Ligand-substitution mode capillary electrophoretic reactor: Extending capillary electrophoretic reactor toward measurement of slow dissociation kinetics with a half-life of hours

Nobuhiko Iki, Mariko Takahashi, Toru Takahashi, Hitoshi Hoshino

研究成果: Article査読

7 被引用数 (Scopus)

抄録

A method employing capillary electrophoresis (CE) was developed to determine the rate constant of the very slow spontaneous dissociation of a complex species. The method uses a CE reactor (CER) to electrophoretically separate components from a complex zone and, thus, spontaneously dissociate a complex. The dissociation is accelerated by ligand substitution (LS) involving a competing ligand added to the electrophoretic buffer. The LSCER method is validated using the dissociation of a Ti(IV)-catechin complex and EDTA as a competing ligand. There is good agreement between the spontaneous dissociation rate constant ( kd = (1.64 ± 0.63) x 10-4 s -1) and the rate constant obtained by a conventional batchwise LS reaction ( kd = (1.43 ± 0.04) x 10-4 s -1). Furthermore, the usefulness of the method is demonstrated using a Ti(IV)-tiron complex, for which kd = (0.51 ± 0.43) x 10 -4 s-1, corresponding to a half-life ( t1/2) of 3.8 h. Notably, a single run of LS-CER for the Ti(IV) complex is completed within 40 min, implying that LS-CER requires a considerably shorter measurement time (roughly equal to t1/2) than conventional CER. LS-CER can be widely applied to determine the spontaneous dissociation rates of inorganic diagnostic and therapeutic reagents as well as of biomolecular complexes.

本文言語English
ページ(範囲)7849-7854
ページ数6
ジャーナルAnalytical Chemistry
81
18
DOI
出版ステータスPublished - 2009 9 15

ASJC Scopus subject areas

  • Analytical Chemistry

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