Lee Jonghwa, Kim Kyeonga, Son Jemin, Lee Hyeseon, Song Jin Han, Lee Taek, Jeon Heungbae, Kim Hyun Soo, Park Si Jae, Yoo Hah Young, Park Chulhwan
Department of Chemical Engineering, Kwangwoon University, Seoul 01897, Korea.
Department of Chemistry, Kwangwoon University, Seoul 01897, Korea.
Antioxidants (Basel). 2022 Jan 27;11(2):242. doi: 10.3390/antiox11020242.
Naringin is a flavonoid found in citrus fruits. It exhibits biological activities, such as anticancer and antioxidant effects, but it suffers from low solubility and low stability in lipophilic systems. These drawbacks lead to difficulties in the commercial application of naringin, but they can be overcome through esterification. In this study, naringin oleate was synthesized by enzymatic esterification and optimal conditions for the reaction were investigated. Experiments were conducted focusing on the following parameters: enzyme type, enzyme concentration, molar ratio of naringin to oleic acid, reaction temperature, and reaction solvent. We further confirmed the degree of esterification based on the difference in the initial and the final naringin concentrations. A conversion of 93.10% was obtained under optimized conditions (Lipozyme TL IM 10 g/L, molar ratio 1:20, reaction temperature 40 °C, acetonitrile as solvent, and 48 h reaction time). Thus, naringin oleate, a high value-added material that overcomes the low hydrophobicity of naringin and enhances its performance, was obtained through esterification of naringin using oleic acid. This study presented a method for the efficient enzymatic synthesis that could ensure high conversion within a shorter reaction time compared with that required in previously reported methods.
柚皮苷是一种存在于柑橘类水果中的黄酮类化合物。它具有抗癌和抗氧化等生物活性,但在亲脂性体系中溶解度低且稳定性差。这些缺点导致柚皮苷在商业应用中存在困难,但可通过酯化作用加以克服。在本研究中,通过酶促酯化反应合成了油酸柚皮苷,并对反应的最佳条件进行了研究。实验重点关注以下参数:酶的类型、酶浓度、柚皮苷与油酸的摩尔比、反应温度和反应溶剂。我们根据柚皮苷初始浓度和最终浓度的差异进一步确定了酯化程度。在优化条件下(脂肪酶TL IM 10 g/L、摩尔比1:20、反应温度40℃、以乙腈为溶剂、反应时间48小时)获得了93.10%的转化率。因此,通过用油酸对柚皮苷进行酯化反应,得到了一种附加值高的物质——油酸柚皮苷,它克服了柚皮苷疏水性低的问题并提高了其性能。本研究提出了一种高效酶促合成方法,与先前报道的方法相比,该方法能在更短的反应时间内确保高转化率。