Soliman Hanaa M, Arafat Shaker M, Basuny Amany M, Shattory Y El-
Oils & Fats Dept., National Research Centre.
Olis & Fats Dept., Food Technology Research Institute, Agricultural Research Center.
J Oleo Sci. 2017 Nov 1;66(11):1263-1271. doi: 10.5650/jos.ess16222. Epub 2017 Oct 11.
A new amphiphilic antioxidant (tannyl stearate) derived from reaction of tannic acid with stearic acid was synthesized in order to improve tannic acid solubility in lipid materials. This reaction gives many products having different degree of esterification (tannyl mono, di, tri, tetra, penta, hexa, hepta……stearate) which were separated using silica gel column chromatography and tentative identification was carried out using thin layer chromatography (TLC). The intrinsic viscosities (η) were used to differentiate between the different molecular weight of the produced esters. Tannyl penta stearate is assumed to be the most suitable amphiphilic antioxidant derivative, where those derivatives with less degree of esterification would be less soluble in fat, and those of higher degree of esterification would exhaust more hydroxyl group that cause decreases of antioxidant activity. The structure of tannyl penta stearate was approved depending on its chemical analysis and spectral data (IR, H NMR,). The emulsification power of tannyl penta stearate was then determined according to method described by El-Sukkary et al., in order to prove its amphiphilic property. Then tannyl penta stearate was tested for its antioxidant and radical scavenging activities in three different manners, those are, lipid oxidation in sunflower oil using Rancimat, (DPPH) free radical scavenging and total antioxidant activity. {Pure tannic acid (T), butylhydroxyanisol (BHA) and butylhydroxytoluene (BHT) were used as reference antioxidant radical saving compounds}. Then tannyl penta stearate was added to sunflower oil, frying process was carried out and all physicochemical parameters of the oil were considered, and compared to other reference antioxidant in order to study the effect of this new antioxidant toward oil stability. Acute oral toxicity of the tannyl penta stearate was carried out using albino mice of 21-25 g body weight to determine its safety according to the method described by Goodman et al.. Also liver and kidney functions of those mice were checked. Thus it could be concluded that the addition of tannyl penta stearate to frying oils offers a good protection against oxidation. The effectiveness of tannyl penta stearate as lipid antioxidant has been attributed mainly to its stability at high temperature. And according to acute lethal toxicity test tannyl penta stearate was found to be a safe compound that can be used as food additive.
为提高单宁酸在脂质材料中的溶解度,合成了一种由单宁酸与硬脂酸反应得到的新型两亲性抗氧化剂(硬脂酰单宁酸)。该反应生成了许多具有不同酯化程度的产物(单硬脂酰单宁酸、二硬脂酰单宁酸、三硬脂酰单宁酸、四硬脂酰单宁酸、五硬脂酰单宁酸、六硬脂酰单宁酸、七硬脂酰单宁酸……),使用硅胶柱色谱法对其进行分离,并采用薄层色谱法(TLC)进行初步鉴定。利用特性粘度(η)区分所生成酯的不同分子量。五硬脂酰单宁酸被认为是最合适的两亲性抗氧化剂衍生物,酯化程度较低的衍生物在脂肪中的溶解度较小,而酯化程度较高的衍生物会消耗更多的羟基,从而导致抗氧化活性降低。根据其化学分析和光谱数据(红外光谱、核磁共振氢谱)确定了五硬脂酰单宁酸的结构。然后根据El-Sukkary等人描述的方法测定了五硬脂酰单宁酸的乳化能力,以证明其两亲性。接着以三种不同方式测试了五硬脂酰单宁酸的抗氧化和自由基清除活性,即使用Rancimat法测定向日葵油中的脂质氧化、(二苯基苦味酰基自由基)DPPH自由基清除以及总抗氧化活性。{使用纯单宁酸(T)、丁基羟基茴香醚(BHA)和丁基羟基甲苯(BHT)作为参考抗氧化自由基清除化合物}。然后将五硬脂酰单宁酸添加到向日葵油中,进行油炸过程,并考虑该油的所有理化参数,与其他参考抗氧化剂进行比较,以研究这种新型抗氧化剂对油稳定性的影响。使用体重为21 - 25 g的白化小鼠,按照Goodman等人描述的方法进行五硬脂酰单宁酸的急性口服毒性试验,以确定其安全性。还检查了这些小鼠的肝肾功能。因此可以得出结论,向煎炸油中添加五硬脂酰单宁酸可提供良好的抗氧化保护。五硬脂酰单宁酸作为脂质抗氧化剂的有效性主要归因于其在高温下的稳定性。根据急性致死毒性试验,发现五硬脂酰单宁酸是一种可作为食品添加剂使用的安全化合物。