Method development in pharmaceutical analysis employing capillary electrochromatography.

Method development in pharmaceutical analysis employing capillary electrochromatography.
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采用毛细管电色谱法进行药物分析的方法开发。

DOI:
10.1002/elps.1150191206
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发表时间:
1998
期刊:
Electrophoresis.
影响因子:
--
通讯作者:
Stobaugh,JF
Stobaugh,JF
中科院分区:
--
文献类型:
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作者:
Angus,PD;Victorino,E;Payne,KM;Demarest,CW;Catalano,T;Stobaugh,JF

文献摘要

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Capillary electrochromatography (CEC) has been employed to explore method development for a series of structurally related polar neutral compounds of pharmaceutical relevance. Capillaries with dimensions of 75 μm ID × 25 cm length (34.5 cm total) were packed with Spherisorb ODS‐1, Hypersil phenyl, and Hypersil MOS (all 3 μm particles) and were compared in the reversed‐phase mode in order to determine which phase provided the best initial performance and thus serve as the phase of choice for additional method development experiments. The various separation parameters examined for their effect on efficiency,k, resolution, and linear velocity included percent and type of organic modifier, buffer concentration, voltage, and temperature. All separations were conducted with an acidic mobile phase (aqueous mobile phase component, pH 3.0). The separation efficiencies obtained were on the order of 200000–260000 plates/m, which equates to reduced plate heights of 1.22 for columns packed with Spherisorb ODS‐1. Repeatable column‐to‐column separation performance was demonstrated.