Identification and quantification of myo-inositol hexakisphosphate in complex environmental matrices using ion chromatography and high-resolution mass spectrometry in comparison to 31P NMR spectroscopy

被引:6
|
作者
McIntyre, Catherine A. [1 ]
Arkell, Jennifer J. L. [1 ]
Arthur, Christopher J. [2 ]
Lawrence, Paul G. [2 ]
Butts, Craig P. [2 ]
Lloyd, Charlotte E. M. [1 ]
Johnes, Penny J. [3 ]
Evershed, Richard P. [1 ]
机构
[1] Univ Bristol, Sch Chem, Organ Geochem Unit, Bristol BS8 1TS, Avon, England
[2] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
[3] Univ Bristol, Sch Geog Sci, Univ Rd, Bristol BS8 1SS, Avon, England
基金
英国自然环境研究理事会; 英国工程与自然科学研究理事会;
关键词
Phytic acid; Soil; Ion chromatography; High-resolution mass spectrometry; NMR; SOIL ORGANIC PHOSPHORUS; INOSITOL PHOSPHATES; QUANTITATIVE-ANALYSIS; PHYTIC ACID; MANURE; EXTRACTION; SEDIMENTS; POULTRY; SPECTRA; PHYTATE;
D O I
10.1016/j.talanta.2019.120188
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Myo-inositol hexakisphosphate, or phytic acid, (myo-IP6) is a key organic phosphorus (P) compound in soils and manures. Determinations of myo-IP6 in soils and manure extracts are frequently performed by P-31 NMR spectroscopy. This approach is time-consuming in terms of both sample preparation and instrument time, with uncertainties existing in relation to accuracy of identification and quantification due to potentially interfering resonances from co-extracted P species. In contrast, ion chromatography (IC) in combination with high-resolution mass spectrometry (HRMS) negative ion, electrospray ionisation (ESI) has been shown to enable highly specific identifications of myo-IP6 isolated from complex mixtures. In this paper, IC and ESI-HRMS were applied to the identification and the quantification of myo-IP6 isolated from soils and manures using NaOH-EDTA extraction, and quantifications based on IC. ESI-HRMS analysis of eluate trapped from IC unequivocally confirmed identification of myo-IP6 from a soil extract. The ion suppression cell of the IC instrument provides isolates of the analyte free of ionic components that would interfere with ESI. The myo-IP6 was identified in the NMR by comparing spectra of extracts of soils with and without authentic myo-IP6 "spiked" prior to extraction. Comparison of quantification via standard addition in IC and NMR analysis gave good correlation (r = 0.955). IC with ESI-HRMS was found to be more sensitive, rapid and reliable for the identification and quantification of myo-IP6 with a limit of detection (LOD) of 0.7 mg kg(-1) and limit of quantification (LOQ) of 2.1 mg kg(-1) using IC versus > 10 mg kg(-1) LOD using P-31 NMR.
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页数:10
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