Liquid and gas chromatography coupled to isotope ratio mass spectrometry for the determination of 13C-valine isotopic ratios in complex biological samples

被引:33
作者
Godin, Jean-Philippe [1 ]
Breuille, Denis [1 ]
Obled, Christiane [2 ]
Papet, Isabelle [2 ]
Schierbeek, Henk [3 ]
Hopfgartner, Gerard [4 ]
Fay, Laurent-Bernard [1 ]
机构
[1] Nestec Ltd, Nestle Res Ctr, CH-1000 Lausanne 26, Switzerland
[2] INRA, Ctr Clermont Ferrand Theix, UMR Unite Nutr Humaine 1019, F-63122 St Genes Champanelle, France
[3] Erasmus MC Sophia Childrens Hosp, Dept Neonatol, NL-3000 CA Rotterdam, Netherlands
[4] Univ Lausanne, Univ Geneva, Sch Pharmaceut Sci, CH-1211 Geneva 4, Switzerland
来源
JOURNAL OF MASS SPECTROMETRY | 2008年 / 43卷 / 10期
关键词
LC-IRMS; GC-C-IRMS; C-13-valine; amino acids; isotope ratio monitoring and bone;
D O I
10.1002/jms.1406
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
On-line gas chromatography-combustion-isotope ratio mass spectrometry (GC-C-IRMS) is commonly used to measure isotopic ratios at natural abundance as well as for tracer studies in nutritional and medical research. However, high-precision C-13 isotopic enrichment can also be measured by liquid chromatography-isotope ratio mass spectrometry (LC-IRMS). Indeed, LC-IRMS can be used, as shown by the new method reported here, to obtain a baseline separation and to measure C-13 isotopic enrichment of underivatised amino acids (Asp, Thr-Ser, Glu, Pro, Gly, Ala, Cys and Val). In case of Val, at natural abundance, the SD(delta C-13) reported with this method was found to be below M. Another key feature of the new LC-IRMS method reported in this paper is the comparison of the LC-IRMS approach with the conventional GC-C-IRMS determination. To perform this comparative study, isotopic enrichments were measured from underivatised Val and its N(O, S)-ethoxycarbonyl ethyl ester derivative. Between 0.0 and 1.0 molar percent excess (MPE) (delta C-13 = -12.3 to 150.8 parts per thousand), the calculated root-mean-square (rms) of SD was 0.38 and 0.46 parts per thousand and the calculated rms of accuracy was 0.023 and 0.005 MPE, respectively, for GC-C-IRMS and LC-IRMS. Both systems measured accurately low isotopic enrichments (0.002 atom percent excess (APE)) with an SD (APE) of 0.0004. To correlate the relative (delta C-13) and absolute (atom%, APE and MPE) isotopic enrichment of Val measured by the GC-C-IRMS and LC-IRMS devices, mathematical equations showing the slope and intercept of the curves were established and validated with experimental data between 0.0 to 2.3 MPE. Finally, both GC-C-IRMS and LC-IRMS instruments were also used to assess isotopic enrichment of protein-bound C-13-Val in tibial epiphysis in a tracer study performed in rats. Isotopic enrichments measured by LC-IRMS and GC-C-IRMS were not statistically different (p > 0.05). The results of this work indicate that the LC-IRMS was successful for high-precision C-13 isotopic measurements in tracer studies giving C-13 isotopic enrichment similar to the GC-C-IRMS but without the step of CC derivatisation. Therefore, for clinical studies requiring high-precision isotopic measurement, the LC-IRMS is the method of choice to measure the isotopic ratio. Copyright (c) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:1334 / 1343
页数:10
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