Ivanova Vanina, Pimpilova Mariya, Stoyanova Maria, Dimcheva Nina
Department of Physical Chemistry, Plovdiv University "Paisii Hilendarski", 24, Tzar Assen Str., 4000 Plovdiv, Bulgaria.
Laboratory of Biologically Active Substances, Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences, 139 Ruski Blvd., 4000 Plovdiv, Bulgaria.
Molecules. 2025 Jan 17;30(2):374. doi: 10.3390/molecules30020374.
Lipid peroxidation is a major process that determines the quality of various oil samples during their use and storage, in which the primary products are hydroperoxides (HP'). HP' are very stable compounds at ambient conditions and are harmful to human health. Therefore, the evaluation of the degree of oil oxidation is an excellent tool for ensuring food safety. The peroxide value (PV) is the main parameter used for quality control in oils. Herein, we propose an alternative electrochemical method to the classical iodometric titration method most widely used for determining the PV. Our approach is based on the electrochemical quantification of hydroperoxides/peroxides in an organic solvent medium (acetonitrile and organic ammonium salt) using a composite electrocatalyst-glassy carbon electrode modified with 2D-nanomaterial graphitic carbon nitride doped with CoO. Calibration was made by the method of standard addition using benzoyl peroxide (BPO) as a model peroxide compound, dissolved in chloroform and added to fresh Rivana-branded anti-cellulite oil, used as a model oil sample. Calibration plots showed a linear response and the very good reproducibility of the analytical result (R ˃ 0.99). Further, in terms of accuracy, the method showed good results, since the BPO quantitative analysis was close to the theoretical response. In addition, the accuracy of the electrochemical method was compared with that of the standard iodometric titration method for determining the PV of vegetable fats (according to a standard method). Finally, using the electrochemical method, the concentration of peroxides was determined in a real sample-an anti-cellulite oil of the trademark Rivana with an expired shelf life.
脂质过氧化是决定各种油样在使用和储存过程中质量的主要过程,其中主要产物是氢过氧化物(HP')。HP'在环境条件下是非常稳定的化合物,对人体健康有害。因此,评估油脂氧化程度是确保食品安全的一项重要手段。过氧化值(PV)是油脂质量控制中使用的主要参数。在此,我们提出了一种替代电化学方法,以取代最广泛用于测定PV的经典碘量滴定法。我们的方法基于在有机溶剂介质(乙腈和有机铵盐)中使用二维纳米材料掺杂CoO的石墨相氮化碳修饰的复合电催化剂-玻碳电极对氢过氧化物/过氧化物进行电化学定量分析。通过标准加入法进行校准,使用过氧化苯甲酰(BPO)作为模型过氧化物化合物,将其溶解在氯仿中并添加到新鲜的Rivana品牌抗橘皮组织油中,用作模型油样。校准曲线显示出线性响应和分析结果的良好重现性(R>0.99)。此外,在准确性方面,该方法显示出良好的结果,因为BPO的定量分析接近理论响应。此外,将电化学方法的准确性与用于测定植物脂肪PV的标准碘量滴定法(根据标准方法)进行了比较。最后,使用电化学方法测定了一个实际样品——保质期已过的Rivana商标抗橘皮组织油中的过氧化物浓度。