[Determination of kojic acid in fermented foods by solid-phase extraction coupled with ultra performance liquid chromatography-tandem mass spectrometry].

IF 1.2 4区 化学 Q4 CHEMISTRY, ANALYTICAL 色谱 Pub Date : 2023-07-01 DOI:10.3724/SP.J.1123.2022.10002
Dong-Yang Chen, Hao Zhang, Lei Zhang, Yi-Hong Wang, Xiao-Dan Wang, Jia-Li Feng, Jing Liang, Xuan Zhong
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Abstract

Kojic acid naturally appears in fermented foods and can be formed during the aerobic fermentation process induced by Aspergillus and Penicillium fungi. It is widely used in the food industry because it exhibits antibacterial and antifungal properties and does not affect food taste. However, recent studies indicate that kojic acid may be a potential carcinogen. Therefore, assessing the health risks of kojic acid in fermented foods are of great importance, and developing a sensitive and accurate analytical method for this compound is a significant endeavor. Much efforts have been devoted to the detection of kojic acid using electrochemistry, high performance liquid chromatography (HPLC), gas chromatography-mass spectrometry (GC-MS), and high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). HPLC and HPLC-MS/MS are the analytical techniques most often employed for this purpose. Of these two methods, HPLC-MS/MS displays excellent sensitivity and is the optimal selective technique. Pretreatment is usually necessary for kojic acid determination because of the complex matrix effects of fermented foods. However, few researches on the determination of kojic acid in food are available, and, to the best of our knowledge, the determination of kojic acid using solid-phase extraction (SPE) pretreatment has not been reported yet. Herein, a convenient, sensitive, and accurate method was developed to determine kojic acid in fermented foods using solid-phase extraction-ultra performance liquid chromatography-tandem mass spectrometry (SPE-UPLC-MS/MS). The pretreatment conditions, such as the extraction solvent, cartridge, rinse solvent, and eluent, were systematically optimized. The samples, including soy sauce, vinegar, liquor, sauce, fermented soya bean, and fermented bean curd, were extracted with 0.1% formic acid-absolute ethyl alcohol and purified using a PRiME HLB cartridge. Kojic acid was separated using an ACQUITY UPLC® BEH C18 column (100 mm×2.1 mm, 1.7 μm) with formic acid-acetonitrile (1∶999, v/v) and formic acid-5 mmol/L ammonium acetate (1∶999, v/v) solutions as the mobile phases under gradient elution mode. MS was performed in electrospray positive ionization (ESI+) and multiple reaction monitoring (MRM) modes. An internal standard method was used for quantification. Under optimized conditions, good linearity was achieved at mass concentrations of 5.0-100.0 μg/L, with a correlation coefficient (r) of 0.9994. The limits of detection and quantification of the method for kojic acid were 2-5 μg/kg and 6-15 μg/kg, respectively. Good recoveries of 86.8%-111.7%, intra-day precisions of 1.0%-7.9% (n=6), and inter-day precisions of 2.7%-10.2% (n=5) were also obtained. The matrix effect was evaluated by establishing a matrix-matching calibration curve, and weak inhibitory effects were found in vinegar and liquor; moderate inhibitory effects in fermented bean curd, fermented soya bean, and soy sauce; and a strong inhibitory effect in sauce. The developed method was used to detect kojic acid in 240 fermented foods, and the results showed that the detection rate of vinegar was the highest, followed by liquor, sauce, soy sauce, fermented soya bean, and fermented bean curd, the contents were 5.69-2272 μg/kg. Matrix interferences can be significantly reduced by optimizing the pretreatment and detection procedures. The proposed method is sensitive, accurate, and can be used to analyze kojic acid in fermented foods.

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[固相萃取-超高效液相色谱-串联质谱法测定发酵食品中的曲酸]。
曲酸天然存在于发酵食品中,可在曲霉和青霉菌诱导的好氧发酵过程中形成。它在食品工业中被广泛应用,因为它具有抗菌和抗真菌的特性,而且不影响食品的味道。然而,最近的研究表明,曲酸可能是一种潜在的致癌物。因此,评估发酵食品中曲酸的健康风险具有重要意义,开发一种灵敏、准确的分析方法是一项重要的工作。电化学、高效液相色谱法(HPLC)、气相色谱-质谱法(GC-MS)、高效液相色谱-串联质谱法(HPLC-MS/MS)检测曲酸的研究已经取得了很大进展。HPLC和HPLC-MS/MS是最常用于此目的的分析技术。两种方法中,HPLC-MS/MS具有良好的灵敏度和最佳的选择性。由于发酵食品的基质效应复杂,测定曲酸通常需要预处理。然而,关于食品中曲酸的测定研究很少,据我们所知,固相萃取(SPE)预处理法测定曲酸还未见报道。建立了一种方便、灵敏、准确的固相萃取-超高效液相色谱-串联质谱(SPE-UPLC-MS/MS)测定发酵食品中曲酸的方法。对提取溶剂、滤筒、漂洗溶剂、洗脱液等预处理条件进行了系统优化。样品包括酱油、醋、白酒、酱油、发酵大豆和腐乳,用0.1%甲酸-无水乙醇提取,用PRiME HLB滤筒纯化。采用ACQUITY UPLC®BEH C18色谱柱(100 mm×2.1 mm, 1.7 μm),甲酸-乙腈(1∶999,v/v)和甲酸-5 mmol/L乙酸铵(1∶999,v/v)为流动相,梯度洗脱方式分离曲酸。质谱采用电喷雾正电离(ESI+)和多反应监测(MRM)模式。采用内标法定量。在优化条件下,质量浓度在5.0 ~ 100.0 μg/L范围内线性良好,相关系数(r)为0.9994。该法对曲酸的检出限为2 ~ 5 μg/kg,定量限为6 ~ 15 μg/kg。加样回收率为86.8% ~ 111.7%,日内精密度为1.0% ~ 7.9% (n=6),日内精密度为2.7% ~ 10.2% (n=5)。通过建立基质匹配校准曲线评价基质效应,在醋和白酒中发现弱抑制作用;对腐乳、豆腐乳、酱油有中等抑制作用;并在酱料中有较强的抑制作用。采用该方法对240种发酵食品中的曲酸进行了检测,结果表明,食醋的曲酸检出率最高,其次为白酒、酱汁、酱油、发酵大豆和发酵豆腐,其含量为5.69 ~ 2272 μg/kg。通过优化预处理和检测程序,可以显著减少基质干扰。该方法灵敏、准确,可用于发酵食品中曲酸的分析。
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来源期刊
色谱
色谱 CHEMISTRY, ANALYTICAL-
CiteScore
1.30
自引率
42.90%
发文量
7198
期刊介绍: "Chinese Journal of Chromatography" mainly reports the basic research results of chromatography, important application results of chromatography and its interdisciplinary subjects and their progress, including the application of new methods, new technologies, and new instruments in various fields, the research and development of chromatography instruments and components, instrument analysis teaching research, etc. It is suitable for researchers engaged in chromatography basic and application technology research in scientific research institutes, master and doctoral students in chromatography and related disciplines, grassroots researchers in the field of analysis and testing, and relevant personnel in chromatography instrument development and operation units. The journal has columns such as special planning, focus, perspective, research express, research paper, monograph and review, micro review, technology and application, and teaching research.
期刊最新文献
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