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Fast simultaneous spectrophotometric determination of naphazoline nitrate and methylparaben by sequential injection chromatography
被引:42
作者:
Chocholous, Petr
[1
]
Satinsky, Dalibor
[1
]
Solich, Petr
[1
]
机构:
[1] Charles Univ Prague, Fac Pharm, Dept Analyt Chem, Hradec Kralove 50005, Czech Republic
来源:
关键词:
sequential injection chromatography;
monolithic column;
naphazoline nitrate;
methylparaben;
spectrophotometric determination;
D O I:
10.1016/j.talanta.2006.02.065
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Fast simultaneous determination of naphazoline nitrate and methylparaben in pharmaceuticals using separation method based on a novel reversed-phase sequential injection chromatography (SIC) is described in this contribution as an alternative to classical HPLC. A Chromolith (TM) Flash RP-18e (25 mm x 4.6 mm) column (Merck (R), Germany) and aFIAlab (R) 3000 system (USA) with a six-port selection valve and 5.Oml syringe pump were used for sequential injection chromatographic separations in our study. The mobile phase used was methanol/water (40:65, v/v), pH 5.2 adjusted with triethylamine 0.8 mu l ml(-1) and acetic acid, at flow rate 0.9 ml min(-1). UV detection provided by DAD detector and two wavelengths were simultaneously monitored for increasing sensitivity of determination. Detector was set up at 220 nm for naphazoline nitrate and 256 run for methylparaben and ethylparaben (IS). There is no necessity to use pre-adjustment of sample of nasal drops (only dilution with mobile phase) so the time of the whole analysis is very short. The validation parameters have shown good results: linearity of determination for both components (naphazoline nitrate and methylparaben), correlation coefficient > 0.999; repeatability of determination (R.S.D.) in the range 0.5-1.6% at three different concentration levels, detection limits 0.02 mu g ml(-1) (naphazoline nitrate) and 0.20 mu g ml(-1) (methylparaben and ethylparaben), and recovery from the pharmaceutical preparations in the range 100.06-102.55%. The chromatographic resolution between peaks of compounds was more than 4.0 and analysis time was less than 4 min under the optimal conditions. The advantages and drawbacks of SIC against classical HPLC are discussed showing that SIC can be an advantageous alternative in many cases. (c) 2006 Elsevier B.V. All rights reserved.
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页码:408 / 413
页数:6
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