Redox speciation of iron, manganese, and copper in cerebrospinal fluid by strong cation exchange chromatography - sector field inductively coupled plasma mass spectrometry

被引:45
|
作者
Solovyev, Nikolay [1 ,2 ]
Vinceti, Marco [3 ]
Grill, Peter [2 ]
Mandrioli, Jessica [4 ]
Michalke, Bernhard [2 ]
机构
[1] St Petersburg State Univ, Inst Chem, St Petersburg, Russia
[2] Helmholtz Zentrum Munchen, German Res Ctr Environm Hlth GmbH, Res Unit Analyt BioGeoChem, Neuherberg, Germany
[3] Univ Modena & Reggio Emilia, Dept Biomed Metab & Neurosci, CREAGEN Res Ctr Environm Genet & Nutr Epidemiol, Modena, Italy
[4] Univ Modena, Azienda Osped, St Agostino Estense Hosp, Dept Neurosci, Modena, Italy
基金
俄罗斯基础研究基金会;
关键词
Cerebrospinal fluid; Speciation; Iron; Manganese; Copper; Cation exchange chromatography - inductively coupled plasma mass spectrometry; AMYOTROPHIC-LATERAL-SCLEROSIS; ION CHROMATOGRAPHY; TRANSITION-METALS; ELEMENT SPECIATION; OXIDATIVE STRESS; ICP-MS; SELENIUM; ALZHEIMERS; PARKINSONS; DISEASE;
D O I
10.1016/j.aca.2017.03.040
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new method of simultaneous redox speciation of iron (II/III), manganese (II/III), and copper (I/II) in cerebrospinal fluid (CSF) has been designed. For the separation of redox species strong cation exchange chromatography (SCX) with isocratic elution was employed. Species were detected using inductively coupled plasma sector field mass spectrometry (ICP-sf-MS), operating at medium resolution. The following parameters were optimized: analytical column, eluent composition and pH, CSF injection volume and dilution factor. Analytical column Dionex IonPac CS5A RFIC 4*250 mm was found to retain and separate species of interest the most effectively under the isocratic elution with a buffer, containing 50 mM ammonium citrate, 7.0 mM pyridine-2,6-dicarboxylic acid at pH = 4.2 and flow rate of 0.8 L min(-1). Injection volume of 50 mu L with CSF sample dilution of 1/3 (v/v) with the eluent was shown to result in minimal matrix suppression. For species identification, retention time matching with standards was used. The stability of metalloproteins (ferritin, transferrin, and ceruloplasmin) under elution conditions was evaluated. For the quantification of redox species, external calibration was employed. To avoid column contamination, a blank was run after measurement and all quantification values were blank subtracted. For recovery checks, species quantification data was verified against total content of an element, measured by dynamic reaction cell ICP-MS. Recoveries (sum of quantified species vs. total element determinations) were 82.5 +/- 22% (Mn), 92 +/- 11% (Fe), and 88.7 +/- 12% (Cu). The method was tested using 38 real CSF samples. Limits of detection (3 sigma) for the CSF samples were 0.5 mu g L-1, 0.6 mg L-1, and 0.8 mu g L-1 for Fe, Mn, and Cu species, respectively. Retention time precision was 1-7.5% (as RSD), whereas peak area RSDs were in the range 5-11%, both depending on the species. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:25 / 33
页数:9
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