Recovering Ga(III) from coordination complexes using pyridine 2,6-dicarboxylic acid chelation ion chromatography

被引:6
|
作者
Staff, K. [1 ,2 ]
Brown, M. B. [2 ]
Hider, R. C. [1 ]
Kong, X. L. [1 ]
Friden, P. [3 ]
Jones, S. A. [1 ]
机构
[1] Kings Coll London, Pharmaceut Sci Res Div, London SE1 9NN, England
[2] Univ Hertfordshire, Sch Pharm, Hatfield AL10 9AB, Herts, England
[3] Transport Pharmaceut Inc, Framingham, MA 01701 USA
关键词
gallium; ion exchange; liquid chromatography; coordination; TRANSITION-METALS; GALLIUM NITRATE; SEPARATION; EXCHANGE; BINDING; INDIUM; MECHANISMS; SPECIATION; ALUMINUM; PLASMA;
D O I
10.1002/bmc.1402
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Ion exchange chelation chromatography is an effective means to extract metals from coordination complexes and biological samples; however there is a lack of data to verify the nature of metal complexes that can be successfully analysed using such a procedure. The aim of this study was to assess the capability of pyridine 2,6-dicarboxylic acid (PDCA) to extract and quantify Ga(III) from a range of environments using standard liquid chromatography apparatus. The PDCA chelation method generated a single Ga(III) peak with a retention time of 2.55 +/- 0.02 min, a precision of <2% and a limit of detection of 110 mu M. Ga(III) hydroxide complexes (highest stability constant 15.66) were used to successfully cross-validate the chelation method with inductively coupled plasma mass spectrometry. The PDCA assay extracted 96.9 +/- 1.2% of the spiked Ga(III) from porcine mucus and 100.7 +/- 2.7% from a citrate complex (stability constant 10.02), but only ca 50% from an EDTA complex (stability constant 22.01). These data suggest that PDCA chelation can be considered a suitable alternative to inductively coupled plasma mass spectrometry for Ga(III) quantification from all but the most strongly bound coordinated complexes i.e. a stability constant of >15. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:1015 / 1022
页数:8
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