Preparation of an iminodiacetic acid-modified capillary and its performance in capillary liquid chromatography and immobilized metal chelate affinity capillary electrophoresis.
Preparation of an iminodiacetic acid-modified capillary and its performance in capillary liquid chromatography and immobilized metal chelate affinity capillary electrophoresis.
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DOI:
10.1016/j.chroma.2004.03.063
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发表时间:
2004-06
期刊:
影响因子:
--
通讯作者:
K. Tsukagoshi;Yasushi Shimadzu;Tatsuhiko Yamane;R. Nakajima
中科院分区:
文献类型:
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作者:
K. Tsukagoshi;Yasushi Shimadzu;Tatsuhiko Yamane;R. Nakajima
We prepared iminodiacetic acid (IDA)-modified and Cu(II)–IDA-modified capillaries through polymerization of N-(vinylbenzylimino)diacetic acid. The fundamental performance of these capillaries was examined in capillary liquid chromatography (LC) and immobilized metal chelate affinity capillary electrophoresis (IMACE). Copper(II), cobalt(II), and hematin were detected at different retention times by means of capillary LC with a chemiluminescence detector, during which the IDA-modified capillary was used. The difference in the retention times was attributed to the difference in the interaction between metal ions or complex and IDA moieties on the inner wall of the capillary. In addition, human serum albumin (HSA) and human serum γ-globulin (HγG) were separated and detected using IMACE with an absorption detector, during which the Cu(II)–IDA-modified capillary was used. The separation of HSA and HγG was achieved through the interaction between proteins and Cu(II) chelate moieties on the inner wall of this capillary.