Greener liquid chromatography using a guard column with micellar mobile phase for separation of some pharmaceuticals and determination of parabens

被引:25
|
作者
Youngvises, Napaporn [1 ,2 ]
Chaida, Thanatcha [1 ,2 ]
Khonyoung, Supada [1 ,2 ]
Kuppithayanant, Nattawan [3 ]
Tiyapongpattana, Warawut [1 ,2 ]
Itharat, Arunporn [4 ]
Jakmunee, Jaroon [5 ,6 ]
机构
[1] Thammasat Univ, Fac Sci & Technol, Dept Chem, Pathum Thani 12120, Thailand
[2] Thammasat Univ, Fac Sci & Technol, Innovat Green Chem Res Ctr, Pathum Thani 12120, Thailand
[3] Rajamangala Univ Technol Thanyaburi, Dept Chem, Fac Sci, Pathum Thani, Thailand
[4] Thammasat Univ, Appl Thai Tradit Med Ctr, Pathum Thani 12120, Thailand
[5] Chiang Mai Univ, Fac Sci, Dept Chem, Chiang Mai 50200, Thailand
[6] Chiang Mai Univ, Fac Sci, Ctr Excellence Innovat Chem, Chiang Mai 50200, Thailand
关键词
Green analytical chromatography; Pharmaceutical; Parabens; Sodium dodecyl sulfate; Guard column; Micelle; COSMETIC PRODUCTS; SIMPLEX OPTIMIZATION; ORGANIC MODIFIER; LC-DETERMINATION; PRESERVATIVES; EXTRACTION; HPLC; ELECTROPHORESIS; SAMPLES;
D O I
10.1016/j.talanta.2012.12.040
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this research, a greener chromatography employing a short column, Zorbax SB C18 cartridge (12.5 x 4.6 mm, 5 mu m) commonly used as a guard column in a reverse phase high performance liquid chromatography (RP-HPLC), was utilized as the analytical column in conjunction with a more eco-friendly micellar mobile phase of sodium dodecyl sulfate (SDS) for separation tertiary mixtures of local anesthetics and antihistamines; and binary mixture of colds drugs; and quaternary mixture of some parabens with different separation conditions. The chromatographic behavior of these analytes was studied to demonstrate separation efficiency of this guard column in a micellar mobile phase. Moreover, this column and SDS mobile phase was exploited for determination of parabens in 64 samples of cosmetic product, both those that were produced locally in the community and those that were commercially manufactured. Linear calibration graphs of the parabens as detected at 254 nm were obtained in the range of 1-100 mu mol L-1 with R-2 > 0.9990. Percentage recoveries were 92.4-109.2 with %RSD <3, and the limit of detection and quantitation were 0.04-0.10 and 0.20-0.80 mu mol L-1, respectively. This analytical system is not only greener but also faster and employing simpler sample preparation than a conventional liquid chromatographic system. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:350 / 359
页数:10
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