Isotopic characterisation of in-house purified progesterone for 13C/12C isotope ratios by multicollector ICP-MS
- 14 January 2010
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of Analytical Atomic Spectrometry
- Vol. 25 (3) , 378-383
- https://doi.org/10.1039/b922642g
Abstract
In this paper, a multicollector inductively coupled mass spectrometer (MC-ICP-MS) has been used for the first time to characterise a steroid sample for carbon isotope ratio traceable to SI. The progesterone sample was purified in house using semi-preparative high performance liquid chromatography (HPLC) and characterised using a multi-method approach. Carbon 13C/ 12C isotope amount ratios have been measured for the progesterone standard and NIST RM materials have been used as QCs to test instrumental performance and linearity over the δ13C range from −46 to +37‰. Internal normalisation by measuring boron 11B/ 10B isotope amount ratios has been used to correct for the effects of instrumental mass bias. Absolute 13C/ 12C ratios have been measured and corrected for instrumental mass bias and full uncertainty budgets have been calculated using the Kragten approach. Alternatively raw ratios have been measured for four isotopic NIST RMs and used for external calibration. This work proves the suitability of the method for the measurement of carbon isotope ratios within the natural range of variation of organic carbon compounds. The potential of the method for the production of isotopic reference standards to be used in metabolic studies, sports science and forensic testing is shown. Measured/corrected value for carbon isotope ratios traceable to the SI for the compound of interest and its combined uncertainty budget (including instrumental error and each parameter contributing to Russell expression for mass bias correction) were found to be 0.010853 ± 0.000011. The main advantages of the method versus conventional Isotope Ratio Mass Spectrometry (IRMS) measurements are that the carbon isotope ratios are measured as C+ instead of CO2 + and therefore an oxygen correction is not required. Moreover, absolute carbon isotope ratios can be measured and expressed as 13C/ 12C instead of δ13C (relative differences in ‰ between a reference standard and the sample).Keywords
This publication has 22 references indexed in Scilit:
- Precise and Traceable 13C/12C Isotope Amount Ratios by Multicollector ICPMSAnalytical Chemistry, 2008
- Reformulated 17O correction of mass spectrometric stable isotope measurements in carbon dioxide and a critical appraisal of historic ‘absolute’ carbon and oxygen isotope ratiosGeochimica et Cosmochimica Acta, 2008
- Determination of Pu isotope concentrations and isotope ratio by inductively coupled plasma mass spectrometry: a review of analytical methodologyJournal of Analytical Atomic Spectrometry, 2007
- A high accuracy primary ratio method for the determination of iodine in complex matrices by double isotope dilution using MC-ICPMS and 129I spikeJournal of Analytical Atomic Spectrometry, 2006
- Forensic applications of isotope ratio mass spectrometry—A reviewForensic Science International, 2006
- Precise determination of the strontium isotope ratios in wine by inductively coupled plasma sector field multicollector mass spectrometry (ICP-SF-MC-MS)Journal of Analytical Atomic Spectrometry, 2001
- Referencing strategies and techniques in stable isotope ratio analysisRapid Communications in Mass Spectrometry, 2001
- Precise sulfur isotope ratio measurements in trace concentration of sulfur by inductively coupled plasma double focusing sector field mass spectrometryJournal of Analytical Atomic Spectrometry, 1999
- Mass spectrometry of inductively coupled plasmasAnalytical Chemistry, 1986
- Isotopic standards for carbon and oxygen and correction factors for mass-spectrometric analysis of carbon dioxideGeochimica et Cosmochimica Acta, 1957