Reversed-phase liquid chromatographic separation of complex samples by optimizing temperature and gradient time I. Peak capacity limitations

被引:147
作者
Dolan, JW
Snyder, LR
Djordjevic, NM
Hill, DW
Waeghe, TJ
机构
[1] LC Resources Inc, Walnut Creek, CA 94596 USA
[2] Novartis Pharma AG, CH-4002 Basel, Switzerland
[3] Univ Connecticut, Microchem Lab, Pasadena, CA 91107 USA
[4] Du Pont Co, Expt Stn, Wilmington, DE 19980 USA
基金
美国国家卫生研究院;
关键词
optimization; peak capacity; temperature effects; gradient elution; computer simulation; mobile phase composition; resolution; selectivity;
D O I
10.1016/S0021-9673(99)00765-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The separation of samples that contain more than 15 to 20 analytes (n>15-20) is typically difficult and usually requires gradient elution. We have examined the reversed-phase liquid chromatographic separation of 24 samples with 8 less than or equal to n less than or equal to 48 as a function of temperature T and gradient time t(G). The required peak capacity was determined for each sample, after selecting T and t(G) for optimum selectivity and maximum sample resolution. Comparison of these results with estimates of the maximum possible peak capacity in reversed-phase gradient elution was used to quantify the maximum value of n for some required sample resolution (when T and t(G) have been optimized). These results were also compared with literature studies of similar isocratic separations as a function of ternary-solvent mobile phase composition, where the proportions of methanol (MeOH), tetrahydrofuran (THF) and water were varied simultaneously. This in turn provides information on the relative effectiveness of these two different method development procedures (optimization of T and t(G) vs. % MeOH and % THF) for changing selectivity and achieving maximum resolution. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1 / 20
页数:20
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