Comparison of UV and charged aerosol detection approach in pharmaceutical analysis of statins

被引:51
作者
Novakova, Lucie [1 ]
Lopez, Sofia Arnal [2 ]
Solichova, Dagmar [3 ,4 ]
Satinsky, Dalibor [1 ]
Kulichova, Bohumila [5 ]
Horna, Ales [5 ,6 ]
Solich, Petr [1 ]
机构
[1] Charles Univ Prague, Fac Pharm, Dept Analyt Chem, Hradec Kralove 50005, Czech Republic
[2] Univ Valencia, Fac Chem, Valencia, Spain
[3] Charles Univ Prague, Dept Metab Care & Gerontol, Fac Med, Hradec Kralove 50005, Czech Republic
[4] Univ Hosp, Hradec Kralove 50005, Czech Republic
[5] Radanal Ltd, Pardubice 53003, Czech Republic
[6] Tomas Bata Univ, Univ Inst, Zlin 76001, Czech Republic
关键词
Atorvastatin; Lovastatin; Simvastatin; HPLC; CAD; Pharmaceutical analysis; COA REDUCTASE INHIBITORS; LIQUID-CHROMATOGRAPHY; BULK DRUG; ATORVASTATIN; HPLC; SIMVASTATIN; IMPURITIES; PRAVASTATIN; LOVASTATIN; TABLETS;
D O I
10.1016/j.talanta.2008.12.057
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
CAD (charged aerosol detector) has recently become a new alternative detection system in HPLC. This detection approach was applied in a new HPLC method for the determination of three of the major statins used in clinical treatment-simvastatin, lovastatin and atorvastatin. The method was optimized and the influence of individual parameters on CAD response and sensitivity was carefully Studied. Chromatography was performed on a Zorbax Eclipse XDB C18 (4.6 mm x 75 min, 3.5 mu m). using acetonitrile and formic acid 0.1%, as mobile phase. The detection was performed using both CAD (20 pA range) and DAD (diode array detector-238 nm) simultaneously connected in series. In terms of linearity, precision and accuracy, the method was validated using tablets containing atorvastatin and simvastatin. The CAD is designated to be a non-linear detector in a wide dynamic range, however, in this application and in the tested concentration range its response was found to be perfectly linear. The limits of quantitation (0.1 mu g/ml) were found to be two times lower than those of UV detection. (C) 2009 Elsevier B.V. All rights reserved
引用
收藏
页码:834 / 839
页数:6
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