{"id":43542,"date":"2020-10-21T00:00:00","date_gmt":"2020-10-21T00:00:00","guid":{"rendered":"https:\/\/discover.restek.com\/uncategorized\/avoid-mycotoxin-quantitation-errors-when-using-stable-isotope-dilution-assay-sida\/"},"modified":"2026-01-03T18:03:41","modified_gmt":"2026-01-03T18:03:41","slug":"avoid-mycotoxin-quantitation-errors-when-using-stable-isotope-dilution-assay-sida","status":"publish","type":"post","link":"https:\/\/discover.restek.com\/it\/articles-ja\/ffar3036\/avoid-mycotoxin-quantitation-errors-when-using-stable-isotope-dilution-assay-sida","title":{"rendered":"Avoid Mycotoxin Quantitation Errors When Using Stable Isotope Dilution Assay (SIDA)"},"content":{"rendered":"\n<p>There are significant benefits to using the stable isotope dilution assay (SIDA) calibration approach for mycotoxin analyses [1], and one of the biggest is being able to use a single calibration curve for multiple matrix types. Compared to making individual matrix-matched calibration standards for each sample type, the time savings offered by the SIDA technique can make up for the relatively high price of isotopically labeled internal standards (IS), especially for high-throughput food safety laboratories that frequently deal with a wide variety of samples. However, labeled standards are not always commercially available for every mycotoxin of interest. Due to these cost and availability issues, labs may be interested in using a practice that is common among many other types of methods that use internal standards: using the same internal standard to calibrate a group of analytes. That approach may seem logical, but in the case of mycotoxin SIDA methods, it can lead to significant errors.<\/p>\n\n\n\n<p>Table I compares the observed concentrations of four different mycotoxins present in two maize flour reference materials to the concentrations reported by the reference material supplier. For the three mycotoxins that were quantified using their corresponding isotopically labeled internal standards, the agreement between the two values is excellent. However, in the case of the mycotoxin zearalenone, we did not have its analogous labeled internal standard, so we quantified it using&nbsp;<sup>13<\/sup>C<sub>17<\/sub>-aflatoxin G1 because it elutes nearby. As the data show, the agreement between the observed results and those reported by the reference material supplier is very poor, which illustrates that similar chromatographic retention alone is not enough to predict the effects of sample preparation and\/or matrix-related changes in ionization efficiency. A more detailed description of Restek\u2019s research on the LC-MS\/MS analysis of mycotoxins in various foods comparing SIDA to matrix-matched calibration is published in a peer-reviewed study [2].<\/p>\n\n\n\n<p>In light of these results, it is strongly recommended that only matching isotopically labeled internal standards be used for quantification in mycotoxin SIDA methods. If matching internal standards are not available, other calibration approaches, such as matrix-matched calibration, should be used.<\/p>\n\n\n\n<h5 class=\"wp-block-heading\"><strong>Table I:<\/strong>&nbsp;Mycotoxin SIDA calibration should only be used for matching analyte and IS pairs.<\/h5>\n\n\n\n<figure class=\"wp-block-table\"><table class=\"has-fixed-layout\"><thead><tr><th><strong>Reference<br>Material<\/strong><\/th><th><strong>Analyte<\/strong><\/th><th><strong>IS<\/strong><\/th><th><strong>Measured<br>Concentration<br>(ng\/g), n=3<\/strong><\/th><th><strong>Assigned<br>Concentration<br>(ng\/g)<\/strong><\/th><th><strong>Percent<br>Accuracy<br>(RSD, %)<\/strong><\/th><\/tr><\/thead><tbody><tr><td>TET017RM<\/td><td>Deoxynivalenol<\/td><td><sup>13<\/sup>C<sub>15<\/sub>-Deoxynivalenol<\/td><td>1867.9 \u00b1 37.36<\/td><td>1971 \u00b1 195<\/td><td>94.8 (2)<\/td><\/tr><tr><td>TET017RM<\/td><td>Aflatoxin B1<\/td><td><sup>13<\/sup>C<sub>17<\/sub>-Aflatoxin B1<\/td><td>8.68 \u00b1 0.434<\/td><td>9.49 \u00b1 0.85<\/td><td>91.4 (5)<\/td><\/tr><tr><td>TET017RM<\/td><td>Ochratoxin A<\/td><td><sup>13<\/sup>C<sub>20<\/sub>-Ochratoxin A<\/td><td>4.48 \u00b1 0.134<\/td><td>4.81 \u00b1 0.75<\/td><td>93.2 (3)<\/td><\/tr><tr><td>TET017RM<\/td><td>Zearalenone<\/td><td><sup>13<\/sup>C<sub>17<\/sub>-Aflatoxin G1<\/td><td>31.26 \u00b1 2.19<sup>a<\/sup><\/td><td>231 \u00b1 25<\/td><td>13.5 (7)<sup>a<\/sup><\/td><\/tr><tr><td>T04301Q<\/td><td>Deoxynivalenol<\/td><td><sup>13<\/sup>C<sub>15<\/sub>-Deoxynivalenol<\/td><td>639.7 \u00b1 19.19<\/td><td>649 \u00b1 222<\/td><td>98.6 (3)<\/td><\/tr><tr><td>T04301Q<\/td><td>Aflatoxin B1<\/td><td><sup>13<\/sup>C<sub>17<\/sub>-Aflatoxin B1<\/td><td>8.69 \u00b1 0.348<\/td><td>9.21 \u00b1 4.05<\/td><td>94.4 (4)<\/td><\/tr><tr><td>T04301Q<\/td><td>Ochratoxin A<\/td><td><sup>13<\/sup>C<sub>20<\/sub>-Ochratoxin A<\/td><td>2.81 \u00b1 0.197<\/td><td>3.03 \u00b1 1.33<\/td><td>92.6 (7)<\/td><\/tr><tr><td>T04301Q<\/td><td>Zearalenone<\/td><td><sup>13<\/sup>C<sub>17<\/sub>-Aflatoxin G1<\/td><td>16.2 \u00b1 0.810<sup>a<\/sup><\/td><td>138.5 \u00b1 59.6<\/td><td>11.7 (5)<sup>a<\/sup><\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><sup>a<\/sup>&nbsp;Results quantified using a nonmatched labeled IS.