Browse > Article
http://dx.doi.org/10.5478/MSL.2011.2.2.037

Accurate Quantification of Saccharin Using Isotope Dilution Liquid Chromatography Mass Spectrometry (ID-LC/MS)  

Lee, Yun-Jung (Division of Metrology for Quality Life, Korea Research Institute of Standards and Science)
Kim, Byung-Joo (Division of Metrology for Quality Life, Korea Research Institute of Standards and Science)
Kim, Jeong-Kwon (Department of Chemistry, Chungnam National University)
Ahn, Seong-Hee (Division of Metrology for Quality Life, Korea Research Institute of Standards and Science)
Publication Information
Mass Spectrometry Letters / v.2, no.2, 2011 , pp. 37-40 More about this Journal
Abstract
Saccharin is a commonly used artificial sweetener in foodstuffs. However, for its carcinogenic dispute, it has been regulated by government bodies. In this study, isotope dilution mass spectrometry (ID-MS) was introduced for the accurate quantification of saccharin. To employ ID-LC/MS, we obtained its isotope analogue, $^{13}C_1$-sodium saccharin, by customized synthesis. Samples were spiked with $^{13}C_1$-sodium saccharin and analyzed with LC/MS in negative mode. Chromatographic conditions were optimized for the adequate chromatographic retention and separation of saccharin with a $C_{18}$ column. MS was operated with electrospray ionization by the selected ion monitoring (SIM) mode of $[M-H]^-$ for saccharin (m/z 182) and $[M-Na]^-$ for its isotope analogue (m/z 183). To validate the ID-LC/MS method for accurate measurement, we prepared a batch of a candidate material by sortifying quasi-tea-drinks with saccharin and analyzed samples gravimetrically fortified in various levels of concentration. The repeatability and reproducibility of this method was tested by analyzing the reference material. Result show that ID-LC/MS is a reliable method for the quantitative analysis of saccharin.
Keywords
Saccharin; Isotope analogue-$^{13}C_1$-sodium saccharin; Isotope dilution mass spectrometry (ID-MS); Repeatability; Reproducibility;
Citations & Related Records
Times Cited By KSCI : 2  (Citation Analysis)
연도 인용수 순위
1 Arnold, D. L.; Krewski, D.; Munro, I. C. Toxicology 1983, 27, 179.   DOI   ScienceOn
2 Oser, B. L. Fd. Chem. Toxic. 1985, 23, 535.   DOI   ScienceOn
3 Remsen, I.; Fahlberg, C. Am. Chem. J. 1879, 1, 426.
4 Kim, B.; Park, S.; Lee, I.; Lim, Y.; Hwang, E.; So, H.-Y. Anal. Bioanal. Chem. 2010, 398, 1035.   DOI
5 Wasik, A.; McCourt, J.; Buchgraber, M. J. Chromatogr. A 2007, 1157, 187.   DOI   ScienceOn
6 Bryan, G. T.; Erturk, E.; Yoshida, O. Science 1970, 168, 1238.   DOI   ScienceOn
7 Holder, C.L.; Bowman, M.C. Toxicol. Lett. 1980, 5, 27.   DOI   ScienceOn
8 Galli, V.; Barbas, C. J. Chromatogr. A 2004, 1048, 207.   DOI   ScienceOn
9 Di Pietra, A. M.; Cavrini, V.; Bonazzi, D.; Benfenati, L. Chromatographia 1990, 30, 215.   DOI
10 Tyler, T. A. J. Assoc. Off. Anal. Chem. 1984, 67, 745.
11 Zhu, Y.; Guo, Y.; Ye, M.; James, F. S. J. Chromatogr. A 2005, 1085, 143.   DOI   ScienceOn
12 Lho, D. S.; Hong, J. K.; Paek, H. K.; Lee, J. A. J. Anal. Toxicol. 1990, 14, 77.   DOI   ScienceOn
13 Heitkemper, D. T.; Jackson, D. S.; Kaine, L. A.; Mulligan, K. A.; Wolnik, K. A. J. Chromatogr. A 1994, 671, 323.   DOI   ScienceOn
14 Thompson, C. O.; Trenerry, V. C.; Kemmery, B. J. Chromatogr. A 1995, 704, 203.   DOI   ScienceOn
15 Boyce, M. C. J. Chromatogr. A 1999, 847, 369.   DOI   ScienceOn
16 Koyama, M.; Yoshida, K.; Uchibori, N.; Wada, I.; Akiyama, K.; Sasaki, T. J. Food Hyg. Soc. Japan 2005, 46, 72.   DOI
17 Yang, D.-J.; Chen, B. J. Agric. Food Chem. 2009, 57, 3022.   DOI   ScienceOn
18 Ferrer, I.; Thyrman, E. M. J. Chromatogr. A 2010, 1217, 4127.   DOI   ScienceOn
19 Lee, I.; Ahn, S.; Kim, B.; Hwang, E.; Kim, Y.-S. Bull. Korean Chem. Soc. 2008, 29, 2125.   DOI   ScienceOn
20 Park, S.; Kim, B.; So, H.-Y.; Kim, Y.-J.; Kim, J. Bull. Korean Chem. Soc. 2007, 28, 737.   DOI   ScienceOn