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Pressurized capillary electrochromatographic assay of trimethoprim impurities using 1 mu m particle-based columns

文献类型:期刊论文

作者Qu, Qi Shu; Mangelings, Debby; Shen, Fei; Hu, Xiao Ya; Yan, Chao; Zhang, Yu Kui; Heyden, Yvan Vander
刊名journal of chromatography a
出版日期2007-10-26
卷号1169期号:1-2页码:228-234
关键词capillary columns micronsized particles pressurized capillary electrochromatography trimethoprim
英文摘要one micrometre silica particles, derivatized with c18, were electrokinetically packed into a 75-mu m-i.d. capillary. the resulting column was evaluated for the separation of trimethoprim (tmp) and its impurities using pressurized capillary electrochromatography (pcec), starting from a capillary liquid chromatographic (clc) separation. these samples require gradient elution when separated by high performance liquid chromatography (hplc), but with the new columns isocratic elution suffices for their separation by clc or pcec. only 70,000 theoretical plates/m for impurity c were achieved using clc mode at relative low pressure (78 bar) although very small particles were utilized. when a voltage above 2 w (50 v/cm) was applied, unknown peaks appeared, which was assumed due to an electrophoretic effect with the unknown peaks resolving as a result of the applied voltage. in order to minimize these unfavorable contributions, only a low voltage was applied, still leading to higher separation performances and shorter separation times than in clc. the optimal analyzing conditions in pcec included a pressure of 78 bar, an applied voltage of i w, and a mobile phase consisting of 80 mm sodium perchlorate (ph 3.1)/methanol (60/40, v/v). these conditions were used to separate and quantify four major impurities in tmp within 22 min. the obtained calibration curves were linear (r > 0.9980) in concentration ranges between 0.005 and 0.1 mg/ml for impurities a and c; 0.02 and 0.10 mg/ml for impurity f; and 0.01 and 0.10 mg/ml for impurity h. the detection limits (s/n = 3) for impurities a, c, f, and h were 0.52, 0.84, 3.18, and 2.41 mu g/ml, respectively. the calibration curves were successfully applied to analyze spiked bulk samples, with mean recoveries ranging from 92% to 110%. the developed method can therefore be considered simple, rapid, and repeatable. (c) 2007 elsevier b.v. all rights reserved.
WOS标题词science & technology ; life sciences & biomedicine ; physical sciences
类目[WOS]biochemical research methods ; chemistry, analytical
研究领域[WOS]biochemistry & molecular biology ; chemistry
关键词[WOS]chromatography-mass-spectrometry ; liquid-chromatography ; electric-field ; separation ; peptides
收录类别SCI
语种英语
WOS记录号WOS:000250316400023
公开日期2015-11-17
源URL[http://159.226.238.44/handle/321008/140700]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
作者单位1.Vrije Univ Brussels, Dept Analyt Chem & Pharmaceut Technol, B-1090 Brussels, Belgium
2.Yangzhou Univ, Coll Chem & Chem Engn, Jiandsu Key Lab Environm Mat & Environm Engn, Yangzhou 225002, Peoples R China
3.Chinese Acad Sci, Dalian Inst Chem Phys, Natl Chromatog R&A Ctr, Dalian 116011, Peoples R China
4.Shanghai Jiao Tong Univ, Sch Pharm, Shanghai 200030, Peoples R China
推荐引用方式
GB/T 7714
Qu, Qi Shu,Mangelings, Debby,Shen, Fei,et al. Pressurized capillary electrochromatographic assay of trimethoprim impurities using 1 mu m particle-based columns[J]. journal of chromatography a,2007,1169(1-2):228-234.
APA Qu, Qi Shu.,Mangelings, Debby.,Shen, Fei.,Hu, Xiao Ya.,Yan, Chao.,...&Heyden, Yvan Vander.(2007).Pressurized capillary electrochromatographic assay of trimethoprim impurities using 1 mu m particle-based columns.journal of chromatography a,1169(1-2),228-234.
MLA Qu, Qi Shu,et al."Pressurized capillary electrochromatographic assay of trimethoprim impurities using 1 mu m particle-based columns".journal of chromatography a 1169.1-2(2007):228-234.

入库方式: OAI收割

来源:大连化学物理研究所

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