<\/p>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<div class=\"wp-block-columns has-background is-layout-flex wp-container-core-columns-is-layout-9d6595d7 wp-block-columns-is-layout-flex\" style=\"background-color:#e4f7fa\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:66.66%\">\n<h3 class=\"wp-block-heading has-text-color has-link-color wp-elements-1489b0bd8c7fa6a213f7f4f1cf134d8f\" style=\"color:#02366d\">Want even better performance when analyzing mycotoxins and other metal-sensitive compounds?<\/h3>\n\n\n\n<p>Learn more at&nbsp;<a href=\"https:\/\/www.restek.com\/articles\/accurately-analyze-metal-sensitive-compounds-with-resteks-new-inert-lc-columns\" target=\"_blank\" rel=\"noopener\">www.restek.com\/inert<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:33.33%\"><div class=\"wp-block-image\">\n<figure class=\"alignright size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"400\" height=\"123\" src=\"https:\/\/discover.restek.com\/wp-content\/uploads\/teaser-product-lc-columns-inert-lc-02.png\" alt=\"\" class=\"wp-image-29764\" title=\"-\" srcset=\"https:\/\/discover.restek.com\/wp-content\/uploads\/teaser-product-lc-columns-inert-lc-02.png 400w, https:\/\/discover.restek.com\/wp-content\/uploads\/teaser-product-lc-columns-inert-lc-02-300x92.png 300w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/><\/figure>\n<\/div><\/div>\n<\/div>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading\">References<\/h2>\n\n\n\n<ol class=\"wp-block-list\">\n<li>K. Zhang, K., M.R. Schaab, G. Southwood, E.R. Tor, L.S. Aston, W. Song, B. Eitzer, S. Majumdar, T. Lapainis, H. Mai, K. Tran, A. El-Demerdash, V. Vega, Y. Cai, J.W. Wong, A.J. Krynitsky, T.H. Begley, A collaborative study: determination of mycotoxins in corn, peanut butter, and wheat flour using stable isotope dilution assay (SIDA) and liquid chromatography-tandem mass spectrometry (LC-MS\/MS), J. of Agric. Food Chem. 65 (33) (2017) 7138\u20137152. DOI: 10.1021\/acs.jafc.6b04872&nbsp;<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jafc.6b04872\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jafc.6b04872<\/a><\/li>\n\n\n\n<li>D. Li, J.A. Steimling, J.D. Konschnik, S. Grossman, T. Kahler, Quantitation of mycotoxins in four food matrices comparing stable isotope dilution assay (SIDA) with matrix-matched calibration methods by LC\u2013MS\/MS, J. AOAC Int. (2019) DOI: 10.5740\/jaoacint.19-0028&nbsp;<a href=\"https:\/\/academic.oup.com\/jaoac\/article-abstract\/102\/6\/1673\/5658363\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/academic.oup.com\/jaoac\/article-abstract\/102\/6\/1673\/5658363<\/a><\/li>\n<\/ol>\n\n\n\n<div style=\"height:100px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Stable isotope dilution assay (SIDA) calibration can offset matrix effects. However, it is critical to use appropriately matched internal standards, as shown in this mycotoxin SIDA analysis.<\/p>\n","protected":false},"author":11,"featured_media":6859,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_kad_blocks_custom_css":"","_kad_blocks_head_custom_js":"","_kad_blocks_body_custom_js":"","_kad_blocks_footer_custom_js":"","_kadence_starter_templates_imported_post":false,"_kad_post_transparent":"","_kad_post_title":"","_kad_post_layout":"","_kad_post_sidebar_id":"","_kad_post_content_style":"","_kad_post_vertical_padding":"","_kad_post_feature":"","_kad_post_feature_position":"","_kad_post_header":false,"_kad_post_footer":false,"footnotes":""},"categories":[789],"tags":[],"industries-application":[2167,2169],"post-badge":[],"resource-type":[],"product-library":[2391,2373,2399,2374],"resource-technique":[2294,2299,2302],"ppma_author":[414],"class_list":["post-43542","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-articles-ja","industries-application-food-beverage","industries-application-food-safety","product-library-lc-columns","product-library-liquid-chromatography-products","product-library-liquid-reference-standards","product-library-reference-standard-products","resource-technique-gas-chromatography-gc","resource-technique-liquid-chromatography","resource-technique-ms-ms"],"acf":[],"taxonomy_info":{"category":[{"value":789,"label":"\u6280\u8853\u8cc7\u6599"}],"industries-application":[{"value":2167,"label":"Food &amp; 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