Ning Xiao-Pan, Yao Qian, Xu Zhong-Xiang, Yin Yao, Liu Han, Zhang Xiao-Yan, Ding Tao, Zhang Yong, Hou Yu, Wang Meng-Ru, Wu Li-Na, Tang Qi-Ting
Animal, Plant and Food Inspection Center, Nanjing Customs, Nanjing 210019, China.
NanoChrom Technologies (Suzhou) Co., Ltd., Suzhou 215123, China.
Se Pu. 2023 Jun 8;41(6):513-519. doi: 10.3724/SP.J.1123.2022.10004.
Seven parabens are widely used in soy sauce, vinegar, jam, oyster sauce, stuffing, and other foods. The long-term intake of large amounts of parabens and similar substances may be harmful to the human body. Therefore, the addition of paraben preservatives to food should be strictly controlled. The current detection method is applicable to single target compound and several food categories, and the experimental pretreatment method involves extraction with anhydrous ethyl ether, which is a toxic reagent. Moreover, interferences in the analysis of parabens via gas chromatography limit the versatility and accuracy of the detection method. Herein, a novel method based on solid-phase extraction (SPE) coupled with high performance liquid chromatography (HPLC) was developed for the determination of seven paraben preservatives (methyl -hydroxybenzoate, ethyl -hydroxybenzoate, propyl -hydroxybenzoate, butyl -hydroxybenzoate, isopropyl -hydroxybenzoate, isobutyl -hydroxybenzoate, and heptyl -hydroxybenzoate) in oyster sauce, shrimp sauce, and fish sauce. Compared with the conventional method, the proposed work enables the determination of more compounds, thereby expanding its scope of application to different food types. This strategy also optimizes the pretreatment method and device parameters. The samples were extracted with methanol and 20% methanol aqueous solution by ultrasonication, respectively, and then centrifuged. The experimental pretreatment method was enriched, and sample clean-up was conducted using a MAX SPE column. The seven parabens were separated using a Chromcore 120 C18 column (150 mm×4.6 mm, 3.0 μm). Gradient elution was performed with acetonitrile-5 mmol/L ammonium acetate aqueous solution as the mobile phase (initial mobile phase volume ratio, 30∶70). The flow rate was 0.7 mL/min, and the column temperature was 35 ℃. A diode array detector with a detection wavelength of 254 nm was also used. The seven paraben preservatives showed good linearity in the range of 0.5-50.0 mg/L, with correlation coefficients greater than 0.9999. The limits of detection (LODs) and quantification (LOQs) for the seven paraben preservatives were 0.2-0.4 mg/kg and 0.5-1.3 mg/kg, respectively. A spiked recovery test was conducted using oyster sauce, shrimp sauce, and fish sauce at three spiked levels of 2, 40, and 200 mg/kg. Good recoveries for the seven paraben preservatives were obtained and the recoveries of the analytes in oyster sauce, shrimp sauce, and fish sauce were 91.0%-102%, 95.5%-106%, and 95.0%-105%, respectively, with relative standard deviations of ≤6.97%. Compared with the liquid-liquid extraction method, the proposed method demonstrated better purification effects. The recoveries of the seven paraben preservatives extracted using this method were also much higher than those obtained from liquid-liquid extraction. We determined the contents of these preservatives in 135 food products using the method established in this study and detected methyl -hydroxybenzoate and ethyl -hydroxybenzoate in soy sauce, vinegar, and pickles. Thus, the established method can be used for the effective determination of seven parabens in aquatic seasoning such as oyster sauce, shrimp sauce, and fish sauce.
七种对羟基苯甲酸酯类物质被广泛应用于酱油、醋、果酱、蚝油、馅料及其他食品中。长期大量摄入对羟基苯甲酸酯类及类似物质可能对人体有害。因此,食品中对羟基苯甲酸酯类防腐剂的添加应受到严格控制。目前的检测方法适用于单一目标化合物及几种食品类别,其实验预处理方法采用无水乙醚萃取,而无水乙醚是一种有毒试剂。此外,气相色谱法分析对羟基苯甲酸酯类时存在的干扰限制了该检测方法的通用性和准确性。在此,本文建立了一种基于固相萃取(SPE)结合高效液相色谱(HPLC)的新方法,用于测定蚝油、虾酱和鱼露中七种对羟基苯甲酸酯类防腐剂(对羟基苯甲酸甲酯、对羟基苯甲酸乙酯、对羟基苯甲酸丙酯、对羟基苯甲酸丁酯、对羟基苯甲酸异丙酯、对羟基苯甲酸异丁酯和对羟基苯甲酸庚酯)。与传统方法相比,本研究建立的方法能够测定更多化合物,从而扩大了其在不同食品类型中的应用范围。该方法还优化了预处理方法和仪器参数。样品分别用甲醇和20%甲醇水溶液超声提取,然后离心。实验预处理方法得到了改进,并采用MAX固相萃取柱进行样品净化。使用Chromcore 120 C18柱(150 mm×4.6 mm,3.0 μm)分离七种对羟基苯甲酸酯类物质。以乙腈-5 mmol/L醋酸铵水溶液为流动相进行梯度洗脱(初始流动相体积比为30∶70)。流速为0.7 mL/min,柱温为35℃。还使用了检测波长为254 nm的二极管阵列检测器。七种对羟基苯甲酸酯类防腐剂在0.5 - 50.0 mg/L范围内呈现良好的线性关系,相关系数大于0.9999。七种对羟基苯甲酸酯类防腐剂的检出限(LOD)和定量限(LOQ)分别为0.2 - 0.4 mg/kg和0.5 - 1.3 mg/kg。采用蚝油、虾酱和鱼露进行加标回收率试验,加标水平为2、40和200 mg/kg。七种对羟基苯甲酸酯类防腐剂均获得了良好的回收率,蚝油、虾酱和鱼露中分析物的回收率分别为91.0% - 102%、95.5% - 106%和95.0% - 105%,相对标准偏差≤6.97%。与液液萃取法相比,本方法具有更好的净化效果。采用本方法萃取的七种对羟基苯甲酸酯类防腐剂的回收率也远高于液液萃取法。我们使用本研究建立的方法测定了135种食品中这些防腐剂的含量,并在酱油、醋和泡菜中检测到了对羟基苯甲酸甲酯和对羟基苯甲酸乙酯。因此,所建立的方法可用于有效测定蚝油、虾酱和鱼露等水产调味料中七种对羟基苯甲酸酯类物质。