All parameters examined are found to be well within the stated guidelines. Naturally aged samples are also tested to determine sample stability. A profile of sample and impurity breakdown was presented. The analysis time was more than halved from just under 20 min (the current European Pharmacopeia Method) to under 8 min (developed method) and the method is applicable for assay and related substance determination.
AB - A selective and sensitive method for the analysis of Miconazole and its associated impurities is developed. The separation is carried out using a Thermo Scientific Hypersil Gold C18 Column (50 mm × 4.6 mm i.d., 1.9 μm particle size) with a mobile phase of acetonitrilemethanolammonium acetate (1.5 w/v) (30:32:38 v/v) at a flow rate of 2.5 mL/min and UV detection at 235 nm. The method is validated according to ICH guidelines with respect to precision, accuracy, linearity, specificity, robustness, and limits of detection and quantification. All parameters examined are found to be well within the stated guidelines. Naturally aged samples are also tested to determine sample stability. A profile of sample and impurity breakdown was presented. The analysis time was more than halved from just under 20 min (the current European Pharmacopeia Method) to under 8 min (developed method) and the method is applicable for assay and related substance determination.
UR - http://www.scopus.com/inward/record.url?scp=84859936475&partnerID=8YFLogxK
U2 - 10.1093/chromsci/bmr047
DO - 10.1093/chromsci/bmr047
M3 - Article
C2 - 22337796
AN - SCOPUS:84859936475
SN - 0021-9665
VL - 50
SP - 199
EP - 205
JO - Journal of Chromatographic Science
JF - Journal of Chromatographic Science
IS - 3
ER -