A fast and accurate micellar electrokinetic capillary chromatography method was developed for quality control of pharmaceutical preparations containing cold remedies as acetaminophen, salicylamide, caffeine, phenylephrine, pseudoephedrine, norephedrine and chlorpheniramine. The method optimization was realized on a Beckman P/ACE System MDQ instrument. The baseline separation of seven analytes was performed in an uncoated fused silica capillary internal diameter (ID)=50 µm using tris-borate (20 mM, pH=8.5) containing sodium dodecyl sulphate 30 mM BGE. On line-UV detection at 214 nm was performed and the applied voltage was 10 kV. The operating temperature was 25°C. After experimental conditions optimization, the proposed method was validated. The evaluated parameters were: precision of migration time and of corrected peak area ratio, linearity range, limit of detection, limit of quantification, accuracy (recovery), ruggedness and applicability. The method was then successfully applied for the analysis of three pharmaceutical preparations containing some of the analytes listed before.

Development and Validation of a MEKC Method for Determination of Nitrogen-Containing Drugs in Pharmaceutical Preparations / Buiarelli, Francesca; Coccioli, Franco; Jasionowska, Renata. - In: ELECTROPHORESIS. - ISSN 0173-0835. - STAMPA. - 29:17(2008), pp. 3519-3523. [10.1002/elps.200700934]

Development and Validation of a MEKC Method for Determination of Nitrogen-Containing Drugs in Pharmaceutical Preparations

BUIARELLI, Francesca;COCCIOLI, Franco;JASIONOWSKA, Renata
2008

Abstract

A fast and accurate micellar electrokinetic capillary chromatography method was developed for quality control of pharmaceutical preparations containing cold remedies as acetaminophen, salicylamide, caffeine, phenylephrine, pseudoephedrine, norephedrine and chlorpheniramine. The method optimization was realized on a Beckman P/ACE System MDQ instrument. The baseline separation of seven analytes was performed in an uncoated fused silica capillary internal diameter (ID)=50 µm using tris-borate (20 mM, pH=8.5) containing sodium dodecyl sulphate 30 mM BGE. On line-UV detection at 214 nm was performed and the applied voltage was 10 kV. The operating temperature was 25°C. After experimental conditions optimization, the proposed method was validated. The evaluated parameters were: precision of migration time and of corrected peak area ratio, linearity range, limit of detection, limit of quantification, accuracy (recovery), ruggedness and applicability. The method was then successfully applied for the analysis of three pharmaceutical preparations containing some of the analytes listed before.
2008
01 Pubblicazione su rivista::01a Articolo in rivista
Development and Validation of a MEKC Method for Determination of Nitrogen-Containing Drugs in Pharmaceutical Preparations / Buiarelli, Francesca; Coccioli, Franco; Jasionowska, Renata. - In: ELECTROPHORESIS. - ISSN 0173-0835. - STAMPA. - 29:17(2008), pp. 3519-3523. [10.1002/elps.200700934]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/17622
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