Iha Maria Helena, Mini Camila Alessandra, Okada Isaura Akemi, Briganti Rita de Cássia, Trucksess Mary W
Center for Chemical Sciences and Bromatological, Regional Laboratory Centre - Adolfo Lutz Institute of Ribeirão Preto VI, Rua Minas, 877, CEP 14085-410, Ribeirão Preto-SP, Brazil.
U.S. Food and Drug Administration, Center for Food Safety and Applied Nutrition, Office of Regulatory Science, 5100 Paint Branch Parkway, College Park, MD, USA.
J Chromatogr A. 2017 Feb 3;1483:1-7. doi: 10.1016/j.chroma.2016.12.040. Epub 2016 Dec 15.
The aim of this study was to investigate the feasibility of using multitime-regenerated immunoaffinity column (IAC) for aflatoxins B, B, G and G in peanut confection. After each use, the IAC was washed immediately with phosphate-buffered saline and stored for >12h prior to reuse. The evaluation procedure consisted of using extracts of naturallycontaminated peanut confection (4 replicates), aflatoxin-free peanut confection (duplicates), and aflatoxin-free peanut confection sample spiked with the 4 aflatoxins (AFT) at 3 levels in 4 replicates. Each day, 18 test extracts were analyzed using 18 designated IACs. After each use, the IACs were regenerated and reused for corresponding test extracts on the following day. This procedure was repeated daily over the course of 9days. Analytical steps included passing the test extracts through the IACs, washing the columns with water, and eluting AFT with methanol. The eluates were diluted with water and were subjected to reversed phase LC separation, post-column photochemical derivatization and fluorescence detection. After eluting AFT, IACs were immediately regenerated by washing with phosphate buffer solution and storing overnight at 8°C for re-use the following day. Results were analyzed using ANOVA and Tukey tests. The numbers of reuse varied for each AF: For AFB AFB, AFGand AFG could be reused for 9, 6, 6 and 0 times, respectively. According to AOAC method performance criteria, recoveries ranging from 70% to 125% are considered acceptable at the spiking levels used in this study.
本研究的目的是探讨使用多次再生免疫亲和柱(IAC)检测花生糖中黄曲霉毒素B₁、B₂、G₁和G₂的可行性。每次使用后,立即用磷酸盐缓冲盐水冲洗IAC,并在重复使用前储存超过12小时。评估程序包括使用天然污染花生糖的提取物(4个重复样)、不含黄曲霉毒素的花生糖(2个重复样)以及不含黄曲霉毒素的花生糖样品,分别添加3种水平的4种黄曲霉毒素(AFT),共4个重复样。每天使用18根指定的IAC分析18个测试提取物。每次使用后,将IAC再生,并在第二天用于相应的测试提取物。此程序在9天内每天重复。分析步骤包括使测试提取物通过IAC、用水冲洗柱子以及用甲醇洗脱AFT。洗脱液用水稀释,然后进行反相液相色谱分离、柱后光化学衍生化和荧光检测。洗脱AFT后,立即用磷酸盐缓冲溶液冲洗IAC使其再生,并在8°C下过夜储存,以便第二天重复使用。使用方差分析和Tukey检验分析结果。每种黄曲霉毒素的重复使用次数各不相同:对于黄曲霉毒素B₁、B₂、G₁和G₂,分别可重复使用9次、6次、6次和0次。根据AOAC方法性能标准,在本研究使用的加标水平下回收率在70%至125%之间被认为是可接受的。